{"id":6534,"date":"2026-06-03T13:22:59","date_gmt":"2026-06-03T17:22:59","guid":{"rendered":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/?post_type=chapter&#038;p=6534"},"modified":"2026-06-10T15:19:48","modified_gmt":"2026-06-10T19:19:48","slug":"white-blood-cells-types-and-roles","status":"web-only","type":"chapter","link":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/chapter\/white-blood-cells-types-and-roles\/","title":{"raw":"Section 2: White Blood Cells - Types and Roles","rendered":"Section 2: White Blood Cells &#8211; Types and Roles"},"content":{"raw":"<h3><span style=\"color: #1f5c99\"><strong>Hematopoiesis:\u00a0 Formation of Blood Cells<\/strong><\/span><\/h3>\r\n<p style=\"text-align: justify\"><span style=\"text-align: initial;font-size: 1em\"><strong>Hematopoiesis<\/strong> is the formation of blood cells.\u00a0 Production begins at day 7 of the embryonic life in the <strong>yolk sac,<\/strong> migrates to the <strong>liver<\/strong> and <strong>spleen<\/strong> at week 7, and moves to the <strong>bone marrow<\/strong> at ~week 20.\u00a0 The pluripotent stem cells giving rise to all blood cell types are called <strong>hemocytoblasts.<\/strong>\u00a0 Their daughter cells differentiate into <strong>erythrocytes<\/strong> (RBCs), <strong>megakaryocytes<\/strong> (platelet precursors), and <strong>leukocytes<\/strong> (WBCs).<\/span><\/p>\r\n\r\n\r\n[caption id=\"attachment_6777\" align=\"alignnone\" width=\"300\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hemopoiesis.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-6777 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hemopoiesis-300x260.png\" alt=\"All the formed elements of the blood arise by differentiation of hematopoietic stem cells in the bone marrow.\" width=\"300\" height=\"260\" \/><\/a> Hematopoiesis:\u00a0 All the formed elements of the blood arise by differentiation of hematopoietic stem cells in the bone marrow.[\/caption]\r\n<p style=\"text-align: justify\"><strong><span style=\"color: #2e75b6\">Red Blood Cells (Erythrocytes)\u00a0<\/span><\/strong><\/p>\r\n<p style=\"text-align: justify\"><strong>Erythropoiesis<\/strong> is the production of RBCs.\u00a0 Developing <strong>erythroblasts<\/strong> become increasingly packed with <strong>hemoglobin.<\/strong>\u00a0 At the <strong>normoblast<\/strong> stage, they lose their nucleus, become <strong>reticulocytes,<\/strong> enter the bloodstream 2-3 days later and mature into <strong>erythrocytes<\/strong> over the following 2 days.\u00a0 Main function:\u00a0 use hemoglobin to transport 98.5% of the oxygen and ~23% of the carbon dioxide in blood.\u00a0 Lifespan ~120 days; aged cells are recycled by macrophages in the liver, bone marrow, and spleen.<\/p>\r\n\r\n[caption id=\"attachment_6524\" align=\"alignnone\" width=\"103\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hematopoiesis_human_diagram-cropped.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-6524 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hematopoiesis_human_diagram-cropped-103x300.png\" alt=\"Erythropoiesis: begins with hemocytoblasts producing proerythroblasts that mature into erythroblasts \u2192 normoblasts reticulocytes erythrocytes. [1] In this diagram, the reticulocyte on the right shows characteristics when stained with methylene blue. [2] The erythrocyte on the right represents its appearance under a light microscope.\" width=\"103\" height=\"300\" \/><\/a> Erythropoiesis: begins with hemocytoblasts producing proerythroblasts that mature into erythroblasts \u2192 normoblasts reticulocytes erythrocytes.<br \/>[1] In this diagram, the reticulocyte on the right shows characteristics when stained with methylene blue.<br \/>[2] The erythrocyte on the right represents its appearance under a light microscope.[\/caption]\r\n\r\n[caption id=\"attachment_6522\" align=\"alignnone\" width=\"231\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-scaled.jpg\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-6522 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-231x300.jpg\" alt=\"Erythrocyte Life Cycle\" width=\"231\" height=\"300\" \/><\/a> Erythrocyte Life Cycle[\/caption]\r\n<p style=\"text-align: justify\">Erythropoiesis is regulated by <strong>erythropoietin (EPO)<\/strong> hormone, secreted by the kidneys in response to low blood-oxygen levels, growth hormone (GH), thyroxine, and testosterone.\u00a0 In an adult, 2-3 million RBCs are produced per second and RBC production requires B vitamins, folate, amino acids and iron.<\/p>\r\n\r\n<div class=\"textbox textbox--key-takeaways\"><header class=\"textbox__header\">\r\n<p class=\"textbox__title\"><strong>Diagnostic Blood Tests<\/strong><\/p>\r\n\r\n<\/header>\r\n<div class=\"textbox__content\">\r\n\r\n<strong><span style=\"color: #2e75b6\">Blood Count Terminology<\/span><\/strong>\r\n<table class=\"grid\" style=\"border-collapse: collapse;width: 100%\" border=\"0\">\r\n<tbody>\r\n<tr>\r\n<td style=\"width: 20.8334%\"><strong>Retic count<\/strong><\/td>\r\n<td style=\"width: 79.1666%\">Proportion of RBCs that are reticulocytes (normal: 1-2%).\r\n\r\nLow retic count (e.g., 0.5%) indicates reduced erythropoiesis.<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 20.8334%\"><strong>Hematocrit<\/strong><\/td>\r\n<td style=\"width: 79.1666%\">Percentage of blood volume made up of formed elements.\r\n\r\nFemales ~42%;\u00a0Males ~46%\u00a0(testosterone stimulates RBC production).<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 20.8334%\"><strong>Leukopenia<\/strong><\/td>\r\n<td style=\"width: 79.1666%\">Reduced WBC production.<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 20.8334%\"><strong>Thrombocytopenia<\/strong><\/td>\r\n<td style=\"width: 79.1666%\">Reduced platelet production.<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 20.8334%\"><strong>Neutrophilia<\/strong><\/td>\r\n<td style=\"width: 79.1666%\">Elevated neutrophil count - common with bacterial infections.<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 20.8334%\"><strong>Neutropenia<\/strong><\/td>\r\n<td style=\"width: 79.1666%\">Decreased neutrophil count - caused by severe infection, nutritional deficiency, congenital defects, autoimmune disease, or cancer.<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 20.8334%\"><strong>Eosinophilia<\/strong><\/td>\r\n<td style=\"width: 79.1666%\">Elevated eosinophil count - caused by helminth infections, allergies, or autoimmune diseases.<\/td>\r\n<\/tr>\r\n<tr>\r\n<td style=\"width: 20.8334%\"><strong>Lymphocytosis<\/strong><\/td>\r\n<td style=\"width: 79.1666%\">Elevated NK, T, and P lymphocytes count - occurs with viral infections.<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<\/div>\r\n<\/div>\r\n\r\n[caption id=\"attachment_6768\" align=\"alignnone\" width=\"300\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/WBC-key.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-6768 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/WBC-key-300x148.png\" alt=\"Five types of leukocytes: from left to right, lymphocyte, basophil, eosinophil, neutrophil, and monocytes.\" width=\"300\" height=\"148\" \/><\/a> Five types of leukocytes: from left to right, lymphocyte, basophil, eosinophil, neutrophil, and monocytes.[\/caption]\r\n\r\n[caption id=\"attachment_6669\" align=\"alignnone\" width=\"300\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Blood-Cells.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-6669 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Blood-Cells-300x297.png\" alt=\"Cells of the blood include (1) monocytes, (2) lymphocytes, (3) neutrophils, (4) red blood cells, and (5) platelets. Note the very similar morphologies of the leukocytes (1, 2, 3). (credit: modification of work by Bruce Wetzel, Harry Schaefer, NCI; scale-bar data from Matt Russell)\" width=\"300\" height=\"297\" \/><\/a> Cells of the blood include (1) monocytes, (2) lymphocytes, (3) neutrophils, (4) red blood cells, and (5) platelets. Note the very similar morphologies of the leukocytes (1, 2, 3). (credit: modification of work by Bruce Wetzel, Harry Schaefer, NCI; scale-bar data from Matt Russell).[\/caption]\r\n\r\n<strong><span style=\"color: #2e75b6\">Platelets (Thrombocytes)\u00a0<\/span><\/strong>\r\n\r\n<strong>Megakaryocytes<\/strong> fragment into ~1,000 anuclear <strong>platelets<\/strong> (thrombocytes).\u00a0 Despite lacking a nucleus, platelet contain ~300 chemicals involved in <strong>hemostasis<\/strong> (blood clotting) and are essential for innate defense and preventing excessive bleeding.\r\n\r\n<strong><span style=\"color: #2e75b6\">White Blood Cell Lineages\u00a0<\/span><\/strong>\r\n\r\nWBCs are classified as either <strong>granulocytes<\/strong> (containing large granules, readily visible with light microscope); also called polymorphonuclear leukocytes (PMNs) or <strong>agranulocytes<\/strong> (containing smaller granules).\u00a0 Granulocytes include: <strong>neutrophils, eosinophils, mast cells<\/strong>, and <strong>basophils.<\/strong> \u00a0Agranulocytes include: <strong>monocytes, macrophages, dendritic cells<\/strong>, Natural Killer lymphocytes (<strong>NK cells<\/strong>), T lymphocytes (<strong>T cells<\/strong>), and B lymphocytes (<strong>B cells<\/strong>).\u00a0 All WBCs perform <strong>amoeboid movement<\/strong> and <strong>diapedesis<\/strong> (emigration from blood vessels into tissue - also termed <strong>extravasation<\/strong> or <strong>transmigration.<\/strong>\r\n<h3><span style=\"color: #1f5c99\"><strong>Granulocytes (Polymorphonuclear Leukocytes, PMNs)<\/strong><\/span><\/h3>\r\n<table class=\"grid landscape\" style=\"border-collapse: collapse;width: 100%;height: 347px\" border=\"0\">\r\n<tbody>\r\n<tr style=\"height: 126px\">\r\n<td class=\"border\" style=\"width: 14.7362%;height: 126px\"><span style=\"color: #032c80\"><strong>Neutrophils<\/strong><\/span><\/td>\r\n<td style=\"width: 85.2638%;height: 126px\">Immature <strong>band cells<\/strong> mature into neutrophils.\r\n\r\nMost abundant WBC (50-70%).\u00a0 2-5 lobed nucleus; stain neutral pink with H&amp;E stain.\u00a0 First responders to sites of damage.\r\n\r\n<strong>Phagocytose<\/strong> bacteria and utilize extensive <strong>lysosomes.<\/strong>\r\n\r\nNeutrophil <strong>Oxidative Bursts<\/strong> exocytose highly toxic, unstable <strong>Reactive Oxygen Species (ROS)<\/strong> from secretory vesicles that <strong>damage bacterial cell walls<\/strong>.\r\n\r\nNeutrophil granules release <strong>lactoferrin<\/strong> (sequesters iron, depriving bacteria of required resource)\r\n\r\nNeutrophils release <strong>defensin<\/strong> and <strong>proteases<\/strong> (degrade pathogen)\r\n\r\nCan also release <strong>NETs<\/strong> (Neutrophil Extracellular Traps - webs of chromatin fibers and toxic enzymes) to trap and destroy microbes extracellularly.\r\n\r\nActive lifespan: 24-48 hours.<\/td>\r\n<\/tr>\r\n<tr style=\"height: 79px\">\r\n<td class=\"shaded\" style=\"width: 14.7362%;height: 79px\"><span style=\"color: #032c80\"><strong>Eosinophils<\/strong><\/span><\/td>\r\n<td class=\"shaded\" style=\"width: 85.2638%;height: 79px\">Stain red with acidic eosin dye;\u00a0 ~2-3% of WBCs.\u00a0 Arrive 2-3 hours after neutrophils.\r\n\r\n<strong>Phagocytose<\/strong> debris and pathogens.\r\n\r\nExocytose <strong>toxins ROS, Eosinophil Cationic Protein (ECP), <\/strong>and <strong>Major Basic Protein (MBP)<\/strong>\u00a0to kill organisms too large to phagocytose (e.g., helminths).\r\n\r\nRelease <strong>cytokines<\/strong> to stimulate mast cell and basophil inflammatory response.\r\n\r\nRelease growth factors (e.g., <strong>VEGF, vascular endothelial growth factor)<\/strong> to support healing.\r\n\r\nRelease <strong>RNases<\/strong> to destroy viruses.\r\n\r\nPlay a role in allergies and asthma<\/td>\r\n<\/tr>\r\n<tr style=\"height: 79px\">\r\n<td class=\"border\" style=\"width: 14.7362%;height: 79px\"><span style=\"color: #032c80\"><strong>Mast cells<\/strong><\/span><\/td>\r\n<td style=\"width: 85.2638%;height: 79px\">Tissue-resident cells, most prevalent in skin dermis, lung mucosa, and GI tract mucosa.\r\n\r\nContain granules with <strong>heparin (anticoagulant)<\/strong> and<strong> histamine<\/strong>.\r\n\r\nActivated by cellular injury;\u00a0 degranulate releasing <strong>pro-inflammatory mediators<\/strong> <strong>(histamine, bradykinins, prostaglandins, leukotrienes).<\/strong><\/td>\r\n<\/tr>\r\n<tr style=\"height: 63px\">\r\n<td class=\"shaded\" style=\"width: 14.7362%;height: 63px\"><span style=\"color: #032c80\"><strong>Basophils<\/strong><\/span><\/td>\r\n<td class=\"shaded\" style=\"width: 85.2638%;height: 63px\">Circulating counterpart to <strong>mast cells<\/strong>.\u00a0 Both contain <strong>heparin<\/strong> and <strong>histamine granules<\/strong> and fulfill similar <strong>pro-inflammatory<\/strong> roles.\u00a0 Basophils circulate the bloodstream rather than residing in tissue.<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\n<strong>*ROS<\/strong> = Reactive Oxygen Species, such as <strong>superoxide, O<sub>2<\/sub><sup>\u2022\u2212<\/sup><\/strong> and <strong>hydroxyl radical HO<sup>\u2022<\/sup><\/strong> are free radicals with <strong>unpaired electrons<\/strong> that damage DNA, lipids and proteins.\r\n\r\n&nbsp;\r\n\r\n[caption id=\"attachment_6513\" align=\"alignnone\" width=\"300\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-production.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-6513 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-production-300x95.png\" alt=\"Neutrophil Production\" width=\"300\" height=\"95\" \/><\/a> Neutrophil Production[\/caption]\r\n\r\n[caption id=\"attachment_2325\" align=\"alignnone\" width=\"150\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/Cardiovascular_system_-_Neutrophil_granulocyte_2_-_Smart-Servier.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-2325 size-thumbnail\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/Cardiovascular_system_-_Neutrophil_granulocyte_2_-_Smart-Servier-150x150.png\" alt=\"Neutrophils circulate the bloodstream and are an essential part of the innate (non-specific) immune system.\" width=\"150\" height=\"150\" \/><\/a> Neutrophils circulate the bloodstream and are an essential part of the innate (non-specific) immune system.[\/caption]\r\n\r\n[caption id=\"attachment_2324\" align=\"alignnone\" width=\"237\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/NeutrophilerAktion.svg_.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-2324 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/NeutrophilerAktion.svg_-237x300.png\" alt=\"Neutrophil (in purple) migrates from the blood vessel into the matrix using diapedesis. Neutrophils can secrete collagenase in the extracellular matrix of tissues to facilitate tissue remodeling, wound healing and immune cell migration. \" width=\"237\" height=\"300\" \/><\/a> Neutrophil (in purple) migrates from the blood vessel into the matrix using diapedesis. Neutrophils can secrete collagenase (green) in the extracellular matrix of tissues to facilitate tissue remodeling, wound healing and immune cell migration.[\/caption]\r\n\r\n[caption id=\"attachment_6514\" align=\"alignnone\" width=\"300\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-activity.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-6514 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-activity-300x226.png\" alt=\"The killing mechanisms of neutrophils: phagocytosis, degranulation, and extracellular traps release.\" width=\"300\" height=\"226\" \/><\/a> The killing mechanisms of neutrophils: phagocytosis, degranulation, and extracellular traps release.[\/caption]\r\n\r\n&nbsp;\r\n\r\n[caption id=\"attachment_5710\" align=\"alignnone\" width=\"1024\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/01\/neutrophils-12-01981-g003-scaled.png\"><img class=\"wp-image-5710 size-large\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/01\/neutrophils-12-01981-g003-1024x675.png\" alt=\"Neutrophil Activation\" width=\"1024\" height=\"675\" \/><\/a> Neutrophil Activation: Neutrophils typically circulate the brainstem until chemokines are secreted by monocytes and macrophages and blood vessel walls stimulate blood vessel endothelial cells to express cell adhesion molecule (selectins) that bind to the carbohydrate ligands on neutrophils. Rolling adhesion of neutrophils occurs, followed by firm attachment and diapedesis in which the neutrophil leaves the blood vessel (extravasation) and enters the tissue. Chemokines released by monocytes and macrophages stimulate chemotaxis of neutrophils to assist in the phagocytosis of debris and any invading bacteria. Neutrophils are able to perform 3 different functions to help contain and eliminate the infecting agent: 1) Phagocytosis (followed by antigen presentation), 2) Secretion of ROS, anti-microbial granules and pro-inflammatory cytokines, and 3) NETosis (in which nuclear or mitochondrial DNA is expelled to trap the pathogen).[\/caption]\r\n\r\n[caption id=\"attachment_6779\" align=\"alignnone\" width=\"300\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/3-granulocytes.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-6779 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/3-granulocytes-300x172.png\" alt=\"Three of the Four Granulocytes (Neutrophils, Eosinophils and Basophils). Granulocytes can be distinguished by the number of lobes in their nuclei and the staining properties of their granules.\" width=\"300\" height=\"172\" \/><\/a> Three of the Four Granulocytes (Neutrophils, Eosinophils and Basophils). Granulocytes can be distinguished by the number of lobes in their nuclei and the staining properties of their granules.[\/caption]\r\n\r\n[caption id=\"attachment_6780\" align=\"alignnone\" width=\"300\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Mast-Cells.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-6780 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Mast-Cells-300x280.png\" alt=\"Mast Cells are granulocytes and function similarly to basophils by inducing and promoting inflammatory responses. This figure shows mast cells in blood. In a blood smear, they are difficult to differentiate from basophils. Unlike basophils that circulate the bloodstream, mast cells migrate from the blood in to patrol various tissues.\" width=\"300\" height=\"280\" \/><\/a> Mast Cells are granulocytes and function similarly to basophils by inducing and promoting inflammatory responses. This figure shows mast cells in blood. In a blood smear, they are difficult to differentiate from basophils. Unlike basophils that circulate the bloodstream, mast cells migrate from the blood in to patrol various tissues.[\/caption]\r\n<h3><span style=\"color: #1f5c99\"><strong>Agranulocytes: Monocytes, Macrophages, and Dendritic Cells<\/strong><\/span><\/h3>\r\n<p style=\"text-align: justify\"><strong>Monocytes<\/strong> are immature macrophages that mature within 1-3 days into <strong>fixed macrophages<\/strong>, <strong>free macrophages<\/strong>, or <strong>dendritic cells<\/strong>.\u00a0 Despite being immature, monocytes can phagocytose bacteria, secrete <strong>cytokines,<\/strong> and act as <strong>Antigen Presenting Cells (APCs)<\/strong>.<\/p>\r\n\r\n<table class=\"grid landscape\" style=\"border-collapse: collapse;width: 100%;height: 125px\" border=\"0\">\r\n<tbody>\r\n<tr style=\"height: 63px\">\r\n<td class=\"border\" style=\"width: 14.7362%;height: 63px\"><span style=\"color: #032c80\"><strong>Fixed macrophages<\/strong><\/span><\/td>\r\n<td style=\"width: 85.2638%;height: 63px\">Patrol tissue beds for debris, cancerous cells, and pathogens.\u00a0 Tissue-specific names:\u00a0 <strong>microglia<\/strong> (brain), <strong>dust cells<\/strong> (lung alveoli), <strong>Kupffer\/stellate cells<\/strong> (liver), <strong>histiocytes<\/strong> (vertebrae), <strong>Langerhans cells<\/strong> (skin).\r\n\r\n<strong>Splenic red pulp macrophages<\/strong> and <strong>liver macrophages<\/strong> recycle millions of RBCs daily in process called erythrophagocytosis.<\/td>\r\n<\/tr>\r\n<tr style=\"height: 31px\">\r\n<td class=\"shaded\" style=\"width: 14.7362%;height: 31px\"><span style=\"color: #032c80\"><strong>Free macrophages<\/strong><\/span><\/td>\r\n<td class=\"shaded\" style=\"width: 85.2638%;height: 31px\">Circulate the bloodstream; enter tissue beds via diapedesis to remove bacteria, cellular debris, and aged neutrophils.<\/td>\r\n<\/tr>\r\n<tr style=\"height: 31px\">\r\n<td class=\"border\" style=\"width: 14.7362%;height: 31px\"><span style=\"color: #032c80\"><strong>Dendritic cells<\/strong><\/span><\/td>\r\n<td style=\"width: 85.2638%;height: 31px\">Reside in tissues exposed to microbes (skin, mucosa).\u00a0 Once activated, migrate to lymph nodes to function as APCs, stimulating T and B lymphocytes.<\/td>\r\n<\/tr>\r\n<\/tbody>\r\n<\/table>\r\nAgranulocytes play important roles in <strong>phagocytosing<\/strong> bacteria, as well as secreting <strong>cytokines<\/strong> (glycoprotein messengers) to induce <strong>inflammation<\/strong> and\u00a0<strong>recruit<\/strong> immune cells to the infected or damaged area.\u00a0 Additionally they release <strong>growth factors<\/strong> to promote tissue repair.\r\n\r\n[caption id=\"attachment_6783\" align=\"alignnone\" width=\"300\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/monocytes.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-6783 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/monocytes-300x123.png\" alt=\"Monocytes are large, agranular white blood cells with a nucleus that lacks lobes. When monocytes leave the bloodstream, they differentiate and become macrophages with tissue-specific properties.\" width=\"300\" height=\"123\" \/><\/a> Monocytes are large, agranular white blood cells with a nucleus that lacks lobes. When monocytes leave the bloodstream, they differentiate and become macrophages with tissue-specific properties.[\/caption]\r\n<h3><span style=\"color: #1f5c99\"><strong>Steps of Phagocytosis<\/strong><\/span><\/h3>\r\n<p style=\"text-align: justify\">Phagocytes <strong>(neutrophils, monocytes, macrophages,<\/strong> <strong>dendritic cells<\/strong>, <strong>eosinophils)<\/strong> remove cellular debris and are able to provide non-specific defence by destroying pathogens through seven ordered steps:<\/p>\r\n\r\n<ul style=\"text-align: justify\">\r\n \t<li><strong>Activation:<\/strong>\u00a0 Pro-inflammatory cytokines activate the phagocyte, enabling pathogen recognition and production of antimicrobial <strong>ROS.<\/strong><\/li>\r\n \t<li><strong>Chemotaxis:<\/strong>\u00a0 Activated phagocytes follow chemokine gradients to the site of infection or injury.<\/li>\r\n \t<li><strong>Recognition and Adherence:<\/strong>\u00a0 <strong>Opsonins<\/strong> (antibodies, lectin, complement proteins) coating the pathogen facilitate phagocyte binding when direct adherence is blocked (e.g., by a bacterial slime capsule).<\/li>\r\n \t<li><strong>Ingestion:<\/strong>\u00a0 The phagocyte extends <strong>pseudopods<\/strong> that encircle the pathogen, forming an internal vesicle called a <strong>phagosome.\u00a0\u00a0<\/strong><\/li>\r\n \t<li><strong>Killing and Recycling:\u00a0<\/strong> The phagosome fuses with a <strong>lysosome \u2192 phagolysosome<\/strong>.\u00a0 Lytic enzymes kill the pathogen and digest its components for recycling, display, or expulsion.<\/li>\r\n \t<li><strong>Antigen Display:<\/strong>\u00a0 Pathogen antigens are coupled to MHC (Major Histocompatibility Complex) molecules and displayed on the phagocyte's surface to activate T and B cells.<\/li>\r\n \t<li><strong>Expulsion:<\/strong>\u00a0 Undigested components are expelled from the cell as waste via exocytosis.<\/li>\r\n<\/ul>\r\n[caption id=\"attachment_2319\" align=\"alignnone\" width=\"300\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/phagocytosis.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-2319 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/phagocytosis-300x211.png\" alt=\"Phagocytosis\" width=\"300\" height=\"211\" \/><\/a> A step-by-step representation of phagocytosis, a form of endocytosis where large particles (e.g., cellular debris or bacteria) are engulfed by a phagocyte (neutrophil, eosinophil, monocyte, macrophage, dendritic cell). In the above diagram, specific cell membrane receptors assist in trapping the bacteria, and then the cell membrane will form extensions (pseudopods) that wrap around the bacteria to form an internal compartment or vesicle called a phagosome. The phagosome will then fuse with a lysosome to form a phagolysosome. The lysosome's lytic enzymes digest the material and kill invading pathogens (e.g., bacteria). The digested contents is then either expelled as waste products through exocytosis or is recycled into cellular components. Examples of phagocytes include several types of White Blood Cells (WBCs, leukocytes): neutrophils, macrophages, monocytes, dendritic cells, eosinophils, and B cells.[\/caption]\r\n\r\n[caption id=\"attachment_5861\" align=\"alignnone\" width=\"300\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/05\/Macrophage-Phagocytosis.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-5861 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/05\/Macrophage-Phagocytosis-300x209.png\" alt=\"\" width=\"300\" height=\"209\" \/><\/a> A macrophage has engulfed (phagocytized) a potentially pathogenic bacterium and then fuses with lysosomes within the cell to destroy the pathogen. Other organelles are present in the cell but for simplicity we do not show them.[\/caption]\r\n<h3><span style=\"color: #1f5c99\"><strong>Agranulocytes: Natural Killer (NK) Cells<\/strong><\/span><\/h3>\r\n<p style=\"text-align: justify\"><strong>Natural Killer (NK ) cells<\/strong> are lymphocytes providing non-specific defense.\u00a0 NK lymphocytes are <strong>cytotoxic<\/strong> (able to kill other cells) and make up 5-20% of lymphocytes.\u00a0 NK cells recognize and destroy damaged, abnormal, cancerous, virally-or bacterially-infected cells, and extracellular pathogens.<\/p>\r\n<p style=\"text-align: justify\">NK cells contain granules of <strong>perforin<\/strong> (pore-forming proteins) and <strong>granzymes<\/strong> (proteases) that are <strong>degranulated<\/strong> near a target cell.\u00a0 Perforin creates portals in the target membrane that if released in high concentration without granzyme can cause a cell to leak in fluid and lyse; though often granzyme are released at the same time and quickly enter the pores and induce <strong>apoptosis<\/strong><strong>.<\/strong>\u00a0 Crucially, NK cells prefer inducing <strong>apoptosis<\/strong> in virally-infected cells rather than lysing them - preventing newly formed virions from escaping into surrounding tissue.<\/p>\r\n<p style=\"text-align: justify\">NK cells also release <strong>alpha-defensins<\/strong> (damaging bacterial cell walls, fungi, and enveloped viruses) and <strong>pro-inflammatory cytokines<\/strong> to activate other WBCs.\u00a0 Together with macrophages, NK cells recycle <strong>senescent cells<\/strong> (cells that have stopped replicating and are at risk of DNA damage due to age).<\/p>\r\n\r\n\r\n[caption id=\"attachment_6785\" align=\"alignnone\" width=\"278\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/NK-cell-perforin-granzyme.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-6785 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/NK-cell-perforin-granzyme-278x300.png\" alt=\"Natural killer (NK) cells are inhibited by the presence of the major histocompatibility cell (MHC) receptor on healthy cells. Cancer cells and virus-infected cells have reduced expression of MHC and increased expression of activating molecules. When a NK cell recognizes decreased MHC and increased activating molecules, it will kill the abnormal cell, typically by inducing apoptosis.\" width=\"278\" height=\"300\" \/><\/a> Natural killer (NK) cells are inhibited by the presence of the major histocompatibility cell (MHC) receptor on healthy cells. Cancer cells and virus-infected cells have reduced expression of MHC and increased expression of activating molecules. When a NK cell recognizes decreased MHC and increased activating molecules, it will kill the abnormal cell, typically by inducing apoptosis.[\/caption]\r\n\r\n[caption id=\"attachment_6784\" align=\"alignnone\" width=\"300\"]<a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/perforin-granzyme.png\" target=\"_blank\" rel=\"noopener\"><img class=\"wp-image-6784 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/perforin-granzyme-300x237.png\" alt=\"Natural killer cell with perforin-containing granules.\" width=\"300\" height=\"237\" \/><\/a> Natural killer cell with perforin-containing granules.[\/caption]\r\n\r\n<div class=\"textbox textbox--key-takeaways\"><header class=\"textbox__header\">\r\n<p class=\"textbox__title\" style=\"text-align: justify\"><strong>Clinical Note:\u00a0 Cancer and Immune Evasion<\/strong><\/p>\r\n\r\n<\/header>\r\n<div class=\"textbox__content\">\r\n<p style=\"text-align: justify\">Cancerous cells or pathogens that evade NK cells can spread through tissue, blood, or lymph, potentially creating damage in multiple locations.\u00a0 Understanding how pathogens and cancers evade innate immunity is a major area of current research.<\/p>\r\n\r\n<\/div>\r\n<\/div>\r\n<h3 style=\"text-align: justify\"><\/h3>","rendered":"<h3><span style=\"color: #1f5c99\"><strong>Hematopoiesis:\u00a0 Formation of Blood Cells<\/strong><\/span><\/h3>\n<p style=\"text-align: justify\"><span style=\"text-align: initial;font-size: 1em\"><strong>Hematopoiesis<\/strong> is the formation of blood cells.\u00a0 Production begins at day 7 of the embryonic life in the <strong>yolk sac,<\/strong> migrates to the <strong>liver<\/strong> and <strong>spleen<\/strong> at week 7, and moves to the <strong>bone marrow<\/strong> at ~week 20.\u00a0 The pluripotent stem cells giving rise to all blood cell types are called <strong>hemocytoblasts.<\/strong>\u00a0 Their daughter cells differentiate into <strong>erythrocytes<\/strong> (RBCs), <strong>megakaryocytes<\/strong> (platelet precursors), and <strong>leukocytes<\/strong> (WBCs).<\/span><\/p>\n<figure id=\"attachment_6777\" aria-describedby=\"caption-attachment-6777\" style=\"width: 300px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hemopoiesis.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-6777 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hemopoiesis-300x260.png\" alt=\"All the formed elements of the blood arise by differentiation of hematopoietic stem cells in the bone marrow.\" width=\"300\" height=\"260\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hemopoiesis-300x260.png 300w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hemopoiesis-1024x888.png 1024w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hemopoiesis-768x666.png 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hemopoiesis-65x56.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hemopoiesis-225x195.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hemopoiesis-350x303.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hemopoiesis.png 1174w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><figcaption id=\"caption-attachment-6777\" class=\"wp-caption-text\">Hematopoiesis:\u00a0 All the formed elements of the blood arise by differentiation of hematopoietic stem cells in the bone marrow.<\/figcaption><\/figure>\n<p style=\"text-align: justify\"><strong><span style=\"color: #2e75b6\">Red Blood Cells (Erythrocytes)\u00a0<\/span><\/strong><\/p>\n<p style=\"text-align: justify\"><strong>Erythropoiesis<\/strong> is the production of RBCs.\u00a0 Developing <strong>erythroblasts<\/strong> become increasingly packed with <strong>hemoglobin.<\/strong>\u00a0 At the <strong>normoblast<\/strong> stage, they lose their nucleus, become <strong>reticulocytes,<\/strong> enter the bloodstream 2-3 days later and mature into <strong>erythrocytes<\/strong> over the following 2 days.\u00a0 Main function:\u00a0 use hemoglobin to transport 98.5% of the oxygen and ~23% of the carbon dioxide in blood.\u00a0 Lifespan ~120 days; aged cells are recycled by macrophages in the liver, bone marrow, and spleen.<\/p>\n<figure id=\"attachment_6524\" aria-describedby=\"caption-attachment-6524\" style=\"width: 103px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hematopoiesis_human_diagram-cropped.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-6524 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hematopoiesis_human_diagram-cropped-103x300.png\" alt=\"Erythropoiesis: begins with hemocytoblasts producing proerythroblasts that mature into erythroblasts \u2192 normoblasts reticulocytes erythrocytes. [1] In this diagram, the reticulocyte on the right shows characteristics when stained with methylene blue. [2] The erythrocyte on the right represents its appearance under a light microscope.\" width=\"103\" height=\"300\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hematopoiesis_human_diagram-cropped-103x300.png 103w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hematopoiesis_human_diagram-cropped-65x189.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hematopoiesis_human_diagram-cropped-225x655.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hematopoiesis_human_diagram-cropped-350x1019.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Hematopoiesis_human_diagram-cropped.png 352w\" sizes=\"auto, (max-width: 103px) 100vw, 103px\" \/><\/a><figcaption id=\"caption-attachment-6524\" class=\"wp-caption-text\">Erythropoiesis: begins with hemocytoblasts producing proerythroblasts that mature into erythroblasts \u2192 normoblasts reticulocytes erythrocytes.<br \/>[1] In this diagram, the reticulocyte on the right shows characteristics when stained with methylene blue.<br \/>[2] The erythrocyte on the right represents its appearance under a light microscope.<\/figcaption><\/figure>\n<figure id=\"attachment_6522\" aria-describedby=\"caption-attachment-6522\" style=\"width: 231px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-scaled.jpg\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-6522 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-231x300.jpg\" alt=\"Erythrocyte Life Cycle\" width=\"231\" height=\"300\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-231x300.jpg 231w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-788x1024.jpg 788w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-768x998.jpg 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-1182x1536.jpg 1182w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-1575x2048.jpg 1575w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-65x84.jpg 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-225x292.jpg 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-350x455.jpg 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/1905_Erythrocyte_Life_Cycle-scaled.jpg 1969w\" sizes=\"auto, (max-width: 231px) 100vw, 231px\" \/><\/a><figcaption id=\"caption-attachment-6522\" class=\"wp-caption-text\">Erythrocyte Life Cycle<\/figcaption><\/figure>\n<p style=\"text-align: justify\">Erythropoiesis is regulated by <strong>erythropoietin (EPO)<\/strong> hormone, secreted by the kidneys in response to low blood-oxygen levels, growth hormone (GH), thyroxine, and testosterone.\u00a0 In an adult, 2-3 million RBCs are produced per second and RBC production requires B vitamins, folate, amino acids and iron.<\/p>\n<div class=\"textbox textbox--key-takeaways\">\n<header class=\"textbox__header\">\n<p class=\"textbox__title\"><strong>Diagnostic Blood Tests<\/strong><\/p>\n<\/header>\n<div class=\"textbox__content\">\n<p><strong><span style=\"color: #2e75b6\">Blood Count Terminology<\/span><\/strong><\/p>\n<table class=\"grid\" style=\"border-collapse: collapse;width: 100%\">\n<tbody>\n<tr>\n<td style=\"width: 20.8334%\"><strong>Retic count<\/strong><\/td>\n<td style=\"width: 79.1666%\">Proportion of RBCs that are reticulocytes (normal: 1-2%).<\/p>\n<p>Low retic count (e.g., 0.5%) indicates reduced erythropoiesis.<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 20.8334%\"><strong>Hematocrit<\/strong><\/td>\n<td style=\"width: 79.1666%\">Percentage of blood volume made up of formed elements.<\/p>\n<p>Females ~42%;\u00a0Males ~46%\u00a0(testosterone stimulates RBC production).<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 20.8334%\"><strong>Leukopenia<\/strong><\/td>\n<td style=\"width: 79.1666%\">Reduced WBC production.<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 20.8334%\"><strong>Thrombocytopenia<\/strong><\/td>\n<td style=\"width: 79.1666%\">Reduced platelet production.<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 20.8334%\"><strong>Neutrophilia<\/strong><\/td>\n<td style=\"width: 79.1666%\">Elevated neutrophil count &#8211; common with bacterial infections.<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 20.8334%\"><strong>Neutropenia<\/strong><\/td>\n<td style=\"width: 79.1666%\">Decreased neutrophil count &#8211; caused by severe infection, nutritional deficiency, congenital defects, autoimmune disease, or cancer.<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 20.8334%\"><strong>Eosinophilia<\/strong><\/td>\n<td style=\"width: 79.1666%\">Elevated eosinophil count &#8211; caused by helminth infections, allergies, or autoimmune diseases.<\/td>\n<\/tr>\n<tr>\n<td style=\"width: 20.8334%\"><strong>Lymphocytosis<\/strong><\/td>\n<td style=\"width: 79.1666%\">Elevated NK, T, and P lymphocytes count &#8211; occurs with viral infections.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<\/div>\n<figure id=\"attachment_6768\" aria-describedby=\"caption-attachment-6768\" style=\"width: 300px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/WBC-key.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-6768 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/WBC-key-300x148.png\" alt=\"Five types of leukocytes: from left to right, lymphocyte, basophil, eosinophil, neutrophil, and monocytes.\" width=\"300\" height=\"148\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/WBC-key-300x148.png 300w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/WBC-key-1024x505.png 1024w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/WBC-key-768x379.png 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/WBC-key-1536x758.png 1536w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/WBC-key-65x32.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/WBC-key-225x111.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/WBC-key-350x173.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/WBC-key.png 1890w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><figcaption id=\"caption-attachment-6768\" class=\"wp-caption-text\">Five types of leukocytes: from left to right, lymphocyte, basophil, eosinophil, neutrophil, and monocytes.<\/figcaption><\/figure>\n<figure id=\"attachment_6669\" aria-describedby=\"caption-attachment-6669\" style=\"width: 300px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Blood-Cells.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-6669 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Blood-Cells-300x297.png\" alt=\"Cells of the blood include (1) monocytes, (2) lymphocytes, (3) neutrophils, (4) red blood cells, and (5) platelets. Note the very similar morphologies of the leukocytes (1, 2, 3). (credit: modification of work by Bruce Wetzel, Harry Schaefer, NCI; scale-bar data from Matt Russell)\" width=\"300\" height=\"297\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Blood-Cells-300x297.png 300w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Blood-Cells-150x150.png 150w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Blood-Cells-768x759.png 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Blood-Cells-65x64.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Blood-Cells-225x222.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Blood-Cells-350x346.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Blood-Cells.png 962w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><figcaption id=\"caption-attachment-6669\" class=\"wp-caption-text\">Cells of the blood include (1) monocytes, (2) lymphocytes, (3) neutrophils, (4) red blood cells, and (5) platelets. Note the very similar morphologies of the leukocytes (1, 2, 3). (credit: modification of work by Bruce Wetzel, Harry Schaefer, NCI; scale-bar data from Matt Russell).<\/figcaption><\/figure>\n<p><strong><span style=\"color: #2e75b6\">Platelets (Thrombocytes)\u00a0<\/span><\/strong><\/p>\n<p><strong>Megakaryocytes<\/strong> fragment into ~1,000 anuclear <strong>platelets<\/strong> (thrombocytes).\u00a0 Despite lacking a nucleus, platelet contain ~300 chemicals involved in <strong>hemostasis<\/strong> (blood clotting) and are essential for innate defense and preventing excessive bleeding.<\/p>\n<p><strong><span style=\"color: #2e75b6\">White Blood Cell Lineages\u00a0<\/span><\/strong><\/p>\n<p>WBCs are classified as either <strong>granulocytes<\/strong> (containing large granules, readily visible with light microscope); also called polymorphonuclear leukocytes (PMNs) or <strong>agranulocytes<\/strong> (containing smaller granules).\u00a0 Granulocytes include: <strong>neutrophils, eosinophils, mast cells<\/strong>, and <strong>basophils.<\/strong> \u00a0Agranulocytes include: <strong>monocytes, macrophages, dendritic cells<\/strong>, Natural Killer lymphocytes (<strong>NK cells<\/strong>), T lymphocytes (<strong>T cells<\/strong>), and B lymphocytes (<strong>B cells<\/strong>).\u00a0 All WBCs perform <strong>amoeboid movement<\/strong> and <strong>diapedesis<\/strong> (emigration from blood vessels into tissue &#8211; also termed <strong>extravasation<\/strong> or <strong>transmigration.<\/strong><\/p>\n<h3><span style=\"color: #1f5c99\"><strong>Granulocytes (Polymorphonuclear Leukocytes, PMNs)<\/strong><\/span><\/h3>\n<table class=\"grid landscape\" style=\"border-collapse: collapse;width: 100%;height: 347px\">\n<tbody>\n<tr style=\"height: 126px\">\n<td class=\"border\" style=\"width: 14.7362%;height: 126px\"><span style=\"color: #032c80\"><strong>Neutrophils<\/strong><\/span><\/td>\n<td style=\"width: 85.2638%;height: 126px\">Immature <strong>band cells<\/strong> mature into neutrophils.<\/p>\n<p>Most abundant WBC (50-70%).\u00a0 2-5 lobed nucleus; stain neutral pink with H&amp;E stain.\u00a0 First responders to sites of damage.<\/p>\n<p><strong>Phagocytose<\/strong> bacteria and utilize extensive <strong>lysosomes.<\/strong><\/p>\n<p>Neutrophil <strong>Oxidative Bursts<\/strong> exocytose highly toxic, unstable <strong>Reactive Oxygen Species (ROS)<\/strong> from secretory vesicles that <strong>damage bacterial cell walls<\/strong>.<\/p>\n<p>Neutrophil granules release <strong>lactoferrin<\/strong> (sequesters iron, depriving bacteria of required resource)<\/p>\n<p>Neutrophils release <strong>defensin<\/strong> and <strong>proteases<\/strong> (degrade pathogen)<\/p>\n<p>Can also release <strong>NETs<\/strong> (Neutrophil Extracellular Traps &#8211; webs of chromatin fibers and toxic enzymes) to trap and destroy microbes extracellularly.<\/p>\n<p>Active lifespan: 24-48 hours.<\/td>\n<\/tr>\n<tr style=\"height: 79px\">\n<td class=\"shaded\" style=\"width: 14.7362%;height: 79px\"><span style=\"color: #032c80\"><strong>Eosinophils<\/strong><\/span><\/td>\n<td class=\"shaded\" style=\"width: 85.2638%;height: 79px\">Stain red with acidic eosin dye;\u00a0 ~2-3% of WBCs.\u00a0 Arrive 2-3 hours after neutrophils.<\/p>\n<p><strong>Phagocytose<\/strong> debris and pathogens.<\/p>\n<p>Exocytose <strong>toxins ROS, Eosinophil Cationic Protein (ECP), <\/strong>and <strong>Major Basic Protein (MBP)<\/strong>\u00a0to kill organisms too large to phagocytose (e.g., helminths).<\/p>\n<p>Release <strong>cytokines<\/strong> to stimulate mast cell and basophil inflammatory response.<\/p>\n<p>Release growth factors (e.g., <strong>VEGF, vascular endothelial growth factor)<\/strong> to support healing.<\/p>\n<p>Release <strong>RNases<\/strong> to destroy viruses.<\/p>\n<p>Play a role in allergies and asthma<\/td>\n<\/tr>\n<tr style=\"height: 79px\">\n<td class=\"border\" style=\"width: 14.7362%;height: 79px\"><span style=\"color: #032c80\"><strong>Mast cells<\/strong><\/span><\/td>\n<td style=\"width: 85.2638%;height: 79px\">Tissue-resident cells, most prevalent in skin dermis, lung mucosa, and GI tract mucosa.<\/p>\n<p>Contain granules with <strong>heparin (anticoagulant)<\/strong> and<strong> histamine<\/strong>.<\/p>\n<p>Activated by cellular injury;\u00a0 degranulate releasing <strong>pro-inflammatory mediators<\/strong> <strong>(histamine, bradykinins, prostaglandins, leukotrienes).<\/strong><\/td>\n<\/tr>\n<tr style=\"height: 63px\">\n<td class=\"shaded\" style=\"width: 14.7362%;height: 63px\"><span style=\"color: #032c80\"><strong>Basophils<\/strong><\/span><\/td>\n<td class=\"shaded\" style=\"width: 85.2638%;height: 63px\">Circulating counterpart to <strong>mast cells<\/strong>.\u00a0 Both contain <strong>heparin<\/strong> and <strong>histamine granules<\/strong> and fulfill similar <strong>pro-inflammatory<\/strong> roles.\u00a0 Basophils circulate the bloodstream rather than residing in tissue.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><strong>*ROS<\/strong> = Reactive Oxygen Species, such as <strong>superoxide, O<sub>2<\/sub><sup>\u2022\u2212<\/sup><\/strong> and <strong>hydroxyl radical HO<sup>\u2022<\/sup><\/strong> are free radicals with <strong>unpaired electrons<\/strong> that damage DNA, lipids and proteins.<\/p>\n<p>&nbsp;<\/p>\n<figure id=\"attachment_6513\" aria-describedby=\"caption-attachment-6513\" style=\"width: 300px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-production.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-6513 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-production-300x95.png\" alt=\"Neutrophil Production\" width=\"300\" height=\"95\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-production-300x95.png 300w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-production-1024x324.png 1024w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-production-768x243.png 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-production-65x21.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-production-225x71.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-production-350x111.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-production.png 1460w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><figcaption id=\"caption-attachment-6513\" class=\"wp-caption-text\">Neutrophil Production<\/figcaption><\/figure>\n<figure id=\"attachment_2325\" aria-describedby=\"caption-attachment-2325\" style=\"width: 150px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/Cardiovascular_system_-_Neutrophil_granulocyte_2_-_Smart-Servier.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2325 size-thumbnail\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/Cardiovascular_system_-_Neutrophil_granulocyte_2_-_Smart-Servier-150x150.png\" alt=\"Neutrophils circulate the bloodstream and are an essential part of the innate (non-specific) immune system.\" width=\"150\" height=\"150\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/Cardiovascular_system_-_Neutrophil_granulocyte_2_-_Smart-Servier-150x150.png 150w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/Cardiovascular_system_-_Neutrophil_granulocyte_2_-_Smart-Servier-65x66.png 65w\" sizes=\"auto, (max-width: 150px) 100vw, 150px\" \/><\/a><figcaption id=\"caption-attachment-2325\" class=\"wp-caption-text\">Neutrophils circulate the bloodstream and are an essential part of the innate (non-specific) immune system.<\/figcaption><\/figure>\n<figure id=\"attachment_2324\" aria-describedby=\"caption-attachment-2324\" style=\"width: 237px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/NeutrophilerAktion.svg_.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2324 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/NeutrophilerAktion.svg_-237x300.png\" alt=\"Neutrophil (in purple) migrates from the blood vessel into the matrix using diapedesis. Neutrophils can secrete collagenase in the extracellular matrix of tissues to facilitate tissue remodeling, wound healing and immune cell migration.\" width=\"237\" height=\"300\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/NeutrophilerAktion.svg_-237x300.png 237w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/NeutrophilerAktion.svg_-810x1024.png 810w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/NeutrophilerAktion.svg_-768x971.png 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/NeutrophilerAktion.svg_-1214x1536.png 1214w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/NeutrophilerAktion.svg_-65x82.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/NeutrophilerAktion.svg_-225x285.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/NeutrophilerAktion.svg_-350x443.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/NeutrophilerAktion.svg_.png 1620w\" sizes=\"auto, (max-width: 237px) 100vw, 237px\" \/><\/a><figcaption id=\"caption-attachment-2324\" class=\"wp-caption-text\">Neutrophil (in purple) migrates from the blood vessel into the matrix using diapedesis. Neutrophils can secrete collagenase (green) in the extracellular matrix of tissues to facilitate tissue remodeling, wound healing and immune cell migration.<\/figcaption><\/figure>\n<figure id=\"attachment_6514\" aria-describedby=\"caption-attachment-6514\" style=\"width: 300px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-activity.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-6514 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-activity-300x226.png\" alt=\"The killing mechanisms of neutrophils: phagocytosis, degranulation, and extracellular traps release.\" width=\"300\" height=\"226\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-activity-300x226.png 300w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-activity-1024x771.png 1024w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-activity-768x578.png 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-activity-65x49.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-activity-225x169.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-activity-350x263.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Neutrophil-activity.png 1216w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><figcaption id=\"caption-attachment-6514\" class=\"wp-caption-text\">The killing mechanisms of neutrophils: phagocytosis, degranulation, and extracellular traps release.<\/figcaption><\/figure>\n<p>&nbsp;<\/p>\n<figure id=\"attachment_5710\" aria-describedby=\"caption-attachment-5710\" style=\"width: 1024px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/01\/neutrophils-12-01981-g003-scaled.png\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-5710 size-large\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/01\/neutrophils-12-01981-g003-1024x675.png\" alt=\"Neutrophil Activation\" width=\"1024\" height=\"675\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/01\/neutrophils-12-01981-g003-1024x675.png 1024w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/01\/neutrophils-12-01981-g003-300x198.png 300w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/01\/neutrophils-12-01981-g003-768x506.png 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/01\/neutrophils-12-01981-g003-1536x1012.png 1536w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/01\/neutrophils-12-01981-g003-2048x1349.png 2048w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/01\/neutrophils-12-01981-g003-65x43.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/01\/neutrophils-12-01981-g003-225x148.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/01\/neutrophils-12-01981-g003-350x231.png 350w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/a><figcaption id=\"caption-attachment-5710\" class=\"wp-caption-text\">Neutrophil Activation: Neutrophils typically circulate the brainstem until chemokines are secreted by monocytes and macrophages and blood vessel walls stimulate blood vessel endothelial cells to express cell adhesion molecule (selectins) that bind to the carbohydrate ligands on neutrophils. Rolling adhesion of neutrophils occurs, followed by firm attachment and diapedesis in which the neutrophil leaves the blood vessel (extravasation) and enters the tissue. Chemokines released by monocytes and macrophages stimulate chemotaxis of neutrophils to assist in the phagocytosis of debris and any invading bacteria. Neutrophils are able to perform 3 different functions to help contain and eliminate the infecting agent: 1) Phagocytosis (followed by antigen presentation), 2) Secretion of ROS, anti-microbial granules and pro-inflammatory cytokines, and 3) NETosis (in which nuclear or mitochondrial DNA is expelled to trap the pathogen).<\/figcaption><\/figure>\n<figure id=\"attachment_6779\" aria-describedby=\"caption-attachment-6779\" style=\"width: 300px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/3-granulocytes.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-6779 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/3-granulocytes-300x172.png\" alt=\"Three of the Four Granulocytes (Neutrophils, Eosinophils and Basophils). Granulocytes can be distinguished by the number of lobes in their nuclei and the staining properties of their granules.\" width=\"300\" height=\"172\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/3-granulocytes-300x172.png 300w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/3-granulocytes-1024x586.png 1024w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/3-granulocytes-768x440.png 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/3-granulocytes-1536x879.png 1536w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/3-granulocytes-65x37.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/3-granulocytes-225x129.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/3-granulocytes-350x200.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/3-granulocytes.png 1724w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><figcaption id=\"caption-attachment-6779\" class=\"wp-caption-text\">Three of the Four Granulocytes (Neutrophils, Eosinophils and Basophils). Granulocytes can be distinguished by the number of lobes in their nuclei and the staining properties of their granules.<\/figcaption><\/figure>\n<figure id=\"attachment_6780\" aria-describedby=\"caption-attachment-6780\" style=\"width: 300px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Mast-Cells.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-6780 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Mast-Cells-300x280.png\" alt=\"Mast Cells are granulocytes and function similarly to basophils by inducing and promoting inflammatory responses. This figure shows mast cells in blood. In a blood smear, they are difficult to differentiate from basophils. Unlike basophils that circulate the bloodstream, mast cells migrate from the blood in to patrol various tissues.\" width=\"300\" height=\"280\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Mast-Cells-300x280.png 300w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Mast-Cells-1024x956.png 1024w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Mast-Cells-768x717.png 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Mast-Cells-65x61.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Mast-Cells-225x210.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Mast-Cells-350x327.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/Mast-Cells.png 1077w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><figcaption id=\"caption-attachment-6780\" class=\"wp-caption-text\">Mast Cells are granulocytes and function similarly to basophils by inducing and promoting inflammatory responses. This figure shows mast cells in blood. In a blood smear, they are difficult to differentiate from basophils. Unlike basophils that circulate the bloodstream, mast cells migrate from the blood in to patrol various tissues.<\/figcaption><\/figure>\n<h3><span style=\"color: #1f5c99\"><strong>Agranulocytes: Monocytes, Macrophages, and Dendritic Cells<\/strong><\/span><\/h3>\n<p style=\"text-align: justify\"><strong>Monocytes<\/strong> are immature macrophages that mature within 1-3 days into <strong>fixed macrophages<\/strong>, <strong>free macrophages<\/strong>, or <strong>dendritic cells<\/strong>.\u00a0 Despite being immature, monocytes can phagocytose bacteria, secrete <strong>cytokines,<\/strong> and act as <strong>Antigen Presenting Cells (APCs)<\/strong>.<\/p>\n<table class=\"grid landscape\" style=\"border-collapse: collapse;width: 100%;height: 125px\">\n<tbody>\n<tr style=\"height: 63px\">\n<td class=\"border\" style=\"width: 14.7362%;height: 63px\"><span style=\"color: #032c80\"><strong>Fixed macrophages<\/strong><\/span><\/td>\n<td style=\"width: 85.2638%;height: 63px\">Patrol tissue beds for debris, cancerous cells, and pathogens.\u00a0 Tissue-specific names:\u00a0 <strong>microglia<\/strong> (brain), <strong>dust cells<\/strong> (lung alveoli), <strong>Kupffer\/stellate cells<\/strong> (liver), <strong>histiocytes<\/strong> (vertebrae), <strong>Langerhans cells<\/strong> (skin).<\/p>\n<p><strong>Splenic red pulp macrophages<\/strong> and <strong>liver macrophages<\/strong> recycle millions of RBCs daily in process called erythrophagocytosis.<\/td>\n<\/tr>\n<tr style=\"height: 31px\">\n<td class=\"shaded\" style=\"width: 14.7362%;height: 31px\"><span style=\"color: #032c80\"><strong>Free macrophages<\/strong><\/span><\/td>\n<td class=\"shaded\" style=\"width: 85.2638%;height: 31px\">Circulate the bloodstream; enter tissue beds via diapedesis to remove bacteria, cellular debris, and aged neutrophils.<\/td>\n<\/tr>\n<tr style=\"height: 31px\">\n<td class=\"border\" style=\"width: 14.7362%;height: 31px\"><span style=\"color: #032c80\"><strong>Dendritic cells<\/strong><\/span><\/td>\n<td style=\"width: 85.2638%;height: 31px\">Reside in tissues exposed to microbes (skin, mucosa).\u00a0 Once activated, migrate to lymph nodes to function as APCs, stimulating T and B lymphocytes.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Agranulocytes play important roles in <strong>phagocytosing<\/strong> bacteria, as well as secreting <strong>cytokines<\/strong> (glycoprotein messengers) to induce <strong>inflammation<\/strong> and\u00a0<strong>recruit<\/strong> immune cells to the infected or damaged area.\u00a0 Additionally they release <strong>growth factors<\/strong> to promote tissue repair.<\/p>\n<figure id=\"attachment_6783\" aria-describedby=\"caption-attachment-6783\" style=\"width: 300px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/monocytes.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-6783 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/monocytes-300x123.png\" alt=\"Monocytes are large, agranular white blood cells with a nucleus that lacks lobes. When monocytes leave the bloodstream, they differentiate and become macrophages with tissue-specific properties.\" width=\"300\" height=\"123\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/monocytes-300x123.png 300w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/monocytes-1024x421.png 1024w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/monocytes-768x315.png 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/monocytes-1536x631.png 1536w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/monocytes-65x27.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/monocytes-225x92.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/monocytes-350x144.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/monocytes.png 1899w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><figcaption id=\"caption-attachment-6783\" class=\"wp-caption-text\">Monocytes are large, agranular white blood cells with a nucleus that lacks lobes. When monocytes leave the bloodstream, they differentiate and become macrophages with tissue-specific properties.<\/figcaption><\/figure>\n<h3><span style=\"color: #1f5c99\"><strong>Steps of Phagocytosis<\/strong><\/span><\/h3>\n<p style=\"text-align: justify\">Phagocytes <strong>(neutrophils, monocytes, macrophages,<\/strong> <strong>dendritic cells<\/strong>, <strong>eosinophils)<\/strong> remove cellular debris and are able to provide non-specific defence by destroying pathogens through seven ordered steps:<\/p>\n<ul style=\"text-align: justify\">\n<li><strong>Activation:<\/strong>\u00a0 Pro-inflammatory cytokines activate the phagocyte, enabling pathogen recognition and production of antimicrobial <strong>ROS.<\/strong><\/li>\n<li><strong>Chemotaxis:<\/strong>\u00a0 Activated phagocytes follow chemokine gradients to the site of infection or injury.<\/li>\n<li><strong>Recognition and Adherence:<\/strong>\u00a0 <strong>Opsonins<\/strong> (antibodies, lectin, complement proteins) coating the pathogen facilitate phagocyte binding when direct adherence is blocked (e.g., by a bacterial slime capsule).<\/li>\n<li><strong>Ingestion:<\/strong>\u00a0 The phagocyte extends <strong>pseudopods<\/strong> that encircle the pathogen, forming an internal vesicle called a <strong>phagosome.\u00a0\u00a0<\/strong><\/li>\n<li><strong>Killing and Recycling:\u00a0<\/strong> The phagosome fuses with a <strong>lysosome \u2192 phagolysosome<\/strong>.\u00a0 Lytic enzymes kill the pathogen and digest its components for recycling, display, or expulsion.<\/li>\n<li><strong>Antigen Display:<\/strong>\u00a0 Pathogen antigens are coupled to MHC (Major Histocompatibility Complex) molecules and displayed on the phagocyte&#8217;s surface to activate T and B cells.<\/li>\n<li><strong>Expulsion:<\/strong>\u00a0 Undigested components are expelled from the cell as waste via exocytosis.<\/li>\n<\/ul>\n<figure id=\"attachment_2319\" aria-describedby=\"caption-attachment-2319\" style=\"width: 300px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/phagocytosis.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-2319 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/phagocytosis-300x211.png\" alt=\"Phagocytosis\" width=\"300\" height=\"211\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/phagocytosis-300x211.png 300w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/phagocytosis-768x540.png 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/phagocytosis-65x46.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/phagocytosis-225x158.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/phagocytosis-350x246.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2024\/09\/phagocytosis.png 932w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><figcaption id=\"caption-attachment-2319\" class=\"wp-caption-text\">A step-by-step representation of phagocytosis, a form of endocytosis where large particles (e.g., cellular debris or bacteria) are engulfed by a phagocyte (neutrophil, eosinophil, monocyte, macrophage, dendritic cell). In the above diagram, specific cell membrane receptors assist in trapping the bacteria, and then the cell membrane will form extensions (pseudopods) that wrap around the bacteria to form an internal compartment or vesicle called a phagosome. The phagosome will then fuse with a lysosome to form a phagolysosome. The lysosome&#8217;s lytic enzymes digest the material and kill invading pathogens (e.g., bacteria). The digested contents is then either expelled as waste products through exocytosis or is recycled into cellular components. Examples of phagocytes include several types of White Blood Cells (WBCs, leukocytes): neutrophils, macrophages, monocytes, dendritic cells, eosinophils, and B cells.<\/figcaption><\/figure>\n<figure id=\"attachment_5861\" aria-describedby=\"caption-attachment-5861\" style=\"width: 300px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/05\/Macrophage-Phagocytosis.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-5861 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/05\/Macrophage-Phagocytosis-300x209.png\" alt=\"\" width=\"300\" height=\"209\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/05\/Macrophage-Phagocytosis-300x209.png 300w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/05\/Macrophage-Phagocytosis-65x45.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/05\/Macrophage-Phagocytosis-225x157.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/05\/Macrophage-Phagocytosis-350x244.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/05\/Macrophage-Phagocytosis.png 629w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><figcaption id=\"caption-attachment-5861\" class=\"wp-caption-text\">A macrophage has engulfed (phagocytized) a potentially pathogenic bacterium and then fuses with lysosomes within the cell to destroy the pathogen. Other organelles are present in the cell but for simplicity we do not show them.<\/figcaption><\/figure>\n<h3><span style=\"color: #1f5c99\"><strong>Agranulocytes: Natural Killer (NK) Cells<\/strong><\/span><\/h3>\n<p style=\"text-align: justify\"><strong>Natural Killer (NK ) cells<\/strong> are lymphocytes providing non-specific defense.\u00a0 NK lymphocytes are <strong>cytotoxic<\/strong> (able to kill other cells) and make up 5-20% of lymphocytes.\u00a0 NK cells recognize and destroy damaged, abnormal, cancerous, virally-or bacterially-infected cells, and extracellular pathogens.<\/p>\n<p style=\"text-align: justify\">NK cells contain granules of <strong>perforin<\/strong> (pore-forming proteins) and <strong>granzymes<\/strong> (proteases) that are <strong>degranulated<\/strong> near a target cell.\u00a0 Perforin creates portals in the target membrane that if released in high concentration without granzyme can cause a cell to leak in fluid and lyse; though often granzyme are released at the same time and quickly enter the pores and induce <strong>apoptosis<\/strong><strong>.<\/strong>\u00a0 Crucially, NK cells prefer inducing <strong>apoptosis<\/strong> in virally-infected cells rather than lysing them &#8211; preventing newly formed virions from escaping into surrounding tissue.<\/p>\n<p style=\"text-align: justify\">NK cells also release <strong>alpha-defensins<\/strong> (damaging bacterial cell walls, fungi, and enveloped viruses) and <strong>pro-inflammatory cytokines<\/strong> to activate other WBCs.\u00a0 Together with macrophages, NK cells recycle <strong>senescent cells<\/strong> (cells that have stopped replicating and are at risk of DNA damage due to age).<\/p>\n<figure id=\"attachment_6785\" aria-describedby=\"caption-attachment-6785\" style=\"width: 278px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/NK-cell-perforin-granzyme.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-6785 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/NK-cell-perforin-granzyme-278x300.png\" alt=\"Natural killer (NK) cells are inhibited by the presence of the major histocompatibility cell (MHC) receptor on healthy cells. Cancer cells and virus-infected cells have reduced expression of MHC and increased expression of activating molecules. When a NK cell recognizes decreased MHC and increased activating molecules, it will kill the abnormal cell, typically by inducing apoptosis.\" width=\"278\" height=\"300\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/NK-cell-perforin-granzyme-278x300.png 278w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/NK-cell-perforin-granzyme-65x70.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/NK-cell-perforin-granzyme-225x243.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/NK-cell-perforin-granzyme-350x378.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/NK-cell-perforin-granzyme.png 759w\" sizes=\"auto, (max-width: 278px) 100vw, 278px\" \/><\/a><figcaption id=\"caption-attachment-6785\" class=\"wp-caption-text\">Natural killer (NK) cells are inhibited by the presence of the major histocompatibility cell (MHC) receptor on healthy cells. Cancer cells and virus-infected cells have reduced expression of MHC and increased expression of activating molecules. When a NK cell recognizes decreased MHC and increased activating molecules, it will kill the abnormal cell, typically by inducing apoptosis.<\/figcaption><\/figure>\n<figure id=\"attachment_6784\" aria-describedby=\"caption-attachment-6784\" style=\"width: 300px\" class=\"wp-caption alignnone\"><a href=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/perforin-granzyme.png\" target=\"_blank\" rel=\"noopener\"><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-6784 size-medium\" src=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/perforin-granzyme-300x237.png\" alt=\"Natural killer cell with perforin-containing granules.\" width=\"300\" height=\"237\" srcset=\"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/perforin-granzyme-300x237.png 300w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/perforin-granzyme-1024x808.png 1024w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/perforin-granzyme-768x606.png 768w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/perforin-granzyme-65x51.png 65w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/perforin-granzyme-225x177.png 225w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/perforin-granzyme-350x276.png 350w, https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-content\/uploads\/sites\/1961\/2026\/06\/perforin-granzyme.png 1236w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><figcaption id=\"caption-attachment-6784\" class=\"wp-caption-text\">Natural killer cell with perforin-containing granules.<\/figcaption><\/figure>\n<div class=\"textbox textbox--key-takeaways\">\n<header class=\"textbox__header\">\n<p class=\"textbox__title\" style=\"text-align: justify\"><strong>Clinical Note:\u00a0 Cancer and Immune Evasion<\/strong><\/p>\n<\/header>\n<div class=\"textbox__content\">\n<p style=\"text-align: justify\">Cancerous cells or pathogens that evade NK cells can spread through tissue, blood, or lymph, potentially creating damage in multiple locations.\u00a0 Understanding how pathogens and cancers evade innate immunity is a major area of current research.<\/p>\n<\/div>\n<\/div>\n<h3 style=\"text-align: justify\"><\/h3>\n<div class=\"media-attributions clear\" prefix:cc=\"http:\/\/creativecommons.org\/ns#\" prefix:dc=\"http:\/\/purl.org\/dc\/terms\/\"><h2>Media Attributions<\/h2><ul><li about=\"https:\/\/openstax.org\/books\/microbiology\/pages\/17-3-cellular-defenses\"><a rel=\"cc:attributionURL\" href=\"https:\/\/openstax.org\/books\/microbiology\/pages\/17-3-cellular-defenses\" property=\"dc:title\">Hemopoiesis<\/a>  &copy;  Nina Parker, Mark Schneegurt, Anh-Hue Thi Tu, Philip Lister, Brian M. Forster    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\">CC BY-NC-SA (Attribution NonCommercial ShareAlike)<\/a> license<\/li><li about=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/6\/69\/Hematopoiesis_%28human%29_diagram.png\"><a rel=\"cc:attributionURL\" href=\"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/6\/69\/Hematopoiesis_%28human%29_diagram.png\" property=\"dc:title\">Hematopoiesis_(human)_diagram cropped<\/a>  &copy;  A. Rad    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-sa\/4.0\/\">CC BY-SA (Attribution ShareAlike)<\/a> license<\/li><li about=\"https:\/\/commons.wikimedia.org\/wiki\/File:1905_Erythrocyte_Life_Cycle_-_svg_for_text_editing.svg#\/media\/File:1905_Erythrocyte_Life_Cycle.jpg\"><a rel=\"cc:attributionURL\" href=\"https:\/\/commons.wikimedia.org\/wiki\/File:1905_Erythrocyte_Life_Cycle_-_svg_for_text_editing.svg#\/media\/File:1905_Erythrocyte_Life_Cycle.jpg\" property=\"dc:title\">1905_Erythrocyte_Life_Cycle<\/a>  &copy;  Open Stax Anatomy and Physiology    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\">CC BY (Attribution)<\/a> license<\/li><li about=\"https:\/\/bio.libretexts.org\/Courses\/Manchester_Community_College_(MCC)\/BIOL_106%3A_Essentials_of_Anatomy_and_Physiology_(Anzalone)\/10%3A_The_Lymphatic_and_Immune_Systems\/10.04%3A_Innate_Immune_System\"><a rel=\"cc:attributionURL\" href=\"https:\/\/bio.libretexts.org\/Courses\/Manchester_Community_College_(MCC)\/BIOL_106%3A_Essentials_of_Anatomy_and_Physiology_(Anzalone)\/10%3A_The_Lymphatic_and_Immune_Systems\/10.04%3A_Innate_Immune_System\" property=\"dc:title\">WBC key<\/a>  &copy;  Leukocytes by Suzanne Wakim licensed CC BY 4.0 adapted from: White Blood Cells, CC BY 3.0, Blausen.com staff (2014). \"Medical gallery of Blausen Medical 2014\". WikiJournal of Medicine 1 (2). DOI:10.15347\/wjm\/2014.010. ISSN 2002-4436. Leukocyte Key by OpenStax College, CC BY 3.0 via Wikimedia Commons    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\">CC BY-NC-SA (Attribution NonCommercial ShareAlike)<\/a> license<\/li><li about=\"https:\/\/openstax.org\/books\/biology-2e\/pages\/42-1-innate-immune-response\"><a rel=\"cc:attributionURL\" href=\"https:\/\/openstax.org\/books\/biology-2e\/pages\/42-1-innate-immune-response\" property=\"dc:title\">Blood Cells<\/a>  &copy;  Mary Ann Clark, Matthew Douglas, Jung Choi    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\">CC BY-NC-SA (Attribution NonCommercial ShareAlike)<\/a> license<\/li><li about=\"https:\/\/doi.org\/10.3389\/fphar.2021.666732\"><a rel=\"cc:attributionURL\" href=\"https:\/\/doi.org\/10.3389\/fphar.2021.666732\" property=\"dc:title\">Neutrophil production<\/a>  &copy;  Gierlikowska, B., Gierlikowki, W., Stachura, A., Demkow, U.    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\">CC BY (Attribution)<\/a> license<\/li><li about=\"https:\/\/commons.wikimedia.org\/wiki\/File:Cardiovascular_system_-_Neutrophil_granulocyte_2_--_Smart-Servier.png\"><a rel=\"cc:attributionURL\" href=\"https:\/\/commons.wikimedia.org\/wiki\/File:Cardiovascular_system_-_Neutrophil_granulocyte_2_--_Smart-Servier.png\" property=\"dc:title\">Private: Neutrophil Granulocyte<\/a>  &copy;  Laboratoires Servier    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-sa\/4.0\/\">CC BY-SA (Attribution ShareAlike)<\/a> license<\/li><li about=\"https:\/\/commons.wikimedia.org\/wiki\/File:NeutrophilerAktion.svg\"><a rel=\"cc:attributionURL\" href=\"https:\/\/commons.wikimedia.org\/wiki\/File:NeutrophilerAktion.svg\" property=\"dc:title\">Private: NeutrophilerAktion.svg<\/a>  &copy;  <a rel=\"dc:creator\" href=\"https:\/\/commons.wikimedia.org\/wiki\/User:DocMario\" property=\"cc:attributionName\">Mario Schubert<\/a>    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/publicdomain\/mark\/1.0\/\">Public Domain<\/a> license<\/li><li about=\"https:\/\/doi.org\/10.3389\/fphar.2021.666732\"><a rel=\"cc:attributionURL\" href=\"https:\/\/doi.org\/10.3389\/fphar.2021.666732\" property=\"dc:title\">Neutrophil activity<\/a>  &copy;  Gierlikowska, B., Gierlikowki, W., Stachura, A., Demkow, U.    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\">CC BY (Attribution)<\/a> license<\/li><li about=\"https:\/\/doi.org\/10.3390\/cells12151981\"><a rel=\"cc:attributionURL\" href=\"https:\/\/doi.org\/10.3390\/cells12151981\" property=\"dc:title\">neutrophils-12-01981-g003<\/a>  &copy;  Tsioumpekou, M., Krijgsman, D., Leusen, J. H. W., & Olofsen, P. A. (2023). The Role of Cytokines in Neutrophil Development, Tissue Homing, Function and Plasticity in Health and Disease. Cells, 12(15), 1981.    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by\/4.0\/\">CC BY (Attribution)<\/a> license<\/li><li about=\"https:\/\/openstax.org\/books\/microbiology\/pages\/17-3-cellular-defenses\"><a rel=\"cc:attributionURL\" href=\"https:\/\/openstax.org\/books\/microbiology\/pages\/17-3-cellular-defenses\" property=\"dc:title\">3 granulocytes<\/a>  &copy;  Nina Parker, Mark Schneegurt, Anh-Hue Thi Tu, Philip Lister, Brian M. Forster (Image Credit: \u201cneutrophil\u201d micrograph: modification of work by Ed Uthman)    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\">CC BY-NC-SA (Attribution NonCommercial ShareAlike)<\/a> license<\/li><li about=\"https:\/\/openstax.org\/books\/microbiology\/pages\/17-3-cellular-defenses\"><a rel=\"cc:attributionURL\" href=\"https:\/\/openstax.org\/books\/microbiology\/pages\/17-3-cellular-defenses\" property=\"dc:title\">Mast Cells<\/a>  &copy;  Nina Parker, Mark Schneegurt, Anh-Hue Thi Tu, Philip Lister, Brian M. Forster    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\">CC BY-NC-SA (Attribution NonCommercial ShareAlike)<\/a> license<\/li><li about=\"https:\/\/openstax.org\/books\/microbiology\/pages\/17-3-cellular-defenses\"><a rel=\"cc:attributionURL\" href=\"https:\/\/openstax.org\/books\/microbiology\/pages\/17-3-cellular-defenses\" property=\"dc:title\">monocytes<\/a>  &copy;  Nina Parker, Mark Schneegurt, Anh-Hue Thi Tu, Philip Lister, Brian M. Forster (Image credit left: modification of work by Armed Forces Institute of Pathology; credit right: modification of work by Centers for Disease Control and Prevention)    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\">CC BY-NC-SA (Attribution NonCommercial ShareAlike)<\/a> license<\/li><li about=\"https:\/\/commons.wikimedia.org\/wiki\/File:Phagocytosis2.png#\/media\/File:Phagocytosis2.png\"><a rel=\"cc:attributionURL\" href=\"https:\/\/commons.wikimedia.org\/wiki\/File:Phagocytosis2.png#\/media\/File:Phagocytosis2.png\" property=\"dc:title\">Private: phagocytosis<\/a>  &copy;  By GrahamColm at English Wikipedia, CC BY-SA 3.0, https:\/\/commons.wikimedia.org\/w\/index.php?curid=6811745    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-sa\/4.0\/\">CC BY-SA (Attribution ShareAlike)<\/a> license<\/li><li about=\"https:\/\/openstax.org\/books\/biology-2e\/pages\/4-4-the-endomembrane-system-and-proteins\"><a rel=\"cc:attributionURL\" href=\"https:\/\/openstax.org\/books\/biology-2e\/pages\/4-4-the-endomembrane-system-and-proteins\" property=\"dc:title\">Macrophage Phagocytosis<\/a>  &copy;  Mary Ann Clark, Matthew Douglas, Jung Choi    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\">CC BY-NC-SA (Attribution NonCommercial ShareAlike)<\/a> license<\/li><li about=\"https:\/\/openstax.org\/books\/microbiology\/pages\/17-3-cellular-defenses\"><a rel=\"cc:attributionURL\" href=\"https:\/\/openstax.org\/books\/microbiology\/pages\/17-3-cellular-defenses\" property=\"dc:title\">NK cell perforin granzyme<\/a>  &copy;  Nina Parker, Mark Schneegurt, Anh-Hue Thi Tu, Philip Lister, Brian M. Forster     <\/li><li about=\"https:\/\/openstax.org\/books\/microbiology\/pages\/17-3-cellular-defenses\"><a rel=\"cc:attributionURL\" href=\"https:\/\/openstax.org\/books\/microbiology\/pages\/17-3-cellular-defenses\" property=\"dc:title\">perforin granzyme<\/a>  &copy;  Nina Parker, Mark Schneegurt, Anh-Hue Thi Tu, Philip Lister, Brian M. Forster (Image credit: modification of work by Rolstad B)    is licensed under a  <a rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\">CC BY-NC-SA (Attribution NonCommercial ShareAlike)<\/a> license<\/li><\/ul><\/div>","protected":false},"author":1370,"menu_order":3,"template":"","meta":{"pb_show_title":"on","pb_short_title":"","pb_subtitle":"","pb_authors":["zoe-soon"],"pb_section_license":"cc-by-nc-sa"},"chapter-type":[],"contributor":[60],"license":[57],"class_list":["post-6534","chapter","type-chapter","status-web-only","hentry","contributor-zoe-soon","license-cc-by-nc-sa"],"part":25,"_links":{"self":[{"href":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-json\/pressbooks\/v2\/chapters\/6534","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-json\/wp\/v2\/users\/1370"}],"version-history":[{"count":18,"href":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-json\/pressbooks\/v2\/chapters\/6534\/revisions"}],"predecessor-version":[{"id":6786,"href":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-json\/pressbooks\/v2\/chapters\/6534\/revisions\/6786"}],"part":[{"href":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-json\/pressbooks\/v2\/parts\/25"}],"metadata":[{"href":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-json\/pressbooks\/v2\/chapters\/6534\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-json\/wp\/v2\/media?parent=6534"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-json\/pressbooks\/v2\/chapter-type?post=6534"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-json\/wp\/v2\/contributor?post=6534"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/pressbooks.bccampus.ca\/pathophysiology\/wp-json\/wp\/v2\/license?post=6534"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}