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-Transporting dissolved gases, nutrients, hormones, and metabolic wastes -Regulating the pH ion composition of interstitial fluids -Restricting fluid losses at injury sites -Defending against toxins and pathogens -Stabilizing body temperature |
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The fluid matrix of blood |
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The percentage of formed elements in a sample of centrifuged blood. |
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Albumins, globulins, and fibrinogen |
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White blood cells (leukocytes) |
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Neutrophils, eosinophils, basophils, lymphocytes, and monocytes |
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About 45% of blood volume, include platelets, white blood cells, and red blood cells |
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Red blood cells (erythrocytes) |
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Most abundant blood cell, essential for the transport of oxygen in the blood |
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Whole blood characteristics |
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-temperature is about 100.4 (38 C.) -5 times as viscous as water -slightly alkaline, pH 7.35-7.45 |
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About 60% of the plasma proteins, major contributors to the osmotic pressure of plasma, transports fatty acids, thyroid hormones, and steroid hormones Most abundant of the plasma proteins |
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About 35% of the plasma proteins antibodies (immunoglobulins) transport globulins |
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1)hormone-binding proteins, ex. thyroid-binding globulin and transthyretin which transport thyroid hormones, and transcortin which transports ACTH
2)Metalloproteins, which transfer metal ions, ex. transferrin, which transports iron
3)Apolipoproteins, which carry triglycerides and other lipids |
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4% of the plasma proteins Functions in clotting Molecules that form clots and produce long, insoluble strands of fibrin |
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Responsible for the cell's ability to transport oxygen and carbon dioxide 2 alpha chains and 2 beta chains |
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Process of producing formed elements by myeloid and lymphoid stem cells |
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Process of separating whole blood for clinical analysis |
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Fluid left after plasma clots |
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iron ions associate with oxygen |
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Low RBC count, Hb content reduced-carry less oxygen, all tissues affected. Weak, lethargic, confused. |
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Hemoglobin conversion and Recycling |
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Phagocytes break Hb into components: Globular proteins to amino acids Heme stripped of iron and converted to biliverdin (green) Biliverdin converted to bilirubin (orange-yellow) |
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RBCs breakdown in urine due to excess hemolysis in bloodstream, urine red/brown. |
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Erythropoieis occurs only in myeloid tissue (red bone marrow in adults) Stem cells mature to become RBCs |
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Hemocytoblasts (stem cells in myeloid tissue) divide to produce _______________. |
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Myeloid stem cells: become RBCs, some WBCs Lymphoid stem cells: become lymphocytes (WBCs) |
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Origins of plasma proteins |
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90% made in liver-albumin, fibrinogen, globulins Antibodies made by plasma cells-B cells Peptide hormones made by endocrine organs |
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Males: 14-18 g/dl Females: 12-16 g/dL |
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Complex quaternary structure (more than 1 polypeptide chain) Four globular protein subunits: 2 alpha & 2 beta chains Each with one molecule of heme (non-protein pigment complex) Each heme contains one iron ion Iron ions associate with oxygen- oxyhemoglobin (HbO2 ) Dissociate easily from oxygen- deoxyhemoglobin Heme whose iron not bound to oxygen |
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Hb releases oxygen Hb bind carbon dioxide and carries it to lungs – Forms carbaminohemoglobin |
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genetic disorder, point mutation in DNA. Changes amino acid inserted into Hb protein from polar to nonpolar |
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RBC formation and turnover |
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Exposed to severe mechanical stress, no repair 1% of circulating RBCs wear out per day About 3 million RBCs enter circulation each second (cool!) Macrophages of liver, spleen, and bone marrow monitor RBCs and engulf them before membranes rupture (hemolyze) |
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Bilirubin transported to liver by albumin Liver excretes bilirubin in bile Bile ducts are blocked, liver cannot absorb or excrete bilirubin Bilirubin diffuses into peripheral tissues Jaundice- yellow skin,sclera |
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Iron removed from heme leaving biliverdin Bound to transport proteins (transferrin) New RBCs use transferrin to make more Hb Excess transferrins removed in spleen, liver Storage proteins (ferritin and hemosiderin) |
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Myeloid stem cell Proerythroblast Erythroblasts Reticulocyte- no nucleus Mature RBC |
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low RBC production due to unavailability of vitamin B12 |
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Formed by liver & kidney when oxygen in peripheral tissues is low (hypoxia) due to disease or high altitude – Anemia, respiratory surfaces lung damaged, blood flow to kidneys decline Stimulate cell division of erythroblasts Speeds up maturation of RBCs |
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any substance that triggers an immune response |
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antigens on surface of RBCs |
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Defend against pathogens Remove toxins and wastes Attack abnormal cells |
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WBC circulation and movement |
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Definition
Most WBCs in connective tissue proper & lymphoid system organs Small numbers in blood 5000 to 10,000 per microliter |
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Characteristics of circulating WBCs |
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Definition
1. Migrate out of bloodstream – Margination- attaching to vessel wall – Diapedesis- squeeze through endothelial cells into surrounding tissue 2. Have amoeboid movement- gliding motion accomplished by flow of cytoplasm 3. Attracted to chemical stimuli- positive chemotaxis 4. Only some are phagocytic: – neutrophils, eosinophils, and monocytes (become macrophages) |
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Neutrophils (polymorphonuclear leukocytes, PMNs) |
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Definition
50–70% of circulating WBCs- most abundant WBC Cytoplasm granules with lysosomal enzymes & bactericides (H2O2 & superoxide- respiratory burst) Live 2-3 days (book ~10 hrs) Usually 1st on scene at injury or infection |
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Phagocytosis- engulf pathogens Digest pathogens Degranulation: defensins (peptides from lysosomes) attack pathogen membranes Release prostaglandins and leukotrienes- inflammation, coordinate response Form pus (yes, that zit on your “friend’s” face is a bunch of neutrophils!) |
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2–4% of circulating WBCs Attack large parasites Excrete toxic compounds Nitric oxide Cytotoxic enzymes Are sensitive to allergens Control inflammation with enzymes that counteract inflammatory effects of neutrophils and mast cells |
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Are less than 1% of circulating WBCs Small & rare Accumulate in damaged tissue Release histamine Dilates blood vessels Release heparin Prevents blood clotting |
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2–8% of circulating WBCs Large and spherical Enter peripheral tissues and become macrophages Engulf large particles and pathogens Secrete substances that attract immune system cells and fibrocytes to injured area |
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20–30% of circulating WBCs Larger than RBCs Migrate in and out of blood Mostly in connective tissues and lymphoid organs Adaptive (acquired) immune defense system- highly specific, memory |
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T cells Cell-mediated immunity- viruses, coordinate immune response (HIV attacks these cells, knocking down the whole defense system) Attack foreign cells directly
B cells Humoral immunity Differentiate into plasma cells- secrete antibodies Bacteria
3. Natural killer (NK) cells Part of innate immune system (not acquired) Detect and destroy abnormal tissue cells (virus & cancers) |
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Abnormally high WBC count (during infection) |
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All blood cells originate from hemocytoblasts which produce myeloid stem cells & lymphoid stem cells |
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Differentiate into progenitor cells- produce all WBCs except lymphocytes |
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Lymphopoiesis: production of lymphocytes |
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Cell fragments involved in human clotting system Nonmammalian vertebrates have thrombocytes (nucleated cells) Circulate for 9–12 days Removed by spleen 1/3 are reserved for emergencies |
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Abnormally low platelet count, bleeding along digestive tract, within skin |
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Abnormally high platelet count in response to infection, inflammation, cancer |
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Three Functions of Platelets: |
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Definition
1. Release important clotting chemicals 2. Temporarily patch damaged vessel walls- platelet plug 3. Actively contract tissue after clot formation-actin & myosin, contract and shrink clot |
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Platelet Production (thrombocytopoiesis) |
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Definition
Occurs in bone marrow Megakaryocytes- giant cells in bone marrow Shed cytoplasm in small membrane-enclosed packets- platelets Stimulated by – Thrombopoietin (TPO) – Interleukin-6 (IL-6) – Multi-CSF |
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A cut triggers vascular spasm that lasts 30 minutes 3 steps of the vascular phase 1. Endothelial cells contract expose basal lamina to bloodstream 2. Endothelial cells release: – chemical factors: ADP, tissue factor, and prostacyclin – local hormones: endothelins- stimulate smooth muscle contraction and cell division 3. Endothelial plasma membranes become “sticky”: – Seal off blood flow |
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Vascular phase,platelet phase, coagulation phase |
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Begins within 15 seconds after injury Platelet adhesion (attachment) To sticky endothelial surfaces To basal lamina To exposed collagen fibers Platelet aggregation (stick together) Forms platelet plug Closes small breaks Activated platelets release clotting compounds Adenosine diphosphate (ADP)-stimulates platelet aggregation & secretion Thromboxane A2 and serotonin- stimulate vascular spasms Clotting factors- blood clotting Platelet-derived growth factor (PDGF)- vessel repair Calcium ions- platelet aggregation |
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Coagulation phase-blood clotting, coagulation |
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Definition
Begins 30 seconds or more after the injury Cascade reactions: – Chain reactions of enzymes and proenzymes – Convert circulating fibrinogen into insoluble fibrin – Require clotting Factors (procoagulants)- proteins or ions in plasma required for normal clotting – Form three pathways |
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Factors that limit the growth of the platelet plug (must be restricted to injury site) |
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Prostacyclin- released by endothelial cells, inhibits platelet aggregation Inhibitory compounds- released by other WBCs Circulating enzymes- break down ADP Negative (inhibitory) feedback: from serotonin Development of blood clot- isolates area |
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Extrinsic pathway-Begins in the vessel wall outside bloodstream Intrinsic pathway-Begins with circulating proenzymes within bloodstream Common pathway- Where intrinsic and extrinsic pathways converge |
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Forms enzyme prothrombinase Converts prothrombin to thrombin Thrombin converts fibrinogen to fibrin Positive Feedback:Thrombin stimulates both TF & PF-3, activating both extrinsic & intrinsic pathways |
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slow process of dissolving clot Thrombin and tissue plasminogen activator (t-PA) activate plasminogen Plasminogen produces plasmin- digests fibrin strands |
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low oxygen levels in tissues |
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