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Blood
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White blood cells Platelets Red blood cells Artery Blood erythrocytes leukocytes thrombocytes
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Deliver O2 Remove metabolic wastes Maintain temperature, pH, and fluid volume Protection from blood loss- platelets Prevent infection- antibodies and WBC Transport hormones Function Blood
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Plasma- 55% Formed elements- 45% Blood Buffy coat- <1%
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90% Water 8% Solutes: Proteins Albumin (60 %) Alpha and Beta Globulins Gamma Globulins fibrinogens Gas Electrolytes Blood Plasma Components-55%
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Organic Nutrients Carbohydrates Amino Acids Lipids Vitamins Hormones Metabolic waste CO2 Urea Blood Plasma Components
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Erythrocytes (red blood cells) Leukocytes (white blood cells) Platelets (thrombocytes) Formed Elements of the Blood-45%
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Erythrocytes
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Erythrocyte 7.5 m in dia Anucleate- so can't reproduce; however, repro in red bone marrow Hematopoiesis- production of RBC Function- transport respiratory gases Hemoglobin- quaternary structure, 2 chains and 2 chains Lack mitochondria. Why? 1 RBC contains 280 million hemoglobin molecules Men- 5 million cells/mm3 Women- 4.5 million cells/mm3 Life span 100-120 days and then destroyed in spleen (RBC graveyard)
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Hemoglobin
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Figure 17.5 Stem cell Hemocytoblast Proerythro- blast Early erythroblast Late erythroblast Normoblast Phase 1 Ribosome synthesis Phase 2 Hemoglobin accumulation Phase 3 Ejection of nucleus Reticulo- cyte Erythro- cyte Committed cell Developmental pathway
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Sickle-cell anemia- HbS results from a change in just one of the 287 amino acids in the b chain in the globin molecule. Found in 1 out of 400 African Americans. Abnormal hemoglobin crystalizes when O2 content of blood is low, causing RBCs to become sickle-shaped. Homozygous for sickle-cell is deadly, but in malaria infested countries, the heterozygous condition is beneficial. RBC Diseases
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Granulocytes Neutrophils- 40-70% Eosinophils- 1-4% Basophils- <1% Agranulocytes Monocytes- 4-8% Lymphocytes- 20-45% Never let monkeys eat bananas 4,000-11,000 cells/mm 3 Types of Leukocytes
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Basophil Eosinophil Neutrophil Lymphocyte Monocyte platelet
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neutrophil RBC eosinophil monocyte lymphocyte basophil monocyte
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ID WBC’s
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Leukocyte Squeezing Through Capillary Wall Diapedesis
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Leukopenia Abnormally low WBC count—drug induced L eukemias C ancerous conditions involving WBCs Named according to the abnormal WBC clone involved M ononucleosis h ighly contagious viral disease caused by Epstein-Barr virus; excessive # of agranulocytes; fatigue, sore throat, recover in a few weeks WBC Diseases
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Platelets Small fragments of megakaryocytes Formation is regulated by thrombopoietin Blue-staining outer region, purple granules Granules contain serotonin, Ca2+, enzymes, ADP, and platelet- derived growth factor (PDGF)
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Figure 17.12 Stem cell Developmental pathway Hemocyto- blast Megakaryoblast Promegakaryocyte MegakaryocytePlatelets
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Hemostasis- stoppage of bleeding Tissue Damage Platelet Plug Clotting Factors Platelets: 250,000-500,000 cells/mm3
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Hemostasis: 4. Coagulation Vessel injury 2. Vascular spasm 3. Platelet plug formation
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Hemostasis ( + feedback) Prothrombin Thrombin Fibrinogen Fibrin Clotting Factors thromboplastin Traps RBC & platelets Platelets release thromboplastin
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Blood Clot Fibrin thread Platelet RBC
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Disorders of Hemostasis Thromboembolytic disorders: undesirable clot formation Bleeding disorders: abnormalities that prevent normal clot formation
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Thromboembolytic Conditions Thrombus: clot that develops and persists in an unbroken blood vessel May block circulation, leading to tissue death Embolus: a thrombus freely floating in the blood stream Pulmonary emboli impair the ability of the body to obtain oxygen Cerebral emboli can cause strokes
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Type A Type B Type AB Type O Blood Types
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Blood type is based on the presence of 2 major antigens in RBC membranes-- A and B Blood typeAntigenAntibody A A anti-B B B anti-A A & B AB no anti body Neither A or B Oanti-A and anti-B Antigen- protein on the surface of a RBC membrane Antibody- proteins made by lymphocytes in plasma which are made in response to the presence of antigens. They attack foreign antigens, which result in clumping (agglutination) Blood Typing
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Type A ABO Blood Types Produces anti-B antibodies b b b b b b b b
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Type B ABO Blood Types Produces anti-A antibodies a a a a a a a a a a
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ABO Blood Types Produces neither anti-A nor anti-B antibodies
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Type O ABO Blood Types Produces both anti-A and anti-B antibodies a a a a a a a a a a b b b b b b b b
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Rh Factor and Pregnancy RH- indicates no protein RH+ indicates protein
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Rh Factor and Pregnancy Rh+ mother w/Rh- baby– no problem Rh- mother w/Rh+ baby– problem Rh- mother w/Rh- father– no problem Rh- mother w/Rh- baby-- no problem RhoGAM used @ 28 weeks
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Type AB- universal recipients Type O- universal donor Rh factor: Rh+ 85% dominant in pop Rh- 15% recessive Blood TypeClumpingAntibody Aantigen Aanti-A serumantibody anti-b Bantigen Banti-B serumantibody anti-a ABantigen A & Banti A & B serum - Oneither A or Bno clumping w/ either anti A or B anti-a, anti-b
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Figure 17.16 Serum Anti-A RBCs Anti-B Type AB (contains agglutinogens A and B; agglutinates with both sera) Blood being tested Type A (contains agglutinogen A; agglutinates with anti-A) Type B (contains agglutinogen B; agglutinates with anti-B) Type O (contains no agglutinogens; does not agglutinate with either serum)
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Blood Type & RhHow Many Have ItFrequency O Rh Positive1 person in 3 37.4% O Rh Negative1 person in 15 6.6% A Rh Positive1 person in 3 35.7% A Rh Negative1 person in 16 6.3% B Rh Positive1 person in 12 8.5% B Rh Negative1 person in 67 1.5% AB Rh Positive1 person in 29 3.4% AB Rh Negative1 person in 167.6%
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ABO Blood Types PhenotypeGenotype Oi i AI A I A or I A i BI B I B or I B i ABI A I B
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Type A and Type B cross IAIA IAIA IBIB i IAi IAIB IAi Punnett square
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