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78 Cards in this Set

  • Front
  • Back
Blood
-specialzed CT
-composed of ECM called plasma plus formed elements (blood cells & platelets)
-involved in maintenance of acid/base levels, transport of CO2, O2, & nutrients, regulation of body temp, immune responses, & clotting
Blood Smear
-drop of blood spread across glass, dried, & stained with Giemsa
Functions of Blood
-Gas Transport
-Acid/Base Levels
-Immune Response
-Blood Clotting
-Body Temperature
-Osmotic Pressure
Hematocrit
-estimate of formed elements in relation to total blood volume
-obtained by centrifuging blood samples in calibrated tubes containing heparin
-top layer --> plasma
-RBC/serum interface --> buffy coat --> highest concentration of WBCs & platelets
-bottom layer = RBCs = 40-45% of total blood volume
Anemia
-reduction in number of RBCs
Polycythemia
-excess of RBCs
Serum
-blood form which clotting elements have bee removed by allowing blood to clot & then centrifuging
Plasma Proteins
-Albumin
-Alpha Globulins
-Beta Globulins
-Gamma-Globulins
-Fibrinogens
Albumin
-most abundant plasma protein
-synthesized in liver
-responsible for ~80% of total osmotic pressure of plasma
Alpha Globulin
-transport bilirubin & steroids
Beta Globulins
-transport iron & copper
Gamma Globulins
-immunoglobulins, or antibodies
-synthsized by plasma cells
Fibrinogens
-synthesized in liver
-act in blood clotting
-responsible for most of the viscosity of plasma
Blood Clotting
-follows a cascade
-initiated by the synthesis & release of thromboplastin by platelets
Blood Cell Formation
-produced & replaced in blood-forming organs (mostly bone marrow)
-have a limited lifespan
Complete Blood Count
-various cells types fit into narrow ranges
-differential leukocyte count can be performed
Differential Leukocyte Count
-Neutrophils (40-75%)
-Lymphocytes (20-50%)
-Monocytes (2-10%)
-Eosinophils (1-6%)
-Basophils (<1%)
Erythrocytes
-annucleate, acidophilic bi-concave disks
-shaped maintained by a cytoskeleton (includes spectrin) that is connected to the lipid bilayer by ankyrin
-essentially membranous bags of hemoglobin & carbonic anhydrase
RBC Antigens
-glycolipids & glycoproteins on surface of RBCs that serve as basis for blood typing
Erythrocytes sensitive to...
osmotic pressure
Hypertonic Environment
-RBCs shrink
-spike-like protuberances are visible (crenation)
Hypotonic Environment
-RBCs swell & burst (hemolysis)
Hemolysis
-can be caused by hypotonic solution or hemolytic agents (hemolysins)
Shape or Erythrocyte
-maintained by a set of specific membrane proteins
Spherocytosis
-ankyrin or spectrin mutations cause the cytoskeleton to separate from the plasmalemma, adopt spherical shape, & are osmotically fragile
-prone to rupture leading to anemia
Splenomegaly
-enlargement of the spleen
-often caused by spherocytosis
-enlarged spleen may be removed to prevent massive bleeding (hemorrhage) that could occur if spleen is damaged by trauma
Sickle Cell Anemia
-mutation in gene coding for beta subunit of hemoglobin
-causes protein to crystallize under low oxygen conditions
-causes cresent shaped RBCs which get caught in capillaries & cause localized anoxia & severe pain
-primarily affects people of African origin
-heterozygous condition appears to protect againt infection by the parasite that causes malaria
RBC Flexibility & Elasticity
-is a function of cell age
-produced in bone marrow & last about 120 days
-phagocytized by macrophages when worn out
-spleen filters out worn out cells & elastic, healthy RBCs return to circulation
Blood Groups
-a person does not have antigens against his or her own blood group
-AB --> universally receiver since that person does not have anitgens against A or B
Agglutination
-clumping of blood if exposed to certain antibodies
-Type A blood agglutinates if combined with antibodies to A antigen
Reticulocytes
-functional but immature form of the erythrocyte
-make up 1-2% of circulating blood population
-slightly larger in diameter than erythrocytes & contain a residual amount of rRNA
-urgent conditions may cause a rise in reticulocytes in bloodstream
Platelets
-derived from megakaryocytes (giant precursor cells in bone marrow)
-small annucleate & have 2 regions (granulomere & hyalomere)
Granulomere
-contains mitochondria, glycogen, lysosomes, & 2 types of membrane-bound granules (dense core & alpha granules)
-dense core granules contain serotonin (a vasoconstrictor), ADP, ATP, & calcium
-alpha granules contain clotting factors
Hyalomere
-rich in bundles of microtubules & microfilaments
-microtubles maintain inactive platelets' flattened shape
-glycocalyx provides necessary adhesive quality for aggregation of platelets
Platelets Play a Crucial Role in Blood Clotting (Coagulation)
-Maintenance of vascular integrity
-Release of blood clotting factors
-Clor retraction & dissolution
Megakaryocytes
-very large, nucleated cells
-cytoplasm is filled with spaces called demarcation zones which outline the future individual platelets
-located in bone marrow (always near venous sinuses)
-extend cytoplasmic processes through walla of venous sinuses which break off to become circulating platelets
Leukocytes
-WBCs --> only true nucleated blood cells
-spherical & have prominent basophilic nuclei
-leave blood vesels by process of dispedesis (except for basophils which remains in blood vessel)
-in CT, they act in cellular & humoral immune responses to foreign agents
Granular Leukocytes
-Neutrophils, eosinophils, basophils
-these cells have multilobulated nuclei & specific granules
between 10 -12 microns in diameter
-short lifespan (1-4 days)
Agranular Leukocytes
-Monocytes & lymphocytes
-these cells habe non-lobulated nuclei & non-specific granules
Neutrophils
-polymorphonuclear leukocytes (PMNs)
-represent 60-70% of WBCs
-active in phagocytosis of invaders
-acitve in acute inflammatory response (appear at site of injury as pain, redness, swelling, & heat)
-bind to glycoproteins on the plasmalemma of virally-invaded cells
-2-5 lobes in nucleus (commonly 3)
-has granules
-contain glycogen to survive in anaerobic conditions
-short lived (spend 4-8 hours in blood, then migrate into tissue where they live for 4-5 days)
-3% of women have Barr Bodies in their neutrophils
Neutrophils Specific Granules
-alkaline phosphatase, collagenase & elastase
-lactoferrin (bacteriostatic agent that bind Fe)
-phagocytins (proteins with bacteriocidal activity)
-lysozymes (enzymes kills bacteria by hydrolyzing components of their cell walls)
-the primary granules are lysosomes --> contain acid hydrolases, antibacterial agents, and myeloperoxidases
Phagocytosis
-neutrophils engulf foreign invaders in membreane-bound organelles
-sepcific granules fuse with and discharge contents into the phagosome
-proton pumps in phagosomes lowers pH (pH and oxidizing agents important in phagocytosis)
-pus is composed of neutrophils and bacterial & cellular debris
Margination of Neutrophils
-neutrophils have selectins on outer surface which bind to selectin receptros on endothelial cells of blood vessels allowing them to move along
Diapedisis
-in response to an inflammatory signals (from basophils & mast cells), neutrophils express integrins that bind to intergrin receptors which anchor the cells
-then migrate between endothelial cells to enter CT
Leukocytosis
-lack of neutrophil integrin CD18 results in poor wound healing because neutrophils can't migrate & instead accumulate in blood
Alpha-1 Antitrypsin
-inhibits proteases once a neutrophil migrates through into CT
-absence of this inhibitor --> chornically high levels of elastase (can lead to emphysema)
Eosinophils
-comprise 2-4% of WBCs
-have bi-lobed nuclei
-have coarse, acidophillic (cherry red) granules
Eosinophil (necessary for)
-phagocytosis of antigens/antibody complexes (in asthma, hay fever, & other allergies)
-destruction of invading parasites
-produce Histminase & Arylsulfatase
Coricosteroids (effect on eosinophils)
-produce a rapid drop in number of blood eosinophils --> reducing inflammation
Major Basic Protein
-comprise ~50% of the protein core of eosinophils specific granules
-function in parasite destruction
Neutrophils & Eosinophils (active)
-circulate in blood
-but active when they enter CT
Basophils
-make up less than 1% of total leukocyte count
-contain coarse, basophilic specific granules
-bi-lobed nucleus
-involved in immediate and delayed hypersensitivity reactions
-mediate anaphylaxis (acute reaction to drugs, food, or other foreign agents)
Development of sensitivity underlying anaphylactic reactions
REVIEW PG. 13 - LECTURE 10
Basophils Specific Granules
-Heparin --> powerful anticoagulant
-Histamine --> quickly & drastically increase the permeability of blood vessels, causes vasodilation, and causes smooth muscle contraction in bronchi
-Leukotrienes (SRS-A) --> for slow, sustained contractions of smooth muscle
Mast Cells vs. Basophils
-Mast cells found in CT; Basophils found in bloodstream
-Basophil is bi-lobed
-2 cell types arise from different stem cells in bone marrow
-Contents of their specific granules ate different
Lymphocytes
-make up 20-30% of WBCs
-smallest are ~size of RBCs (7-8 microns in diameter)
-mediate immunological responses
-T-Cells & B-Cells
T-Cells
-Thymus-differentiated
-most numerous lymphocytes
-important for cell-mediated immune reactions
-significant decrease in helper cells in HIV
B-Cells
-lymphocyte
-upon activation, migrate into CT & transform into plasma cells which manufacture antibodies responsible for humoral (antibody-mediated) immune reactions
-Some activated B-;ymphocytes give rise to memory B cells --> maintain and individuals immunity for an extended time
Monocytes
-3-8% of total leukocytes
-largest in size of peripheral blood elements (17 micron diameter)
-kidney-shaped nucleus
-migrate into tissue to become active macrophages
-macrophages are part of diffuse lymphoid nodules which are found in many organs --> lung (alveolar macrophages), liver (Kupffer cells), CT, spleen, bone marrow
-monocytes/macrophages play an essential role in recognition & presentation of antigens to lymphocytes during immune responses, and in antigen disposal
Anemias
-decrease in hemoglobin levels either due to a drop in RBC populations (due to hemorrhage) or to the inability to manufacture hemoglobin itself
-Vitamin B12 Deficiency is a common cause of anemia (necessary for heme biosynthesis)
Vitamin B12 Deficiency
-common cause of anemia
-necessary for heme biosynthesis
Thrombocytopenia
-low platelet count, probably due to autoimmunity against platelets
-this condition leads to easy bruising and an increased risk of stroke (bleeding from blood vessels in the brain)
Leukemias
-uncontrolled proliferation (cancer) of various leukocytes or their immature precursors
-these precursors eventually spill out into the peripheral blood
Erythroblastosis Fetalis
-Several different "Rh" antigens on erythrocytes from the basis for the Rh blood grouping
-EF is caused by an immune attack on erythrocytes of an Rh+ fetus by anti-Rh antibodies of the mother
-This occurs when an Rh- woman has had a previous Rh+ child and therefore has developed antibodies against the Rh series of RBC surface antigens
Hemophilia
-Hereditary absence of clotting factor VIII, passed by mothers to their male children
AIDS
-HIV virus infects & kills T-helper cells
-as a result, infected individuals eventually become incapable of mounting immune responses against bacterial or viral infections
SSRIs (Specific Serotonin Reuptake Inhibitors)
-Drugs used primarily as anit-depressants
-also used as illegal euphorics (Ecstasy)
-inhibit serotonin uptake by neurons and platelets
-depletion of serotonin from platelets causes decreased coagulation ability, which leads to increased clotting time
Neutrophils (Peripheral Blood Cell Granules)
-Alkaline Phosphatase
-Collagenase, Elastase
-Lactoferrin
-Phagocytins
-Lysozymes
Eosinophils (Peripheral Blood Cell Granules)
-Major Basic Proteins
-Hydrolytic Enzymes
-Histaminase
-Arylsulfatase
Basophils (Peripheral Blood Cell Granules)
-Heparin
-Histamine
-Leukotrienes (SRS-A)
-Serotonin
Platelets (Peripheral Blood Cell Granules)
-Serotonin
-ADP
-ATP
-Blood-Clotting Factors
Erythrocyte (Diameter/Population/Lifespan)
-7.5 microns
-5 million/mL (male)
-4.5 million/mL (female)
-120 days
Platelet (Diameter/Population/Lifespan)
-3 microns
-200,000-400,000/mL
-4-6 days
Monocyte (Diameter/Population/Lifespan)
-17 microns
-3-8% of leukocytes
-long lifespan
Lymphocyte (Diameter/Population/Lifespan)
-7-8 microns
-20-30% of leukocytes
-variable lifespan
Neutrophil (Diameter/Population/Lifespan)
-10-12 microns
-60-70% of leukocytes
-1-4 days
Eosinphils
-10-12 microns
-2-4% of leukocytes
-1-4 days
Basophils
-10-12 microns
-0-1% of leukocytes
-1-4 days