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24 Cards in this Set

  • Front
  • Back

blood composition

cellular


-erythrocytes (hematocrit: males 44%, females 40%, infants 50%)


-leukocytes


-granulocytes


-lymphocytes


-platelets



plasma


-clotting factors


-immunoglobulins


-albumin

RBC size and features

-small (7-8 microns in diameter; 0.8 microns thick at center, 1.6 microns thick at edge)


-biconcave disk (center is central palet)


-stains acidophilic


-anucleated


-same diameter as leukocyte nucleus


-too small : microcytic; too big: macrocytic


-variation in size = anisocytosis

reticulocytes

-young RBC


-anucleated, but slightly basophilic due to remaining mRNA being translated to hemoglobin


-slightly larger


-normally about 1% of the RBC population (increases during high RBC production)

function of RBCs

transport oxygen


-requires ability to bind oxygen tightly in the lung and release it at the tissues --> hemoglobin


-they are deformed (squished) through capillaries with smaller diameter to allow interaction of membranes and gas exchange to take place

Hgb

hemoglobin


-tetramer; two alpha and two beta chains


-each subunit binds a heme


-heme is a ferrous (Fe2+) binding ring structure, where the iron binds oxygen


-binds oxygen coopratively (relaxed state has high affinity, taut state has low affinity)


-affinity is altered by allosteric factors (e.g. temp, pH, 2,3-DPG, and pCO2); right shift during metabolic action

hemoglobin isoforms

-fetus makes HgbF (alpha1gamma2) (resistant to 2,3-DPG)


-embryo makes many isoforms


-adult makes mostly HgbA (alpha2beta2)


-small amount of HgbA2 in adults (alpha2delta2)


-mutations in the beta chain cause hemoglobinopathies such as HgbS (sickle), which alters the solubility --> pathology

RBC life span

-120 days


-100,000 circulations


-produces wear and tear --> macrophages will remove bad RBCs at capillaries

RBC specializations

-highly specialized membrane: cholesterol and phospholipids with transporters for glucose, ions, and bicarbonate


-specialized cytoskeleton: includes spectrin (supportive hexagonal meshwork just below membrane) which forms complexes with ankyrin and band4.1 which are anchored to integral membrane proteins band 3 and glycophorin C

RBC shape

-biconcave discs


-many potential (generally problematic) variations; e.g. elliptocytes, spherocytes, target cells, sickle cells, schistocytes


-variation in shape = poikilocytosis

anisocytosis

variation is size of RBCs

poikilocytosis

variation in shape of RBCs

routinely measured RBC parameters

-mean cell volume


-mean cell hemoglobin


-mean cell hemoglobin concentration


-red cell distribution width (measure of the distribution of mean cell volume)

2,3-DPG

2,3-diphosphoglycerate


-derived from glycolytic intermediates


-regulates the affinity of Hgb for O2


-shifts curve rightward, causing O2 to dissociate more rapidly


-made in response to increased hypoxia, anemia


-takes hours to days to increase amounts --> adaptive response

CO poisoning

-binds heme iron with higher affinity than O2


-shifts O2 dissociation curve left

methemoglobin

-iron in ferric state due to oxidative stress (drugs, toxins)


-cannot transport oxygen


-cyt B5 can reduce ferric iron back to ferrous with NADH

RBC handling of other ROS

-superoxide dismutase


-catalase


-glutathione (reduces hydrogen peroxide; uses NADPH from pentose pathway to recycle back)

hemoglobin A1C

-glycated Hb


-nonenzymatic


-proportional to blood glucose levels


-integrated measure of glucose control over prolonged period

the spleen role in RBC

-cell that has lost flexibility cannot squeeze between the specialized endothelial cells


-most of cell becomes bilirubin and goes to liver to be degraded

spectrin

-band 1


-gives the RBC its elasticity


-all around the membrane in a meshwork

ankyrin

anchors spectrin to membrane

band 3

-anion exchanger important for moving bicarbonate in and out


-integral membrane protein

band 4.1

-anchors spectrin to the membrane


-binds to integral membrane proteins

hereditary elliptocytosis

-due to spectrin mutations


-most patients are asymptomatic


-confers resistance to malaria

herediitary spherocytosis

-abnormal RBC shape


-shortened lifespan


-caused by mutations in: spectrin, ankyrin, or band 3