Term
|
Definition
| process by which mature blood cells develop from precursor cells |
|
|
Term
| vascular sinuses of bone marrow of certain bones esp. flat bones of skull, ribs, sternum, vertebrae, pelvis and some long bones |
|
Definition
| location of hematopoiesis in adult humans |
|
|
Term
|
Definition
|
|
Term
| blood islands in yolk sac |
|
Definition
| where hematopoiesis occurs in fetus 1st (during first trimester) |
|
|
Term
| liver and lymphatic tissue |
|
Definition
| where hematopoeisis occurs in second trimester of fetus |
|
|
Term
|
Definition
| where hematopoeisis occurs in last month of pregnancy |
|
|
Term
| restricted primarily to marrow cavities |
|
Definition
| where hematopoeisis occurs at birth |
|
|
Term
|
Definition
| what happens to number of active hematopoeisis sites with age |
|
|
Term
|
Definition
| type of marrow that is active, contains large number of RBC's |
|
|
Term
|
Definition
| inactive bone marrow, more in adults |
|
|
Term
|
Definition
| specialized CT in fluid extracellular matrix (plasma) |
|
|
Term
|
Definition
primary vehicle for transport of nutrients, O2, CO2, waste products, and hormones also functions in thermo regulation and homeostasis |
|
|
Term
|
Definition
| average volume of blood in adults |
|
|
Term
|
Definition
| liquid, extracellular matrix, ~55% of blood volume |
|
|
Term
|
Definition
| percentages of contents of blood(plasma?) ____% water, ____% electrolytes(Na, Ca, K, HCO3), ____% protein |
|
|
Term
|
Definition
| plasma without clotting factors |
|
|
Term
|
Definition
| albumin, globulins, fibrinogens |
|
|
Term
|
Definition
|
|
Term
|
Definition
| location of albumin synthesis |
|
|
Term
|
Definition
| function as transport protein for insoluble metabolites (ex: fatty acids) |
|
|
Term
|
Definition
| responsible for maintaining colloid osmotic pressure in blood vessels |
|
|
Term
|
Definition
| large molecules, used as transport proteins for lipids and heavy metal ions |
|
|
Term
|
Definition
| largest fraction of globulins, aka antibodies |
|
|
Term
|
Definition
| location of antibody/immunoglobulin synthesis |
|
|
Term
|
Definition
|
|
Term
|
Definition
| polymer of fibrinogen that forms during clotting |
|
|
Term
|
Definition
| location of fibrinogen synthesis |
|
|
Term
|
Definition
| cleaved to thrombin to catalyze fibrinogen to become fibrin |
|
|
Term
|
Definition
|
|
Term
|
Definition
| where formed elements are made via hematopoeisis |
|
|
Term
|
Definition
| volume of RBC's ___% in males, ____% in females |
|
|
Term
|
Definition
| same as hematocrit (+/- buffy coat depending on source) |
|
|
Term
|
Definition
| WBC's and platelets (1-2%) |
|
|
Term
|
Definition
| drop of blood smeared, air dried, stained with modified Romanovsky method (ex: Wright Giemsa) |
|
|
Term
|
Definition
|
|
Term
|
Definition
| diameter of a RBC, used as a reference to measure other things |
|
|
Term
|
Definition
| shape of RBC's that allows deformability and resiliency, also increase surface area for gas exchange |
|
|
Term
|
Definition
| primary structural protein in RBC's |
|
|
Term
|
Definition
| binds to inner surface of RBS plasma membrane |
|
|
Term
|
Definition
|
|
Term
|
Definition
| iron containing pigment involved in O2 and CO2 transport in RBC's |
|
|
Term
|
Definition
| Hemoglobin has __ # polypeptide chains with __ # Fe containing heme groups |
|
|
Term
|
Definition
| number of Hb molecules which transport O2 in RBC's |
|
|
Term
|
Definition
| results from decreased iron or blood loss |
|
|
Term
|
Definition
| disease resulting from a single AA substitution (Valine for Glutamic Acid) causing change in structure of Hb molecule |
|
|
Term
| position 6 of beta globulin chain |
|
Definition
| where AA is substituted in sickle cell anemia |
|
|
Term
|
Definition
| causes damage to endothelial cells of capillary walls due to rough edges, more fragile, easily damaged |
|
|
Term
| enucleated & organelles degenerate |
|
Definition
| what happens to RBC's b4 they are released into blood stream |
|
|
Term
|
Definition
| occasional basophillic nuclear remnants visible within cytoplasm of RBC's |
|
|
Term
|
Definition
| immature RBC's with stippled cytoplasm, still have some rRNA. Slightly larger than mature RBC's |
|
|
Term
|
Definition
|
|
Term
|
Definition
| trends in RBC production cell size ___, loss of nucleus and organelles, ____ in Hb |
|
|
Term
|
Definition
| increased number of reticulocytes in circulation associated with chronic blood loss, or hemlytic anemia (left shift) |
|
|
Term
|
Definition
| on a scale of RBC maturity with most mature to the right and least mature to the left, what happens with chronic blood loss/hemolytic anemia |
|
|
Term
|
Definition
| with iron deficient anemia, RBC's are small ( _____) and pale staining (_______) |
|
|
Term
|
Definition
| outer cell membrane with cytoplasm, Hb, and a few enzymes. No mitochondria |
|
|
Term
|
Definition
|
|
Term
|
Definition
| the only way RBC's can make energy |
|
|
Term
|
Definition
| remove senescent(old) RBC's from circulation |
|
|
Term
|
Definition
| another name for platelets |
|
|
Term
|
Definition
| small non-nucleated cells containing few organelles |
|
|
Term
|
Definition
| large polyploid cells in bone marrow with single multi-lobed nucleus |
|
|
Term
| megakaryocytes in bone marrow |
|
Definition
| where/what platelets come from |
|
|
Term
|
Definition
| pleated areas in the cytoplasm of megakaryocytes where platelets tear off. |
|
|
Term
|
Definition
| lifespan of human platelets |
|
|
Term
|
Definition
| function in blood clotting, form physical plugs at the site of vascular damage |
|
|
Term
|
Definition
result of cascade interaction between plasma proteins and coagulation factors
occurs only if endothelial lining of vessel is injured |
|
|
Term
|
Definition
| faster pathway of coagulation |
|
|
Term
|
Definition
| slower pathway of coagulation because it requires numerous clotting factors (von Willebrand's, factor VIII) and longer cascade reaction |
|
|
Term
|
Definition
| initiated by release of tissue thromboplastin as a result of tissue damage |
|
|
Term
|
Definition
| initiated by exposure of collagen |
|
|
Term
| Factor 12 -> factor 11 -> factor 9 -> (with help of factor 8) |
|
Definition
| intrinsic pathway of coagulation cascade to factor X |
|
|
Term
|
Definition
| extrinsic pathway of coagulation cascade to factor X |
|
|
Term
| 10-> 5 -> 2 (prothrombin to thrombin) -> 1 (fibrinogen) |
|
Definition
| coagulation cascadde from factor X onward |
|
|
Term
| when wall of blood vessel breaks, tissue injury results |
|
Definition
|
|
Term
|
Definition
| what platelets mechanically adhere to |
|
|
Term
|
Definition
| potent vasoconstrictor-constricts sm muscle in damaged vessel to minimize blood loss |
|
|
Term
|
Definition
| point where factor X is activated in coagulation cascade |
|
|
Term
|
Definition
| results in conversion of prothrombin to thrombin, which converts soluble fibrinogen to insoluble fibrin |
|
|
Term
|
Definition
| results in conversion of prothrombin to thrombin, which converts soluble fibrinogen to insoluble fibrin |
|
|
Term
|
Definition
| net that forms and traps platelets and RBC's |
|
|
Term
|
Definition
| exhaustion of fibrinogen and removal of thrombin from blood during conversion of fibrinogen to fibrin |
|
|
Term
| antithrombin 3 and heparin |
|
Definition
|
|
Term
| heart attack, stroke, disseminated intervascular coagulation (DIC) |
|
Definition
| result of inappropriate clot formation |
|
|
Term
|
Definition
| deficiency of clotting factors, so blood can't clot |
|
|
Term
|
Definition
| hemphilia is due to a defect in (intrinsic or extrinsic) pathway |
|
|
Term
|
Definition
| deficiency in clotting factor 8 |
|
|
Term
|
Definition
| deficiency in clotting factor 9 |
|
|
Term
|
Definition
| deficiency in clotting factor 11 |
|
|
Term
|
Definition
| deficiency in von willebrand's clotting factor |
|
|