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Clot removal
protected by the clot, the endothelium and surrounding tunic are restored by new tissue, and the clot is then removed, mainly dissolved by the proteolytic enzyme plasmin, which is formed continuously through the local action of plasminogen activators from the endothelium on plasminogen from plasma.
Aspirin
an anti-inflammatory agent that contains an inhibitory effect on platelet function and blood coagulation because they block the local prostaglandin synthesis.
Bleeding disorders
it results from abnormally slow blood clotting.
Glycoprotein Ib deficiency
a disease directly related to a defect in the platelets that is a rare autosomal recessive, involving a factor on the platelet surface needed to bind subendothelial collagen.
Blood
a specialized connective tissue consisting of cells and fluid extracellular material called plasma.
Serum
a pale yellow liquid that contains growth factors and other proteins released from platelets during clot formation, which confer biological properties very different from those of plasma.
Hematocrit
erythrocytes that comprise the sedimented material, and their volume, normally about 44% of the total blood volume in healthy adults.
Buffy coat
a thin gray-white layer between the plasma and the hematocrit, about 1% of the volume, consists of leukocytes and platelets, both less dense than erythrocytes.
Plasma
an aqueous solution, pH 7.4, containing substances of low or high molecular weight that make up 7% of its volume.
Electrolytes
it includes nutrients, respiratory gases, nitrogenous waste products, hormones and inorganic ions.
Albumin
it is the most abundant plasma protein; it is made in the liver and serves primarily to maintain the osmotic pressure of the blood.
Globulins
known as a and b globulins; it is made by the liver and other cells, includes transferrin and other transport factors; fibronectin; prothrombin and other coagulation factors.
Immunoglobulins
known as antibodies or y-globulins; secreted by plasma cells in many locations.
Fibrinogen
the largest plasma protein; made in the liver which during clotting, polymerizes insoluble, cross-linked fibers of fibrin that block blood loss from small vessels.
Complement proteins
comprises a defensive system important in inflammation and destruction of microorganisms.
Water
92% of plasma; it is the solvent in which formed elements are suspended and proteins and solutes are dissolved.
Plasma proteins
7% of plasma; all proteins serve to buffer against pH changes.
Albumin plasma
58% of plasma proteins; exerts osmotic force to retain fluid within the microvasculature; contributes to blood’s viscosity; binds and transports some fatty acids, electrolytes, hormones and drugs.
a-Globulins; b-Globulins
transports lipids and some metal ions; transports iron ions and lipids in bloodstream.
y-Globulins
are antibodies with various immune functions.
Erythrocytes
are terminally differentiated structures lacking nuclei and completely filled with the O2-carrying protein hemoglobin.
Anemia
is the condition of having a concentration of erythrocytes below the normal range.
Sickle cell anemia
is caused by a homozygous mutation causing an amino acid substitution in hemoglobin, which renders the mature RBCs deformed and slightly rigid and can lead to capillary blockage.
Leukocytes
it leaves the blood and migrate to the tissue where they become functional and perform various activities related to immunity.
Granulocytes
possesses two major types of abundant cytoplasmic granules: lysosomes (often called azurophilic granules in blood cells) and specific granules that bind neutral, basic, or acidic stains.
Agranulocytes
it lacks specific granules but do contain some azurophilic granules.
Neutrophils
constitute about 50%-70% of circulating leukocytes, a figure that includes slightly immature forms released to the circulation.
Diapedesis
the process which the leukocytes send extensions through the openings between the endothelial cells, migrate out of the venules into the surrounding tissue space, and head directly for the site of injury or invasion.
Azurophilic primary granules
large, dense vesicles with a major role in both killing and degrading engulfed microorganisms.
Myeloperoxidase
generates hypochlorite and other agent toxic to bacteria.
Lysozyme
it degrades components of bacterial cell walls.
Defensins
small cysteine-rich proteins that bind and disrupt the cell membranes of many types of bacteria and other microorganisms.
Specific secondary granules
smaller and less dense, stain faintly pink, and have diverse functions, including secretion of various ECM-degrading enzymes.
Pus
a viscous, usually yellow collection of fluid from apoptotic neutrophils, bacteria, semi-digested material, and tissue fluid.
Eosinophils
far less numerous than neutrophils, constituting only 1%-4% of leukocytes; particularly abundant in connective tissue of intestinal lining and at sites of chronic inflammation.
Basophils
12-15 μm in diameter but make up less than 1% of circulating leukocytes and are therefore difficult to find in normal blood smears.
Leukotrienes
lipid-derived proinflammatory factors.
Lymphocytes
the most abundant type of agranulocytes in normal blood smears, it constitutes a family of leukocytes with spherical nuclei.
Lymphomas
are a group of disorders involving neoplastic proliferation of lymphocytes or the failure of these cells to undergo apoptosis.
Monocytes
precursor cells of macrophages, osteoclasts, microglia, and other cells of the mononuclear phagocyte system in connective tissue of nearly all organs.
Acute inflammation
usually short-lived as macrophages and undergo apoptosis or leave the site, but chronic inflammation usually involves the continued recruitment of monocytes.
Platelets
are very small nonnucleated, membranebound cell fragments only 2-4 μm in diameter.
Megakaryocytes
a giant polyploid bone marrow cells.
Alpha granules
are larger (300-500 nm in diameter) and contain platelet-derived growth factor (PDGF), platelet factor 4, and several other platelet-specific proteins.