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Untitled - D Ank Unlimited

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clotting system 180 coated vesicle<br />

Most clostridial diseases do not induce protective immunity<br />

because the amount of toxin required to produce disease<br />

is less than that necessary to induce an immunologic<br />

response. Even though systemic immunity does not follow<br />

an episode of the disease, tetanus toxoid can induce immunity<br />

that may last for 5 years. Tetanus immunoglobulin is<br />

also valuable for passive immunization in suspected cases.<br />

Antibotulinum toxin antibody is available for laboratory<br />

workers. Intravenous administration of γ globulin containing<br />

high titers of antibody to C. difficile toxin has been<br />

useful in the therapy of patients with relapsing C. difficile<br />

diarrhea.<br />

clotting system<br />

A mixture of cells, their fragments, zymogens, zymogen<br />

activation products and naturally occurring inhibitors,<br />

adhesive and structural proteins, phospholipids, lipids,<br />

cyclic and noncyclic nucleotides, hormones, and inorganic<br />

cations, all of which normally maintain blood flow.<br />

With disruption of the monocellular layer of endothelial<br />

cells lining a vessel wall, the subendothelial layer is<br />

exposed, bleeding occurs, and a cascade of events is<br />

initiated that leads to clot formation. These homeostatic<br />

reactions lead to formation of the primary platelet plug<br />

followed by a clot that mainly contains crosslinked<br />

fibrin (secondary hemostasis). After the blood vessel is<br />

repaired, the clot is dissolved by fibrinolysis. Refer also<br />

to coagulation system.<br />

cluster of differentiation (CD)<br />

The designation of antigens on the surfaces of leukocytes by<br />

their reactions with clusters of monoclonal antibodies. The<br />

antigens are designated as clusters of differentiation (CDs).<br />

clusterin (serum protein SP-40,40)<br />

A complement regulatory protein that inhibits membrane<br />

attack complex (MAC) formation by blocking the fluid<br />

phase of the MAC. Its substrate is C5b67.<br />

clustering<br />

Monomeric antigens, monovalent lectins, and monovalent<br />

antibody to mIg, and other membrane components<br />

neither cap on the cell surface nor produce large clusters.<br />

Multivalent ligand binding is necessary for clustering and<br />

for capping. Clustering, unlike capping, is a passive redistribution<br />

process. Spotting or patching does not require a cell<br />

to be living or metabolically active. Clustering is affected<br />

by the factors that control phenomena occurring in a threedimensional<br />

fluid aqueous phase and also by physicochemical<br />

properties of plasma membranes. The outcome of<br />

cluster formation is influenced by physiological interactions<br />

between the membrane proteins.<br />

CMI<br />

Abbreviation for cell-mediated immunity.<br />

CMK-BRL-1<br />

Chemokine β receptor-like 1 is a member of the G proteincoupled<br />

receptor family, the chemokine receptor branch<br />

of the rhodopsin family. It is expressed on neutrophils and<br />

monocytes but not on eosinophils. It may be found in brain,<br />

placenta, lung, liver, and pancreas.<br />

CML<br />

Abbreviation for chronic myelogenous leukemia.<br />

CNS prophylaxis<br />

The intrathecal administration of chemotherapeutic<br />

agents or localized CNS and brain irradiation to block<br />

tumor cell invasion.<br />

Cμ<br />

An immunoglobulin μ chain constant region. The corresponding<br />

exon is designated Cμ.<br />

c-myb<br />

A protooncogene that codes for the 75- to 89-kDa phosphoprotein<br />

designated c-Myb in the nucleus, which immature<br />

hematopoietic cells express during differentiation. When<br />

casein kinase II phosphorylates Myb at an N terminal<br />

site, the union of Myb to DNA and continued activation<br />

are blocked. This phosphorylation site is deleted during<br />

oncogenic transformation, which permits Myb to combine<br />

with DNA.<br />

c-myb gene<br />

A gene that encodes formation of a DNA-binding protein<br />

that acts during early growth and differentiation stages<br />

of normal cells. A c-myb gene is expressed mainly in<br />

hematopoietic cells, especially bone marrow hematopoietic<br />

precursor cells, but it is greatest in the normal murine thymus.<br />

The highest c-myb expression is in the double-negative<br />

thymocyte subpopulation.<br />

c-myc gene<br />

Refer to myc.<br />

coagglutination<br />

The interaction of immunoglobulin (IgG) antibodies with<br />

the surfaces of protein-A-containing Staphylococcus aureus<br />

microorganisms through their Fc regions, followed by interaction<br />

of the Fab regions of these same antibody molecules<br />

with surface antigens of bacteria for which they are specific.<br />

Thus, when the appropriate reagents are all present, coagglutination<br />

will take place in which the Y-shaped antibody<br />

molecule will serve as a bridge between staphylococci and<br />

the coagglutinated microorganism for which it is specific.<br />

coagulation, invertebrate<br />

A mechanism in higher invertebrates in which lipopolysaccharide<br />

combines with a pattern recognition receptor to<br />

activate three proteases of a zymogen cascade that leads<br />

to crosslinking of coagulogen protein in hemolymph to<br />

produce a clot. This halts loss of body fluids and isolates<br />

pathogenic microorganisms that may have gained access to<br />

the injured site. It may occur after V(D)J recombination and<br />

non-homologous end joining repair.<br />

coagulation system<br />

A cascade of interactions among 12 proteins in blood<br />

serum that culminates in the generation of fibrin, which<br />

prevents bleeding from blood vessels whose integrity has<br />

been interrupted.<br />

coated pit<br />

A depression in a cell membrane coated with clathrin.<br />

Hormones such as insulin and epidermal growth factor may<br />

bind to their receptors in coated pits or migrate toward the<br />

pits following binding of the ligand at another site. After<br />

the aggregation of complexes of receptor and ligand in the<br />

coated pits, they invaginate and bud off as coated vesicles<br />

containing the receptor–ligand complexes. These structures,<br />

called receptosomes, migrate into cells by endocytosis.<br />

Following association with GERL structures, they fuse with<br />

lysosomes where receptors and ligands are degraded.<br />

coated vesicle<br />

Vesicles in the cytoplasm usually encircled by a coat of<br />

protein-containing clathrin molecules. Coated vesicles<br />

originate from coated pits and are important for protein<br />

secretion and receptor-mediated endocytosis. Coated

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