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macrophage colony-stimulating factor (M-CSF) 474 macrophage inflammatory protein 1α (MIP-1α)<br />

Human macrophage colony-stimulating factor (M-CSF).<br />

Resolution = 2.5 Å.<br />

Cys<br />

96<br />

Cys<br />

54<br />

COOH<br />

Cys<br />

121<br />

Cys<br />

88<br />

NH 2<br />

Three-dimensional structure of dimeric human recombinant macrophage<br />

colony-stimulating factor (M-CSF; α form, soluble). Resolution = 2.5 Å.<br />

macrophage colony-stimulating factor (M-CSF)<br />

Facilitates growth, differentiation, and survival and serves as<br />

an activating mechanism for macrophages and their precursors.<br />

It is derived from numerous sources such as lymphocytes,<br />

monocytes, endothelial cells, fibroblasts, epithelial<br />

cells, osteoblasts, and myoblasts. X-ray crystallography of<br />

recombinant CSF reveals a structure in which four α helices<br />

are placed end to end in two bundles. Human and mouse<br />

M-CSF share 82% homology in the N terminal 227 amino<br />

acids of the mature sequence; there is only 47% homology<br />

in the remainder of the molecular structure. M-CSF derived<br />

from humans and from mice was formerly called colonystimulating<br />

factor 1 (CSF-1). M-CSF is homodimeric and is<br />

secreted as an 80- to 100-kDa glycoprotein or a 130- to 160kDa<br />

chondroitin sulfate proteoglycan, or it is expressed as<br />

a biologically active, cell surface membrane, 68- to 86-kDa<br />

glycoprotein. Both forms are present in the blood circulation.<br />

The cell surface participates in local regulation, but the<br />

proteoglycan form may be sequestered to specific sites. The<br />

CSF-1 receptor mediates the effects of CSF-1. This receptor<br />

is expressed on osteoclasts and tissue macrophages, their<br />

precursors, embryonic cells, decidual cells, and trophoblasts.<br />

Circulating CSF-1 is postulated to be derived from endothelial<br />

cells that line small blood vessels.<br />

Macrophage cytophilic antibody.<br />

macrophage cytophilic antibody<br />

A cytophilic antibody that becomes anchored to the Fc<br />

receptors on macrophage surfaces. It can be demonstrated<br />

by the immunocytoadherence test.<br />

macrophage functional assays<br />

Tests of macrophage function. (1) Chemotaxis, in which<br />

macrophages are placed in one end of a Boyden chamber<br />

and a chemoattractant is added to the other end; macrophage<br />

migration toward the chemoattractant is assayed.<br />

(2) Lysis, in which macrophages acting against radiolabeled<br />

tumor cells or bacterial cells in suspension can be measured<br />

after suitable incubation by measuring the radioactivity of<br />

the supernatant. (3) Phagocytosis, in which the radioactivity<br />

of macrophages that have ingested a radiolabeled target can<br />

be assayed.<br />

macrophage immunity<br />

Cellular immunity.<br />

macrophage inflammatory peptide 2 (MIP-2)<br />

Interleukin-8 (IL8) type II receptor competitor and<br />

chemoattractant also involved in hematopoietic colony<br />

formation as a costimulator. It also degranulates murine<br />

neutrophils. The inflammatory activities of MIP-2 are very<br />

similar to those of IL8.<br />

macrophage inflammatory protein 1 (MIP-1)<br />

A chemokine of the β (CC) family and endogenous feverinducing<br />

substance that binds heparin and is resistant to<br />

cyclooxygenase inhibition. Macrophages stimulated by

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