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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1981-3-24
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pubmed:abstractText |
Macrophage Fc receptors (FcR) are essential for antibody-dependent cellular cytotoxicity and for optimal phagocytosis of opsonized particulate antigens. Culture in the presence of conditioned medium from mixed leukocyte cultures (MLC-CM) resulted in a dose- and time-dependent increase (up to 10-fold) in FcR-dependent binding of 125I-labeled IgG1 to promyelocytic HL-60 cells, macrophage-like U-937 cells, and normal cultured human monocytes. FcR increase in HL-60 cells was blocked by cycloheximide (100 microM) and was accompanied by a slight decrease in binding affinity. Since cell volume did not change, the increase in FcR probably represents an increase in the surface density of FcR sites. MLC-CM prepared with or without serum were equally effective in augmenting FcR sites, whereas only serum-containing MLC-CM caused morphologic change of U-937 and HL-60 cells.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
126
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
666-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:6450248-Antibody Specificity,
pubmed-meshheading:6450248-Antibody-Dependent Cell Cytotoxicity,
pubmed-meshheading:6450248-Binding Sites,
pubmed-meshheading:6450248-Biological Transport,
pubmed-meshheading:6450248-Culture Media,
pubmed-meshheading:6450248-Humans,
pubmed-meshheading:6450248-Lymphocyte Culture Test, Mixed,
pubmed-meshheading:6450248-Macrophages,
pubmed-meshheading:6450248-Receptors, Fc,
pubmed-meshheading:6450248-Rosette Formation,
pubmed-meshheading:6450248-Time Factors
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pubmed:year |
1981
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pubmed:articleTitle |
MLC-conditioned media stimulate an increase in Fc receptors on human macrophages.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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