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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1991-8-30
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pubmed:abstractText |
Incubation of peritoneal macrophages in vitro before fixation increased their ability to present exogenous peptides to 3A9 T hybridoma cells. The enhanced level of presentation correlated with a greatly increased, peptide-specific adhesion of 3A9 cells to the macrophages, whereas peptide-independent adhesion was minimal and essentially unaltered. 3A9 cells exhibited rapid peptide-specific adhesion (plateau by 5 to 10 min) and deadhesion (complete reversal by 5 min). Peptide-specific adhesion was blocked by anti-I-Ak and anti-LFA-1. Interaction of T cell receptors and CD-4 with peptide-I-Ak complexes appeared to provide little direct contribution to the avidity of T cell-macrophage adhesion, but activated a LFA-1-mediated adhesion mechanism. In addition, anti-T cell receptor, anti-CD3, and anti-CD4 antibodies themselves activated LFA-1-dependent adhesion in the absence of peptide. Unlike the peptide-induced adhesion, this adhesion was similar for macrophages whether or not they were incubated in vitro before fixation. We conclude that the different macrophage populations supported LFA-1-mediated adhesion equally. Therefore, the enhancement of T cell stimulation observed after in vitro incubation of macrophages was due to increased peptide presentation and consequently increased triggering of LFA-1-mediated adhesion. Mechanisms may exist to regulate the effectiveness with which peptide-class II MHC complexes are displayed for T cell recognition.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD4,
http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Lymphocyte Function-Associated...,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Antigen, T-Cell
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
147
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
767-73
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1861073-Animals,
pubmed-meshheading:1861073-Antibody Specificity,
pubmed-meshheading:1861073-Antigens,
pubmed-meshheading:1861073-Antigens, CD4,
pubmed-meshheading:1861073-Cell Adhesion,
pubmed-meshheading:1861073-Dose-Response Relationship, Drug,
pubmed-meshheading:1861073-Gene Expression Regulation,
pubmed-meshheading:1861073-Histocompatibility Antigens,
pubmed-meshheading:1861073-Hybridomas,
pubmed-meshheading:1861073-Interleukin-2,
pubmed-meshheading:1861073-Lymphocyte Function-Associated Antigen-1,
pubmed-meshheading:1861073-Macrophages,
pubmed-meshheading:1861073-Mice,
pubmed-meshheading:1861073-Mice, Inbred CBA,
pubmed-meshheading:1861073-Receptors, Antigen, T-Cell
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pubmed:year |
1991
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pubmed:articleTitle |
Modulation of antigen presentation and peptide-MHC-specific, LFA-1-dependent T cell-macrophage adhesion.
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pubmed:affiliation |
Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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