Source:http://linkedlifedata.com/resource/pubmed/id/11747372
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2001-12-18
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pubmed:abstractText |
Human retinal pigment epithelial (RPE) cells are capable of presenting bacterial superantigens (SAg) to T cells in vitro by ligation of MHC class II molecules on RPE cells with the T cell receptor. The purpose of this study was to evaluate the involvement of adhesion molecules in presentation of SAg. Cultured human fetal and adult RPE cells were treated with interferon-gamma (IFN-gamma, 500 U ml(-1) for 72 hr) and afterwards pulsed with the SAg staphylococcal enterotoxin A (SEA, 500 ng ml(-1) for 2 hr) followed by coculture with freshly obtained T cells isolated from peripheral blood. Proliferation was measured by (3)H-thymidine incorporation assay. In selected experiments, either RPE or T cells were pre-treated with blocking antibodies specific for cell surface molecules. For comparison, dendritic cells were used as superantigen presenting cells for T cells. This study showed that presentation of SEA by RPE cells to resting T cells was dependent on the presence of the molecules CD2, CD58 and CD18, CD54. The cycling status of T cells was decisive, thus resting T cells but not activated T cells were capable to proliferate in response to SEA presentation. Proliferation of T cells induced by adult RPE cells was comparable to the proliferation induced by dendritic cells at concentrations of SAg above 100 ng ml(-1), but at concentrations of SAg below 10 ng ml(-1) the response was significantly lower for SAg presented by RPE cells compared to dendritic cells. The results demonstrate that CD2-CD58 and CD18-CD54 interactions are critical for SAg presentation by RPE cells to T cells. The findings thus suggest that also presentation of peptides to resting T cells by RPE cells may be dependent upon these interactions.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD18,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD2,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD58,
http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Adhesion Molecule-1,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Superantigens
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0014-4835
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pubmed:author | |
pubmed:copyrightInfo |
(C) 2001 Academic Press.
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pubmed:issnType |
Print
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pubmed:volume |
73
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
723-33
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:11747372-Antibodies, Monoclonal,
pubmed-meshheading:11747372-Antigen Presentation,
pubmed-meshheading:11747372-Antigens, CD,
pubmed-meshheading:11747372-Antigens, CD18,
pubmed-meshheading:11747372-Antigens, CD2,
pubmed-meshheading:11747372-Antigens, CD58,
pubmed-meshheading:11747372-Cell Division,
pubmed-meshheading:11747372-Cell Separation,
pubmed-meshheading:11747372-Cells, Cultured,
pubmed-meshheading:11747372-Flow Cytometry,
pubmed-meshheading:11747372-Humans,
pubmed-meshheading:11747372-Intercellular Adhesion Molecule-1,
pubmed-meshheading:11747372-Interferon-gamma,
pubmed-meshheading:11747372-Pigment Epithelium of Eye,
pubmed-meshheading:11747372-Statistics, Nonparametric,
pubmed-meshheading:11747372-Superantigens,
pubmed-meshheading:11747372-T-Lymphocytes
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pubmed:year |
2001
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pubmed:articleTitle |
Superantigen presentation by human retinal pigment epithelial cells to T cells is dependent on CD2-CD58 and CD18-CD54 molecule interactions.
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pubmed:affiliation |
Institute of Medical Anatomy, The Panum Institute, University of Copenhagen, Copenhagen, Denmark.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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