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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6312
|
pubmed:dateCreated |
1991-4-9
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pubmed:abstractText |
Endothelial cell leukocyte adhesion molecule-1 (ELAM-1) has been described as an inducible endothelial cell-adhesion molecule for neutrophils, and is believed to have a key role in the extravasation of these cells at sites of acute inflammation. Here we report that ELAM-1-transfected COS cells also bind a unique skin-associated subset of circulating memory T cells defined by the expression of the cutaneous lymphocyte-associated antigen. T cells expressing this antigen bind at least as well as neutrophils to expressed ELAM-1, whereas other lymphocytes in the peripheral blood bind poorly, or not at all. Immunohistological survey of chronically inflamed tissue specimens revealed that vascular expression of ELAM-1 occurs at cutaneous sites in preference to noncutaneous sites. We conclude that at sites of chronic inflammation, ELAM-1 may function as a skin vascular addressin, a tissue-selective endothelial cell-adhesion molecule for skin-homing memory T lymphocytes.
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pubmed:commentsCorrections | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0028-0836
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
28
|
pubmed:volume |
349
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
796-9
|
pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1705666-Animals,
pubmed-meshheading:1705666-Cell Adhesion,
pubmed-meshheading:1705666-Cell Adhesion Molecules,
pubmed-meshheading:1705666-Cell Line,
pubmed-meshheading:1705666-E-Selectin,
pubmed-meshheading:1705666-Humans,
pubmed-meshheading:1705666-Neutrophils,
pubmed-meshheading:1705666-Skin,
pubmed-meshheading:1705666-T-Lymphocyte Subsets,
pubmed-meshheading:1705666-T-Lymphocytes,
pubmed-meshheading:1705666-Transfection
|
pubmed:year |
1991
|
pubmed:articleTitle |
ELAM-1 is an adhesion molecule for skin-homing T cells.
|
pubmed:affiliation |
Department of Pathology, Stanford University School of Medicine, California 94305.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
|