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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6320
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pubmed:dateCreated |
1991-5-31
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pubmed:abstractText |
CD43 (sialophorin, leukosialin, leukocyte large sialoglycoprotein), a heavily sialylated molecule found on most leukocytes and platelets, was initially identified as a major glycoprotein of mouse, rat and human T cells. CD43 expression is defective on the T cells of males with the Wiskott-Aldrich syndrome, an X chromosome-linked recessive immunodeficiency disorder. Affected males are susceptible to opportunistic infections and do not respond to polysaccharide antigens, reflecting defects in cytotoxic and helper T-cell functions. Anti-CD43 monoclonal antibodies have a modest costimulatory effect on T cells, natural killer cells, B cells and monocytes, and one such antibody has been shown to activate T cells directly. To investigate a possible physiological role for CD43, a complementary DNA encoding the human protein was introduced into an antigen-responsive murine T-cell hybridoma. We observed that CD43 enhances the antigen-specific activation of T cells and that the intracellular domain of CD43, which is hyperphosphorylated during T-cell activation, is required for this function. We also found that antigen-presenting cells can bind specifically to immobilized purified CD43 and that the binding can be inhibited by liposomes containing CD43 as well as by anti-CD43 monoclonal antibodies.
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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, CD43,
http://linkedlifedata.com/resource/pubmed/chemical/Sialoglycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Spn protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/UN1 sialoglycoprotein, human
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0028-0836
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
25
|
pubmed:volume |
350
|
pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
706-9
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pubmed:dateRevised |
2011-9-7
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pubmed:meshHeading |
pubmed-meshheading:2023632-Animals,
pubmed-meshheading:2023632-Antibodies, Monoclonal,
pubmed-meshheading:2023632-Antigens, CD,
pubmed-meshheading:2023632-Antigens, CD43,
pubmed-meshheading:2023632-B-Lymphocytes,
pubmed-meshheading:2023632-Cell Line,
pubmed-meshheading:2023632-Cell Membrane,
pubmed-meshheading:2023632-Cloning, Molecular,
pubmed-meshheading:2023632-Humans,
pubmed-meshheading:2023632-Lymphocyte Activation,
pubmed-meshheading:2023632-Male,
pubmed-meshheading:2023632-Mice,
pubmed-meshheading:2023632-Plasmids,
pubmed-meshheading:2023632-Sialoglycoproteins,
pubmed-meshheading:2023632-T-Lymphocytes,
pubmed-meshheading:2023632-Transfection,
pubmed-meshheading:2023632-Wiskott-Aldrich Syndrome
|
pubmed:year |
1991
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pubmed:articleTitle |
Enhancement of T-cell activation by the CD43 molecule whose expression is defective in Wiskott-Aldrich syndrome.
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pubmed:affiliation |
Division of Pediatric Oncology, Dana Farber Cancer Institute, Boston, Massachusetts.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|