Source:http://linkedlifedata.com/resource/pubmed/id/12810075
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2003-6-17
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pubmed:abstractText |
Growing evidence suggests that the immunomodulatory heme oxygenase-1 (HO-1) may have an important role in regulating T-cell responses. In this study, we investigated whether CD4(+)CD25(-) and CD4(+)CD25(+) T cells of human CD4(+) subpopulation could differentially express HO-1. Our results obtained from qualitative reverse transcriptase-polymerase chain reaction and quantitative flow cytometry analyses revealed that the CD4(+)CD25(+) T cells constitutively express HO-1 and that T cell stimulation with plate-bound anti-CD3 in combination with soluble anti-CD28 not only induced HO-1 gene expression in the CD4(+)CD25(-) T cells but also up-regulated HO-1 gene expression in the CD4(+)CD25(+) T cells. Our further studies showed that CD28 signal alone was enough to induce HO-1 expression and CD3 signal, of which signal alone did not induce HO-1 expression, was required at least for full HO-1 expression in both CD25(-) and CD25(+) subsets of human CD4(+) T cells. In addition, transfection of human Jurkat T cells with HO-1 suppressed the cellular proliferation, and this effect was reversed by zinc protoporphyrin, a specific HO competitive inhibitor. Taken together, we have first reported that human CD4(+)CD25(+) regulatory T cells constitutively express HO-1 and that HO-1 inhibits Jurkat T cell proliferation.
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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/Antigens, CD28,
http://linkedlifedata.com/resource/pubmed/chemical/HMOX1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Heme Oxygenase (Decyclizing),
http://linkedlifedata.com/resource/pubmed/chemical/Heme Oxygenase-1,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-2
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0006-291X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
4
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pubmed:volume |
306
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
701-5
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12810075-Antigens, CD28,
pubmed-meshheading:12810075-CD4-Positive T-Lymphocytes,
pubmed-meshheading:12810075-Cell Division,
pubmed-meshheading:12810075-Gene Expression Regulation, Enzymologic,
pubmed-meshheading:12810075-Heme Oxygenase (Decyclizing),
pubmed-meshheading:12810075-Heme Oxygenase-1,
pubmed-meshheading:12810075-Humans,
pubmed-meshheading:12810075-Immunomagnetic Separation,
pubmed-meshheading:12810075-Jurkat Cells,
pubmed-meshheading:12810075-Membrane Proteins,
pubmed-meshheading:12810075-Receptors, Interleukin-2,
pubmed-meshheading:12810075-T-Lymphocyte Subsets
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pubmed:year |
2003
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pubmed:articleTitle |
Differential expressions of heme oxygenase-1 gene in CD25- and CD25+ subsets of human CD4+ T cells.
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pubmed:affiliation |
Medicinal Resources Research Center (MRRC), Wonkwang University, Iksan, 570-749, Chonbuk, Republic of Korea.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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