Source:http://linkedlifedata.com/resource/pubmed/id/15495158
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2004-12-1
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pubmed:abstractText |
The transcription factor c-Maf controls IL-4 gene expression in CD4(+) T cells, and its expression is up-regulated in human asthmatic airways after allergen challenge. In the present study, we addressed the role of c-Maf in asthma by studying transgenic (Tg) mice overexpressing c-Maf in CD4(+) T cells under the control of the CD2 promoter. As shown, lung CD4(+) T cells of c-maf-Tg mice produced more IL-5 at the early stage (day 2) of culture in the presence of IL-4 than wild-type control cells. Consistently, c-maf-Tg mice spontaneously showed increased IL-5 expression and eosinophils in the bronchial alveolar lavage fluid (BALF) and activated IL-5 signal transduction via Raf-1 and Ras in lung eosinophils. Finally, IL-13 was suppressed in the BALF of c-maf-Tg mice and in supernatants of Tg lung CD4(+) T cells cultured in the presence of IL-2. Consistently, retroviral overexpression of c-Maf suppressed IL-13 production in developing lung Th2 cells. In summary, c-Maf induces IL-5 production in lung CD4(+) T cells at an early stage, but along with IL-2 suppresses IL-13 production in differentiating lung Th2 cells, thereby explaining the finding that overexpression of c-Maf does not cause airway hyperresponsiveness, a hallmark feature of asthma.
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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/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-5,
http://linkedlifedata.com/resource/pubmed/chemical/Maf protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-maf,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0014-2980
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
34
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3401-12
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15495158-Animals,
pubmed-meshheading:15495158-Cell Differentiation,
pubmed-meshheading:15495158-Cell Division,
pubmed-meshheading:15495158-DNA-Binding Proteins,
pubmed-meshheading:15495158-Eosinophils,
pubmed-meshheading:15495158-Interleukin-4,
pubmed-meshheading:15495158-Interleukin-5,
pubmed-meshheading:15495158-Leucine Zippers,
pubmed-meshheading:15495158-Lung,
pubmed-meshheading:15495158-Mice,
pubmed-meshheading:15495158-Mice, Transgenic,
pubmed-meshheading:15495158-Proto-Oncogene Proteins,
pubmed-meshheading:15495158-Proto-Oncogene Proteins c-maf,
pubmed-meshheading:15495158-Th2 Cells,
pubmed-meshheading:15495158-Transcription Factors
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pubmed:year |
2004
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pubmed:articleTitle |
A stage-specific functional role of the leucine zipper transcription factor c-Maf in lung Th2 cell differentiation.
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pubmed:affiliation |
Laboratory of Cellular and Molecular Lung Immunology, I Medical Clinic, Mainz, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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