Source:http://linkedlifedata.com/resource/pubmed/id/17330136
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2007-4-25
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pubmed:abstractText |
Primary immune response to pathogens involves the maturation of antigen-presenting dendritic cells (DC). Bacterial lipopolysacharride (LPS) is a potent inducer of DC maturation, whereas the transforming growth factor beta (TGFbeta) attenuates much of this process. Here, we analyzed the global gene expression pattern in LPS-treated bone marrow derived DC during inhibition of their maturation process by TGFbeta. Exposure of DC to LPS induces a pronounced cell response, manifested in altered expression of a large number of genes. Interestingly, TGFbeta did not affect most of the LPS responding genes. Nevertheless, analysis identified a subset of genes that did respond to TGFbeta, among them the two inflammatory cytokines interleukin (IL)-12 and IL-18. Expression of IL-12, the major proinflammatory cytokine secreted by mature DC, was downregulated by TGFbeta, whereas the expression level of the proinflammatory cytokine IL-18, known to potentiate the IL-12 effect, was upregulated. Expression of the peroxisome proliferator-activated receptor gamma (PPARgamma) increased in response to TGFbeta, concomitantly with reduced expression of chemokine receptor 7 (CCR7). This finding supports the possibility that TGFbeta-dependent inhibition of CCR7 expression in DC is mediated by PPARgamma.
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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/Granulocyte-Macrophage...,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-12,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-18,
http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1466-4879
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
239-44
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:17330136-Animals,
pubmed-meshheading:17330136-Cell Differentiation,
pubmed-meshheading:17330136-Dendritic Cells,
pubmed-meshheading:17330136-Gene Expression,
pubmed-meshheading:17330136-Gene Expression Profiling,
pubmed-meshheading:17330136-Granulocyte-Macrophage Colony-Stimulating Factor,
pubmed-meshheading:17330136-Interleukin-12,
pubmed-meshheading:17330136-Interleukin-18,
pubmed-meshheading:17330136-Lipopolysaccharides,
pubmed-meshheading:17330136-Mice,
pubmed-meshheading:17330136-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:17330136-Recombinant Proteins,
pubmed-meshheading:17330136-Transforming Growth Factor beta
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pubmed:year |
2007
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pubmed:articleTitle |
TGFbeta-dependent gene expression profile during maturation of dendritic cells.
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pubmed:affiliation |
Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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