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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6622
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pubmed:dateCreated |
1997-4-7
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pubmed:abstractText |
For cells of the innate immune system to mount a host defence response to infection, they must recognize products of microbial pathogens such as lipopolysaccharide (LPS), the endotoxin secreted by Gram-negative bacteria. These cellular responses require intracellular signalling pathways, such as the four MAP kinase (MAPK) pathways. In mammalian cells the MAPK p38 is thought to play an important role in the regulation of cellular responses during infection through its effects on the expression of proinflammatory molecules. One means of understanding the role of p38 in these responses is to identify proteins with functions regulated by p38-catalysed phosphorylation. Here we demonstrate a link between the p38 pathway and a member of the myocyte-enhancer factor 2 (MEF2) group of transcription factors. We found that in monocytic cells, LPS increases the transactivation activity of MEF2C through p38-catalysed phosphorylation. One consequence of MEF2C activation is increased c-jun gene transcription. Our results show that p38 may influence host defence and inflammation by maintaining the balance of c-Jun protein consumed during infection.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Calcium-Calmodulin-Dependent...,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/Luciferases,
http://linkedlifedata.com/resource/pubmed/chemical/MADS Domain Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/MEF2C protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Myogenic Regulatory Factors,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/myocyte-specific enhancer-binding...,
http://linkedlifedata.com/resource/pubmed/chemical/p38 Mitogen-Activated Protein...
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0028-0836
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
386
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
296-9
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:9069290-Binding Sites,
pubmed-meshheading:9069290-Calcium-Calmodulin-Dependent Protein Kinases,
pubmed-meshheading:9069290-Cell Line,
pubmed-meshheading:9069290-DNA, Complementary,
pubmed-meshheading:9069290-DNA-Binding Proteins,
pubmed-meshheading:9069290-Genes, Reporter,
pubmed-meshheading:9069290-Genes, jun,
pubmed-meshheading:9069290-Humans,
pubmed-meshheading:9069290-Inflammation,
pubmed-meshheading:9069290-Lipopolysaccharides,
pubmed-meshheading:9069290-Luciferases,
pubmed-meshheading:9069290-MADS Domain Proteins,
pubmed-meshheading:9069290-Mitogen-Activated Protein Kinases,
pubmed-meshheading:9069290-Monocytes,
pubmed-meshheading:9069290-Myogenic Regulatory Factors,
pubmed-meshheading:9069290-Phosphorylation,
pubmed-meshheading:9069290-RNA, Messenger,
pubmed-meshheading:9069290-Recombinant Fusion Proteins,
pubmed-meshheading:9069290-Transcription Factors,
pubmed-meshheading:9069290-Transfection,
pubmed-meshheading:9069290-p38 Mitogen-Activated Protein Kinases
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pubmed:year |
1997
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pubmed:articleTitle |
Activation of the transcription factor MEF2C by the MAP kinase p38 in inflammation.
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pubmed:affiliation |
Department of Immunology, The Scripps Research Institute, La Jolla, California 92037, USA. jhan@scripps.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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