Source:http://linkedlifedata.com/resource/pubmed/id/17088249
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2007-1-1
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pubmed:abstractText |
Recognition of lipopolysaccharide (LPS) by Toll-like receptor (TLR)4 initiates an intracellular signaling pathway leading to the activation of nuclear factor-kappaB (NF-kappaB). Although LPS-induced activation of NF-kappaB is critical to the induction of an efficient immune response, excessive or prolonged signaling from TLR4 can be harmful to the host. Therefore, the NF-kappaB signal transduction pathway demands tight regulation. In the present study, we describe the human protein Listeria INDuced (LIND) as a novel A20-binding inhibitor of NF-kappaB activation (ABIN) that is related to ABIN-1 and -2 and, therefore, is further referred to as ABIN-3. Similar to the other ABINs, ABIN-3 binds to A20 and inhibits NF-kappaB activation induced by tumor necrosis factor, interleukin-1, and 12-O-tetradecanoylphorbol-13-acetate. However, unlike the other ABINs, constitutive expression of ABIN-3 could not be detected in different human cells. Treatment of human monocytic cells with LPS strongly induced ABIN-3 mRNA and protein expression, suggesting a role for ABIN-3 in the LPS/TLR4 pathway. Indeed, ABIN-3 overexpression was found to inhibit NF-kappaB-dependent gene expression in response to LPS/TLR4 at a level downstream of TRAF6 and upstream of IKKbeta. NF-kappaB inhibition was mediated by the ABIN-homology domain 2 and was independent of A20 binding. Moreover, in vivo adenoviral gene transfer of ABIN-3 in mice reduced LPS-induced NF-kappaB activity in the liver, thereby partially protecting mice against LPS/D-(+)-galactosamine-induced mortality. Taken together, these results implicate ABIN-3 as a novel negative feedback regulator of LPS-induced NF-kappaB activation.
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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/Adaptor Proteins, Signal Transducing,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa B,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/TLR4 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/TNIP1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/TNIP2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/TNIP3 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Toll-Like Receptor 4
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0021-9258
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pubmed:author |
pubmed-author:Adib-ConquyMinouM,
pubmed-author:BeyaertRudiR,
pubmed-author:CarpentierIsabelleI,
pubmed-author:CavaillonJean-MarcJM,
pubmed-author:CornelisSigridS,
pubmed-author:El BakkouriKarimK,
pubmed-author:HaegmanMiraM,
pubmed-author:HeyninckKarenK,
pubmed-author:KreikeMarjaM,
pubmed-author:SandersMatthewM,
pubmed-author:Van HuffelSofieS,
pubmed-author:VerhelstKellyK,
pubmed-author:VerstrepenLynnL,
pubmed-author:WullaertAndyA
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pubmed:issnType |
Print
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pubmed:day |
5
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pubmed:volume |
282
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
81-90
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pubmed:dateRevised |
2010-9-10
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pubmed:meshHeading |
pubmed-meshheading:17088249-Adaptor Proteins, Signal Transducing,
pubmed-meshheading:17088249-Amino Acid Sequence,
pubmed-meshheading:17088249-DNA-Binding Proteins,
pubmed-meshheading:17088249-Gene Expression Regulation,
pubmed-meshheading:17088249-Humans,
pubmed-meshheading:17088249-Lipopolysaccharides,
pubmed-meshheading:17088249-Listeria,
pubmed-meshheading:17088249-Molecular Sequence Data,
pubmed-meshheading:17088249-Monocytes,
pubmed-meshheading:17088249-NF-kappa B,
pubmed-meshheading:17088249-Protein Binding,
pubmed-meshheading:17088249-Proteins,
pubmed-meshheading:17088249-RNA, Messenger,
pubmed-meshheading:17088249-Sequence Homology, Amino Acid,
pubmed-meshheading:17088249-Toll-Like Receptor 4
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pubmed:year |
2007
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pubmed:articleTitle |
LIND/ABIN-3 is a novel lipopolysaccharide-inducible inhibitor of NF-kappaB activation.
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pubmed:affiliation |
Unit of Molecular Signal Transduction in Inflammation, Department for Molecular Biomedical Research, Flanders Interuniversity Institute for Biotechnology, Ghent University, Belgium.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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