Source:http://linkedlifedata.com/resource/pubmed/id/10201981
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rdf:type | |
lifeskim:mentions |
umls-concept:C0014597,
umls-concept:C0017262,
umls-concept:C0021753,
umls-concept:C0021853,
umls-concept:C0079633,
umls-concept:C0079904,
umls-concept:C0086418,
umls-concept:C0185117,
umls-concept:C0812246,
umls-concept:C1314939,
umls-concept:C1456820,
umls-concept:C1522538,
umls-concept:C1879547,
umls-concept:C2611812,
umls-concept:C2911684
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pubmed:issue |
8
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pubmed:dateCreated |
1999-5-6
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pubmed:abstractText |
Cytokine signaling involves the participation of many adaptor proteins, including the docking protein TNF receptor-associated factor-2 (TRAF-2), which is believed to transmit the TNF-alpha signal through both the I kappa B/NF-kappa B and c-Jun N-terminal kinase (JNK)/stress-related protein kinase (SAPK) pathways. The physiological role of TRAF proteins in cytokine signaling in intestinal epithelial cells (IEC) is unknown. We characterized the effect of a dominant-negative TRAF-2 delivered by an adenoviral vector (Ad5dnTRAF-2) on the cytokine signaling cascade in several IEC and also investigated whether inhibiting the TRAF-2-transmitting signal blocked TNF-alpha-induced NF-kappa B and IL-8 gene expression. A high efficacy and level of Ad5dnTRAF-2 gene transfer were obtained in IEC using a multiplicity of infection of 50. Ad5dnTRAF-2 expression prevented TNF-alpha-induced, but not IL-1 beta-induced, I kappa B alpha degradation and NF-kappa B activation in NIH-3T3 and IEC-6 cells. TNF-alpha-induced JNK activation was also inhibited in Ad5dnTRAF-2-infected HT-29 cells. Induction of IL-8 gene expression by TNF-alpha was partially inhibited in Ad5dnTRAF-2-transfected HT-29, but not in control Ad5LacZ-infected, cells. Surprisingly, IL-1 beta-mediated IL-8 gene expression was also inhibited in HT-29 cells as measured by Northern blot and ELISA. We concluded that TRAF-2 is partially involved in TNF-alpha-mediated signaling through I kappa B/NF-kappa B in IEC. In addition, our data suggest that TRAF-2 is involved in IL-1 beta signaling in HT-29 cells. Manipulation of cytokine signaling pathways represents a new approach for inhibiting proinflammatory gene expression in IEC.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-8,
http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa B,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor,
http://linkedlifedata.com/resource/pubmed/chemical/TNF Receptor-Associated Factor 2,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
162
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4447-54
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:10201981-Adenoviruses, Human,
pubmed-meshheading:10201981-Cell Transformation, Viral,
pubmed-meshheading:10201981-Epithelial Cells,
pubmed-meshheading:10201981-Gene Expression Regulation,
pubmed-meshheading:10201981-Genetic Vectors,
pubmed-meshheading:10201981-HT29 Cells,
pubmed-meshheading:10201981-Humans,
pubmed-meshheading:10201981-Interleukin-1,
pubmed-meshheading:10201981-Interleukin-8,
pubmed-meshheading:10201981-Intestinal Mucosa,
pubmed-meshheading:10201981-NF-kappa B,
pubmed-meshheading:10201981-Proteins,
pubmed-meshheading:10201981-Receptors, Tumor Necrosis Factor,
pubmed-meshheading:10201981-Signal Transduction,
pubmed-meshheading:10201981-TNF Receptor-Associated Factor 2,
pubmed-meshheading:10201981-Tumor Necrosis Factor-alpha
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pubmed:year |
1999
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pubmed:articleTitle |
TNF receptor-associated factor-2 is involved in both IL-1 beta and TNF-alpha signaling cascades leading to NF-kappa B activation and IL-8 expression in human intestinal epithelial cells.
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pubmed:affiliation |
Department of Medicine, Center for Gastrointestinal Biology and Disease, University of North Carolina, Chapel Hill 27599, USA. job@med.unc.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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