Source:http://linkedlifedata.com/resource/pubmed/id/17609291
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2007-8-31
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pubmed:abstractText |
Exposure of renal tubular epithelial cells (TEC) to IFN-gamma/TNF-alpha leads to Fas/FasL-mediated self-injury, which contributes to allograft rejection. Indoleamine 2,3-dioxygenase (IDO) converts tryptophan to N-formyl-kynurenine and contributes to immune privilege in tissues by increasing Fas-mediated T cell apoptosis. However, renal expression of IDO and its role in promoting Fas-mediated TEC death have not been examined. IDO expression was analyzed by RT-PCR and Western blot. Apoptosis was measured by fluorescence-activated cell sorting analysis and terminal deoxytransferase-mediated dUTP nick end labeling. We demonstrated that functional IDO is expressed in TEC and is increased by IFN-gamma/TNF-alpha exposure. Increased IDO activity promoted TEC apoptosis, whereas inhibition of IDO by its specific inhibitor 1-methyl-d-tryptophan attenuated IFN-gamma/TNF-alpha-mediated TEC apoptosis and augmented TEC survival. Transgenic expression of IDO resulted in increased TEC apoptosis in the absence of proinflammatory cytokine exposure, supporting a central role for IDO in TEC injury. Inhibition of IDO-mediated TEC death by a caspase-8-specific inhibitor (Z-IETD-FMK), as well as the absence of an IDO effect in Fas-deficient and FasL-deficient TEC, supports a Fas/FasL-dependent, caspase-8-mediated mechanism for IDO-enhanced TEC death. These data suggest that renal IDO expression may be deleterious during renal inflammation, because it enhances TEC self-injury through Fas/FasL interactions. Thus attenuation of IDO may represent a novel strategy to promote kidney function following ischemia and renal allograft rejection.
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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/Antigens, CD95,
http://linkedlifedata.com/resource/pubmed/chemical/Fas Ligand Protein,
http://linkedlifedata.com/resource/pubmed/chemical/Indoleamine-Pyrrole 2,3,-Dioxygenase,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1931-857X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
293
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
F801-12
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pubmed:dateRevised |
2011-4-28
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pubmed:meshHeading |
pubmed-meshheading:17609291-Animals,
pubmed-meshheading:17609291-Antigens, CD95,
pubmed-meshheading:17609291-Apoptosis,
pubmed-meshheading:17609291-Cells, Cultured,
pubmed-meshheading:17609291-Epithelial Cells,
pubmed-meshheading:17609291-Fas Ligand Protein,
pubmed-meshheading:17609291-Gene Expression Regulation, Enzymologic,
pubmed-meshheading:17609291-Indoleamine-Pyrrole 2,3,-Dioxygenase,
pubmed-meshheading:17609291-Interferon-gamma,
pubmed-meshheading:17609291-Kidney Tubules,
pubmed-meshheading:17609291-Mice,
pubmed-meshheading:17609291-Mice, Inbred C3H,
pubmed-meshheading:17609291-Mice, Inbred C57BL,
pubmed-meshheading:17609291-Tumor Necrosis Factor-alpha,
pubmed-meshheading:17609291-Up-Regulation
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pubmed:year |
2007
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pubmed:articleTitle |
Proapoptotic activity of indoleamine 2,3-dioxygenase expressed in renal tubular epithelial cells.
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pubmed:affiliation |
Department of Medicine and Microbiology, The University of Western Ontario, London, Ontario, Canada.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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