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dc.contributor.authorWang, X. F.zh_CN
dc.contributor.authorOno, K.zh_CN
dc.contributor.authorKim, S. O.zh_CN
dc.contributor.authorKravchenko, V.zh_CN
dc.contributor.authorLin, S. C.zh_CN
dc.contributor.authorHan, J. H.zh_CN
dc.contributor.author韩家淮zh_CN
dc.date.accessioned2013-12-12T02:24:41Z
dc.date.available2013-12-12T02:24:41Z
dc.date.issued2001zh_CN
dc.identifier.citationEmbo Reports,2(7):628-633zh_CN
dc.identifier.issn1469-221Xzh_CN
dc.identifier.otherISI:000169964500017zh_CN
dc.identifier.urihttps://dspace.xmu.edu.cn/handle/2288/65771
dc.description.abstractWe used retrovirus insertion-mediated random mutagenesis and tumor necrosis factor (TNF) selection to generate TNF-resistant lines from L929 cells. The metaxin gene, which encodes a protein located on the outer membrane of mitochondria, was identified to be the gene disrupted in one of the resistant lines. The requirement of metaxin in TNF-induced cell death of L929 was confirmed by the restoration of TNF sensitivity after ectopic reconstitution of metaxin expression. Analysis of the cell death induced by other stimuli revealed that metaxin deficiency-mediated death resistance was selective to certain stimuli. Studies using deletion mutants of metaxin showed that mitochondrial association of metaxin is required for the function of metaxin. Over-expression of truncated metaxin lacking the mitochondria anchoring sequence mimicked metaxin deficiency in wild-type cells. Interfering with metaxin prevented TNF-induced necrotic cell death in L929 cells and apoptosis in MCF-7 cells. Our work has thus defined a novel component in the death pathway used by TNF and some other death stimuli.zh_CN
dc.language.isoen_USzh_CN
dc.subjectOUTER-MEMBRANEzh_CN
dc.subjectAPOPTOSISzh_CN
dc.subjectRECEPTORzh_CN
dc.subjectIMPORTzh_CN
dc.titleMetaxin is required for tumor necrosis factor-induced cell deathzh_CN
dc.typeArticlezh_CN


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