The mouse cell surface protein TOSO regulates Fas/Fas ligand-induced apoptosis through its binding to fas-associated death domain

被引:33
|
作者
Song, YH
Jacob, CO
机构
[1] Univ So Calif, Sch Med, Dept Med, Los Angeles, CA 90089 USA
[2] Univ So Calif, Sch Med, Dept Mol Microbiol & Immunol, Los Angeles, CA 90089 USA
关键词
D O I
10.1074/jbc.M413609200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mouse TOSO, the homologue of human TOSO gene, was cloned and characterized in the present study. Using immunofluorescence confocal microscopy we localized TOSO to the cytoplasmic membrane of expressing cells. Using stably transfected mouse TOSO ( mTOSO)- expressing Jurkat cells, we show that TOSO protects cells from Fas/ Fas ligand- and tumor necrosis factor-induced apoptosis but not from TNF-related apoptosis-inducing ligand-induced apoptosis. The Fas-induced activation of caspase-8 was significantly inhibited by the expression of mTOSO. Using deletion mutants and glutathione S- transferase pull-down approaches, we have shown that mTOSO regulates apoptosis by directly binding to Fasassociated death domain through its C-terminal domain, suggesting the disruption of death-inducing signaling complex formation as mechanism of action. Furthermore, we have expressed mTOSO in transgenic mice and show that mTOSO overexpressing primary T lymphocytes are resistant to Fas/Fas ligand-induced apoptosis.
引用
收藏
页码:9618 / 9626
页数:9
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