NADE, a p75NTR-associated cell death executor, is involved in signal transduction mediated by the common neurotrophin receptor p75NTR

被引:164
作者
Mukai, J
Hachiya, T
Shoji-Hoshino, S
Kimura, MT
Nadano, D
Suvanto, P
Hanaoka, T
Li, Y
Irie, S
Greene, LA
Sato, TA
机构
[1] Columbia Univ Coll Phys & Surg, Dept Otolaryngol Head & Neck Surg & Pathol, Div Mol Oncol, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[3] RIKEN, Tsukuba Life Sci Ctr, Oncol Mol Lab, Tsukuba, Ibaraki 3050074, Japan
[4] Med & Biol Labs Co Ltd, Ina Lab, Nagano 3960002, Japan
[5] ZAIYA Inc, Kyoto 6008815, Japan
[6] Tottori Univ, Sch Life Sci, Dept Mol & Cell Genet, Tottori 683, Japan
关键词
D O I
10.1074/jbc.C000140200
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
The low affinity neurotrophin receptor p75NTR can mediate cell survival as well as cell death of neural cells by NGF and other neurotrophins. To elucidate p75NTR-mediated signal transduction, we screened p75NTR-associated proteins by a yeast two-hybrid system. We identified one positive clone and named NADE (p75NTR-associated cell death executor). Mouse NADE has marked homology to the human HGR74 protein. NADE specifically binds to the cell-death domain of p75NTR, Go-expression of NADE and p75NTR induced caspase-2 and caspase-3 activities and the fragmentation of nuclear DNA in 293T cells. However, in the absence of p75NTR, NADE failed to induce apoptosis, suggesting that NADE expression is necessary but insufficient for p75NTR-mediated apoptosis, Furthermore, p75NTR/ NADE-induced cell death was dependent on NGF but not BDNF, NT-3, or NT-4/5, and the recruitment of NADE to p75NTR (intracellular domain) was dose-dependent. We obtained similar results from PC12 cells, nnr5 cells, and oligodendrocytes. Taken together, NADE is the first signaling adaptor molecule identified in the involvement of p75NTR-mediated apoptosis induced by NGF, and it may play an important role in the pathogenesis of neurogenetic diseases.
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收藏
页码:17566 / 17570
页数:5
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