Requirement of the familial Alzheimer's disease gene PS2 for apoptosis - Opposing effect of ALG-3

被引:127
作者
Vito, P
Wolozin, B
Ganjei, JK
Iwasaki, K
Lacana, E
DAdamio, L
机构
[1] NIAID,T CELL MOL BIOL UNIT,CELLULAR & MOL IMMUNOL LAB,NIH,BETHESDA,MD 20892
[2] NIMH,UNIV ALZHEIMER BIOL,CLIN SCI LAB,BETHESDA,MD 20892
关键词
D O I
10.1074/jbc.271.49.31025
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
ALG-3, a truncated mouse homologue of the chromosome I familial Alzheimer's disease gene PS2, rescues T hybridoma 3DO cells from T-cell receptor-induced apoptosis by inhibiting Fas ligand induction and Fas signaling, Here we show that ALG-3 transfected 3DO cells express a COOH-terminal PS2 polypeptide, Overexpression of PS2 in ALG-3 transfected 3DO cells reconstitutes sensitivity to receptor-induced cell death, suggesting that the artificial PS2 polypeptide functions as a dominant negative mutant of PS2, ALG-3 and antisense PS2 protect PC12 cells from glutamate-induced apoptosis but not from death induced by hydrogen peroxide or the free radical MPP(+). Thus, the PS2 gene is required for some forms of cell death in diverse cell types, and its function is opposed by ALG-3.
引用
收藏
页码:31025 / 31028
页数:4
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