Participation of Presenilin 2 in apoptosis: Enhanced basal activity conferred by an Alzheimer mutation

被引:403
作者
Wolozin, B
Iwasaki, K
Vito, P
Ganjei, JK
Lacana, E
Sunderland, T
Zhao, BY
Kusiak, JW
Wasco, V
DAdamio, L
机构
[1] NIMH,UNIT ALZHEIMER BIOL,CLIN SCI LAB,BETHESDA,MD 20892
[2] NIAID,T CELL MOL BIOL UNIT,CELLULAR & MOL IMMUNOL LAB,BETHESDA,MD 20892
[3] NIA,MOL NEUROBIOL UNIT,BALTIMORE,MD 21224
[4] NINCDS,CELLULAR NEUROBIOL BRANCH,GERONTOL RES CTR,BALTIMORE,MD 21224
[5] HARVARD UNIV,SCH MED,MASSACHUSETTS GEN HOSP E,DEPT NEUROL,GENET & AGING UNIT,CHARLESTOWN,MA 02139
[6] NIH,T CELL MOL BIOL UNIT,CELLULAR & MOL IMMUNOL LAB,BETHESDA,MD 20892
关键词
D O I
10.1126/science.274.5293.1710
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Overexpression of the familial Alzheimer's disease gene Presenilin 2 (PS2) in nerve growth factor-differentiated PC12 cells increased apoptosis induced by trophic factor withdrawal or beta-amyloid. Transfection of antisense PS2 conferred protection against apoptosis induced by trophic withdrawal in nerve growth factor-differentiated or amyloid precursor protein-expressing PC12 cells, The apoptotic cell death induced by PS2 protein was sensitive to pertussis toxin, suggesting that heterotrimeric GTP-binding proteins are involved, A PS2 mutation associated with familial Alzheimer's disease was found to generate a molecule with enhanced basal apoptotic activity, This gain of function might accelerate the process of neurodegeneration that occurs in Alzheimer's disease, leading to the earlier age of onset characteristic a familial Alzheimer's disease.
引用
收藏
页码:1710 / 1713
页数:4
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