BCL-2 PREVENTS KILLING OF NEURONAL CELLS BY GLUTAMATE BUT NOT BY AMYLOID-BETA PROTEIN

被引:83
作者
BEHL, C
HOVEY, L
KRAJEWSKI, S
SCHUBERT, D
REED, JC
机构
[1] SALK INST BIOL STUDIES,LA JOLLA,CA 92037
[2] LA JOLLA CANC RES FDN,CANC RES CTR,ONCOGNE & TUMOR SUPPRESSOR GENE PROGRAM,LA JOLLA,CA 92037
关键词
D O I
10.1006/bbrc.1993.2571
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 26-kDa protein encoded by the bcl-2 gene is a regulator of cell survival and blocks cell death induced by numerous stimuli. Amyloid beta protein (ABP) and glutamate are believed to play important roles in the neuronal cell death that occurs in Alzheimer′s disease and stroke, respectively. Glutamate induces apoptosis in some neuronal cell systems, but it remains controversial whether ABP-mediated cell death occurs through apoptosis or necrosis. To further explore the pathways for cell death that are activated by these neurotoxins, we examined the effects of elevated levels of the p26-Bcl-2 protein on the susceptibility of neuronal cell lines to killing by glutamate and ABP. Gene transfer methods were used to elevate p26-Bcl-2 protein levels in the rat nerve lines PC-12 and B50 and the human neuroblastoma IMR-5. Bcl-2 protected all 3 cell lines from glutamate induced cell death but had no effect on killing mediated by ABP. © 1993 Academic Press. All rights reserved.
引用
收藏
页码:949 / 956
页数:8
相关论文
共 25 条
[1]   VITAMIN-E PROTECTS NERVE-CELLS FROM AMYLOID BETA-PROTEIN TOXICITY [J].
BEHL, C ;
DAVIS, J ;
COLE, GM ;
SCHUBERT, D .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 186 (02) :944-950
[2]   GLUTAMATE-INDUCED NEURONAL DEATH IS NOT A PROGRAMMED CELL-DEATH IN CEREBELLAR CULTURE [J].
DESSI, F ;
CHARRIAUTMARLANGUE, C ;
KHRESTCHATISKY, M ;
BENARI, Y .
JOURNAL OF NEUROCHEMISTRY, 1993, 60 (05) :1953-1955
[3]   SEGREGATION OF A MISSENSE MUTATION IN THE AMYLOID PRECURSOR PROTEIN GENE WITH FAMILIAL ALZHEIMERS-DISEASE [J].
GOATE, A ;
CHARTIERHARLIN, MC ;
MULLAN, M ;
BROWN, J ;
CRAWFORD, F ;
FIDANI, L ;
GIUFFRA, L ;
HAYNES, A ;
IRVING, N ;
JAMES, L ;
MANT, R ;
NEWTON, P ;
ROOKE, K ;
ROQUES, P ;
TALBOT, C ;
PERICAKVANCE, M ;
ROSES, A ;
WILLIAMSON, R ;
ROSSOR, M ;
OWEN, M ;
HARDY, J .
NATURE, 1991, 349 (6311) :704-706
[4]  
Greene L. A., 1982, ADV CELL NEUROBIOL, P373, DOI DOI 10.1016/B978-0-12-008303-9.50016-5
[5]  
HANADA M, 1993, IN PRESS CANCER RES
[6]   AN INVIVO MODEL FOR THE NEURODEGENERATIVE EFFECTS OF BETA-AMYLOID AND PROTECTION BY SUBSTANCE-P [J].
KOWALL, NW ;
BEAL, MF ;
BUSCIGLIO, J ;
DUFFY, LK ;
YANKNER, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :7247-7251
[7]  
KRAJEWSKI S, 1993, IN PRESS CANCER RES
[8]   GLUTAMATE TRIGGERS INTERNUCLEOSOMAL DNA CLEAVAGE IN NEURONAL CELLS [J].
KURE, S ;
TOMINAGA, T ;
YOSHIMOTO, T ;
TADA, K ;
NARISAWA, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 179 (01) :39-45
[9]   THE PROTOONCOGENE BCL-2 INHIBITS APOPTOSIS IN PC12 CELLS [J].
MAH, SP ;
ZHONG, LT ;
LIU, Y ;
ROGHANI, A ;
EDWARDS, RH ;
BREDESEN, DE .
JOURNAL OF NEUROCHEMISTRY, 1993, 60 (03) :1183-1186
[10]   BETA-AMYLOID PEPTIDES DESTABILIZE CALCIUM HOMEOSTASIS AND RENDER HUMAN CORTICAL-NEURONS VULNERABLE TO EXCITOTOXICITY [J].
MATTSON, MP ;
CHENG, B ;
DAVIS, D ;
BRYANT, K ;
LIEBERBURG, I ;
RYDEL, RE .
JOURNAL OF NEUROSCIENCE, 1992, 12 (02) :376-389