BCL-X IS EXPRESSED IN EMBRYONIC AND POSTNATAL NEURAL TISSUES AND FUNCTIONS TO PREVENT NEURONAL CELL-DEATH

被引:267
作者
GONZALEZGARCIA, M
GARCIA, I
DING, LY
OSHEA, S
BOISE, LH
THOMPSON, CB
NUNEZ, G
机构
[1] UNIV MICHIGAN,SCH MED,DEPT PATHOL & ANAT,ANN ARBOR,MI 48109
[2] UNIV MICHIGAN,SCH MED,DEPT CELL BIOL,ANN ARBOR,MI 48109
[3] CTR MED UNIV GENEVA,DEPT PATHOL,CH-1211 GENEVA 4,SWITZERLAND
[4] UNIV CHICAGO,HOWARD HUGHES MED INST,CHICAGO,IL 60637
[5] UNIV CHICAGO,DEPT MED,CHICAGO,IL 60637
[6] UNIV CHICAGO,DEPT MOLEC GENET & CELL BIOL,CHICAGO,IL 60637
关键词
APOPTOSIS; BCL-2; NEURONAL SURVIVAL;
D O I
10.1073/pnas.92.10.4304
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
Previous studies have implicated the bcl-2 protooncogene as a potential regulator of neuronal survival, However, mice lacking functional bcl-2 exhibited normal development and maintenance of the central nervous system (CNS), Since bcl-2 appears dispensable for neuronal survival, we have examined the expression and function of bcl-x, another member of the bcl-2 family of death regulatory genes, Bcl-2 is expressed in neuronal tissues during embryonic development but is down-regulated in the adult CNS. In contrast, Bcl-x(L) expression is retained in neurons of the adult CNS, Two different forms of bcl-x mRNA and their corresponding products, Bcl-x(L) and Bcl-x(beta), were expressed in embryonic and adult neurons of the CNS, Microinjection of bcl-x(L) and bcl-x(beta) cDNAs into primary sympathetic neurons inhibited their death induced by nerve growth factor withdrawal, Thus, Bcl-x proteins appear to play an important role in the regulation of neuronal survival in the adult CNS.
引用
收藏
页码:4304 / 4308
页数:5
相关论文
共 26 条
[11]   BCL-2 FUNCTIONS IN AN ANTIOXIDANT PATHWAY TO PREVENT APOPTOSIS [J].
HOCKENBERY, DM ;
OLTVAI, ZN ;
YIN, XM ;
MILLIMAN, CL ;
KORSMEYER, SJ .
CELL, 1993, 75 (02) :241-251
[12]   BCL2 PROTEIN IS TOPOGRAPHICALLY RESTRICTED IN TISSUES CHARACTERIZED BY APOPTOTIC CELL-DEATH [J].
HOCKENBERY, DM ;
ZUTTER, M ;
HICKEY, W ;
NAHM, M ;
KORSMEYER, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :6961-6965
[13]   BCL-2 INHIBITION OF NEURAL DEATH - DECREASED GENERATION OF REACTIVE OXYGEN SPECIES [J].
KANE, DJ ;
SARAFIAN, TA ;
ANTON, R ;
HAHN, H ;
GRALLA, EB ;
VALENTINE, JS ;
ORD, T ;
BREDESEN, DE .
SCIENCE, 1993, 262 (5137) :1274-1277
[14]  
KRAJEWSKI S, 1993, CANCER RES, V53, P4701
[15]  
LEBRUN DP, 1993, AM J PATHOL, V142, P743
[16]   INHIBITORS OF PROTEIN-SYNTHESIS AND RNA-SYNTHESIS PREVENT NEURONAL DEATH CAUSED BY NERVE GROWTH-FACTOR DEPRIVATION [J].
MARTIN, DP ;
SCHMIDT, RE ;
DISTEFANO, PS ;
LOWRY, OH ;
CARTER, JG ;
JOHNSON, EM .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :829-844
[17]   DEVELOPMENTAL REGULATION OF THE BCL-2-PROTEIN AND SUSCEPTIBILITY TO CELL-DEATH IN B-LYMPHOCYTES [J].
MERINO, R ;
DING, LY ;
VEIS, DJ ;
KORSMEYER, SJ ;
NUNEZ, G .
EMBO JOURNAL, 1994, 13 (03) :683-691
[18]  
MERRY DE, 1994, DEVELOPMENT, V120, P301
[19]  
MONAGHAN P, 1993, J HISTOCHEM CYTOCHEM, V40, P1819
[20]   TARGETED DISRUPTION OF BCL-2-ALPHA-BETA IN MICE - OCCURRENCE OF GRAY HAIR, POLYCYSTIC KIDNEY-DISEASE, AND LYMPHOCYTOPENIA [J].
NAKAYAMA, K ;
NAKAYAMA, K ;
NEGISHI, I ;
KUIDA, K ;
SAWA, H ;
LOH, DY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (09) :3700-3704