Mood stabilizers, glycogen synthase kinase-3β and cell survival

被引:117
作者
Jope, RS [1 ]
Bijur, GN [1 ]
机构
[1] Univ Alabama, Dept Psychiat & Behav Neurobiol, Sparks Ctr, Birmingham, AL 35294 USA
关键词
apoptosis; CREB; lithium; bipolar disorder; neuroprotection; beta-catenin;
D O I
10.1038/sj.mp.4001017
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
Glycogen synthase kinase-3beta (GSK3beta) is a central figure in many intracellular signaling systems and is directly regulated by lithium. Substantial evidence now indicates that an important property of the mood stabilizer, lithium, is to influence GSK3beta-linked signaling pathways. This raises the possibility that other mood stabilizers act in a similar manner, which may include modulation of signaling systems leading to GSK3beta, direct regulation of GSK3beta or regulation of signaling intermediates downstream of GSK3beta, Downstream targets of GSK3beta, and thus potential targets of mood stabilizers, are several key transcription factors, including beta-catenin, AP-1, cyclic AMP-response element binding protein, NFkappaB, Myc, heat shock factor-1, nuclear factor of activated T-cells and CCAAT/enhancer-binding proteins. GSK3beta also is an important modulator of cell death, which may be a consequence of its regulatory effects on transcription factor activities. GSK3beta facilitates apoptosis, and lithium's inhibition of GSK3beta supports cell survival. Thus, signaling systems determining cell fate appear to be important targets of mood stabilizers, and these may include signaling pathways encompassing GSK3beta, including transcription factors regulated by GSK3beta.
引用
收藏
页码:S35 / S45
页数:11
相关论文
共 112 条
[61]  
LI X, 2001, IN PRESS BIPOLAR DIS
[62]   Calcineurin binds the transcription factor NFAT1 and reversibly regulates its activity [J].
Loh, C ;
Shaw, KTY ;
Carew, J ;
Viola, JPB ;
Luo, C ;
Perrino, BA ;
Rao, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (18) :10884-10891
[63]   Lithium reduces tau phosphorylation: Effects in living cells and in neurons at therapeutic concentrations [J].
Lovestone, S ;
Davis, DR ;
Webster, MT ;
Kaech, S ;
Brion, JP ;
Matus, A ;
Anderton, BH .
BIOLOGICAL PSYCHIATRY, 1999, 45 (08) :995-1003
[64]   INSULIN REGULATES TRANSCRIPTION OF THE CCAAT/ENHANCER BINDING-PROTEIN (C/EBP) ALPHA-GENE, BETA-GENE, AND DELTA-GENE IN FULLY-DIFFERENTIATE 3T3-L1 ADIPOCYTES [J].
MACDOUGALD, OA ;
CORNELIUS, P ;
LIU, R ;
LANE, MD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (02) :647-654
[65]   HIV-1 Tat-mediated activation of glycogen synthase kinase-3β contributes to Tat-mediated neurotoxicity [J].
Maggirwar, SB ;
Tong, N ;
Ramirez, S ;
Gelbard, HA ;
Dewhurst, S .
JOURNAL OF NEUROCHEMISTRY, 1999, 73 (02) :578-586
[66]   GLYCOGEN-SYNTHASE KINASE-3 AND THE ALZHEIMER-LIKE STATE OF MICROTUBULE-ASSOCIATED PROTEIN TAU [J].
MANDELKOW, EM ;
DREWES, G ;
BIERNAT, J ;
GUSTKE, N ;
VANLINT, J ;
VANDENHEEDE, JR ;
MANDELKOW, E .
FEBS LETTERS, 1992, 314 (03) :315-321
[67]   Different mechanisms of protection against apoptosis by valproate and Li+ [J].
Mora, A ;
González-Polo, RA ;
Fuentes, JM ;
Soler, G ;
Centeno, F .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 266 (03) :886-891
[68]  
Morimoto RI, 1997, ESSAYS BIOCHEM, V32, P17
[69]   Lithium inhibits Alzheimer's disease-like tau protein phosphorylation in neurons [J].
MunozMontano, JR ;
Moreno, FJ ;
Avila, J ;
DiazNido, J .
FEBS LETTERS, 1997, 411 (2-3) :183-188
[70]   MOLECULAR ANALYSIS OF THE C-MYC LOCUS IN NORMAL TISSUE AND IN AVIAN-LEUKOSIS VIRUS-INDUCED LYMPHOMAS [J].
NEEL, BG ;
GASIC, GP ;
ROGLER, CE ;
SKALKA, AM ;
JU, G ;
HISHINUMA, F ;
PAPAS, T ;
ASTRIN, SM ;
HAYWARD, WS .
JOURNAL OF VIROLOGY, 1982, 44 (01) :158-166