Gadd153 sensitizes cells to endoplasmic reticulum stress by down-regulating Bc12 and perturbing the cellular redox state

被引:1616
作者
McCullough, KD
Martindale, JL
Klotz, LO
Aw, TY
Holbrook, NJ
机构
[1] NIA, Cell Stress & Aging Sect, Biol Chem Lab, NIH, Baltimore, MD 21224 USA
[2] Louisiana State Univ, Hlth Sci Ctr, Dept Mol & Cellular Physiol, Shreveport, LA 71130 USA
关键词
D O I
10.1128/MCB.21.4.1249-1259.2001
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
gadd153, also known as chop, is a highly stress-inducible gene that is robustly expressed following disruption of homeostasis in the endoplasmic reticulum (ER) (so-called ER stress). Although all reported types of ER stress induce expression of Gadd153, its role in the stress response has remained largely undefined. Several studies have correlated Gadd153 expression with cell death, but a mechanistic link between Gadd153 and apoptosis has never been demonstrated. To address this issue we employed a cell model system in which Gadd153 is constitutively overexpressed, as well as two cell lines in which Gadd153 expression is conditional. In all cell lines, overexpression of Gadd153 sensitized cells to ER stress. Investigation of the mechanisms contributing to this effect revealed that elevated Gadd153 expression results in the down-regulation of Bc12 expression, depletion of cellular glutathione, and exaggerated production of reactive oxygen species. Restoration of Bc12 expression in Gadd153-overexpressing cells led to replenishment of glutathione and a reduction in levels of reactive oxygen species, and it protected cells from ER stress-induced cell death. We conclude that Gadd153 sensitizes cells to ER stress through mechanisms that involve down-regulation of Bc12 and enhanced oxidant injury.
引用
收藏
页码:1249 / 1259
页数:11
相关论文
共 45 条
[1]  
Alarcon RM, 1996, CANCER RES, V56, P4315
[2]  
ANDERSON ME, 1985, METHOD ENZYMOL, V113, P548
[3]   Glutathione therapy: From prodrugs to genes [J].
Anderson, ME ;
Luo, JL .
SEMINARS IN LIVER DISEASE, 1998, 18 (04) :415-424
[4]   Integration of endoplasmic reticulum signaling in health and disease [J].
Aridor, M ;
Balch, WE .
NATURE MEDICINE, 1999, 5 (07) :745-751
[5]   REGULATION OF THE C/EBP-RELATED GENE GADD153 BY GLUCOSE DEPRIVATION [J].
CARLSON, SG ;
FAWCETT, TW ;
BARTLETT, JD ;
BERNIER, M ;
HOLBROOK, NJ .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (08) :4736-4744
[6]  
Chen CH, 1996, ONCOGENE, V13, P1659
[7]   A ROLE FOR DEREGULATED C-MYC EXPRESSION IN APOPTOSIS OF EPSTEIN-BARR VIRUS-IMMORTALIZED B-CELLS [J].
CHERNEY, BW ;
BHATIA, K ;
TOSATO, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (26) :12967-12971
[8]   Fas-mediated apoptosis is modulated by intracellular glutathione in human T cells [J].
Chiba, T ;
Takahashi, S ;
Sato, N ;
Ishii, S ;
Kikuchi, K .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (05) :1164-1169
[9]   Recent trends in glutathione biochemistry - Glutathione-protein interactions: A molecular link between oxidative stress and cell proliferation? [J].
Cotgreave, IA ;
Gerdes, RG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 242 (01) :1-9
[10]   ALPHA-ADRENERGIC MODULATION OF GLUTATHIONE METABOLISM IN ISOLATED RAT HEPATOCYTES [J].
ESTRELA, JM ;
GIL, F ;
VILA, JM ;
VINA, J .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (06) :E801-E805