Specific up-regulation of GADD153/CHOP in 1-methyl-4-phenyl-pyridinium-treated SH-SY5Y cells

被引:31
作者
Conn, KJ
Gao, WW
Ullman, MD
McKeon-O'Malley, C
Eisenhauer, PB
Fine, RE
Wells, JM
机构
[1] Vet Adm Med Ctr, Dept Vet Affairs, Bedford, MA 01730 USA
[2] Boston Univ, Sch Med, Dept Neurol, Boston, MA 02118 USA
[3] Boston Univ, Sch Med, Dept Psychiat, Boston, MA 02118 USA
[4] Univ Massachusetts, Sch Med, Shriver Ctr, Waltham, MA USA
[5] Boston Univ, Sch Med, Dept Biochem, Boston, MA 02118 USA
关键词
1-methyl-4-phenyl-pyridinium; Parkinson's disease; gene expression; apoptosis; endoplasmic reticulum;
D O I
10.1002/jnr.10252
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Growth arrest DNA damage-inducible 153 (GADD153) expression was increased in 1-methyl-4-phenyl-pyridinium (MPP+)-treated human SH-SY5Y neuroblastoma cells as determined by gene microarray analysis. GADD153 expression increased after 24 hr of MPP+ (1 mM) exposure and preceded activation of caspase 3. Comparison of GADD153 expression among cultures treated with other toxins whose primary mode of action is either via mitochondrial impairment (rotenone) or via oxidative stress (6-hydroxydopamine or hydrogen peroxide) showed that GADD153 was uniquely up-regulated by MPP+. Together these data suggest that a cellular mechanism distinct from mitochondrial impairment or oxidative stress contributes significantly to the upregulation of GADD153 by MPP+ and that GADD153 may function as an inducer of apoptosis following MPP-exposure. Published 2002 Wiley-Liss, Inc.
引用
收藏
页码:755 / 760
页数:6
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