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.
机构:
Harvard Univ, Mol Endocrinol Lab, Sch Med, Massachusetts Gen Hosp,Howard Hughes Med Inst, Boston, MA 02114 USAHarvard Univ, Mol Endocrinol Lab, Sch Med, Massachusetts Gen Hosp,Howard Hughes Med Inst, Boston, MA 02114 USA
Schmitt-Ney, M
Habener, JF
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Harvard Univ, Mol Endocrinol Lab, Sch Med, Massachusetts Gen Hosp,Howard Hughes Med Inst, Boston, MA 02114 USAHarvard Univ, Mol Endocrinol Lab, Sch Med, Massachusetts Gen Hosp,Howard Hughes Med Inst, Boston, MA 02114 USA
机构:
Harvard Univ, Mol Endocrinol Lab, Sch Med, Massachusetts Gen Hosp,Howard Hughes Med Inst, Boston, MA 02114 USAHarvard Univ, Mol Endocrinol Lab, Sch Med, Massachusetts Gen Hosp,Howard Hughes Med Inst, Boston, MA 02114 USA
Schmitt-Ney, M
Habener, JF
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h-index: 0
机构:
Harvard Univ, Mol Endocrinol Lab, Sch Med, Massachusetts Gen Hosp,Howard Hughes Med Inst, Boston, MA 02114 USAHarvard Univ, Mol Endocrinol Lab, Sch Med, Massachusetts Gen Hosp,Howard Hughes Med Inst, Boston, MA 02114 USA