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RNASET2 is required for ROS propagation during oxidative stress-mediated cell death
被引:31
|作者:
Caputa, G.
[1
]
Zhao, S.
[1
]
Criado, A. E. G.
[1
]
Ory, D. S.
[1
]
Duncan, J. G.
[2
]
Schaffer, J. E.
[1
]
机构:
[1] Washington Univ, Sch Med, Diabet Cardiovasc Dis Ctr, Dept Internal Med, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
来源:
CELL DEATH AND DIFFERENTIATION
|
2016年
/
23卷
/
02期
关键词:
PALMITATE-INDUCED APOPTOSIS;
CYSTIC LEUKOENCEPHALOPATHY;
INSULIN-RESISTANCE;
NAD(P)H OXIDASE;
ACTIVATION;
EXPRESSION;
PROTECTS;
CYTOTOXICITY;
MECHANISMS;
TOXICITY;
D O I:
10.1038/cdd.2015.105
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:
RNASET2 is a ubiquitously expressed acidic ribonuclease that has been implicated in diverse pathophysiological processes including tumorigeneis, vitiligo, asthenozoospermia, and neurodegeneration. Prior studies indicate that RNASET2 is induced in response to oxidative stress and that overexpression of RNASET2 sensitizes cells to reactive oxygen species (ROS)-induced cell death through a mechanism that is independent of catalytic activity. Herein, we report a loss-of-function genetic screen that identified RNASET2 as an essential gene for lipotoxic cell death. Haploinsufficiency of RNASET2 confers increased antioxidant capacity and generalized resistance to oxidative stress-mediated cell death in cultured cells. This function is critically dependent on catalytic activity. Furthermore, knockdown of RNASET2 in the Drosophila fat body confers increased survival in the setting of oxidative stress inducers. Together, these findings demonstrate that RNASET2 regulates antioxidant tone and is required for physiological ROS responses.
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页码:347 / 357
页数:11
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