Arsenite stabilizes HIF-1α protein through p85α-mediated up-regulation of inducible Hsp70 protein expression

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作者
Wei Guo
Zhuo Yang
Qing Xia
Jinyi Liu
Yonghui Yu
Jingxia Li
Zhenghong Zuo
Dongyun Zhang
Xueyong Li
Xianglin Shi
Chuanshu Huang
机构
[1] New York University School of Medicine,Nelson Institute of Environmental Medicine
[2] Wuhan University,Oversea Laboratory, Center for Medical Research
[3] University of Kentucky,Graduate Center for Toxicology
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Hsp70; HIF-1α; p85α; Akt; Arsenite;
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摘要
Hypoxia-inducible factor-1α (HIF-1α) has been reported to regulate over 100 gene expressions in response to hypoxia and other stress conditions. In the present study, we found that arsenite could induce HIF-1α protein accumulation in both mouse epidermal Cl41 cells and mouse embryonic fibroblasts (MEFs). Knockout of p85α, a regulatory subunit of PI-3K, in MEFs (p85α−/−) dramatically decreased the arsenite-induced HIF-1α accumulation, indicating that p85α is crucial for arsenite effects on the stabilization of HIF-1α protein. Our further studies suggest that arsenite could induce inducible Hsp70 expression, and transfection of inducible Hsp70 into p85α−/− MEFs could restore HIF-1α protein accumulation. Moreover, the results using EMSA and Supershift assays indicate that p85α is crucial for arsenite-induced activation of the heat-shock transcription factor 1 (HSF-1), which is responsible for transcription of inducible Hsp70. Taken together, p85α-mediated HIF-1α stabilization upon arsenite exposure is specifically through HSF-1 activation and subsequent up-regulation of the inducible Hsp70 expression.
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页码:475 / 488
页数:13
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