| Literature DB >> 26514935 |
Ran Chen1, Liang Deng2, Xinxin Yu1, Xiuxiu Wang1, Liye Zhu3, Tao Yu3, Yiheng Zhang1, Bo Zhou1, Wentao Xu3, Liang Chen4, Haoshu Luo5.
Abstract
Ochratoxin A (OTA) is a mycotoxin which has been shown to be nephrotoxic, hepatotoxic, and immunotoxic to animals, and mainly exists in the mildew grain. MicroRNAs (miRNAs) regulate a wide variety of cellular processes. However, the toxic effects of OTA on the germ cell and whether miRNAs mediate the effects of OTA-induced GC-2 cell apoptosis are still not clear. In the present study, OTA treatment resulted in a dose-dependent increase apoptosis in GC-2 cells. MiR-122 was increased in the OTA-treated GC-2 cells. It showed that Bcl-w was down-regulated after OTA treatment, and caspase-3 was obviously activated. Cyclin G1 (CCNG1) was significantly decreased, and inversely the expression of p53 was increased. Inhibition of miR-122 partly relieved the OTA-induced GC-2 cell apoptosis. These results indicate that OTA induces GC-2 cell apoptosis by causing the increase of caspase-3 activity and that miR-122 partly mediates the OTA-induced cell apoptosis.Entities:
Keywords: Cell apoptosis; GC-2 cell; Ochratoxin A; miR-122
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Year: 2015 PMID: 26514935 DOI: 10.1016/j.tiv.2015.10.011
Source DB: PubMed Journal: Toxicol In Vitro ISSN: 0887-2333 Impact factor: 3.500