2,5-己二酮通过PI3K/Akt/mTOR通路诱导VSC4.1细胞自噬死亡

IF 3.743 Q2 Biochemistry, Genetics and Molecular Biology Molecular BioSystems Pub Date : 2017-07-28 DOI:10.1039/C7MB00001D
Huai Guan, Hua Piao, Zhiqiang Qian, Xueying Zhou, Yijie Sun, Chenxue Gao, Shuangyue Li and Fengyuan Piao
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引用次数: 17

摘要

2,5-己二酮(HD)是正己烷的重要生物活性代谢物,介导母体化合物的神经毒性。越来越多的证据表明,过度激活的自噬可导致自噬神经元死亡;然而,过度自噬是否参与hd诱导的神经毒性尚不清楚。为了研究HD对VSC4.1细胞自噬的影响及其潜在机制,我们分别用5、15和25 mM HD处理VSC4.1细胞24 h。我们的研究结果表明,HD诱导VSC4.1细胞过度自噬呈剂量依赖性,并且在PI3K激活剂、Akt激活剂或mTOR激活剂存在时,过度自噬明显减轻。这些结果表明,HD通过抑制PI3K/Akt/mTOR信号通路诱导VSC4.1细胞过度自噬。LDH检测显示,HD导致VSC4.1细胞死亡呈浓度依赖性增加,而自噬抑制剂PIK-III可显著降低HD的死亡率。这些结果也表明HD通过信号通路诱导VSC4.1细胞自噬死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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2,5-Hexanedione induces autophagic death of VSC4.1 cells via a PI3K/Akt/mTOR pathway

2,5-Hexanedione (HD) is an important bioactive metabolite of n-hexane, which mediates the neurotoxicity of the parent compound. Increasing evidence suggests that over-activated autophagy can lead to autophagic neuronal death; however, whether the excessive autophagy is involved in HD-induced neurotoxicity remains unknown. To investigate the effect of HD on autophagy and to find its underlying mechanism, we respectively treated VSC4.1 cells with 5, 15 and 25 mM HD for 24 h. Our results show that HD induced excessive autophagy of VSC4.1 cells in a dose-dependent manner, also, the over-activated autophagy was significantly mitigated in the presence of PI3K activator or Akt activator or mTOR activator. These results indicate that HD induces excessive autophagy of VSC4.1 cells by repressing the PI3K/Akt/mTOR signaling pathway. LDH assay showed that HD contributed to a concentration dependent increase in VSC4.1 cell death, which was significantly reduced by the administration of PIK-III, an autophagy inhibitor. These results also indicate that HD induces autophagic death of VSC4.1 cells via the signaling pathway.

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来源期刊
Molecular BioSystems
Molecular BioSystems 生物-生化与分子生物学
CiteScore
2.94
自引率
0.00%
发文量
0
审稿时长
2.6 months
期刊介绍: Molecular Omics publishes molecular level experimental and bioinformatics research in the -omics sciences, including genomics, proteomics, transcriptomics and metabolomics. We will also welcome multidisciplinary papers presenting studies combining different types of omics, or the interface of omics and other fields such as systems biology or chemical biology.
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