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天然除虫菊素通过激活 AMPK/mTOR 通路诱导 HepG2 细胞自噬。

Natural pyrethrins induce autophagy of HepG2 cells through the activation of AMPK/mTOR pathway.

机构信息

Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, Shanghai, 200237, China.

College of Life and Environmental Sciences, Shanghai Normal University, Shanghai, 200234, China.

出版信息

Environ Pollut. 2018 Oct;241:1091-1097. doi: 10.1016/j.envpol.2018.06.049. Epub 2018 Jun 18.

Abstract

Natural pyrethrins, one kind of insects' neural toxin, have been used worldwide for the control of pests of crops, livestock, and human beings. However, their specific mechanisms of action are incompletely understood and hence further investigation is required. Here we used a series of experiments including colony formation, fluorescent staining, western blotting, enzyme activity detection, immunofluorescence analysis, and real-time quantitative PCR (QPCR) to investigate whether natural pyrethrins (0-40 μg/mL) are able to modulate autophagy process through AMPK/mTOR signaling pathway, in order to reveal their cytotoxic mechanisms. The results showed that natural pyrethrins markedly inhibited the proliferation of HepG2 cells in both concentration- and time-dependent manners. Particularly, natural pyrethrins could induce the resulting autophagosome, and the intensification of LC3-II formation and translocation, the accumulation of Beclin-1 and the reduction of p62 and thus autophagy. We clarified that natural pyrethrins induced the abnormal level of oxidation reduction metabolism, leading to mitochondrial permeability transition pore (mPTP) opening, ATP depletion and mitochondria eliminating by autophagy. Moreover, the phosphorylation levels of AMPK were significantly enhanced, and the mTOR and p70s6k phosphorylation were drastically decreased. These results showed that natural pyrethrins induced autophagy of HepG2 cells and activation of the AMPK/mTOR signaling pathway might have potential risk to human health.

摘要

天然除虫菊酯是一种昆虫神经毒素,已被广泛用于防治农作物、家畜和人类害虫。然而,其作用机制尚不完全清楚,因此需要进一步研究。在这里,我们使用了一系列实验,包括集落形成实验、荧光染色实验、Western blot 实验、酶活性检测实验、免疫荧光分析实验和实时定量 PCR(QPCR)实验,以研究天然除虫菊酯(0-40μg/mL)是否能够通过 AMPK/mTOR 信号通路调节自噬过程,从而揭示其细胞毒性机制。结果表明,天然除虫菊酯能够以浓度和时间依赖性方式显著抑制 HepG2 细胞的增殖。特别是,天然除虫菊酯能够诱导自噬体的形成,增强 LC3-II 的形成和转位,增加 Beclin-1 的积累,减少 p62 的积累,从而诱导自噬。我们阐明了天然除虫菊酯诱导氧化还原代谢异常水平,导致线粒体通透性转换孔(mPTP)开放、ATP 耗竭和线粒体通过自噬消除。此外,AMPK 的磷酸化水平显著增强,而 mTOR 和 p70s6k 的磷酸化水平则明显降低。这些结果表明,天然除虫菊酯诱导了 HepG2 细胞的自噬,并激活了 AMPK/mTOR 信号通路,这可能对人类健康有潜在风险。

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