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在小鼠精母细胞中,共济失调毛细血管扩张症突变基因(ATM)向腺苷酸活化蛋白激酶(AMPK)发出信号以促进自噬,并对镉诱导的活性氧(ROS)作出反应,正向调节DNA损伤。

ATM signals to AMPK to promote autophagy and positively regulate DNA damage in response to cadmium-induced ROS in mouse spermatocytes.

作者信息

Li Renyan, Luo Xue, Zhu Yijian, Zhao Letian, Li Lianbing, Peng Qiang, Ma Mingfu, Gao Yanfei

机构信息

Chongqing Institute of Population and Family Planning, Key Laboratory of Birth Defects and Reproductive Health, Chongqing, China.

Institute of Tropical Medicine, Third Military Medical University, Chongqing, China.

出版信息

Environ Pollut. 2017 Dec;231(Pt 2):1560-1568. doi: 10.1016/j.envpol.2017.09.044. Epub 2017 Sep 28.

Abstract

Cadmium (Cd) is a toxic heavy metal and harmful to human health due to its ability to accumulate in organs. Previous studies have shown that Cd can induce DNA damage and autophagy. Autophagy can stabilize genetic material and DNA integrity. The aim of the present study was to determine the exact mechanism and role of autophagy induced by Cd in spermatozoa cells. Mouse spermatocyte-derived cells (GC-2) were treated with 20 μM Cd chloride for 24 h. The level of reactive oxygen species (ROS), DNA damage, autophagy and the expression of the molecular signaling pathway ATM/AMP-activated protein kinase (AMPK)/mTOR were determined. The results showed that Cd induced autophagy and DNA damage in GC-2 cells via ROS generation, and the autophagy signal pathway AMPK/mTOR was activated by ATM which is a DNA damage sensor. Melatonin, a well-known antioxidant, ameliorated DNA damage, and inhibited autophagy via the AMPK/mTOR signal pathway. Furthermore, after inhibition of autophagy by knockdown of AMPKα, increased DNA damage by Cd treatment was observed in GC-2 cells. These findings demonstrated the protective role of autophagy in DNA damage and suggested that the mechanism of autophagy induced by Cd was through the ATM/AMPK/mTOR signal pathway in spermatozoa cells.

摘要

镉(Cd)是一种有毒重金属,因其能够在器官中蓄积而对人体健康有害。先前的研究表明,镉可诱导DNA损伤和自噬。自噬能够稳定遗传物质和DNA完整性。本研究的目的是确定镉在精子细胞中诱导自噬的确切机制和作用。用20μM氯化镉处理小鼠精母细胞衍生细胞(GC-2)24小时。测定活性氧(ROS)水平、DNA损伤、自噬以及分子信号通路ATM/AMP活化蛋白激酶(AMPK)/mTOR的表达。结果表明,镉通过产生活性氧在GC-2细胞中诱导自噬和DNA损伤,并且自噬信号通路AMPK/mTOR被作为DNA损伤传感器的ATM激活。褪黑素是一种著名的抗氧化剂,可改善DNA损伤,并通过AMPK/mTOR信号通路抑制自噬。此外,在通过敲低AMPKα抑制自噬后,在GC-2细胞中观察到镉处理导致的DNA损伤增加。这些发现证明了自噬在DNA损伤中的保护作用,并表明镉诱导自噬的机制是通过精子细胞中的ATM/AMPK/mTOR信号通路。

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