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The Protective Effect of Autophagy on DNA Damage in Mouse Spermatocyte-Derived Cells Exposed to 1800 MHz Radiofrequency Electromagnetic Fields

机译:自噬对1800MHz射频电磁场暴露于小鼠精子细胞衍生细胞DNA损伤的保护作用

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摘要

Background/Aims: The effects of exposure to radiofrequency electromagnetic fields (RF-EMFs) on the male reproductive system have raised public concern and studies have shown that exposure to RF-EMFs can induce DNA damage and autophagy. However, there are no related reports on the role of autophagy in DNA damage in spermatocytes, especially after exposure to RF-EMFs. The aim of the present study was to determine the mechanism and role of autophagy induced by RF-EMFs in spermatozoa cells. Methods: Mouse spermatocyte-derived cells (GC-2) were exposed to RF-EMFs 4 W/kg for 24 h. The level of reactive oxygen species (ROS) was determined by ROS assay kit. Comet assay was utilized to detect DNA damage. Autophagy was detected by three indicators: LC3II/LC3I, autophagic vacuoles, and GFP-LC3 dots, which were measured by western blot, transmission electron microscopy, and transfection with GFP-LC3, respectively. The expression of the molecular signaling pathway AMP-activated protein kinase (AMPK)/mTOR was determined by western blot. Results: The results showed that RF-EMFs induced autophagy and DNA damage in GC-2 cells via ROS generation, and the autophagy signaling pathway AMPK/mTOR was activated by ROS generation. Furthermore, following inhibition of autophagy by knockdown of AMPKα, increased DNA damage was observed in GC-2 cells following RF-EMFs exposure, and overexpression of AMPKα promoted autophagy and attenuated DNA damage. Conclusions: These findings demonstrated that the autophagy which was induced by RF-EMFs via the AMPK/mTOR signaling pathway could prevent DNA damage in spermatozoa cells.
机译:背景/目的:暴露于男性生殖系统都提出了公众的关注和研究射频电磁场(RF-电磁场)的影响已经表明,暴露于RF-电磁场可诱导DNA损伤和自噬。然而,没有关于自噬在精子细胞DNA损伤中的作用的相关报告,特别是在暴露于RF-EMF后。本研究的目的是确定RF-EMF在精子细胞中诱导的自噬的机制和作用。方法:将小鼠精子细胞衍生的细胞(GC-2)暴露于RF-EMF 4W / kg 24小时。通过ROS测定试剂盒测定反应性氧物质(ROS)的水平。使用彗星测定来检测DNA损伤。通过三种指标检测到自噬:LC3II / LC3I,自噬液压液压和GFP-LC3点,其分别通过蛋白质印迹,透射电子显微镜测量和用GFP-LC3转染。通过蛋白质印迹测定分子信令途径AMP活化蛋白激酶(AMPK)/ mTOR的表达。结果:结果表明,RF-EMF通过ROS产生诱导GC-2细胞中的自噬和DNA损伤,并通过ROS产生激活自噬信号通路AMPK / MTOR。此外,随着AMPKα的敲低抑制自噬后,在RF-EMF暴露后,在GC-2细胞中观察到增加的DNA损伤,并且AMPKα的过表达促进了自噬并减弱了DNA损伤。结论:这些研究结果表明,通过AMPK / MTOR信号传导途径由RF-EMF诱导的自噬能防止细菌细胞中的DNA损伤。

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