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镍纳米颗粒诱导 GC-1 细胞凋亡中 PI3K/AKT/mTOR 信号通路的作用及其机制。

Effect and mechanism of PI3K/AKT/mTOR signaling pathway in the apoptosis of GC-1 cells induced by nickel nanoparticles.

机构信息

Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing, 210009, China.

Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing, 210009, China.

出版信息

Chemosphere. 2020 Sep;255:126913. doi: 10.1016/j.chemosphere.2020.126913. Epub 2020 Apr 27.

Abstract

Nickel nanoparticles (Ni NPs) have a wide range of application prospects, but there is still a lack of their safety evaluation for the reproductive system. Nowadays, male reproductive health has been widely concerned because of the increasing incidence of male infertility. Studies have shown that Ni NPs can cause male reproductive toxicity. The purpose of this study was to investigate the toxicity of Ni NPs on GC-1 cells, a mouse spermatogonia cell line, and to explore the possible mechanism underlying the induction of apoptosis via PI3K/AKT/mTOR signaling pathway. The cell ultrastructure was firstly observed under a transmission electron microscope. Then, cell proliferation, cycle and apoptosis were detected by CCK-8 and flow cytometry, respectively. Furthermore, the expression levels of related proteins and genes were determined by Western blot and Reverse transcription-polymerase chain reaction, respectively. The results showed that Ni NPs could not only cause changes in cell ultrastructure, decreased survival rate and arrested G1 phase cell cycle, but also activated apoptosis pathway by inhibiting the PI3K/AKT/mTOR signaling pathway. The results of this study provide novel insights to explore the mechanisms of reproductive toxicity of Ni NPs and are of great significance to develop safety evaluation criteria for Ni NPs.

摘要

镍纳米颗粒(Ni NPs)具有广泛的应用前景,但它们对生殖系统的安全性评估仍然缺乏。如今,由于男性不育症的发病率不断上升,男性生殖健康受到了广泛关注。研究表明,Ni NPs 可导致雄性生殖毒性。本研究旨在探讨 Ni NPs 对 GC-1 细胞(一种小鼠精原细胞系)的毒性作用,并通过 PI3K/AKT/mTOR 信号通路探索诱导细胞凋亡的可能机制。首先通过透射电子显微镜观察细胞超微结构。然后,通过 CCK-8 和流式细胞术分别检测细胞增殖、细胞周期和细胞凋亡。此外,通过 Western blot 和逆转录-聚合酶链反应分别测定相关蛋白和基因的表达水平。结果表明,Ni NPs 不仅可引起细胞超微结构改变、降低存活率和使 G1 期细胞周期阻滞,还可通过抑制 PI3K/AKT/mTOR 信号通路激活细胞凋亡途径。本研究结果为探讨 Ni NPs 生殖毒性的机制提供了新的见解,对制定 Ni NPs 的安全性评价标准具有重要意义。

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