Institute of Toxicology, College of Medicine, National Taiwan University, Taipei 100, Taiwan; Department of Occupational Safety and Health, College of Health Care and Management, Chung Shan Medical University, Taichung, 402, Taiwan.
Department of Occupational Safety and Health, College of Health Care and Management, Chung Shan Medical University, Taichung, 402, Taiwan; Department of Occupational Medicine, Chung Shan Medical University Hospital, Taichung, 402, Taiwan.
Toxicology. 2019 Sep 1;425:152245. doi: 10.1016/j.tox.2019.152245. Epub 2019 Jul 19.
Epidemiological studies have positively linked mercury exposure and neurodegenerative diseases (ND). Methylmercury (MeHg), an organic form of mercury, is a ubiquitous and potent environmental neurotoxicant that easily crosses the blood-brain barrier and causes irreversible injury to the central nervous system (CNS). However, the molecular mechanisms underlying MeHg-induced neurotoxicity remain unclear. Here, the present study found that Neuro-2a cells underwent apoptosis in response to MeHg (1-5 μM), which was accompanied by increased phosphatidylserine (PS) exposure on the outer cellular membrane leaflets, caspase-3 activity, and the activation of caspase cascades and poly (ADP-ribose) polymerase (PARP). Exposure of Neuro-2a cells to MeHg also triggered endoplasmic reticulum (ER) stress, which was identified via several key molecules (including: glucose-regulated protein (GRP)78, GRP94, C/EBP homologous protein (CHOP) X-box binding protein(XBP)-1, protein kinase R-like ER kinase (PERK), eukaryotic initiation factor 2α (eIF2α), inositol-requiring enzyme(IRE)-1, activation transcription factor(AFT)4, and ATF6. Transfection with GRP78-, GRP94-, CHOP-, and XBP-1-specific small interfering (si)RNA significantly suppressed the expression of these proteins, and attenuated cytotoxicity and caspase-12, -7, and -3 activation in MeHg-exposed cells. Furthermore, MeHg dramatically decreased Akt phosphorylation, and the overexpression of activation of Akt1 (myr-Akt1) could significantly prevent MeHg-induced Akt inactivation, as well as apoptotic and ER stress-related signals. Pretreatment with the antioxidant N-acetylcysteine (NAC) effectively prevented MeHg-induced neuronal cell reactive oxygen species (ROS) generation, apoptotic and ER stress-related signals, and Akt inactivation. Collectively, these results indicate that MeHg exerts its cytotoxicity in neurons by inducing ROS-mediated Akt inactivation up-regulated ER stress, which induces apoptosis and ultimately leads to cell death.
流行病学研究已经证实,汞暴露与神经退行性疾病(ND)之间存在正相关关系。甲基汞(MeHg)是一种有机形式的汞,是一种普遍存在且具有强大毒性的环境神经毒素,它很容易穿过血脑屏障,对中枢神经系统(CNS)造成不可逆转的损伤。然而,MeHg 诱导神经毒性的分子机制尚不清楚。本研究发现,Neuro-2a 细胞在 MeHg(1-5 μM)的作用下发生凋亡,同时伴有细胞膜外叶磷脂酰丝氨酸(PS)暴露增加、半胱氨酸天冬氨酸蛋白酶-3(caspase-3)活性增加以及 caspase 级联和多聚(ADP-核糖)聚合酶(PARP)的激活。Neuro-2a 细胞暴露于 MeHg 还会引发内质网(ER)应激,通过几种关键分子(包括葡萄糖调节蛋白(GRP)78、GRP94、C/EBP 同源蛋白(CHOP)X 盒结合蛋白(XBP)-1、蛋白激酶 R 样内质网激酶(PERK)、真核起始因子 2α(eIF2α)、肌醇需求酶 1(IRE)-1、激活转录因子(AFT)4 和 ATF6)来识别。用 GRP78、GRP94、CHOP 和 XBP-1 的特异性小干扰(si)RNA 转染可显著抑制这些蛋白的表达,并减弱 MeHg 暴露细胞的细胞毒性和 caspase-12、-7 和 -3 的激活。此外,MeHg 显著降低 Akt 磷酸化,过表达 Akt1(myr-Akt1)可显著防止 MeHg 诱导的 Akt 失活以及凋亡和 ER 应激相关信号。抗氧化剂 N-乙酰半胱氨酸(NAC)预处理可有效防止 MeHg 诱导的神经元细胞活性氧(ROS)生成、凋亡和 ER 应激相关信号以及 Akt 失活。总之,这些结果表明,MeHg 通过诱导 ROS 介导的 Akt 失活来发挥其在神经元中的细胞毒性,上调 ER 应激,诱导细胞凋亡,最终导致细胞死亡。