甲基汞通过小胶质细胞中的 ASK1/p38 信号通路诱导 TNF-α 表达,从而诱导神经元细胞死亡。
Methylmercury induces neuronal cell death by inducing TNF-α expression through the ASK1/p38 signaling pathway in microglia.
机构信息
Laboratory of Molecular and Biochemical Toxicology, Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Aoba-ku, Aramaki, Sendai, Miyagi, 980-8578, Japan.
Laboratory of Molecular Biology and Metabolism, Graduate School of Pharmaceutical Sciences, Tohoku University, 6-3 Aoba, Aoba-ku, Sendai, Miyagi, 980-8578, Japan.
出版信息
Sci Rep. 2021 May 10;11(1):9832. doi: 10.1038/s41598-021-89210-7.
We recently found that tumor necrosis factor-α (TNF-α) may be involved in neuronal cell death induced by methylmercury in the mouse brain. Here, we examined the cells involved in the induction of TNF-α expression by methylmercury in the mouse brain by in situ hybridization. TNF-α-expressing cells were found throughout the brain and were identified as microglia by immunostaining for ionized calcium binding adaptor molecule 1 (Iba1). Methylmercury induced TNF-α expression in mouse primary microglia and mouse microglial cell line BV2. Knockdown of apoptosis signal-regulating kinase 1 (ASK1), an inflammatory cytokine up-regulator that is responsible for reactive oxygen species (ROS), decreased methylmercury-induced TNF-α expression through decreased phosphorylation of p38 MAP kinase in BV2 cells. Suppression of methylmercury-induced reactive oxygen species (ROS) by antioxidant treatment largely abolished the induction of TNF-α expression and phosphorylation of p38 by methylmercury in BV2 cells. Finally, in mouse brain slices, the TNF-α antagonist (WP9QY) inhibited neuronal cell death induced by methylmercury, as did the p38 inhibitor SB203580 and liposomal clodronate (a microglia-depleting agent). These results indicate that methylmercury induces mitochondrial ROS that are involved in activation of the ASK1/p38 pathway in microglia and that this is associated with induction of TNF-α expression and neuronal cell death.
我们最近发现肿瘤坏死因子-α(TNF-α)可能参与了甲基汞诱导的小鼠大脑神经元细胞死亡。在这里,我们通过原位杂交技术研究了甲基汞诱导小鼠大脑中 TNF-α表达的相关细胞。TNF-α 表达细胞遍布整个大脑,并通过对离子钙结合衔接分子 1(Iba1)的免疫染色鉴定为小胶质细胞。甲基汞诱导小鼠原代小胶质细胞和小鼠小胶质细胞系 BV2 中 TNF-α 的表达。凋亡信号调节激酶 1(ASK1)的敲低,作为一种负责活性氧(ROS)的炎症细胞因子上调物,通过降低 BV2 细胞中 p38 MAP 激酶的磷酸化,降低了甲基汞诱导的 TNF-α 表达。抗氧化剂处理抑制甲基汞诱导的活性氧(ROS),在很大程度上消除了 BV2 细胞中 TNF-α 表达和 p38 的磷酸化。最后,在小鼠脑切片中,TNF-α 拮抗剂(WP9QY)抑制了甲基汞诱导的神经元细胞死亡,p38 抑制剂 SB203580 和脂质体氯膦酸盐(一种小胶质细胞耗竭剂)也有同样的效果。这些结果表明,甲基汞诱导的线粒体 ROS 参与了小胶质细胞中 ASK1/p38 途径的激活,这与 TNF-α 表达和神经元细胞死亡的诱导有关。
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