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Identification of Cells Involved in the Induction of TNF-A Expression by Methylmercury in the Mouse Brain and Its Molecular Mechanisms

机译:鉴定小鼠脑中甲基汞诱导TNF-A表达的细胞及其分子机制

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Methylmercury is an environmental pollutant that causes neurotoxicity. Recently, we found that tumor necrosis factor-a (TNF-a; inflammatory cytokine) is selectively induced in the brain of mice administered methylmercury. Although TNF-a may be involved in the neurotoxicity caused by methylmercury, the mechanisms involved in the induction of TNF-a expression by methylmercury are unknown. In this study, we aimed to identify cells involved in the induction of TNF-a expression by methylmercury in mice brain, to elucidate the underlying molecular mechanisms. Seven days after subcutaneous injection of C57BL6 mice with methylmercuric chloride (25 mg/kg), TNF-a mRNA levels were determined in the brain tissues by in situ hybridization. We found that TNF-a was hardly expressed in the saline-administered group, whereas TNF-a-expressing cells were observed in the whole area of the brain in the methylmercury-treated group. It was reported that astrocytes and microglial cells are involved in the induction of TNF-a expression. Therefore, we performed immunostaining using antibodies specific for GFAP or IBA1, which are specifically expressed in astrocytes and microglial cells, respectively. The TNF-a-expressing cells did not overlap with the GFAP-positive cells, but with the IBAl-positive cells. The results suggest that microglial cells are mainly involved in the induction of TNF-a expression by methylmercury in the mouse brain. In addition, methylmercury induced TNF-a expression in mouse microglial cell line BV2. MAP kinases such as JNK, ERK, and p38 are known to be involved in the induction of TNF-a expression in microglial cells. We found that all three MAP kinases were phosphorylated by methylmercury treatment. Moreover, when the cells were pretreated with specific inhibitors, only the p38 inhibitor suppressed the induction of TNF-a expression by methylmercury. These results indicate that methylmercury may induce TNF-a expression via activation of p38 in microglial cells.
机译:甲基汞是一种导致神经毒性的环境污染物。最近,我们发现肿瘤坏死因子-A(TNF-A;炎症细胞因子)在给予甲基汞的小鼠的脑中被选择性地诱导。虽然TNF-A可以参与由甲基汞引起的神经毒性,但是甲基汞诱导TNF-A表达的机制未知。在这项研究中,我们旨在鉴定甲基汞在小鼠脑中甲基汞诱导TNF-A表达的细胞,以阐明潜在的分子机制。通过原位杂交在脑组织中测定皮下注射甲基镁(25mg / kg)后七天的C57BL6小鼠。用脑组织测定TNF-A mRNA水平。我们发现TNF-A几乎不在盐水施用的基团中表达,而在甲基汞治疗组大脑的整个区域中观察到TNF-A表达细胞。据报道,星形胶质细胞和小胶质细胞参与诱导TNF-A表达。因此,我们使用针对GFAP或IBA1特异的抗体进行免疫抑制,其分别以星形胶质细胞和小胶质细胞特异性地表达。 TNF-A表达的细胞与GFAP阳性细胞没有重叠,而是用IBAL阳性细胞重叠。结果表明,小胶质细胞主要参与在小鼠脑中甲基汞的TNF-A表达的诱导。此外,甲基汞在小鼠小胶质细胞系BV2中诱导TNF-A表达。已知地图激酶如JNK,ERK和P38涉及诱导TNF-A在微胶质细胞中的表达。我们发现所有三种地图激酶通过甲基汞处理磷酸化。此外,当用特异性抑制剂预处理细胞,只有P38抑制剂抑制甲基汞的TNF-A表达的诱导。这些结果表明,通过在微胶质细胞中激活P38,甲基汞可以诱导TNF-A表达。

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