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暴露于甲基汞的普通狨猴小脑的蛋白质组学分析。

Proteomic Analysis of Cerebellum in Common Marmoset Exposed to Methylmercury.

作者信息

Shao Yueting, Yamamoto Megumi, Figeys Daniel, Ning Zhibin, Chan Hing Man

机构信息

*Natural Resources and Environmental Studies Program, University of Northern British Columbia, Prince George, British Columbia V2N 4Z9, Canada.

Department of Basic Medical Science, National Institute for Minamata Disease, Minamata, Kumamoto 867-0008, Japan.

出版信息

Toxicol Sci. 2015 Jul;146(1):43-51. doi: 10.1093/toxsci/kfv069. Epub 2015 Mar 25.

Abstract

The cerebellum is known as the major target regions of methylmercury (MeHg) toxicity, but the mechanisms are still not fully understood. We studied the effects of MeHg exposure in the cerebellum of common marmoset (Callithrix jacchus) using a shotgun proteomic approach with liquid chromatography coupled to mass spectrometry. A total of 1000 common proteins were identified in all samples, and 102 proteins were significantly differentially expressed in the cerebellum of common marmoset with orally dosed MeHg (1.5 mg MeHg/kg body weight for 2 weeks) compared with those of the control group. Functional enrichment analysis and pathway predictions showed that the differentially expressed proteins were involved in carbohydrate derivative metabolic process, ion transport including synaptic transmission, cell development, and calcium signaling pathway. Cellular component enrichment analysis showed that they were mainly distributed in plasma membrane, excitatory synapse, and synaptic membrane. These results indicate that synaptic transmission and calcium signaling pathways are the core functions affected by MeHg. We found a total of 21 novel proteins affected by MeHg in synaptic transmission and calcium signaling pathways. DLG4: (PSD95) and MIR-19A/MIR-19B were found to be potential key targets leading to the multiple effects of MeHg neurotoxicity. These results show the global effects of MeHg on cellular functions and pathways leading to neurological deficits in common marmoset.

摘要

小脑是甲基汞(MeHg)毒性的主要靶区,但相关机制仍未完全明确。我们采用液相色谱-质谱联用的鸟枪法蛋白质组学方法,研究了普通狨猴(Callithrix jacchus)小脑暴露于MeHg后的影响。在所有样本中共鉴定出1000种常见蛋白质,与对照组相比,口服给予MeHg(1.5 mg MeHg/kg体重,持续2周)的普通狨猴小脑中,有102种蛋白质存在显著差异表达。功能富集分析和通路预测表明,差异表达的蛋白质参与碳水化合物衍生物代谢过程、包括突触传递在内的离子转运、细胞发育和钙信号通路。细胞成分富集分析表明,它们主要分布在质膜、兴奋性突触和突触膜中。这些结果表明,突触传递和钙信号通路是受MeHg影响的核心功能。我们在突触传递和钙信号通路中总共发现了21种受MeHg影响的新蛋白质。发现DLG4(PSD95)和MIR-19A/MIR-19B是导致MeHg神经毒性产生多种效应的潜在关键靶点。这些结果显示了MeHg对普通狨猴细胞功能和导致神经功能缺损的通路的整体影响。

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