TFEB 介导的自噬-溶酶体功能障碍在锰神经毒性中的作用

IF 2.9 Q2 TOXICOLOGY
Jiaqiao Lu , Peng Su , Fang Zhao , Kailun Yu , Xunbo Yang , Hui Lv , Diya Wang , Jianbin Zhang
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引用次数: 0

摘要

长期摄入过量的锰会对神经系统造成不可逆的损伤,主要影响黑质-纹状体通路。通过模拟锰暴露的小鼠模型,我们深入研究了锰对中枢神经运动系统的影响,发现自噬-溶酶体功能障碍是锰诱导神经毒性的关键因素。我们的研究揭示了 TFEB 在锰引发的神经元自噬功能障碍中发挥作用背后的分子机制,为锰诱导蛋白质异常积累的细胞和分子机制提供了见解。这项研究为今后旨在防范锰神经毒性的工作奠定了重要的理论基础。此外,TFEB有望成为锰暴露的早期分子生物标志物,为暴露于锰的人群提供先期防护和临床治疗的坚实基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The role of TFEB-mediated autophagy-lysosome dysfunction in manganese neurotoxicity

The role of TFEB-mediated autophagy-lysosome dysfunction in manganese neurotoxicity

Excessive long-term manganese intake can inflict irreversible damage to the nervous system, with a predominant effect on the substantia nigra-striatum pathway. Through a mouse model simulating manganese exposure, we delved into its implications on the central nervous motor system, uncovering autophagy-lysosome dysfunction as a pivotal factor in manganese-induced neurotoxicity. Our research illuminated the molecular mechanisms behind TFEB’s role in manganese-triggered neuronal autophagy dysfunction, offering insights into the cellular and molecular mechanisms of manganese-induced abnormal protein accumulation. This study lays a significant theoretical foundation for future endeavors aimed at safeguarding against manganese neurotoxicity. Furthermore, TFEB emerges as a potential early molecular biomarker for manganese exposure, providing a solid basis for preemptive protection and clinical treatment for populations exposed to manganese.

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来源期刊
Current Research in Toxicology
Current Research in Toxicology Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
4.70
自引率
3.00%
发文量
33
审稿时长
82 days
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