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 Current Research in Toxicology Pub Date : 2024-01-01 DOI:10.1016/j.crtox.2024.100193
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。

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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
期刊最新文献
Editorial Board Contents Evaluation of the diphenyl herbicide, oxyfluorfen, for effects on thyroid hormones in the juvenile rat Ethylene dimethanesulfonate effects on gene promoter activities related to the endocrine function of immortalized Leydig cell lines R2C and MA-10 Placental transfer of tofacitinib in the ex vivo dual-side human placenta perfusion model
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