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TFEB介导的自噬-溶酶体功能障碍在锰神经毒性中的作用。

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

作者信息

Lu Jiaqiao, Su Peng, Zhao Fang, Yu Kailun, Yang Xunbo, Lv Hui, Wang Diya, Zhang Jianbin

机构信息

Department of Occupational and Environmental Health, the Ministry of Education Key Lab of Hazard Assessment and Control in Special Operational Environment, School of Public Health, Fourth Military Medical University, No.169 Chang Le West Rd., Xi'an, Shaanxi 710032, China.

Department of Health Service Teaching and Research, Dalian Health Service Training Center of Chinese PLA, Da Lian 116001, China.

出版信息

Curr Res Toxicol. 2024 Sep 11;7:100193. doi: 10.1016/j.crtox.2024.100193. eCollection 2024.

Abstract

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.

摘要

长期过量摄入锰会对神经系统造成不可逆转的损害,对黑质-纹状体通路影响尤为显著。通过模拟锰暴露的小鼠模型,我们深入研究了其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。我们的研究阐明了转录因子EB(TFEB)在锰引发的神经元自噬功能障碍中作用的分子机制,为锰诱导异常蛋白质积累的细胞和分子机制提供了见解。本研究为未来预防锰神经毒性的努力奠定了重要的理论基础。此外,TFEB成为锰暴露的潜在早期分子生物标志物,为锰暴露人群的预防性保护和临床治疗提供了坚实依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/283b/11459403/2cd05733019d/ga1.jpg

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