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α-突触核蛋白毒性机制:最新进展与展望

Mechanisms of alpha-synuclein toxicity: An update and outlook.

作者信息

Brás Inês Caldeira, Xylaki Mary, Outeiro Tiago Fleming

机构信息

Department of Experimental Neurodegeneration, Center for Biostructural Imaging of Neurodegeneration, University Medical Center Göttingen, Göttingen, Germany.

Department of Experimental Neurodegeneration, Center for Biostructural Imaging of Neurodegeneration, University Medical Center Göttingen, Göttingen, Germany; Max Planck Institute for Experimental Medicine, Göttingen, Germany; Institute of Neuroscience, The Medical School, Newcastle University, Newcastle upon Tyne, United Kingdom.

出版信息

Prog Brain Res. 2020;252:91-129. doi: 10.1016/bs.pbr.2019.10.005. Epub 2019 Nov 23.

Abstract

Alpha-synuclein (aSyn) was identified as the main component of inclusions that define synucleinopathies more than 20 years ago. Since then, aSyn has been extensively studied in an attempt to unravel its roles in both physiology and pathology. Today, studying the mechanisms of aSyn toxicity remains in the limelight, leading to the identification of novel pathways involved in pathogenesis. In this chapter, we address the molecular mechanisms involved in synucleinopathies, from aSyn misfolding and aggregation to the various cellular effects and pathologies associated. In particular, we review our current understanding of the mechanisms involved in the spreading of aSyn between different cells, from the periphery to the brain, and back. Finally, we also review recent studies on the contribution of inflammation and the gut microbiota to pathology in synucleinopathies. Despite significant advances in our understanding of the molecular mechanisms involved, we still lack an integrated understanding of the pathways leading to neurodegeneration in PD and other synucleinopathies, compromising our ability to develop novel therapeutic strategies.

摘要

20多年前,α-突触核蛋白(aSyn)被确定为定义突触核蛋白病的包涵体的主要成分。从那时起,人们对aSyn进行了广泛研究,试图阐明其在生理和病理过程中的作用。如今,研究aSyn毒性机制仍然备受关注,这使得人们发现了与发病机制相关的新途径。在本章中,我们将探讨突触核蛋白病所涉及的分子机制,从aSyn的错误折叠和聚集到与之相关的各种细胞效应和病理变化。特别地,我们回顾了目前对aSyn在不同细胞间传播机制的理解,这种传播从外周到大脑,再返回。最后,我们还回顾了关于炎症和肠道微生物群对突触核蛋白病病理影响的最新研究。尽管我们对所涉及的分子机制有了重大进展,但我们仍然缺乏对导致帕金森病和其他突触核蛋白病神经退行性变途径的综合理解,这削弱了我们开发新治疗策略的能力。

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