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α-突触核蛋白 2.0 - 迈向细胞类型特异性发病机制。

α-Synuclein 2.0 - Moving towards Cell Type Specific Pathophysiology.

机构信息

Institute of Neurophysiology, Goethe University, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.

Department of Medical Neurobiology, Institute of Medical Research Israel-Canada, The Faculty of Medicine, The Hebrew University of Jerusalem, 9112102 Jerusalem, Israel.

出版信息

Neuroscience. 2019 Aug 1;412:248-256. doi: 10.1016/j.neuroscience.2019.06.005. Epub 2019 Jun 14.

Abstract

Since the landmark discovery that point mutations in the α-synuclein gene (SNCA) cause familial Parkinson's disease (PD) more than 2 decades ago, extensive research has been conducted to unravel the molecular and cellular mechanisms by which α-synuclein drives PD pathogenesis resulting in selective neurodegeneration of vulnerable neuronal populations. Current interest focuses on the identification of relevant toxic α-synuclein conformers and their interaction with basic cellular functions. In this context, seminal advances have been made in defining mechanisms of α-synuclein's toxicity in neurons, but many open questions remain regarding its neuronal subtype pathophysiology, as well as the defining the most disease relevant conformations. Moreover, we still only have a partial understanding of the full spectrum of α-synuclein's physiological functions both in neurons and in other cells. In this short review, we focus on cell-specific responses to α-synuclein with a focus on the toxic conformers of α-synuclein. We will not discuss more general cellular death pathways, which have been comprehensively covered by a number of elegant recent reviews.

摘要

自从 20 多年前发现 α-突触核蛋白基因(SNCA)点突变导致家族性帕金森病(PD)以来,人们进行了广泛的研究,以揭示 α-突触核蛋白驱动 PD 发病机制的分子和细胞机制,导致脆弱神经元群体的选择性神经退行性变。目前的研究重点是确定相关的有毒 α-突触核蛋白构象及其与基本细胞功能的相互作用。在这方面,在定义神经元中 α-突触核蛋白毒性的机制方面取得了重大进展,但关于其神经元亚型发病机制以及确定最相关疾病构象的问题仍然很多。此外,我们仍然只是部分了解 α-突触核蛋白在神经元和其他细胞中的全部生理功能。在这篇简短的综述中,我们重点关注α-突触核蛋白对特定细胞的反应,特别关注α-突触核蛋白的有毒构象。我们不会讨论更一般的细胞死亡途径,这些途径已经被一些优雅的最新综述全面涵盖。

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