Suppr超能文献

细胞模型作为研究α-突触核蛋白在帕金森病中作用的工具。

Cellular models as tools for the study of the role of alpha-synuclein in Parkinson's disease.

作者信息

Lázaro Diana F, Pavlou Maria Angeliki S, Outeiro Tiago Fleming

机构信息

Department of Experimental Neurodegeneration, Center for Nanoscale Microscopy and Molecular Physiology of the Brain, University Medical Center Göttingen, 37073 Göttingen, Germany.

Department of Experimental Neurodegeneration, Center for Nanoscale Microscopy and Molecular Physiology of the Brain, University Medical Center Göttingen, 37073 Göttingen, Germany; Max Planck Institute for Experimental Medicine, Goettingen, Germany.

出版信息

Exp Neurol. 2017 Dec;298(Pt B):162-171. doi: 10.1016/j.expneurol.2017.05.007. Epub 2017 May 16.

Abstract

Neurodegenerative diseases are highly debilitating conditions characterised primarily by progressive neuronal loss and impairment of the nervous system. Parkinson's disease (PD) is one of the most common of these disorders, affecting 1-2% of the population above the age of 65. Although the underlying mechanisms of PD have been extensively studied, we still lack a full understanding of the molecular underpinnings of the disease. Thus, the in vitro and in vivo models currently used are able to only partially recapitulate the typical phenotypes of the disease. Here, we review various cell culture models currently used to study the molecular basis of PD, with a focus on alpha-synuclein-associated molecular pathologies. We also discuss how different cell models may constitute powerful tools for high-throughput screening of molecules capable of modulating alpha-synuclein toxicity.

摘要

神经退行性疾病是极具致残性的病症,主要特征为神经元进行性丧失和神经系统损害。帕金森病(PD)是这些疾病中最常见的一种,影响65岁以上人群的1%-2%。尽管对PD的潜在机制已进行了广泛研究,但我们仍未完全了解该疾病的分子基础。因此,目前使用的体外和体内模型仅能部分重现该疾病的典型表型。在此,我们综述了目前用于研究PD分子基础的各种细胞培养模型,重点关注与α-突触核蛋白相关的分子病理学。我们还讨论了不同的细胞模型如何可能成为高通量筛选能够调节α-突触核蛋白毒性的分子的有力工具。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验