Suppr超能文献

α-突触核蛋白功能丧失是帕金森病病理的一个促成因素吗?来自非人类灵长类动物的证据。

Is Alpha-Synuclein Loss-of-Function a Contributor to Parkinsonian Pathology? Evidence from Non-human Primates.

作者信息

Collier Timothy J, Redmond D Eugene, Steece-Collier Kathy, Lipton Jack W, Manfredsson Fredric P

机构信息

Department of Translational Science & Molecular Medicine, Michigan State UniversityGrand Rapids, MI, USA; Hauenstein Neuroscience Center, Mercy Health Saint Mary'sGrand Rapids, MI, USA.

Departments of Psychiatry & Neurosurgery, Yale University School of MedicineNew Haven, CT, USA; Axion Research FoundationHamden, CT, USA.

出版信息

Front Neurosci. 2016 Jan 29;10:12. doi: 10.3389/fnins.2016.00012. eCollection 2016.

Abstract

Accumulation of alpha-synuclein (α-syn) in Lewy bodies and neurites of midbrain dopamine neurons is diagnostic for Parkinson's disease (PD), leading to the proposal that PD is a toxic gain-of-function synucleinopathy. Here we discuss the alternative viewpoint that α-syn displacement from synapses by misfolding and aggregation results in a toxic loss-of-function. In support of this hypothesis we provide evidence from our pilot study demonstrating that knockdown of endogenous α-syn in dopamine neurons of non-human primates reproduces the pattern of nigrostriatal degeneration characteristic of PD.

摘要

α-突触核蛋白(α-syn)在路易小体和中脑多巴胺神经元的神经突中积累是帕金森病(PD)的诊断依据,这使得人们提出PD是一种有毒性的功能获得性突触核蛋白病。在此,我们讨论另一种观点,即α-syn因错误折叠和聚集而从突触中被置换,导致有毒性的功能丧失。为支持这一假设,我们提供了来自初步研究的证据,表明在非人类灵长类动物的多巴胺神经元中敲低内源性α-syn可重现PD特征性的黑质纹状体变性模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fb0/4731516/f43b752bec99/fnins-10-00012-g0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验