Collier Timothy J, Redmond D Eugene, Steece-Collier Kathy, Lipton Jack W, Manfredsson Fredric P
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.
Front Neurosci. 2016 Jan 29;10:12. doi: 10.3389/fnins.2016.00012. eCollection 2016.
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.
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。