Laboratory of Neurogenetics, National Institute on Aging, NIH, Building 35, Room 1A116, MSC 3707, 35 Convent Drive, Bethesda, MD 20982-3707, USA.
Mol Neurodegener. 2009 Feb 4;4:9. doi: 10.1186/1750-1326-4-9.
alpha-Synuclein is a small protein that has special relevance for understanding Parkinson disease and related disorders. Not only is alpha-synuclein found in Lewy bodies characteristic of Parkinson disease, but also mutations in the gene for alpha-synuclein can cause an inherited form of Parkinson disease and expression of normal alpha-synuclein can increase the risk of developing Parkinson disease in sporadic, or non-familial, cases. Both sporadic and familial Parkinson disease are characterized by substantial loss of several groups of neurons, including the dopaminergic cells of the substantia nigra that are the target of most current symptomatic therapies. Therefore, it is predicted that alpha-synuclein, especially in its mutant forms or under conditions where its expression levels are increased, is a toxic protein in the sense that it is associated with an increased rate of neuronal cell death. This review will discuss the experimental contexts in which alpha-synuclein has been demonstrated to be toxic. I will also outline what is known about the mechanisms by which alpha-synuclein triggers neuronal damage, and identify some of the current gaps in our knowledge about this subject. Finally, the therapeutic implications of toxicity of alpha-synuclein will be discussed.
α-突触核蛋白是一种小蛋白,对理解帕金森病和相关疾病具有特殊意义。不仅帕金森病特征性的路易小体中存在α-突触核蛋白,而且α-突触核蛋白基因的突变也可导致遗传性帕金森病,而正常α-突触核蛋白的表达可增加散发的(即非家族性的)帕金森病的发病风险。散发性和家族性帕金森病的特征是包括黑质多巴胺能神经元在内的几组神经元大量丧失,这些神经元是大多数目前对症治疗的靶点。因此,有人推测α-突触核蛋白,特别是其突变形式或在其表达水平升高的情况下,是一种毒性蛋白,因为它与神经元细胞死亡速率的增加有关。这篇综述将讨论已经证明α-突触核蛋白具有毒性的实验背景。我还将概述已知的α-突触核蛋白引发神经元损伤的机制,并确定我们对这一主题的认识中的一些当前空白。最后,将讨论α-突触核蛋白毒性的治疗意义。