Department of Genetics and Evolution, Sciences III, University of Geneva, 30 Quai Ernest-Ansermet, CH-1211 Geneva-4, Switzerland.
Int J Mol Sci. 2018 Oct 26;19(11):3343. doi: 10.3390/ijms19113343.
Parkinson's disease (PD) is the most common cause of movement disorders and is characterized by the progressive loss of dopaminergic neurons in the substantia nigra. It is increasingly recognized as a complex group of disorders presenting widely heterogeneous symptoms and pathology. With the exception of the rare monogenic forms, the majority of PD cases result from an interaction between multiple genetic and environmental risk factors. The search for these risk factors and the development of preclinical animal models are in progress, aiming to provide mechanistic insights into the pathogenesis of PD. This review summarizes the studies that capitalize on modeling sporadic (i.e., nonfamilial) PD using and discusses their methodologies, new findings, and future perspectives.
帕金森病(PD)是运动障碍最常见的原因,其特征是黑质中多巴胺能神经元进行性丧失。它越来越被认为是一组复杂的疾病,表现出广泛异质的症状和病理学。除了罕见的单基因形式外,大多数 PD 病例是由多种遗传和环境风险因素相互作用引起的。目前正在寻找这些风险因素,并开发临床前动物模型,旨在为 PD 的发病机制提供机制见解。本综述总结了利用 和讨论其方法学、新发现和未来展望来模拟散发性(即非家族性)PD 的研究。