Friesen Erik L, De Snoo Mitch L, Rajendran Luckshi, Kalia Lorraine V, Kalia Suneil K
Krembil Research Institute, Toronto Western Hospital, University Health Network, 60 Leonard Avenue, Toronto, ON, Canada.
Department of Laboratory Medicine and Pathobiology, University of Toronto, 1 King's College Circle, Toronto, ON, Canada.
Parkinsons Dis. 2017;2017:5015307. doi: 10.1155/2017/5015307. Epub 2017 Aug 21.
Parkinson's disease (PD) is the second most common neurodegenerative disorder and is characterized by the presence of pathological intracellular aggregates primarily composed of misfolded -synuclein. This pathology implicates the molecular machinery responsible for maintaining protein homeostasis (proteostasis), including molecular chaperones, in the pathobiology of the disease. There is mounting evidence from preclinical and clinical studies that various molecular chaperones are downregulated, sequestered, depleted, or dysfunctional in PD. Current therapeutic interventions for PD are inadequate as they fail to modify disease progression by ameliorating the underlying pathology. Modulating the activity of molecular chaperones, cochaperones, and their associated pathways offers a new approach for disease modifying intervention. This review will summarize the potential of chaperone-based therapies that aim to enhance the neuroprotective activity of molecular chaperones or utilize small molecule chaperones to promote proteostasis.
帕金森病(PD)是第二常见的神经退行性疾病,其特征是存在主要由错误折叠的α-突触核蛋白组成的病理性细胞内聚集体。这种病理学表明,负责维持蛋白质稳态(蛋白质平衡)的分子机制,包括分子伴侣,参与了该疾病的病理生物学过程。临床前和临床研究中有越来越多的证据表明,在帕金森病中,各种分子伴侣被下调、隔离、耗尽或功能失调。目前针对帕金森病的治疗干预措施并不充分,因为它们无法通过改善潜在病理来改变疾病进展。调节分子伴侣、辅助分子伴侣及其相关途径的活性为疾病修饰干预提供了一种新方法。本综述将总结基于伴侣蛋白的疗法的潜力,这些疗法旨在增强分子伴侣的神经保护活性或利用小分子伴侣来促进蛋白质稳态。