Neuroregeneration Laboratories, Harvard Medical School, McLean Hospital Belmont, Massachusetts, 02478.
Shire 300 Shire Way, Lexington, Massachusetts, 02421.
Ann Clin Transl Neurol. 2015 Apr;2(4):433-8. doi: 10.1002/acn3.177. Epub 2015 Feb 6.
The principal risk factor for developing most adult onset neurodegenerative diseases is aging, with incidence rising significantly after age 50. Despite research efforts, the causes of Parkinson's disease (PD) remain unknown. As neurons age, they show signs of diminished lysosomal and mitochondrial function, including increased oxidative stress and accumulation of misfolded proteins, and these changes become exacerbated PD. We show that activity of the lysosomal hydrolase glucocerebrosidase gradually diminishes with age in the substantia nigra and putamen of healthy controls. This reduction is comparable to glucocerebrosidase activity in GBA1-mutation carrier PD patients. These data, demonstrate for the first time that an age-dependent reduction in glucocerebrosidase activity may lower the threshold for developing PD.
导致大多数成人发病的神经退行性疾病的主要风险因素是衰老,发病率在 50 岁后显著上升。尽管进行了研究,但帕金森病 (PD) 的病因仍不清楚。随着神经元衰老,其溶酶体和线粒体功能会出现减弱的迹象,包括氧化应激增加和错误折叠蛋白堆积,这些变化在 PD 中变得更加严重。我们发现,在健康对照者的黑质和纹状体中,溶酶体水解酶葡萄糖脑苷脂酶的活性随年龄的增长而逐渐降低。这种减少与 GBA1 基因突变携带者 PD 患者的葡萄糖脑苷脂酶活性相当。这些数据首次表明,葡萄糖脑苷脂酶活性的年龄依赖性降低可能降低了发生 PD 的阈值。