Hennis Meghan R, Seamans Katherine W, Marvin Marian A, Casey Bradford H, Goldberg Matthew S
Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America.
Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America ; Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Texas, United States of America.
PLoS One. 2013 Dec 26;8(12):e84894. doi: 10.1371/journal.pone.0084894. eCollection 2013.
Parkinson's disease (PD) is a progressive neurodegenerative disease characterized by loss of neurons in the substantia nigra that project to the striatum and release dopamine. The cause of PD remains uncertain, however, evidence implicates mitochondrial dysfunction and oxidative stress. Although most cases of PD are sporadic, 5-10% of cases are caused by inherited mutations. Loss-of-function mutations in Parkin and DJ-1 were the first to be linked to recessively inherited Parkinsonism. Surprisingly, mice bearing similar loss-of-function mutations in Parkin and DJ-1 do not show age-dependent loss of nigral dopaminergic neurons or depletion of dopamine in the striatum. Although the normal cellular functions of Parkin and DJ-1 are not fully understood, we hypothesized that loss-of-function mutations in Parkin and DJ-1 render cells more sensitive to mitochondrial dysfunction and oxidative stress. To test this hypothesis, we crossed mice deficient for Parkin and DJ-1 with mice deficient for the mitochondrial antioxidant protein Mn-superoxide dismutase (SOD2) or the cytosolic antioxidant protein Cu-Zn-superoxide dismutase (SOD1). Aged Parkin -/-) DJ-1(-/-) and Mn-superoxide dismutase triple deficient mice have enhanced performance on the rotorod behavior test. Cu/Zn-superoxide dismutase triple deficient mice have elevated levels of dopamine in the striatum in the absence of nigral cell loss. Our studies demonstrate that on a Parkin/DJ-1 null background, mice that are also deficient for major antioxidant proteins do not have progressive loss of dopaminergic neurons but have behavioral and striatal dopamine abnormalities.
帕金森病(PD)是一种进行性神经退行性疾病,其特征是黑质中投射到纹状体并释放多巴胺的神经元丧失。然而,PD的病因仍不确定,不过有证据表明与线粒体功能障碍和氧化应激有关。虽然大多数PD病例是散发性的,但5-10%的病例是由遗传突变引起的。Parkin和DJ-1的功能丧失突变是最早与隐性遗传帕金森症相关的。令人惊讶的是,在Parkin和DJ-1中携带类似功能丧失突变的小鼠并未表现出黑质多巴胺能神经元随年龄增长的丧失或纹状体中多巴胺的耗竭。虽然Parkin和DJ-1的正常细胞功能尚未完全了解,但我们推测Parkin和DJ-1的功能丧失突变使细胞对线粒体功能障碍和氧化应激更敏感。为了验证这一假设,我们将缺乏Parkin和DJ-1的小鼠与缺乏线粒体抗氧化蛋白锰超氧化物歧化酶(SOD2)或胞质抗氧化蛋白铜锌超氧化物歧化酶(SOD1)的小鼠进行杂交。老年的Parkin -/-) DJ-1(-/-)和锰超氧化物歧化酶三重缺陷小鼠在转棒行为测试中的表现增强。在没有黑质细胞丢失的情况下,铜/锌超氧化物歧化酶三重缺陷小鼠纹状体中的多巴胺水平升高。我们的研究表明,在Parkin/DJ-1基因缺失的背景下,同时缺乏主要抗氧化蛋白的小鼠没有多巴胺能神经元的进行性丧失,但有行为和纹状体多巴胺异常。