Department of Neurology, University of California at Los Angeles David Geffen School of Medicine, Los Angeles, CA 90095, USA.
Neurotoxicology. 2010 Aug;31(4):367-72. doi: 10.1016/j.neuro.2010.04.006. Epub 2010 Apr 22.
The etiology of Parkinson's disease is unclear but appears to involve mitochondrial dysfunction, proteasome inhibition, and environmental toxins. It has been shown that pesticides, including the complex I inhibitor rotenone, cause proteasome inhibition but the mechanism of rotenone-induced proteasome dysfunction remains largely unknown. In this study, we examined the role of mitochondrial inhibition, oxidative stress, and microtubule dysfunction as potential mediators of rotenone-induced proteasome inhibition. Proteasome activity (26S) was measured in HEK and SK-N-MC cells expressing an EGFP-U degron fusion protein that is selectively degraded by the proteasome. We found that complexes I and III inhibition led to the production of peroxides and decreased proteasome activity. We also found that rotenone increased nitric oxide production and nitric oxide and peroxynitrites led to proteasome inhibition. The effects of rotenone were attenuated by anti-oxidants and nitric oxide synthase inhibition. Since rotenone can also inhibit microtubule assembly, we tested a specific MT inhibitor and found it led to proteasome dysfunction. Rotenone also led to a decrease in 20S proteasome activity and 20S proteasome subunit immunoreactivity without a change in subunit mRNA. Together, these data suggest that rotenone-induced decreases in proteasome activity are due to increased degradation of proteasome components secondary to oxidative damage and possibly microtubule dysfunction.
帕金森病的病因尚不清楚,但似乎涉及线粒体功能障碍、蛋白酶体抑制和环境毒素。已经表明,包括复合物 I 抑制剂鱼藤酮在内的杀虫剂会导致蛋白酶体抑制,但鱼藤酮诱导的蛋白酶体功能障碍的机制在很大程度上仍不清楚。在这项研究中,我们研究了线粒体抑制、氧化应激和微管功能障碍作为鱼藤酮诱导的蛋白酶体抑制的潜在介质的作用。用表达 EGFP-U 降解结构域融合蛋白的 HEK 和 SK-N-MC 细胞测量蛋白酶体活性(26S),该融合蛋白可被蛋白酶体选择性降解。我们发现复合物 I 和 III 的抑制导致过氧化物的产生和蛋白酶体活性的降低。我们还发现鱼藤酮增加了一氧化氮的产生,而一氧化氮和过氧亚硝酸盐导致蛋白酶体抑制。抗氧化剂和一氧化氮合酶抑制可减弱鱼藤酮的作用。由于鱼藤酮还可以抑制微管组装,我们测试了一种特定的 MT 抑制剂,发现它导致了蛋白酶体功能障碍。鱼藤酮还导致 20S 蛋白酶体活性和 20S 蛋白酶体亚基免疫反应性降低,而亚基 mRNA 没有变化。总之,这些数据表明,鱼藤酮诱导的蛋白酶体活性降低是由于氧化损伤和可能的微管功能障碍导致蛋白酶体成分的降解增加所致。