Hol Elly M, Fischer David F, Ovaa Huib, Scheper Wiep
Netherlands Institute for Neuroscience, Research Group Cellular Quality Control, Meibergdreef 47, 1105 BA Amsterdam, The Netherlands.
Expert Rev Neurother. 2006 Sep;6(9):1337-47. doi: 10.1586/14737175.6.9.1337.
Ubiquitinated protein aggregates are observed in the brains of Alzheimer's, Parkinson's and Huntington's disease patients and in other neurodegenerative disorders. These aggregates indicate that the ubiquitin proteasome system may be impaired in these diseases. To date no therapy is available that specifically targets this system, although preventing aggregate formation or stimulating the degradation of already formed aggregates by targeting components of the ubiquitin proteasome system is an attractive therapeutic approach. Here, we review the role of the ubiquitin proteasome system in aggregate formation with respect to neurodegenerative diseases, discussing the unfolded protein response, endoplasmic reticulum-associated degradation, aggresome formation and accumulation as well as aggregation and neurotoxicity of proteins involved in neurodegeneration. The potential of pharmacological intervention within this system in patients suffering from neurodegenerative diseases will be evaluated.
在阿尔茨海默病、帕金森病和亨廷顿病患者以及其他神经退行性疾病患者的大脑中观察到泛素化蛋白聚集体。这些聚集体表明泛素蛋白酶体系统在这些疾病中可能受损。尽管通过靶向泛素蛋白酶体系统的组分来防止聚集体形成或刺激已形成聚集体的降解是一种有吸引力的治疗方法,但迄今为止尚无专门针对该系统的疗法。在此,我们综述泛素蛋白酶体系统在神经退行性疾病聚集体形成中的作用,讨论未折叠蛋白反应、内质网相关降解、聚集体的形成和积累以及神经退行性变相关蛋白的聚集和神经毒性。将评估该系统内药物干预对神经退行性疾病患者的潜力。