Iwatsubo T, Yamaguchi H, Fujimuro M, Yokosawa H, Ihara Y, Trojanowski J Q, Lee V M
Department of Neuropathology and Neuroscience, Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.
Am J Pathol. 1996 May;148(5):1517-29.
Lewy bodies (LBs) are the pathological hallmarks of degenerating neurons in the brains of patients with Parkinson's disease and diffuse Lewy body disease. We developed a novel purification procedure for LBs using sucrose density separation followed by fluorescence-activated particle sorting, and we raised > 15 monoclonal antibodies to LBs purified from diffuse Lewy body disease brains. The monoclonal antibody that stained the largest number of LBs most intensely did not recognize ubiquitin in free or monoubiquitinated forms nor the ubiquitin conjugating enzymes, but it did react with polyubiquitin chains as well as with high molecular weight polyubiquitinated LB-derived proteins. Thus, these results suggest that LBs contain polyubiquitin chains. Although polyubiquitination of LB proteins may trigger ubiquitin-proteasome proteolytic pathways, the incomplete activation of these pathways could play a mechanistic role in the formation of LBs in neurodegenerative diseases.
路易小体(LBs)是帕金森病和弥漫性路易体病患者大脑中神经元退化的病理标志。我们开发了一种用于路易小体的新型纯化程序,先采用蔗糖密度分离,然后进行荧光激活颗粒分选,并且我们制备了超过15种针对从弥漫性路易体病大脑中纯化出的路易小体的单克隆抗体。染色路易小体数量最多且强度最大的单克隆抗体既不识别游离形式或单泛素化形式的泛素,也不识别泛素结合酶,但它确实与多聚泛素链以及高分子量的多聚泛素化路易小体衍生蛋白发生反应。因此,这些结果表明路易小体含有多聚泛素链。尽管路易小体蛋白的多聚泛素化可能触发泛素 - 蛋白酶体蛋白水解途径,但这些途径的不完全激活可能在神经退行性疾病中路易小体的形成中发挥机制性作用。