Suppr超能文献

遗传性还原小体肌病中的未折叠蛋白反应与聚集体形成

Unfolded protein response and aggresome formation in hereditary reducing-body myopathy.

作者信息

Liewluck Teerin, Hayashi Yukiko K, Ohsawa Maki, Kurokawa Rumi, Fujita Masako, Noguchi Satoru, Nonaka Ikuya, Nishino Ichizo

机构信息

Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, 4-1-1 Ogawa-Higashi, Kodaira, Tokyo 187-8502, Japan.

出版信息

Muscle Nerve. 2007 Mar;35(3):322-6. doi: 10.1002/mus.20691.

Abstract

Reducing-body myopathy (RBM) is a rare myopathy characterized by the presence of unique sarcoplasmic inclusions called reducing bodies (RBs). We characterized the aggresomal features of RBs that contained gamma-tubulin, ubiquitin, and endoplasmic reticulum (ER) chaperones, together with a set of membrane proteins, in a family with hereditary RBM. Increased messenger ribonucleic acid and protein levels of a molecular chaperone, glucose-related protein 78, were also observed. These results suggest that the unfolded protein response caused by the accumulation of misfolded proteins in the endoplasmic reticulum plays an important role in the formation of RBs.

摘要

减体重性肌病(RBM)是一种罕见的肌病,其特征是存在称为减体重小体(RB)的独特肌浆内包涵体。我们对一个遗传性RBM家系中含有γ-微管蛋白、泛素和内质网(ER)伴侣蛋白以及一组膜蛋白的RB的聚集体特征进行了表征。还观察到一种分子伴侣葡萄糖相关蛋白78的信使核糖核酸和蛋白质水平升高。这些结果表明,内质网中错误折叠蛋白的积累所引发的未折叠蛋白反应在RB的形成中起重要作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验