https://scholars.lib.ntu.edu.tw/handle/123456789/531480
標題: | Deconstructing pompe disease by analyzing single muscle fibers: To see a world in a grain of sand... | 作者: | Raben N. Takikita S. Pittis M.G. Bembi B. Marie S.K.N. Roberts A. Page L. Kishnani P.S. Schoser B.G.H. YIN-HSIU CHIEN Ralston E. Nagaraju K. Plotz P.H. |
關鍵字: | Autophagosome; Glycogen storage; Lysosomal storage disorder; Lysosome; Metabolic disorder; Myopathy; Skeletal muscle | 公開日期: | 2007 | 出版社: | Taylor and Francis Inc. | 卷: | 3 | 期: | 6 | 起(迄)頁: | 546-552 | 來源出版物: | Autophagy | 摘要: | Autophagy is a major pathway for delivery of proteins and organelles to lysosomes where they are degraded and recycled. We have previously shown excessive autophagy in a mouse model of Pompe disease (glycogen storage disease type II), a devastating myopathy caused by a deficiency of the glycogen-degrading lysosomal enzyme acid α-glucosidase. The autophagic buildup constituted a major pathological component in skeletal muscle and interfered with delivery of the therapeutic enzyme. To assess the role of autophagy in the pathogenesis of the human disease, we have analyzed vesicles of the lysosomal-degradative pathway in isolated single muscle fibers from Pompe patients. Human myofibers showed abundant autophagosome formation and areas of autophagic buildup of a wide range of sizes. In patients, as in the mouse model, the enormous autophagic buildup causes greater skeletal muscle damage than the enlarged, glycogen-filled lysosomes outside the autophagic regions. Clearing or preventing autophagic buildup seems, therefore, a necessary target of Pompe disease therapy. ?2007 Landes Bioscience. |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-34548621869&doi=10.4161%2fauto.4591&partnerID=40&md5=2cf0c38e3989ea822767d78864048b11 https://scholars.lib.ntu.edu.tw/handle/123456789/531480 |
ISSN: | 1554-8627 | DOI: | 10.4161/auto.4591 | SDG/關鍵字: | alpha glucosidase; animal experiment; animal model; article; autophagy; cell organelle; controlled study; glycogen storage disease type 2; glycogen storage disease type 3; lysosome; mouse; muscle cell; muscle injury; myopathy; nonhuman; pathogenesis; phagosome; protein degradation; skeletal muscle |
顯示於: | 醫學系 |
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