MISC

2007年3月

Different pattern of HSP47 expression in skeletal muscle of patients with neuromuscular diseases

NEUROMUSCULAR DISORDERS
  • Itsuro Higuchi
  • ,
  • Akihiro Hashiguchi
  • ,
  • Eiji Matsuura
  • ,
  • Keiko Higashi
  • ,
  • Tadafumi Shiraishi
  • ,
  • Noriko Hirata
  • ,
  • Kimiyoshi Arimura
  • ,
  • Mitsuhiro Osame

17
3
開始ページ
221
終了ページ
226
記述言語
英語
掲載種別
DOI
10.1016/j.nmd.2006.11.008
出版者・発行元
PERGAMON-ELSEVIER SCIENCE LTD

Heat shock protein (HSP) 47, a collagen-specific molecular chaperone, is involved in the processing and secretion of procollagens, and its expression is increased in various fibrotic diseases. However, its involvement in muscle diseases is unknown. In this study, we analyzed HSP47 expression in muscular dystrophies and other muscle diseases. We found an overexpression of HSP47 in fibrous connective tissue and in the adjacent muscle membrane in various muscular dystrophies. However, in Ullrich congenital muscular dystrophy (UCMD), the overexpression of HSP47 was found only in the connective tissue, and not in the muscle membrane. The overexpression of HSP47 was found only in the muscle membrane in the case of active inflammatory myopathy. In particular, HSP47 was strongly expressed in the membrane of regenerating fibers. We found that HSP47 in the muscle membrane locates in the basement membrane with confocal microscopy. Our findings suggest that HSP47 may be involved in the repair or regeneration of muscle fibers in addition to the fibrotic change in the connective tissue. (C) 2007 Elsevier B.V. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/j.nmd.2006.11.008
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000246119600004&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.nmd.2006.11.008
  • ISSN : 0960-8966
  • Web of Science ID : WOS:000246119600004

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