Literature DB >> 10679961

Plasma membrane cytoskeleton of muscle: a fine structural analysis.

S C Watkins1, M J Cullen, E P Hoffman, L Billington.   

Abstract

The discovery of dystrophin and its definition as the causative molecule in Duchenne Muscular Dystrophy has led to a renewed interest in the molecular structure of the muscle fiber plasma membrane and its association with the extracellular basal lamina. The original identification of dystrophin gave credence to the possibility that the plasma membrane of the muscle fiber may be highly organized and involved in maintaining appropriate homeostasis in this actively contracting cellular system. In this review, we examine the currently known members of the muscle fiber plasma membrane cytoskeleton and the interactions that occur between the different members of this complex using histological, electron microscopic, and confocal methods. From our studies and others cited in this review, it is clear that the dystrophin cytoskeletal complex is not completely understood and component molecules continue to be discovered. Perhaps equally importantly, currently defined molecules (such as alpha-actinin or neuronal nitric oxide synthase) are being recognized as being specifically associated with the complex. What is striking from all of the studies, to date, is that while we are able to identify members of the dystrophin cytoskeletal complex and while we are able to associate mutations of individual molecules with disease(s), we are still unable to truly define the roles of each of the molecules in maintaining the normal physiology of the muscle fiber. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10679961     DOI: 10.1002/(SICI)1097-0029(20000201/15)48:3/4<131::AID-JEMT2>3.0.CO;2-G

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  2 in total

1.  Brain dystrophin-glycoprotein complex: persistent expression of beta-dystroglycan, impaired oligomerization of Dp71 and up-regulation of utrophins in animal models of muscular dystrophy.

Authors:  K Culligan; L Glover; P Dowling; K Ohlendieck
Journal:  BMC Cell Biol       Date:  2001-02-02       Impact factor: 4.241

2.  Mutation types and aging differently affect revertant fiber expansion in dystrophic mdx and mdx52 mice.

Authors:  Yusuke Echigoya; Joshua Lee; Merryl Rodrigues; Tetsuya Nagata; Jun Tanihata; Ashkan Nozohourmehrabad; Dharminder Panesar; Bailey Miskew; Yoshitsugu Aoki; Toshifumi Yokota
Journal:  PLoS One       Date:  2013-07-24       Impact factor: 3.240

  2 in total

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