Literature DB >> 16051092

Postnatal changes in sarcolemmal organization in the mdx mouse.

Patrick Reed1, Robert J Bloch.   

Abstract

The tibialis anterior muscles of mdx mice degenerate between 3 and 4 weeks after birth and then partially recover. We show that the membrane cytoskeleton at the mdx sarcolemma is disorganized at 18-days postnatal, and becomes more disorganized at 4 weeks compared to earlier or later times. Mdx muscle at 18 days have few central nuclei, suggesting that it has not yet sustained significant damage. The variance of myofiber diameter confirms that the mdx pathology is greatest at 4 weeks, when the sarcolemma is most disorganized. Sarcolemmal disorganization in the mdx does not involve contractile structures, nor is it seen in age-matched controls. In revertant mdx fibers expressing dystrophin, sarcolemmal organization is similar to controls. Our results suggest that the absence of dystrophin results in the disorganization of the sarcolemma, even in 18-day-old mice, and that the extent of disorganization is greater when the myopathy is most severe.

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Year:  2005        PMID: 16051092     DOI: 10.1016/j.nmd.2005.03.007

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  9 in total

1.  Biomechanics of the sarcolemma and costameres in single skeletal muscle fibers from normal and dystrophin-null mice.

Authors:  K P García-Pelagio; R J Bloch; A Ortega; H González-Serratos
Journal:  J Muscle Res Cell Motil       Date:  2011-02-11       Impact factor: 2.698

2.  Genomic removal of a therapeutic mini-dystrophin gene from adult mice elicits a Duchenne muscular dystrophy-like phenotype.

Authors:  Nalinda B Wasala; Yi Lai; Jin-Hong Shin; Junling Zhao; Yongping Yue; Dongsheng Duan
Journal:  Hum Mol Genet       Date:  2016-04-22       Impact factor: 6.150

3.  Physiology, structure, and susceptibility to injury of skeletal muscle in mice lacking keratin 19-based and desmin-based intermediate filaments.

Authors:  Richard M Lovering; Andrea O'Neill; Joaquin M Muriel; Benjamin L Prosser; John Strong; Robert J Bloch
Journal:  Am J Physiol Cell Physiol       Date:  2011-01-05       Impact factor: 4.249

4.  CT-GalNAc transferase overexpression in adult mice is associated with extrasynaptic utrophin in skeletal muscle fibres.

Authors:  Margaret Durko; Carol Allen; Josephine Nalbantoglu; George Karpati
Journal:  J Muscle Res Cell Motil       Date:  2010-08-13       Impact factor: 2.698

5.  Progressive resistance voluntary wheel running in the mdx mouse.

Authors:  Jarrod A Call; James N McKeehen; Susan A Novotny; Dawn A Lowe
Journal:  Muscle Nerve       Date:  2010-12       Impact factor: 3.217

6.  Microcurrent electrical neuromuscular stimulation facilitates regeneration of injured skeletal muscle in mice.

Authors:  Hiroto Fujiya; Yuji Ogura; Yoshitaka Ohno; Ayumi Goto; Ayane Nakamura; Kazuya Ohashi; Daiki Uematsu; Haruhito Aoki; Haruki Musha; Katsumasa Goto
Journal:  J Sports Sci Med       Date:  2015-05-08       Impact factor: 2.988

Review 7.  Targeting the Muscle-Bone Unit: Filling Two Needs with One Deed in the Treatment of Duchenne Muscular Dystrophy.

Authors:  Antoine Boulanger Piette; Dounia Hamoudi; Laetitia Marcadet; Françoise Morin; Anteneh Argaw; Leanne Ward; Jérôme Frenette
Journal:  Curr Osteoporos Rep       Date:  2018-10       Impact factor: 5.096

8.  Destabilization of the dystrophin-glycoprotein complex without functional deficits in alpha-dystrobrevin null muscle.

Authors:  Tina M Bunnell; Michele A Jaeger; Daniel P Fitzsimons; Kurt W Prins; James M Ervasti
Journal:  PLoS One       Date:  2008-07-02       Impact factor: 3.240

9.  Dystropathology increases energy expenditure and protein turnover in the mdx mouse model of duchenne muscular dystrophy.

Authors:  Hannah G Radley-Crabb; Juan C Marini; Horacio A Sosa; Liliana I Castillo; Miranda D Grounds; Marta L Fiorotto
Journal:  PLoS One       Date:  2014-02-19       Impact factor: 3.240

  9 in total

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