Literature DB >> 1557946

The fate of dystrophin during the degeneration and regeneration of the soleus muscle of the rat.

R Vater1, M J Cullen, L V Nicholson, J B Harris.   

Abstract

Immunocytochemistry and Western blotting were used to monitor the fate of dystrophin in the soleus muscle of the rat during a cycle of degeneration and regeneration induced by inoculation of the muscle with the venom of Notechis scutatus scutatus (the Australian tiger snake). In control muscle dystrophin was localised close to the plasma membrane. Dystrophin began to break down 3-6 h after venom inoculation, giving a characteristic discontinuous labelling pattern. At 12 h dystrophin was absent from the plasma membrane, and by 1 day the architecture of the muscle fibers had completely broken down. By 2 days post inoculation regeneration had commenced. The regenerating myofibres possessed well-organised myofibrils and the plasma membrane was intact. Dystrophin was detected by Western blot at 3 days, but was not seen in sections until regeneration of the muscle was well advanced, at 4 days post inoculation. The results suggested that although dystrophin was present in the myofibres at 3 days, it was not incorporated into the plasma membrane until 4 days post inoculation. This may be due to the influence of the functional reinnervation of the regenerating fibres, which occurs at 4-5 days, or to the growing fibres reaching a critical diameter.

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Year:  1992        PMID: 1557946     DOI: 10.1007/bf00308473

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  39 in total

1.  Glycoprotein complex anchoring dystrophin to sarcolemma.

Authors:  M Yoshida; E Ozawa
Journal:  J Biochem       Date:  1990-11       Impact factor: 3.387

Review 2.  Dystrophin abnormalities in Duchenne/Becker muscular dystrophy.

Authors:  E P Hoffman; L M Kunkel
Journal:  Neuron       Date:  1989-01       Impact factor: 17.173

3.  Muscular dystrophy in a litter of golden retriever dogs.

Authors:  J N Kornegay; S M Tuler; D M Miller; D C Levesque
Journal:  Muscle Nerve       Date:  1988-10       Impact factor: 3.217

4.  Immunoelectron microscopic localization of dystrophin in myofibres.

Authors:  S C Watkins; E P Hoffman; H S Slayter; L M Kunkel
Journal:  Nature       Date:  1988-06-30       Impact factor: 49.962

5.  Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface.

Authors:  E Bonilla; C E Samitt; A F Miranda; A P Hays; G Salviati; S DiMauro; L M Kunkel; E P Hoffman; L P Rowland
Journal:  Cell       Date:  1988-08-12       Impact factor: 41.582

6.  Dystrophin is localized to the plasma membrane of human skeletal muscle fibers by electron-microscopic cytochemical study.

Authors:  S Carpenter; G Karpati; E Zubrzycka-Gaarn; D E Bulman; P N Ray; R G Worton
Journal:  Muscle Nerve       Date:  1990-05       Impact factor: 3.217

7.  Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide.

Authors:  K Arahata; S Ishiura; T Ishiguro; T Tsukahara; Y Suhara; C Eguchi; T Ishihara; I Nonaka; E Ozawa; H Sugita
Journal:  Nature       Date:  1988-06-30       Impact factor: 49.962

8.  Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophy.

Authors:  L V Nicholson; K Davison; M A Johnson; C R Slater; C Young; S Bhattacharya; D Gardner-Medwin; J B Harris
Journal:  J Neurol Sci       Date:  1989-12       Impact factor: 3.181

9.  Dystrophin in skeletal muscle. I. Western blot analysis using a monoclonal antibody.

Authors:  L V Nicholson; K Davison; G Falkous; C Harwood; E O'Donnell; C R Slater; J B Harris
Journal:  J Neurol Sci       Date:  1989-12       Impact factor: 3.181

10.  Cell fractionation studies indicate that dystrophin is a protein of surface membranes of skeletal muscle.

Authors:  G Salviati; R Betto; S Ceoldo; E Biasia; E Bonilla; A F Miranda; S Dimauro
Journal:  Biochem J       Date:  1989-03-15       Impact factor: 3.857

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  6 in total

1.  Muscle fibre breakdown in venom-induced muscle degeneration.

Authors:  J B Harris; R Vater; M Wilson; M J Cullen
Journal:  J Anat       Date:  2003-04       Impact factor: 2.610

2.  Fetal microchimeric cells in a fetus-treats-its-mother paradigm do not contribute to dystrophin production in serially parous mdx females.

Authors:  Elke Jane Seppanen; Samantha Susan Hodgson; Kiarash Khosrotehrani; George Bou-Gharios; Nicholas M Fisk
Journal:  Stem Cells Dev       Date:  2012-08-06       Impact factor: 3.272

3.  The fate of desmin and titin during the degeneration and regeneration of the soleus muscle of the rat.

Authors:  R Vater; M J Cullen; J B Harris
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

4.  The expression of vimentin in satellite cells of regenerating skeletal muscle in vivo.

Authors:  R Vater; M J Cullen; J B Harris
Journal:  Histochem J       Date:  1994-12

5.  Immunogold localization of the 43-kDa dystroglycan at the plasma membrane in control and dystrophic human muscle.

Authors:  M J Cullen; J Walsh; L V Nicholson
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

6.  Distribution of myosin heavy chain isoforms in muscular dystrophy: insights into disease pathology.

Authors:  Aaron M Beedle
Journal:  Musculoskelet Regen       Date:  2016-07-05
  6 in total

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