Literature DB >> 2000106

Dystrophin expression in myotubes formed by the fusion of normal and dystrophic myoblasts.

J Huard1, C Labrecque, G Dansereau, L Robitaille, J P Tremblay.   

Abstract

Mdx mouse dystrophy is characterized by the absence in the muscle cytoplasmic membrane of a high molecular weight protein called dystrophin. A possible avenue for treatment of muscular dystrophies is to inject normal myoblasts in a dystrophic muscle to form hybrid muscle fibers. Hybrid myotubes were formed in vitro by the fusion of normal rat and dystrophic mouse (mdx) myoblasts. Staining with Hoechst dye 33258 permitted the clear distinction of mouse and rat nuclei. Immunostaining demonstrated that dystrophin was present over the entire membrane of all hybrid myotubes even when nuclei ratio normal/dystrophic was low.

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Year:  1991        PMID: 2000106     DOI: 10.1002/mus.880140213

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  14 in total

1.  Lack of myoblasts migration between transplanted and host muscles of mdx and normal mice.

Authors:  P D Moens; M C Van-Schoor; G Maréchal
Journal:  J Muscle Res Cell Motil       Date:  1996-02       Impact factor: 2.698

Review 2.  Satellite Cells in Muscular Dystrophy - Lost in Polarity.

Authors:  Natasha C Chang; Fabien P Chevalier; Michael A Rudnicki
Journal:  Trends Mol Med       Date:  2016-05-05       Impact factor: 11.951

3.  In vivo fusion of circulating fluorescent cells with dystrophin-deficient myofibers results in extensive sarcoplasmic fluorescence expression but limited dystrophin sarcolemmal expression.

Authors:  Fabrice Chretien; Patrick A Dreyfus; Christo Christov; Philippe Caramelle; Jean-Léon Lagrange; Bénédicte Chazaud; Romain K Gherardi
Journal:  Am J Pathol       Date:  2005-06       Impact factor: 4.307

4.  Visualization of the subsarcolemmal cytoskeleton network of mouse skeletal muscle cells by en face views and application to immunoelectron localization of dystrophin.

Authors:  C Berthier; J Amsellem; S Blaineau
Journal:  J Muscle Res Cell Motil       Date:  1995-10       Impact factor: 2.698

5.  Functional improvement of damaged adult mouse muscle by implantation of primary myoblasts.

Authors:  A Irintchev; M Langer; M Zweyer; R Theisen; A Wernig
Journal:  J Physiol       Date:  1997-05-01       Impact factor: 5.182

6.  Contractile properties of skinned muscle fibres from young and adult normal and dystrophic (mdx) mice.

Authors:  D A Williams; S I Head; G S Lynch; D G Stephenson
Journal:  J Physiol       Date:  1993-01       Impact factor: 5.182

7.  Ca2+ levels in myotubes grown from the skeletal muscle of dystrophic (mdx) and normal mice.

Authors:  A J Bakker; S I Head; D A Williams; D G Stephenson
Journal:  J Physiol       Date:  1993-01       Impact factor: 5.182

8.  Heterokaryon myotubes with normal mouse and Duchenne nuclei exhibit sarcolemmal dystrophin staining and efficient intracellular free calcium control.

Authors:  W F Denetclaw; G Bi; D V Pham; R A Steinhardt
Journal:  Mol Biol Cell       Date:  1993-09       Impact factor: 4.138

9.  Inhibition of CD26/DPP-IV enhances donor muscle cell engraftment and stimulates sustained donor cell proliferation.

Authors:  Maura H Parker; Carol Loretz; Ashlee E Tyler; Lauren Snider; Rainer Storb; Stephen J Tapscott
Journal:  Skelet Muscle       Date:  2012-02-16       Impact factor: 4.912

10.  Activation of Notch signaling during ex vivo expansion maintains donor muscle cell engraftment.

Authors:  Maura H Parker; Carol Loretz; Ashlee E Tyler; William J Duddy; John K Hall; Bradley B Olwin; Irwin D Bernstein; Rainer Storb; Stephen J Tapscott
Journal:  Stem Cells       Date:  2012-10       Impact factor: 6.277

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