Literature DB >> 16584859

Adenoviral mediated MyoD gene transfer into fibroblasts: myogenic disease diagnosis.

Isao Fujii1, Makoto Matsukura, Makoto Ikezawa, Satoru Suzuki, Takashi Shimada, Teruhisa Miike.   

Abstract

MyoD, a master regulatory gene for myogenesis, converts mesoderm derived cells to the skeletal muscle phenotype MyoD gene transfer into skin fibroblasts has been attempted in an effort to diagnose genetic muscle diseases. Although the gene transduction efficiency of adenoviral gene delivery systems is higher than that of various other systems, the rate of myo-conversion is insignificant. Since high adenovirus doses are cytotoxic and exogenous MyoD expression is insufficient for skin fibroblasts to re-differentiate into muscle cells, we constructed the novel adeno-MyoD vector, Ad.CAGMyoD using the recombinant CAG promoter. Even at a lower multiplicities of infection most skin fibroblasts infected with Ad.CAGMyoD could convert into myotubes without vector-induced cytotoxicity. The converted cells expressed muscle-specific desmin and full-length dystrophin, both of which were detected by Western blotting. Genetic and immunohistochemical analyses using skin fibroblasts and our vector system are reliable and useful for the clinical diagnosis of genetic muscle diseases.

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Year:  2006        PMID: 16584859     DOI: 10.1016/j.braindev.2005.12.007

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  9 in total

1.  In vitro and in vivo study of human amniotic fluid-derived stem cell differentiation into myogenic lineage.

Authors:  Jean Gekas; Guillaume Walther; Daniel Skuk; Emmanuel Bujold; Isabelle Harvey; Olivier François Bertrand
Journal:  Clin Exp Med       Date:  2010-03       Impact factor: 3.984

2.  A method to facilitate and monitor expression of exogenous genes in the rat kidney using plasmid and viral vectors.

Authors:  Peter R Corridon; George J Rhodes; Ellen C Leonard; David P Basile; Vincent H Gattone; Robert L Bacallao; Simon J Atkinson
Journal:  Am J Physiol Renal Physiol       Date:  2013-03-06

3.  Transcription factor rational design improves directed differentiation of human mesenchymal stem cells into skeletal myocytes.

Authors:  Manuel A F V Gonçalves; Josephine M Janssen; Quynh G Nguyen; Takis Athanasopoulos; Stephen D Hauschka; George Dickson; Antoine A F de Vries
Journal:  Mol Ther       Date:  2011-01-25       Impact factor: 11.454

4.  Plasmonic fusion between fibroblasts and skeletal muscle cells for skeletal muscle regeneration.

Authors:  Limor Minai; Dvir Yelin
Journal:  Biomed Opt Express       Date:  2022-01-06       Impact factor: 3.732

5.  Incomplete MyoD-induced transdifferentiation is associated with chromatin remodeling deficiencies.

Authors:  Dinesh Manandhar; Lingyun Song; Ami Kabadi; Jennifer B Kwon; Lee E Edsall; Melanie Ehrlich; Koji Tsumagari; Charles A Gersbach; Gregory E Crawford; Raluca Gordân
Journal:  Nucleic Acids Res       Date:  2017-11-16       Impact factor: 16.971

6.  Myoblasts derived from normal hESCs and dystrophic hiPSCs efficiently fuse with existing muscle fibers following transplantation.

Authors:  Sébastien Goudenege; Carl Lebel; Nicolas B Huot; Christine Dufour; Isao Fujii; Jean Gekas; Joël Rousseau; Jacques P Tremblay
Journal:  Mol Ther       Date:  2012-09-18       Impact factor: 11.454

7.  Functional validation and expression analysis of myotubes converted from skin fibroblasts using a simple direct reprogramming strategy.

Authors:  Fukuko Horio; Hidetoshi Sakurai; Yutaka Ohsawa; Shiho Nakano; Makoto Matsukura; Isao Fujii
Journal:  eNeurologicalSci       Date:  2016-11-03

8.  SREBP-1 transcription factors regulate skeletal muscle cell size by controlling protein synthesis through myogenic regulatory factors.

Authors:  Kevin Dessalle; Vanessa Euthine; Stéphanie Chanon; Joffrey Delarichaudy; Isao Fujii; Sophie Rome; Hubert Vidal; Georges Nemoz; Chantal Simon; Etienne Lefai
Journal:  PLoS One       Date:  2012-11-30       Impact factor: 3.240

9.  Myogenic progenitor cells derived from human induced pluripotent stem cell are immune-tolerated in humanized mice.

Authors:  Basma Benabdallah; Cynthia Désaulniers-Langevin; Marie-Lyn Goyer; Chloé Colas; Chantale Maltais; Yuanyi Li; Jean V Guimond; Jacques P Tremblay; Elie Haddad; Christian Beauséjour
Journal:  Stem Cells Transl Med       Date:  2020-09-02       Impact factor: 6.940

  9 in total

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