Literature DB >> 16198565

ADAM12 overexpression does not improve outcome in mice with laminin alpha2-deficient muscular dystrophy.

Ling T Guo1, G Diane Shelton, Ulla M Wewer, Eva Engvall.   

Abstract

We have recently shown that overexpression of ADAM12 results in increased muscle regeneration and significantly reduced pathology in mdx, dystrophin deficient mice. In the present study, we tested the effect of overexpressing ADAM12 in dy(W) laminin-deficient mice. dy mice have a very severe clinical phenotype and would be expected to benefit greatly from enhanced regeneration. We found that dy(W) mice overexpressing ADAM12 indeed have increased muscle regeneration, as evidenced by increased numbers of muscle fibers expressing fetal myosin. However, overexpression of ADAM12 had no significant effect on overall health, as evidenced by body weight, and did not improve muscle pathology.

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Year:  2005        PMID: 16198565     DOI: 10.1016/j.nmd.2005.06.019

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


  6 in total

1.  Transgenic overexpression of ADAM12 suppresses muscle regeneration and aggravates dystrophy in aged mdx mice.

Authors:  Louise Helskov Jørgensen; Charlotte Harken Jensen; Ulla M Wewer; Henrik Daa Schrøder
Journal:  Am J Pathol       Date:  2007-11       Impact factor: 4.307

2.  Overexpression of Galgt2 reduces dystrophic pathology in the skeletal muscles of alpha sarcoglycan-deficient mice.

Authors:  Rui Xu; Sarah DeVries; Marybeth Camboni; Paul T Martin
Journal:  Am J Pathol       Date:  2009-06-04       Impact factor: 4.307

3.  Overexpression of the cytotoxic T cell (CT) carbohydrate inhibits muscular dystrophy in the dyW mouse model of congenital muscular dystrophy 1A.

Authors:  Rui Xu; Kumaran Chandrasekharan; Jung Hae Yoon; Marybeth Camboni; Paul T Martin
Journal:  Am J Pathol       Date:  2007-07       Impact factor: 4.307

4.  Increasing alpha 7 beta 1-integrin promotes muscle cell proliferation, adhesion, and resistance to apoptosis without changing gene expression.

Authors:  Jianming Liu; Dean J Burkin; Stephen J Kaufman
Journal:  Am J Physiol Cell Physiol       Date:  2007-11-28       Impact factor: 4.249

Review 5.  A Family of Laminin α2 Chain-Deficient Mouse Mutants: Advancing the Research on LAMA2-CMD.

Authors:  Kinga I Gawlik; Madeleine Durbeej
Journal:  Front Mol Neurosci       Date:  2020-04-21       Impact factor: 5.639

6.  ACE2 is augmented in dystrophic skeletal muscle and plays a role in decreasing associated fibrosis.

Authors:  Cecilia Riquelme; María José Acuña; Javiera Torrejón; Daniela Rebolledo; Daniel Cabrera; Robson A Santos; Enrique Brandan
Journal:  PLoS One       Date:  2014-04-02       Impact factor: 3.240

  6 in total

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