Literature DB >> 23777246

Bone marrow transplantation in dysferlin-deficient mice results in a mild functional improvement.

Bàrbara Flix1, Xavier Suárez-Calvet, Jordi Díaz-Manera, Eva Santos-Nogueira, Renzo Mancuso, Jordi Barquinero, Miquel Navas, Xavier Navarro, Isabel Illa, Eduard Gallardo.   

Abstract

Dysferlinopathies are caused by mutations in the DYSF gene. Dysferlin is a protein mainly expressed in the skeletal muscle and monocytes. Cell therapy constitutes a promising tool for the treatment of muscular dystrophies. The aim of our study was to evaluate the effect of bone marrow transplantation (BMT) using the A/J Dysf(prmd) mouse model of dysferlinopathy. For that purpose, we studied dysferlin expression by western blot and/or immunohistochemistry in transplanted mice and controls. Computerized analyses of locomotion and electrophysiological techniques were also performed to test the functional improvement. We observed dysferlin expression in splenocytes, but not in the skeletal muscle of the transplanted mice. However, the locomotion test, electromyography studies, and muscle histology showed an improvement in all transplanted mice that was more significant in the animals transplanted with dysferlin⁺/⁺ cells. In conclusion, although BMT restores dysferlin expression in monocytes, but not in skeletal muscle, muscle function was partially recovered. We propose that the slight improvement observed in the functional studies could be related with factors, such as the hepatocyte growth factor, released after BMT that prevented muscle degeneration.

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Year:  2013        PMID: 23777246      PMCID: PMC3804083          DOI: 10.1089/scd.2013.0049

Source DB:  PubMed          Journal:  Stem Cells Dev        ISSN: 1547-3287            Impact factor:   3.272


  59 in total

1.  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

2.  A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathy.

Authors:  Mengfatt Ho; Eduard Gallardo; Diane McKenna-Yasek; Noemi De Luna; Isabel Illa; Robert H Brown
Journal:  Ann Neurol       Date:  2002-01       Impact factor: 10.422

3.  Hepatocyte growth factor mobilizes non-bone marrow-derived circulating mesoangioblasts.

Authors:  Masayoshi Iwasaki; Masamichi Koyanagi; Hans Kossmann; Nadejda Monsefi; Stefan Rupp; Janina Trauth; Patrick Paulus; Rebekka Goetz; Stefan Momma; Marc Tjwa; Kisho Ohtani; Reinhard Henschler; Dietmar Schranz; Giulio Cossu; Kai Zacharowski; Sven Martens; Andreas M Zeiher; Stefanie Dimmeler
Journal:  Eur Heart J       Date:  2010-12-29       Impact factor: 29.983

4.  Sigma-1R agonist improves motor function and motoneuron survival in ALS mice.

Authors:  Renzo Mancuso; Sara Oliván; Amaya Rando; Caty Casas; Rosario Osta; Xavier Navarro
Journal:  Neurotherapeutics       Date:  2012-10       Impact factor: 7.620

5.  Human umbilical cord blood cells differentiate into muscle in sjl muscular dystrophy mice.

Authors:  Kimi Y Kong; Jingmei Ren; Morey Kraus; Seth P Finklestein; Robert H Brown
Journal:  Stem Cells       Date:  2004       Impact factor: 6.277

6.  Genetic ablation of complement C3 attenuates muscle pathology in dysferlin-deficient mice.

Authors:  Renzhi Han; Ellie M Frett; Jennifer R Levy; Erik P Rader; John D Lueck; Dimple Bansal; Steven A Moore; Rainer Ng; Daniel Beltrán-Valero de Bernabé; John A Faulkner; Kevin P Campbell
Journal:  J Clin Invest       Date:  2010-11-08       Impact factor: 14.808

7.  Partial dysferlin reconstitution by adult murine mesoangioblasts is sufficient for full functional recovery in a murine model of dysferlinopathy.

Authors:  J Díaz-Manera; T Touvier; A Dellavalle; R Tonlorenzi; F S Tedesco; G Messina; M Meregalli; C Navarro; L Perani; C Bonfanti; I Illa; Y Torrente; G Cossu
Journal:  Cell Death Dis       Date:  2010-08-05       Impact factor: 8.469

8.  Dysferlin is expressed in human placenta but does not associate with caveolin.

Authors:  Dale D Vandré; William E Ackerman; Douglas A Kniss; Arun K Tewari; Miki Mori; Toshihiro Takizawa; John M Robinson
Journal:  Biol Reprod       Date:  2007-06-06       Impact factor: 4.285

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.  Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy.

Authors:  J Liu; M Aoki; I Illa; C Wu; M Fardeau; C Angelini; C Serrano; J A Urtizberea; F Hentati; M B Hamida; S Bohlega; E J Culper; A A Amato; K Bossie; J Oeltjen; K Bejaoui; D McKenna-Yasek; B A Hosler; E Schurr; K Arahata; P J de Jong; R H Brown
Journal:  Nat Genet       Date:  1998-09       Impact factor: 38.330

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  2 in total

1.  Inhibition of inflammation with celastrol fails to improve muscle function in dysferlin-deficient A/J mice.

Authors:  Blythe C Dillingham; Margaret E Benny Klimek; Ramkishore Gernapudi; Sree Rayavarapu; Eduard Gallardo; Jack H Van der Meulen; Sarah Jordan; Beryl Ampong; Heather Gordish-Dressman; Christopher F Spurney; Kanneboyina Nagaraju
Journal:  J Neurol Sci       Date:  2015-06-24       Impact factor: 3.181

2.  Nintedanib decreases muscle fibrosis and improves muscle function in a murine model of dystrophinopathy.

Authors:  Patricia Piñol-Jurado; Xavier Suárez-Calvet; Esther Fernández-Simón; Eduard Gallardo; Natalia de la Oliva; Anna Martínez-Muriana; Pedro Gómez-Gálvez; Luis M Escudero; María Pérez-Peiró; Lutz Wollin; Noemi de Luna; Xavier Navarro; Isabel Illa; Jordi Díaz-Manera
Journal:  Cell Death Dis       Date:  2018-07-10       Impact factor: 8.469

  2 in total

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