Could utrophin rescue the myocardium of patients with dystrophin gene mutations?

Marina Fanin, Paola Melacini, Corrado Angelini, Gian Antonio Danieli

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

The spontaneous up-regulation of utrophin, observed in dystrophin-deficient skeletal muscle fibers, may decrease the susceptibility of such fibers to necrosis. It has been reported that the utrophin-rescued double-mutant mdx mouse always develops a lethal cardiomyopathy. We report two patients with severe dilated cardiomyopathy due to dystrophin gene mutations: the first was a manifesting Duchenne muscular dystrophy carrier and the second a patient affected with moderate Becker muscular dystrophy. We studied their explanted heart specimen and/or endomyocardial biopsies by immunohistochemistry and Western blot for both dystrophin and utrophin. Utrophin was found to be over-expressed in these specimens. Our results suggest that in these patients the up-regulation of utrophin in dystrophin-deficient cardiomyocytes was unable to prevent the development of life threatening myocardial dysfunction. These findings seem to dampen the enthusiasm raised by the prospect of DMD treatment by utrophin rescue in skeletal muscle fibers, as the myocardium would still remain severely affected.

Original languageEnglish
Pages (from-to)1501-1508
Number of pages8
JournalJournal of Molecular and Cellular Cardiology
Volume31
Issue number8
DOIs
Publication statusPublished - Aug 1999

Fingerprint

Utrophin
Dystrophin
Myocardium
Mutation
Genes
Duchenne Muscular Dystrophy
Skeletal Muscle Fibers
Up-Regulation
Inbred mdx Mouse
Dilated Cardiomyopathy
Cardiomyopathies
Cardiac Myocytes
Necrosis
Western Blotting
Immunohistochemistry
Biopsy

Keywords

  • Cardiomyopathy
  • Dystrophin
  • Dystrophin-associated proteins
  • Muscular dystrophy
  • Utrophin

ASJC Scopus subject areas

  • Molecular Biology
  • Cardiology and Cardiovascular Medicine

Cite this

Could utrophin rescue the myocardium of patients with dystrophin gene mutations? / Fanin, Marina; Melacini, Paola; Angelini, Corrado; Danieli, Gian Antonio.

In: Journal of Molecular and Cellular Cardiology, Vol. 31, No. 8, 08.1999, p. 1501-1508.

Research output: Contribution to journalArticle

Fanin, Marina ; Melacini, Paola ; Angelini, Corrado ; Danieli, Gian Antonio. / Could utrophin rescue the myocardium of patients with dystrophin gene mutations?. In: Journal of Molecular and Cellular Cardiology. 1999 ; Vol. 31, No. 8. pp. 1501-1508.
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