A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy

Sheng Li, En Kimura, Rainer Ng, Brent M. Fall, Leonard Meuse, Morayma Reyes, John A. Faulkner, Jeffrey S. Chamberlain

Research output: Contribution to journalArticle

38 Scopus citations

Abstract

A promising approach for treating Duchenne muscular dystrophy (DMD) is by autologous cell transplantation of myogenic stem cells transduced with a therapeutic expression cassette. Development of this method has been hampered by a low frequency of cellular engraftment, the difficulty of tracing transplanted cells, the rapid loss of autologous cells carrying marker genes that are unable to halt muscle necrosis and the difficulty of stable transfer of a large dystrophin gene into myogenic stem cells. We engineered a 5.7 miniDys-GFP fusion gene by replacing the dystrophin C-terminal domain (ΔCT) with an eGFP coding sequence and removing much of the dystrophin central rod domain (ΔH2-R19). In a transgenic mdx4Cvmouse expressing the miniDys-GFP fusion protein under the control of a skeletal muscle-specific promoter, the green fusion protein localized on the sarcolemma, where it assembled the dystrophin-glycoprotein complex and completely prevented the development of dystrophy in transgenic mdx4Cv muscles. When myogenic and other stem cells from these mice were transplanted into mdx4Cv recipients, donor cells can be readily identified in skeletal muscle by direct green fluorescence or by using antibodies against GFP or dystrophin. In mdx4Cv mice reconstituted with bone marrow cells from the transgenic mice, we monitored engraftment in various muscle groups and found the number of miniDys-GFP+ fibers increased with time. We suggest that these transgenic mdx 4Cv mice are highly useful for developing autologous cell therapies for DMD.

Original languageEnglish (US)
Pages (from-to)1610-1622
Number of pages13
JournalHuman molecular genetics
Volume15
Issue number10
DOIs
StatePublished - May 15 2006
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

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