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Dystrophin expression improves myofiber survival in <i>mdx</i> muscle following intramuscular plasmid DNA injection
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1993
Year
Muscle FunctionPathologyCytoskeletonCellular PhysiologyMuscle PhysiologyMuscle InjurySkeletal MuscleMdx MusclePlasmid DnaMdx Mouse MuscleHealth SciencesNeuromuscular PhysiologyNeuromuscular PathologyCell BiologyPhysiologyDystrophin ExpressionDegenerative DiseaseMedicineNeuromusculoskeletal Disorder
Expression of Becker-like and full-length human dystrophins was stable for at least 6 months in mdx mouse muscle following intramuscular plasmid DNA injection. Intramuscular injection of a single plasmid DNA encoding both luciferase and dystrophin resulted in stable luciferase expression for at least 2 months in mdx muscle, whereas injection of plasmid DNA encoding only luciferase did not result in stable luciferase expression. These results suggest that expression of either full-length or Becker-like dystrophins protects mdx mouse myofibers from degeneration.