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Muscle Nerve ; 54(4): 763-8, 2016 10.
Article in English | MEDLINE | ID: mdl-26998682

ABSTRACT

INTRODUCTION: Duchenne muscular dystrophy (DMD) is caused by loss of the structural protein, dystrophin, resulting in muscle fragility. Muscle stem cell (MuSC) transplantation is a potential therapy for DMD. It is unknown whether donor-derived muscle fibers are structurally innervated. METHODS: Green fluorescent protein (GFP)-expressing MuSCs were transplanted into the tibials anterior of adult dystrophic mdx/mTR mice. Three weeks later the neuromuscular junction was labeled by immunohistochemistry. RESULTS: The percent overlap between pre- and postsynaptic immunolabeling was greater in donor-derived GFP(+) myofibers, and fewer GFP(+) myofibers were identified as denervated compared with control GFP(-) fibers (P = 0.001 and 0.03). GFP(+) fibers also demonstrated acetylcholine receptor fragmentation and expanded endplate area, indicators of muscle reinnervation (P = 0.008 and 0.033). CONCLUSION: It is unclear whether GFP(+) fibers are a result of de novo synthesis or fusion with damaged endogenous fibers. Either way, donor-derived fibers demonstrate clear histological innervation. Muscle Nerve 54: 763-768, 2016.


Subject(s)
Muscle Cells/transplantation , Muscle, Skeletal/innervation , Muscular Dystrophy, Duchenne/physiopathology , Muscular Dystrophy, Duchenne/therapy , Stem Cell Transplantation/methods , Animals , Mice , Mice, Inbred mdx , Mice, Transgenic , Muscle Cells/chemistry , Muscle Fibers, Skeletal/chemistry , Muscle Fibers, Skeletal/transplantation , Muscle, Skeletal/chemistry , Muscular Dystrophy, Animal/physiopathology , Muscular Dystrophy, Animal/therapy
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