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Muscle as a putative producer of acid alpha-glucosidase for glycogenosis type II gene therapy.

Abstract
Glycogenosis type II (GSD II) is a lysosomal disorder affecting skeletal and cardiac muscle. In the infantile form of the disease, patients display cardiac impairment, which is fatal before 2 years of life. Patients with juvenile or adult forms can present diaphragm involvement leading to respiratory failure. The enzymatic defect in GSD II results from mutations in the acid alpha-glucosidase (GAA) gene, which encodes a 76 kDa protein involved in intralysosomal glycogen hydrolysis. We previously reported the use of an adenovirus vector expressing GAA (AdGAA) for the transduction of myoblasts and myotubes cultures from GSD II patients. Transduced cells secreted GAA in the medium, and GAA was internalized by receptor-mediated capture, allowing glycogen hydrolysis in untransduced cells. In this study, using a GSD II mouse model, we evaluated the feasibility of GSD II gene therapy using muscle as a secretary organ. Adenovirus vector encoding AdGAA was injected in the gastrocnemius of neonates. We detected a strong expression of GAA in the injected muscle, secretion into plasma, and uptake by peripheral skeletal muscle and the heart. Moreover, glycogen content was decreased in these tissues. Electron microscopy demonstrated the disappearance of destruction foci, normally present in untreated mice. We thus demonstrate for the first time that muscle can be considered as a safe and easily accessible organ for GSD II gene therapy.
AuthorsE Martin-Touaux, J P Puech, D Château, C Emiliani, E J Kremer, N Raben, B Tancini, A Orlacchio, A Kahn, L Poenaru
JournalHuman molecular genetics (Hum Mol Genet) Vol. 11 Issue 14 Pg. 1637-45 (Jul 01 2002) ISSN: 0964-6906 [Print] England
PMID12075008 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Glycogen
  • alpha-Glucosidases
  • Glucan 1,4-alpha-Glucosidase
Topics
  • Adenoviridae (genetics)
  • Animals
  • Genetic Therapy (methods)
  • Genetic Vectors (pharmacology)
  • Glucan 1,4-alpha-Glucosidase (genetics, metabolism)
  • Glycogen (metabolism)
  • Glycogen Storage Disease Type II (genetics, therapy)
  • Injections, Intramuscular
  • Lysosomes (drug effects, metabolism)
  • Mice
  • Mice, Knockout
  • Microscopy, Electron
  • Muscle, Skeletal (drug effects, metabolism, pathology)
  • alpha-Glucosidases

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