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Adeno-Associated Virus-Mediated Gene Therapy in the Mashlool, Atp1a3Mashl/+, Mouse Model of Alternating Hemiplegia of Childhood.
Hunanyan, Arsen S; Kantor, Boris; Puranam, Ram S; Elliott, Courtney; McCall, Angela; Dhindsa, Justin; Pagadala, Promila; Wallace, Keri; Poe, Jordan; Gunduz, Talha; Asokan, Aravind; Koeberl, Dwight D; ElMallah, Mai K; Mikati, Mohamad A.
Afiliación
  • Hunanyan AS; Division of Pediatric Neurology and Developmental Medicine, Department of Pediatrics, Duke University, Durham, North Carolina, USA.
  • Kantor B; Viral Vector Core, Department of Neurobiology, Duke University, Durham, North Carolina, USA.
  • Puranam RS; Department of Neurobiology, Duke University, Durham, North Carolina, USA.
  • Elliott C; Division of Pediatric Neurology and Developmental Medicine, Department of Pediatrics, Duke University, Durham, North Carolina, USA.
  • McCall A; Division of Pediatric Pulmonary Medicine, Department of Pediatrics, Duke University, Durham, North Carolina, USA.
  • Dhindsa J; Division of Pediatric Pulmonary Medicine, Department of Pediatrics, Duke University, Durham, North Carolina, USA.
  • Pagadala P; Department of Clinical and Translational Science Institute, Duke University, Durham, North Carolina, USA.
  • Wallace K; Division of Pediatric Neurology and Developmental Medicine, Department of Pediatrics, Duke University, Durham, North Carolina, USA.
  • Poe J; Viral Vector Core, Department of Neurobiology, Duke University, Durham, North Carolina, USA.
  • Gunduz T; Division of Pediatric Neurology and Developmental Medicine, Department of Pediatrics, Duke University, Durham, North Carolina, USA.
  • Asokan A; Department of Surgery, Duke University, Durham, North Carolina, USA.
  • Koeberl DD; Molecular Genetics and Microbiology, Duke University, Durham, North Carolina, USA.
  • ElMallah MK; Division of Medical Genetics, Department of Pediatrics, Duke University, Durham, North Carolina, USA.
  • Mikati MA; Division of Pediatric Pulmonary Medicine, Department of Pediatrics, Duke University, Durham, North Carolina, USA.
Hum Gene Ther ; 32(7-8): 405-419, 2021 04.
Article en En | MEDLINE | ID: mdl-33577387
Alternating Hemiplegia of Childhood (AHC) is a devastating autosomal dominant disorder caused by ATP1A3 mutations, resulting in severe hemiplegia and dystonia spells, ataxia, debilitating disabilities, and premature death. Here, we determine the effects of delivering an extra copy of the normal gene in a mouse model carrying the most common mutation causing AHC in humans, the D801N mutation. We used an adeno-associated virus serotype 9 (AAV9) vector expressing the human ATP1A3 gene under the control of a human Synapsin promoter. We first demonstrated that intracerebroventricular (ICV) injection of this vector in wild-type mice on postnatal day 10 (P10) results in increases in ouabain-sensitive ATPase activity and in expression of reporter genes in targeted brain regions. We then tested this vector in mutant mice. Simultaneous intracisterna magna and bilateral ICV injections of this vector at P10 resulted, at P40, in reduction of inducible hemiplegia spells, improvement in balance beam test performance, and prolonged survival of treated mutant mice up to P70. Our study demonstrates, as a proof of concept, that gene therapy can induce favorable effects in a disease caused by a mutation of the gene of a protein that is, at the same time, an ATPase enzyme, a pump, and a signal transduction factor.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dependovirus / Hemiplejía Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: Hum Gene Ther Asunto de la revista: GENETICA MEDICA / TERAPEUTICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Dependovirus / Hemiplejía Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Animals Idioma: En Revista: Hum Gene Ther Asunto de la revista: GENETICA MEDICA / TERAPEUTICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos