| Literature DB >> 28053186 |
Chang Xie1,2, Xue-Min Gong2, Jie Luo1, Bo-Liang Li2, Bao-Liang Song3.
Abstract
Niemann-Pick type C (NPC) disease is a fatal inherited neurodegenerative disorder caused by loss-of-function mutations in the NPC1 or NPC2 gene. There is no effective way to treat NPC disease. In this study, we used adeno-associated virus (AAV) serotype 9 (AAV9) to deliver a functional NPC1 gene systemically into NPC1-/- mice at postnatal day 4. One single AAV9-NPC1 injection resulted in robust NPC1 expression in various tissues, including brain, heart, and lung. Strikingly, AAV9-mediated NPC1 delivery significantly promoted Purkinje cell survival, restored locomotor activity and coordination, and increased the lifespan of NPC1-/- mice. Our work suggests that AAV-based gene therapy is a promising means to treat NPC disease.Entities:
Keywords: Niemann-Pick type C disease; Niemann-Pick type C1; adeno-associated virus serotype 9; blood-brain barrier; cholesterol; gene therapy; lysosomal storage diseases
Mesh:
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Year: 2017 PMID: 28053186 PMCID: PMC5335581 DOI: 10.1194/jlr.M071274
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922