| Literature DB >> 27793778 |
Allison M Bradbury1, Tiffany A Peterson2, Amanda L Gross2, Stephen Z Wells3, Victoria J McCurdy4, Karen G Wolfe5, John C Dennis5, Brandon L Brunson5, Heather Gray-Edwards2, Ashley N Randle2, Aime K Johnson3, Edward E Morrison5, Nancy R Cox6, Henry J Baker2, Miguel Sena-Esteves7, Douglas R Martin4.
Abstract
Sandhoff disease (SD) is a lysosomal storage disorder characterized by the absence of hydrolytic enzyme β-N-acetylhexosaminidase (Hex), which results in storage of GM2 ganglioside in neurons and unremitting neurodegeneration. Neuron loss initially affects fine motor skills, but rapidly progresses to loss of all body faculties, a vegetative state, and death by five years of age in humans. A well-established feline model of SD allows characterization of the disease in a large animal model and provides a means to test the safety and efficacy of therapeutic interventions before initiating clinical trials. In this study, we demonstrate a robust central nervous system (CNS) inflammatory response in feline SD, primarily marked by expansion and activation of the microglial cell population. Quantification of major histocompatibility complex II (MHC-II) labeling revealed significant up-regulation throughout the CNS with areas rich in white matter most severely affected. Expression of the leukocyte chemokine macrophage inflammatory protein-1 alpha (MIP-1α) was also up-regulated in the brain. SD cats were treated with intracranial delivery of adeno-associated viral (AAV) vectors expressing feline Hex, with a study endpoint 16weeks post treatment. AAV-mediated gene delivery repressed the expansion and activation of microglia and normalized MHC-II and MIP-1α levels. These data reiterate the profound inflammatory response in SD and show that neuroinflammation is abrogated after AAV-mediated restoration of enzymatic activity.Entities:
Keywords: AAV gene therapy; cytokines/chemokines; lysosomal storage disorder; microglia activation; neurodegenerative disease; neuroinflammation
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Year: 2016 PMID: 27793778 PMCID: PMC5154837 DOI: 10.1016/j.neuroscience.2016.10.047
Source DB: PubMed Journal: Neuroscience ISSN: 0306-4522 Impact factor: 3.590