| Literature DB >> 35121108 |
Antonella Capuozzo1, Sandro Montefusco1, Vincenzo Cacace1, Martina Sofia1, Alessandra Esposito1, Gennaro Napolitano2, Eduardo Nusco1, Elena Polishchuk1, Maria Teresa Pizzo1, Maria De Risi1, Elvira De Leonibus3, Nicolina Cristina Sorrentino4, Diego Luis Medina5.
Abstract
Mucopolysaccharidosis type IIIA (MPS-IIIA) is an autosomal recessive disorder caused by mutations in SGSH involved in the degradation of heparan sulfate. MPS-IIIA presents severe neurological symptoms such as progressive developmental delay and cognitive decline, for which there is currently no treatment. Brain targeting represents the main challenge for therapeutics to treat MPS-IIIA, and the development of small-molecule-based treatments able to reach the CNS could be a relevant advance for therapy. Using cell-based high content imaging to survey clinically approved drugs in MPS-IIIA cells, we identified fluoxetine, a selective serotonin reuptake inhibitor. Fluoxetine increases lysosomal and autophagic functions via TFEB activation through a RagC-dependent mechanism. Mechanistically, fluoxetine increases lysosomal exocytosis in mouse embryonic fibroblasts from MPS-IIIA mice, suggesting that this process may be responsible for heparan sulfate clearance. In vivo, fluoxetine ameliorates somatic and brain pathology in a mouse model of MPS-IIIA by decreasing the accumulation of glycosaminoglycans and aggregated autophagic substrates, reducing inflammation, and slowing down cognitive deterioration. We repurposed fluoxetine for potential therapeutics to treat human MPS-IIIA disease.Entities:
Keywords: MPS-IIIA; TFEB; autophagy; drug repurposing; fluoxetine; high content imaging; lysosomal exocytosis; lysosomal storage disorders
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Year: 2022 PMID: 35121108 PMCID: PMC9077373 DOI: 10.1016/j.ymthe.2022.01.037
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 12.910