| Literature DB >> 32154600 |
Federica Naso1, Daniela Intartaglia1, Danila Falanga1, Chiara Soldati1, Elena Polishchuk1, Giuliana Giamundo1, Paola Tiberi1, Elena Marrocco1, Paolo Scudieri1, Chiara Di Malta1, Ivana Trapani1, Edoardo Nusco1, Francesco Giuseppe Salierno1, Enrico Maria Surace1,2, Luis Jv Galietta1,2, Sandro Banfi1,3, Alberto Auricchio1,2, Andrea Ballabio1,2,4,5, Diego Luis Medina1, Ivan Conte1,6.
Abstract
Vertebrate vision relies on the daily phagocytosis and lysosomal degradation of photoreceptor outer segments (POS) within the retinal pigment epithelium (RPE). However, how these events are controlled by light is largely unknown. Here, we show that the light-responsive miR-211 controls lysosomal biogenesis at the beginning of light-dark transitions in the RPE by targeting Ezrin, a cytoskeleton-associated protein essential for the regulation of calcium homeostasis. miR-211-mediated down-regulation of Ezrin leads to Ca2+ influx resulting in the activation of calcineurin, which in turn activates TFEB, the master regulator of lysosomal biogenesis. Light-mediated induction of lysosomal biogenesis and function is impaired in the RPE from miR-211-/- mice that show severely compromised vision. Pharmacological restoration of lysosomal biogenesis through Ezrin inhibition rescued the miR-211-/- phenotype, pointing to a new therapeutic target to counteract retinal degeneration associated with lysosomal dysfunction.Entities:
Keywords: Ezrin; RPE; TFEB; autophagy; miR-211
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Year: 2020 PMID: 32154600 PMCID: PMC7156966 DOI: 10.15252/embj.2019102468
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598