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Reversible induction of mitophagy by an optogenetic bimodular system

Autophagy-mediated degradation of mitochondria (mitophagy) is a key process in cellular quality control. Although mitophagy impairment is involved in several patho-physiological conditions, valuable methods to induce mitophagy with low toxicity in vivo are still lacking. Herein, we describe a new op...

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Detalles Bibliográficos
Autores principales: D’Acunzo, Pasquale, Strappazzon, Flavie, Caruana, Ignazio, Meneghetti, Giacomo, Di Rita, Anthea, Simula, Luca, Weber, Gerrit, Del Bufalo, Francesca, Dalla Valle, Luisa, Campello, Silvia, Locatelli, Franco, Cecconi, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449392/
https://www.ncbi.nlm.nih.gov/pubmed/30948710
http://dx.doi.org/10.1038/s41467-019-09487-1
Descripción
Sumario:Autophagy-mediated degradation of mitochondria (mitophagy) is a key process in cellular quality control. Although mitophagy impairment is involved in several patho-physiological conditions, valuable methods to induce mitophagy with low toxicity in vivo are still lacking. Herein, we describe a new optogenetic tool to stimulate mitophagy, based on light-dependent recruitment of pro-autophagy protein AMBRA1 to mitochondrial surface. Upon illumination, AMBRA1-RFP-sspB is efficiently relocated from the cytosol to mitochondria, where it reversibly mediates mito-aggresome formation and reduction of mitochondrial mass. Finally, as a proof of concept of the biomedical relevance of this method, we induced mitophagy in an in vitro model of neurotoxicity, fully preventing cell death, as well as in human T lymphocytes and in zebrafish in vivo. Given the unique features of this tool, we think it may turn out to be very useful for a wide range of both therapeutic and research applications.