Reversible induction of mitophagy by an optogenetic bimodular system
Authors:
- Pasquale D’aCunzoPDPasquale D’aCunzo
- Flavie StrappazzonFSFlavie Strappazzon
- Ignazio CaruanaICIgnazio Caruana
- Giacomo MeneghettiGMGiacomo Meneghetti
- Luca SimulaLSLuca Simula
- Gerrit WeberGWGerrit Weber
- Francesca Del BufaloFBFrancesca Del Bufalo
- Luisa Dalla ValleLuisa Dalla Valle
- Silvia CampelloSCSilvia Campello
- Francesco CecconiFCFrancesco Cecconi
Open Access
- 4 April 2019
- journal article
- research article
- Published by Springer Nature in Nature Communications
- Vol. 10 (1) , 1533
Abstract
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.Keywords
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