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Tkatch, T.* ; Greotti, E.* ; Baranauskas, G.* ; Pendin, D.* ; Roy, S.* ; Nita, L.I.* ; Wettmarshausen, J. ; Prigge, M.* ; Yizhar, O.* ; Shirihai, O.S.* ; Fishman, D.* ; Hershfinkel, M.* ; Fleidervish, I.A.* ; Perocchi, F. ; Pozzan, T.* ; Sekler, I.*

Optogenetic control of mitochondrial metabolism and Ca2+ signaling by mitochondria-targeted opsins.

Proc. Natl. Acad. Sci. U.S.A. 114, E5167-E5176 (2017)
Verlagsversion Forschungsdaten DOI PMC
Open Access Gold
Key mitochondrial functions such as ATP production, Ca2+ uptake and release, and substrate accumulation depend on the proton electrochemical gradient (ΔμH+) across the inner membrane. Although several drugs can modulate ΔμH+, their effects are hardly reversible, and lack cellular specificity and spatial resolution. Although channelrhodopsins are widely used to modulate the plasma membrane potential of excitable cells, mitochondria have thus far eluded optogenetic control. Here we describe a toolkit of optometabolic constructs based on selective targeting of channelrhodopsins with distinct functional properties to the inner mitochondrial membrane of intact cells. We show that our strategy enables a light-dependent control of the mitochondrial membrane potential (Δψm) and coupled mitochondrial functions such as ATP synthesis by oxidative phosphorylation, Ca2+ dynamics, and respiratory metabolism. By directly modulating Δψm, the mitochondriatargeted opsinswere used to control complex physiological processes such as spontaneous beats in cardiac myocytes and glucose-dependent ATP increase in pancreatic β-cells. Furthermore, our optometabolic tools allow modulation of mitochondrial functions in single cells and defined cell regions.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Ca Signaling 2+ ; Mitochondria ; Mitochondrial Membrane Potential ; Optogenetic; Permeability Transition Pore; Endoplasmic-reticulum; Cell-differentiation; Calcium Uniporter; Optical Control; Indicators; Channels; Death; Channelrhodopsin-2; Determinants
Sprache englisch
Veröffentlichungsjahr 2017
HGF-Berichtsjahr 2017
ISSN (print) / ISBN 0027-8424
e-ISSN 1091-6490
Zeitschrift Proceedings of the National Academy of Sciences of the United States of America
Quellenangaben Band: 114, Heft: 26, Seiten: E5167-E5176 Artikelnummer: , Supplement: ,
Verlag National Academy of Sciences
Verlagsort Washington
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Diabetes and Obesity (IDO)
POF Topic(s) 30501 - Systemic Analysis of Genetic and Environmental Factors that Impact Health
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-553000-001
DOI 10.1073/pnas.1703623114
WOS ID WOS:000404108400020
Scopus ID 85021395235
PubMed ID 28611221
Erfassungsdatum 2017-07-14
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