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dc.contributor.authorMahecic, Dora
dc.contributor.authorCarlini, Lina
dc.contributor.authorKleele, Tatjana
dc.contributor.authorColom Diego, Adai
dc.contributor.authorGoujon, Antoine
dc.contributor.authorMatile, Stefan
dc.contributor.authorRoux, Aurelien
dc.contributor.authorManley, Suliana
dc.date.accessioned2021-05-19T08:17:22Z
dc.date.available2021-05-19T08:17:22Z
dc.date.issued2021-04-13
dc.identifier.citationCell Reports 35(2) : (2021) // Article ID 108947es_ES
dc.identifier.issn2211-1247
dc.identifier.urihttp://hdl.handle.net/10810/51484
dc.description.abstractDuring mitochondrial fission, key molecular and cellular factors assemble on the outer mitochondrial membrane, where they coordinate to generate constriction. Constriction sites can eventually divide or reverse upon disassembly of the machinery. However, a role for membrane tension in mitochondrial fission, although speculated, has remained undefined. We capture the dynamics of constricting mitochondria in mammalian cells using live-cell structured illumination microscopy (SIM). By analyzing the diameters of tubules that emerge from mitochondria and implementing a fluorescence lifetime-based mitochondrial membrane tension sensor, we discover that mitochondria are indeed under tension. Under perturbations that reduce mitochondrial tension, constrictions initiate at the same rate, but are less likely to divide. We propose a model based on our estimates of mitochondrial membrane tension and bending energy in living cells which accounts for the observed probability distribution for mitochondrial constrictions to divide.es_ES
dc.description.sponsorshipThis work was supported in part by the National Centre of Competence in Research Chemical Biology (S. Manley, S. Matile, and A.R.). S. Manley also acknowledges SNSF Project Grant 31003A_182429 (to T.K. and D.M). T.K. received funding from the European Molecular Biology Organization (ALTF-739-2016) and the Munich Cluster for Systems Neurology (SyNergy). A.C. received funding from MCIU, MINECO G19/P66, RYC-18/02, and T1270-19es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectfluorescence lifetimees_ES
dc.subjectfluorescent tension sensores_ES
dc.subjectmembrane tensiones_ES
dc.subjectmicrotubuleses_ES
dc.subjectmitochondrial divisiones_ES
dc.subjectmitochondrial dynamicses_ES
dc.subjectsuper-resolution microscopyes_ES
dc.titleMitochondrial Membrane Tension Governs Fissiones_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderThis is an open access article distributed under the terms of the Creative Commons CC-BY licensees_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S2211124721002618?via%3Dihubes_ES
dc.identifier.doi10.1016/j.celrep.2021.108947
dc.departamentoesBioquímica y biología moleculares_ES
dc.departamentoeuBiokimika eta biologia molekularraes_ES


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This is an open access article distributed under the terms of the Creative Commons CC-BY license
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