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Mitochondrial network complexity emerges from fission/fusion dynamics

Mitochondrial networks exhibit a variety of complex behaviors, including coordinated cell-wide oscillations of energy states as well as a phase transition (depolarization) in response to oxidative stress. Since functional and structural properties are often interwinded, here we characterized the str...

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Autores principales: Zamponi, Nahuel, Zamponi, Emiliano, Cannas, Sergio A., Billoni, Orlando V., Helguera, Pablo R., Chialvo, Dante R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762699/
https://www.ncbi.nlm.nih.gov/pubmed/29321534
http://dx.doi.org/10.1038/s41598-017-18351-5
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author Zamponi, Nahuel
Zamponi, Emiliano
Cannas, Sergio A.
Billoni, Orlando V.
Helguera, Pablo R.
Chialvo, Dante R.
author_facet Zamponi, Nahuel
Zamponi, Emiliano
Cannas, Sergio A.
Billoni, Orlando V.
Helguera, Pablo R.
Chialvo, Dante R.
author_sort Zamponi, Nahuel
collection PubMed
description Mitochondrial networks exhibit a variety of complex behaviors, including coordinated cell-wide oscillations of energy states as well as a phase transition (depolarization) in response to oxidative stress. Since functional and structural properties are often interwinded, here we characterized the structure of mitochondrial networks in mouse embryonic fibroblasts using network tools and percolation theory. Subsequently we perturbed the system either by promoting the fusion of mitochondrial segments or by inducing mitochondrial fission. Quantitative analysis of mitochondrial clusters revealed that structural parameters of healthy mitochondria laid in between the extremes of highly fragmented and completely fusioned networks. We confirmed our results by contrasting our empirical findings with the predictions of a recently described computational model of mitochondrial network emergence based on fission-fusion kinetics. Altogether these results offer not only an objective methodology to parametrize the complexity of this organelle but also support the idea that mitochondrial networks behave as critical systems and undergo structural phase transitions.
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spelling pubmed-57626992018-01-17 Mitochondrial network complexity emerges from fission/fusion dynamics Zamponi, Nahuel Zamponi, Emiliano Cannas, Sergio A. Billoni, Orlando V. Helguera, Pablo R. Chialvo, Dante R. Sci Rep Article Mitochondrial networks exhibit a variety of complex behaviors, including coordinated cell-wide oscillations of energy states as well as a phase transition (depolarization) in response to oxidative stress. Since functional and structural properties are often interwinded, here we characterized the structure of mitochondrial networks in mouse embryonic fibroblasts using network tools and percolation theory. Subsequently we perturbed the system either by promoting the fusion of mitochondrial segments or by inducing mitochondrial fission. Quantitative analysis of mitochondrial clusters revealed that structural parameters of healthy mitochondria laid in between the extremes of highly fragmented and completely fusioned networks. We confirmed our results by contrasting our empirical findings with the predictions of a recently described computational model of mitochondrial network emergence based on fission-fusion kinetics. Altogether these results offer not only an objective methodology to parametrize the complexity of this organelle but also support the idea that mitochondrial networks behave as critical systems and undergo structural phase transitions. Nature Publishing Group UK 2018-01-10 /pmc/articles/PMC5762699/ /pubmed/29321534 http://dx.doi.org/10.1038/s41598-017-18351-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zamponi, Nahuel
Zamponi, Emiliano
Cannas, Sergio A.
Billoni, Orlando V.
Helguera, Pablo R.
Chialvo, Dante R.
Mitochondrial network complexity emerges from fission/fusion dynamics
title Mitochondrial network complexity emerges from fission/fusion dynamics
title_full Mitochondrial network complexity emerges from fission/fusion dynamics
title_fullStr Mitochondrial network complexity emerges from fission/fusion dynamics
title_full_unstemmed Mitochondrial network complexity emerges from fission/fusion dynamics
title_short Mitochondrial network complexity emerges from fission/fusion dynamics
title_sort mitochondrial network complexity emerges from fission/fusion dynamics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762699/
https://www.ncbi.nlm.nih.gov/pubmed/29321534
http://dx.doi.org/10.1038/s41598-017-18351-5
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