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Mitochondrial cellular organization and shape fluctuations are differentially modulated by cytoskeletal networks
The interactions between mitochondria and the cytoskeleton have been found to alter mitochondrial function; however, the mechanisms underlying this phenomenon are largely unknown. Here, we explored how the integrity of the cytoskeleton affects the cellular organization, morphology and mobility of mi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008531/ https://www.ncbi.nlm.nih.gov/pubmed/36906690 http://dx.doi.org/10.1038/s41598-023-31121-w |
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author | Fernández Casafuz, Agustina Belén De Rossi, María Cecilia Bruno, Luciana |
author_facet | Fernández Casafuz, Agustina Belén De Rossi, María Cecilia Bruno, Luciana |
author_sort | Fernández Casafuz, Agustina Belén |
collection | PubMed |
description | The interactions between mitochondria and the cytoskeleton have been found to alter mitochondrial function; however, the mechanisms underlying this phenomenon are largely unknown. Here, we explored how the integrity of the cytoskeleton affects the cellular organization, morphology and mobility of mitochondria in Xenopus laevis melanocytes. Cells were imaged in control condition and after different treatments that selectively affect specific cytoskeletal networks (microtubules, F-actin and vimentin filaments). We observed that mitochondria cellular distribution and local orientation rely mostly on microtubules, positioning these filaments as the main scaffolding of mitochondrial organization. We also found that cytoskeletal networks mold mitochondria shapes in distinct ways: while microtubules favor more elongated organelles, vimentin and actin filaments increase mitochondrial bending, suggesting the presence of mechanical interactions between these filaments and mitochondria. Finally, we identified that microtubule and F-actin networks play opposite roles in mitochondria shape fluctuations and mobility, with microtubules transmitting their jittering to the organelles and F-actin restricting the organelles motion. All our results support that cytoskeleton filaments interact mechanically with mitochondria and transmit forces to these organelles molding their movements and shapes. |
format | Online Article Text |
id | pubmed-10008531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100085312023-03-13 Mitochondrial cellular organization and shape fluctuations are differentially modulated by cytoskeletal networks Fernández Casafuz, Agustina Belén De Rossi, María Cecilia Bruno, Luciana Sci Rep Article The interactions between mitochondria and the cytoskeleton have been found to alter mitochondrial function; however, the mechanisms underlying this phenomenon are largely unknown. Here, we explored how the integrity of the cytoskeleton affects the cellular organization, morphology and mobility of mitochondria in Xenopus laevis melanocytes. Cells were imaged in control condition and after different treatments that selectively affect specific cytoskeletal networks (microtubules, F-actin and vimentin filaments). We observed that mitochondria cellular distribution and local orientation rely mostly on microtubules, positioning these filaments as the main scaffolding of mitochondrial organization. We also found that cytoskeletal networks mold mitochondria shapes in distinct ways: while microtubules favor more elongated organelles, vimentin and actin filaments increase mitochondrial bending, suggesting the presence of mechanical interactions between these filaments and mitochondria. Finally, we identified that microtubule and F-actin networks play opposite roles in mitochondria shape fluctuations and mobility, with microtubules transmitting their jittering to the organelles and F-actin restricting the organelles motion. All our results support that cytoskeleton filaments interact mechanically with mitochondria and transmit forces to these organelles molding their movements and shapes. Nature Publishing Group UK 2023-03-11 /pmc/articles/PMC10008531/ /pubmed/36906690 http://dx.doi.org/10.1038/s41598-023-31121-w Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Fernández Casafuz, Agustina Belén De Rossi, María Cecilia Bruno, Luciana Mitochondrial cellular organization and shape fluctuations are differentially modulated by cytoskeletal networks |
title | Mitochondrial cellular organization and shape fluctuations are differentially modulated by cytoskeletal networks |
title_full | Mitochondrial cellular organization and shape fluctuations are differentially modulated by cytoskeletal networks |
title_fullStr | Mitochondrial cellular organization and shape fluctuations are differentially modulated by cytoskeletal networks |
title_full_unstemmed | Mitochondrial cellular organization and shape fluctuations are differentially modulated by cytoskeletal networks |
title_short | Mitochondrial cellular organization and shape fluctuations are differentially modulated by cytoskeletal networks |
title_sort | mitochondrial cellular organization and shape fluctuations are differentially modulated by cytoskeletal networks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008531/ https://www.ncbi.nlm.nih.gov/pubmed/36906690 http://dx.doi.org/10.1038/s41598-023-31121-w |
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