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Mitochondria Localize to the Cleavage Furrow in Mammalian Cytokinesis
Mitochondria are dynamic organelles with multiple cellular functions, including ATP production, calcium buffering, and lipid biosynthesis. Several studies have shown that mitochondrial positioning is regulated by the cytoskeleton during cell division in several eukaryotic systems. However, the distr...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3749163/ https://www.ncbi.nlm.nih.gov/pubmed/23991162 http://dx.doi.org/10.1371/journal.pone.0072886 |
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author | Lawrence, Elizabeth J. Mandato, Craig A. |
author_facet | Lawrence, Elizabeth J. Mandato, Craig A. |
author_sort | Lawrence, Elizabeth J. |
collection | PubMed |
description | Mitochondria are dynamic organelles with multiple cellular functions, including ATP production, calcium buffering, and lipid biosynthesis. Several studies have shown that mitochondrial positioning is regulated by the cytoskeleton during cell division in several eukaryotic systems. However, the distribution of mitochondria during mammalian cytokinesis and whether the distribution is regulated by the cytoskeleton has not been examined. Using live spinning disk confocal microscopy and quantitative analysis of mitochondrial fluorescence intensity, we demonstrate that mitochondria are recruited to the cleavage furrow during cytokinesis in HeLa cells. After anaphase onset, the mitochondria are recruited towards the site of cleavage furrow formation, where they remain enriched as the furrow ingresses and until cytokinesis completion. Furthermore, we show that recruitment of mitochondria to the furrow occurs in multiple mammalian cells lines as well as in monopolar, bipolar, and multipolar divisions, suggesting that the mechanism of recruitment is conserved and robust. Using inhibitors of cytoskeleton dynamics, we show that the microtubule cytoskeleton, but not actin, is required to transport mitochondria to the cleavage furrow. Thus, mitochondria are specifically recruited to the cleavage furrow in a microtubule-dependent manner during mammalian cytokinesis. Two possible reasons for this could be to localize mitochondrial function to the furrow to facilitate cytokinesis and / or ensure accurate mitochondrial inheritance. |
format | Online Article Text |
id | pubmed-3749163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37491632013-08-29 Mitochondria Localize to the Cleavage Furrow in Mammalian Cytokinesis Lawrence, Elizabeth J. Mandato, Craig A. PLoS One Research Article Mitochondria are dynamic organelles with multiple cellular functions, including ATP production, calcium buffering, and lipid biosynthesis. Several studies have shown that mitochondrial positioning is regulated by the cytoskeleton during cell division in several eukaryotic systems. However, the distribution of mitochondria during mammalian cytokinesis and whether the distribution is regulated by the cytoskeleton has not been examined. Using live spinning disk confocal microscopy and quantitative analysis of mitochondrial fluorescence intensity, we demonstrate that mitochondria are recruited to the cleavage furrow during cytokinesis in HeLa cells. After anaphase onset, the mitochondria are recruited towards the site of cleavage furrow formation, where they remain enriched as the furrow ingresses and until cytokinesis completion. Furthermore, we show that recruitment of mitochondria to the furrow occurs in multiple mammalian cells lines as well as in monopolar, bipolar, and multipolar divisions, suggesting that the mechanism of recruitment is conserved and robust. Using inhibitors of cytoskeleton dynamics, we show that the microtubule cytoskeleton, but not actin, is required to transport mitochondria to the cleavage furrow. Thus, mitochondria are specifically recruited to the cleavage furrow in a microtubule-dependent manner during mammalian cytokinesis. Two possible reasons for this could be to localize mitochondrial function to the furrow to facilitate cytokinesis and / or ensure accurate mitochondrial inheritance. Public Library of Science 2013-08-21 /pmc/articles/PMC3749163/ /pubmed/23991162 http://dx.doi.org/10.1371/journal.pone.0072886 Text en © 2013 Lawrence, Mandato http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lawrence, Elizabeth J. Mandato, Craig A. Mitochondria Localize to the Cleavage Furrow in Mammalian Cytokinesis |
title | Mitochondria Localize to the Cleavage Furrow in Mammalian Cytokinesis |
title_full | Mitochondria Localize to the Cleavage Furrow in Mammalian Cytokinesis |
title_fullStr | Mitochondria Localize to the Cleavage Furrow in Mammalian Cytokinesis |
title_full_unstemmed | Mitochondria Localize to the Cleavage Furrow in Mammalian Cytokinesis |
title_short | Mitochondria Localize to the Cleavage Furrow in Mammalian Cytokinesis |
title_sort | mitochondria localize to the cleavage furrow in mammalian cytokinesis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3749163/ https://www.ncbi.nlm.nih.gov/pubmed/23991162 http://dx.doi.org/10.1371/journal.pone.0072886 |
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