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Mitochondria-cytoskeleton associations in mammalian cytokinesis

BACKGROUND: The role of the cytoskeleton in regulating mitochondrial distribution in dividing mammalian cells is poorly understood. We previously demonstrated that mitochondria are transported to the cleavage furrow during cytokinesis in a microtubule-dependent manner. However, the exact subset of s...

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Autores principales: Lawrence, E. J., Boucher, E., Mandato, C. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812650/
https://www.ncbi.nlm.nih.gov/pubmed/27030796
http://dx.doi.org/10.1186/s13008-016-0015-4
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author Lawrence, E. J.
Boucher, E.
Mandato, C. A.
author_facet Lawrence, E. J.
Boucher, E.
Mandato, C. A.
author_sort Lawrence, E. J.
collection PubMed
description BACKGROUND: The role of the cytoskeleton in regulating mitochondrial distribution in dividing mammalian cells is poorly understood. We previously demonstrated that mitochondria are transported to the cleavage furrow during cytokinesis in a microtubule-dependent manner. However, the exact subset of spindle microtubules and molecular machinery involved remains unknown. METHODS: We employed quantitative imaging techniques and structured illumination microscopy to analyse the spatial and temporal relationship of mitochondria with microtubules and actin of the contractile ring during cytokinesis in HeLa cells. RESULTS: Superresolution microscopy revealed that mitochondria were associated with astral microtubules of the mitotic spindle in cytokinetic cells. Dominant-negative mutants of KIF5B, the heavy chain of kinesin-1 motor, and of Miro-1 disrupted mitochondrial transport to the furrow. Live imaging revealed that mitochondrial enrichment at the cell equator occurred simultaneously with the appearance of the contractile ring in cytokinesis. Inhibiting RhoA activity and contractile ring assembly with C3 transferase, caused mitochondrial mislocalisation during division. CONCLUSIONS: Taken together, the data suggest a model in which mitochondria are transported by a microtubule-mediated mechanism involving equatorial astral microtubules, Miro-1, and KIF5B to the nascent actomyosin contractile ring in cytokinesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13008-016-0015-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-48126502016-03-31 Mitochondria-cytoskeleton associations in mammalian cytokinesis Lawrence, E. J. Boucher, E. Mandato, C. A. Cell Div Research BACKGROUND: The role of the cytoskeleton in regulating mitochondrial distribution in dividing mammalian cells is poorly understood. We previously demonstrated that mitochondria are transported to the cleavage furrow during cytokinesis in a microtubule-dependent manner. However, the exact subset of spindle microtubules and molecular machinery involved remains unknown. METHODS: We employed quantitative imaging techniques and structured illumination microscopy to analyse the spatial and temporal relationship of mitochondria with microtubules and actin of the contractile ring during cytokinesis in HeLa cells. RESULTS: Superresolution microscopy revealed that mitochondria were associated with astral microtubules of the mitotic spindle in cytokinetic cells. Dominant-negative mutants of KIF5B, the heavy chain of kinesin-1 motor, and of Miro-1 disrupted mitochondrial transport to the furrow. Live imaging revealed that mitochondrial enrichment at the cell equator occurred simultaneously with the appearance of the contractile ring in cytokinesis. Inhibiting RhoA activity and contractile ring assembly with C3 transferase, caused mitochondrial mislocalisation during division. CONCLUSIONS: Taken together, the data suggest a model in which mitochondria are transported by a microtubule-mediated mechanism involving equatorial astral microtubules, Miro-1, and KIF5B to the nascent actomyosin contractile ring in cytokinesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13008-016-0015-4) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-18 /pmc/articles/PMC4812650/ /pubmed/27030796 http://dx.doi.org/10.1186/s13008-016-0015-4 Text en © Lawrence et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lawrence, E. J.
Boucher, E.
Mandato, C. A.
Mitochondria-cytoskeleton associations in mammalian cytokinesis
title Mitochondria-cytoskeleton associations in mammalian cytokinesis
title_full Mitochondria-cytoskeleton associations in mammalian cytokinesis
title_fullStr Mitochondria-cytoskeleton associations in mammalian cytokinesis
title_full_unstemmed Mitochondria-cytoskeleton associations in mammalian cytokinesis
title_short Mitochondria-cytoskeleton associations in mammalian cytokinesis
title_sort mitochondria-cytoskeleton associations in mammalian cytokinesis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4812650/
https://www.ncbi.nlm.nih.gov/pubmed/27030796
http://dx.doi.org/10.1186/s13008-016-0015-4
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