Cargando…

Microtubules Are Essential for Mitochondrial Dynamics–Fission, Fusion, and Motility–in Dictyostelium discoideum

Mitochondrial function is dependent upon mitochondrial structure which is in turn dependent upon mitochondrial dynamics, including fission, fusion, and motility. Here we examined the relationship between mitochondrial dynamics and the cytoskeleton in Dictyostelium discoideum. Using time-lapse analys...

Descripción completa

Detalles Bibliográficos
Autores principales: Woods, Laken C., Berbusse, Gregory W., Naylor, Kari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4801864/
https://www.ncbi.nlm.nih.gov/pubmed/27047941
http://dx.doi.org/10.3389/fcell.2016.00019
_version_ 1782422629821448192
author Woods, Laken C.
Berbusse, Gregory W.
Naylor, Kari
author_facet Woods, Laken C.
Berbusse, Gregory W.
Naylor, Kari
author_sort Woods, Laken C.
collection PubMed
description Mitochondrial function is dependent upon mitochondrial structure which is in turn dependent upon mitochondrial dynamics, including fission, fusion, and motility. Here we examined the relationship between mitochondrial dynamics and the cytoskeleton in Dictyostelium discoideum. Using time-lapse analysis, we quantified mitochondrial fission, fusion, and motility in the presence of cytoskeleton disrupting pharmaceuticals and the absence of the potential mitochondria-cytoskeleton linker protein, CluA. Our results indicate that microtubules are essential for mitochondrial movement, as well as fission and fusion; actin plays a less significant role, perhaps selecting the mitochondria for transport. We also suggest that CluA is not a linker protein but plays an unidentified role in mitochondrial fission and fusion. The significance of our work is to gain further insight into the role the cytoskeleton plays in mitochondrial dynamics and function. By better understanding these processes we can better appreciate the underlying mitochondrial contributions to many neurological disorders characterized by altered mitochondrial dynamics, structure, and/or function.
format Online
Article
Text
id pubmed-4801864
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-48018642016-04-04 Microtubules Are Essential for Mitochondrial Dynamics–Fission, Fusion, and Motility–in Dictyostelium discoideum Woods, Laken C. Berbusse, Gregory W. Naylor, Kari Front Cell Dev Biol Physiology Mitochondrial function is dependent upon mitochondrial structure which is in turn dependent upon mitochondrial dynamics, including fission, fusion, and motility. Here we examined the relationship between mitochondrial dynamics and the cytoskeleton in Dictyostelium discoideum. Using time-lapse analysis, we quantified mitochondrial fission, fusion, and motility in the presence of cytoskeleton disrupting pharmaceuticals and the absence of the potential mitochondria-cytoskeleton linker protein, CluA. Our results indicate that microtubules are essential for mitochondrial movement, as well as fission and fusion; actin plays a less significant role, perhaps selecting the mitochondria for transport. We also suggest that CluA is not a linker protein but plays an unidentified role in mitochondrial fission and fusion. The significance of our work is to gain further insight into the role the cytoskeleton plays in mitochondrial dynamics and function. By better understanding these processes we can better appreciate the underlying mitochondrial contributions to many neurological disorders characterized by altered mitochondrial dynamics, structure, and/or function. Frontiers Media S.A. 2016-03-22 /pmc/articles/PMC4801864/ /pubmed/27047941 http://dx.doi.org/10.3389/fcell.2016.00019 Text en Copyright © 2016 Woods, Berbusse and Naylor. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Woods, Laken C.
Berbusse, Gregory W.
Naylor, Kari
Microtubules Are Essential for Mitochondrial Dynamics–Fission, Fusion, and Motility–in Dictyostelium discoideum
title Microtubules Are Essential for Mitochondrial Dynamics–Fission, Fusion, and Motility–in Dictyostelium discoideum
title_full Microtubules Are Essential for Mitochondrial Dynamics–Fission, Fusion, and Motility–in Dictyostelium discoideum
title_fullStr Microtubules Are Essential for Mitochondrial Dynamics–Fission, Fusion, and Motility–in Dictyostelium discoideum
title_full_unstemmed Microtubules Are Essential for Mitochondrial Dynamics–Fission, Fusion, and Motility–in Dictyostelium discoideum
title_short Microtubules Are Essential for Mitochondrial Dynamics–Fission, Fusion, and Motility–in Dictyostelium discoideum
title_sort microtubules are essential for mitochondrial dynamics–fission, fusion, and motility–in dictyostelium discoideum
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4801864/
https://www.ncbi.nlm.nih.gov/pubmed/27047941
http://dx.doi.org/10.3389/fcell.2016.00019
work_keys_str_mv AT woodslakenc microtubulesareessentialformitochondrialdynamicsfissionfusionandmotilityindictyosteliumdiscoideum
AT berbussegregoryw microtubulesareessentialformitochondrialdynamicsfissionfusionandmotilityindictyosteliumdiscoideum
AT naylorkari microtubulesareessentialformitochondrialdynamicsfissionfusionandmotilityindictyosteliumdiscoideum