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Nano-positioning and tubulin conformation contribute to axonal transport regulation of mitochondria along microtubules

Correct spatiotemporal distribution of organelles and vesicles is crucial for healthy cell functioning and is regulated by intracellular transport mechanisms. Controlled transport of bulky mitochondria is especially important in polarized cells such as neurons that rely on these organelles to locall...

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Autores principales: Van Steenbergen, Valérie, Lavoie-Cardinal, Flavie, Kazwiny, Youcef, Decet, Marianna, Martens, Tobie, Verstreken, Patrik, Boesmans, Werend, De Koninck, Paul, Vanden Berghe, Pieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659393/
https://www.ncbi.nlm.nih.gov/pubmed/36322761
http://dx.doi.org/10.1073/pnas.2203499119
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author Van Steenbergen, Valérie
Lavoie-Cardinal, Flavie
Kazwiny, Youcef
Decet, Marianna
Martens, Tobie
Verstreken, Patrik
Boesmans, Werend
De Koninck, Paul
Vanden Berghe, Pieter
author_facet Van Steenbergen, Valérie
Lavoie-Cardinal, Flavie
Kazwiny, Youcef
Decet, Marianna
Martens, Tobie
Verstreken, Patrik
Boesmans, Werend
De Koninck, Paul
Vanden Berghe, Pieter
author_sort Van Steenbergen, Valérie
collection PubMed
description Correct spatiotemporal distribution of organelles and vesicles is crucial for healthy cell functioning and is regulated by intracellular transport mechanisms. Controlled transport of bulky mitochondria is especially important in polarized cells such as neurons that rely on these organelles to locally produce energy and buffer calcium. Mitochondrial transport requires and depends on microtubules that fill much of the available axonal space. How mitochondrial transport is affected by their position within the microtubule bundles is not known. Here, we found that anterograde transport, driven by kinesin motors, is susceptible to the molecular conformation of tubulin in neurons both in vitro and in vivo. Anterograde velocities negatively correlate with the density of elongated tubulin dimers like guanosine triphosphate (GTP)-tubulin. The impact of the tubulin conformation depends primarily on where a mitochondrion is positioned, either within or at the rim of microtubule bundle. Increasing elongated tubulin levels lowers the number of motile anterograde mitochondria within the microtubule bundle and increases anterograde transport speed at the microtubule bundle rim. We demonstrate that the increased kinesin velocity and density on microtubules consisting of elongated dimers add to the increased mitochondrial dynamics. Our work indicates that the molecular conformation of tubulin contributes to the regulation of mitochondrial motility and as such to the local distribution of mitochondria along axons.
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spelling pubmed-96593932023-05-02 Nano-positioning and tubulin conformation contribute to axonal transport regulation of mitochondria along microtubules Van Steenbergen, Valérie Lavoie-Cardinal, Flavie Kazwiny, Youcef Decet, Marianna Martens, Tobie Verstreken, Patrik Boesmans, Werend De Koninck, Paul Vanden Berghe, Pieter Proc Natl Acad Sci U S A Biological Sciences Correct spatiotemporal distribution of organelles and vesicles is crucial for healthy cell functioning and is regulated by intracellular transport mechanisms. Controlled transport of bulky mitochondria is especially important in polarized cells such as neurons that rely on these organelles to locally produce energy and buffer calcium. Mitochondrial transport requires and depends on microtubules that fill much of the available axonal space. How mitochondrial transport is affected by their position within the microtubule bundles is not known. Here, we found that anterograde transport, driven by kinesin motors, is susceptible to the molecular conformation of tubulin in neurons both in vitro and in vivo. Anterograde velocities negatively correlate with the density of elongated tubulin dimers like guanosine triphosphate (GTP)-tubulin. The impact of the tubulin conformation depends primarily on where a mitochondrion is positioned, either within or at the rim of microtubule bundle. Increasing elongated tubulin levels lowers the number of motile anterograde mitochondria within the microtubule bundle and increases anterograde transport speed at the microtubule bundle rim. We demonstrate that the increased kinesin velocity and density on microtubules consisting of elongated dimers add to the increased mitochondrial dynamics. Our work indicates that the molecular conformation of tubulin contributes to the regulation of mitochondrial motility and as such to the local distribution of mitochondria along axons. National Academy of Sciences 2022-11-02 2022-11-08 /pmc/articles/PMC9659393/ /pubmed/36322761 http://dx.doi.org/10.1073/pnas.2203499119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Van Steenbergen, Valérie
Lavoie-Cardinal, Flavie
Kazwiny, Youcef
Decet, Marianna
Martens, Tobie
Verstreken, Patrik
Boesmans, Werend
De Koninck, Paul
Vanden Berghe, Pieter
Nano-positioning and tubulin conformation contribute to axonal transport regulation of mitochondria along microtubules
title Nano-positioning and tubulin conformation contribute to axonal transport regulation of mitochondria along microtubules
title_full Nano-positioning and tubulin conformation contribute to axonal transport regulation of mitochondria along microtubules
title_fullStr Nano-positioning and tubulin conformation contribute to axonal transport regulation of mitochondria along microtubules
title_full_unstemmed Nano-positioning and tubulin conformation contribute to axonal transport regulation of mitochondria along microtubules
title_short Nano-positioning and tubulin conformation contribute to axonal transport regulation of mitochondria along microtubules
title_sort nano-positioning and tubulin conformation contribute to axonal transport regulation of mitochondria along microtubules
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659393/
https://www.ncbi.nlm.nih.gov/pubmed/36322761
http://dx.doi.org/10.1073/pnas.2203499119
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