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Active diffusion and microtubule-based transport oppose myosin forces to position organelles in cells

Even distribution of peroxisomes (POs) and lipid droplets (LDs) is critical to their role in lipid and reactive oxygen species homeostasis. How even distribution is achieved remains elusive, but diffusive motion and directed motility may play a role. Here we show that in the fungus Ustilago maydis ∼...

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Autores principales: Lin, Congping, Schuster, Martin, Guimaraes, Sofia Cunha, Ashwin, Peter, Schrader, Michael, Metz, Jeremy, Hacker, Christian, Gurr, Sarah Jane, Steinberg, Gero
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895713/
https://www.ncbi.nlm.nih.gov/pubmed/27251117
http://dx.doi.org/10.1038/ncomms11814
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author Lin, Congping
Schuster, Martin
Guimaraes, Sofia Cunha
Ashwin, Peter
Schrader, Michael
Metz, Jeremy
Hacker, Christian
Gurr, Sarah Jane
Steinberg, Gero
author_facet Lin, Congping
Schuster, Martin
Guimaraes, Sofia Cunha
Ashwin, Peter
Schrader, Michael
Metz, Jeremy
Hacker, Christian
Gurr, Sarah Jane
Steinberg, Gero
author_sort Lin, Congping
collection PubMed
description Even distribution of peroxisomes (POs) and lipid droplets (LDs) is critical to their role in lipid and reactive oxygen species homeostasis. How even distribution is achieved remains elusive, but diffusive motion and directed motility may play a role. Here we show that in the fungus Ustilago maydis ∼95% of POs and LDs undergo diffusive motions. These movements require ATP and involve bidirectional early endosome motility, indicating that microtubule-associated membrane trafficking enhances diffusion of organelles. When early endosome transport is abolished, POs and LDs drift slowly towards the growing cell end. This pole-ward drift is facilitated by anterograde delivery of secretory cargo to the cell tip by myosin-5. Modelling reveals that microtubule-based directed transport and active diffusion support distribution, mobility and mixing of POs. In mammalian COS-7 cells, microtubules and F-actin also counteract each other to distribute POs. This highlights the importance of opposing cytoskeletal forces in organelle positioning in eukaryotes.
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spelling pubmed-48957132016-08-18 Active diffusion and microtubule-based transport oppose myosin forces to position organelles in cells Lin, Congping Schuster, Martin Guimaraes, Sofia Cunha Ashwin, Peter Schrader, Michael Metz, Jeremy Hacker, Christian Gurr, Sarah Jane Steinberg, Gero Nat Commun Article Even distribution of peroxisomes (POs) and lipid droplets (LDs) is critical to their role in lipid and reactive oxygen species homeostasis. How even distribution is achieved remains elusive, but diffusive motion and directed motility may play a role. Here we show that in the fungus Ustilago maydis ∼95% of POs and LDs undergo diffusive motions. These movements require ATP and involve bidirectional early endosome motility, indicating that microtubule-associated membrane trafficking enhances diffusion of organelles. When early endosome transport is abolished, POs and LDs drift slowly towards the growing cell end. This pole-ward drift is facilitated by anterograde delivery of secretory cargo to the cell tip by myosin-5. Modelling reveals that microtubule-based directed transport and active diffusion support distribution, mobility and mixing of POs. In mammalian COS-7 cells, microtubules and F-actin also counteract each other to distribute POs. This highlights the importance of opposing cytoskeletal forces in organelle positioning in eukaryotes. Nature Publishing Group 2016-06-02 /pmc/articles/PMC4895713/ /pubmed/27251117 http://dx.doi.org/10.1038/ncomms11814 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Lin, Congping
Schuster, Martin
Guimaraes, Sofia Cunha
Ashwin, Peter
Schrader, Michael
Metz, Jeremy
Hacker, Christian
Gurr, Sarah Jane
Steinberg, Gero
Active diffusion and microtubule-based transport oppose myosin forces to position organelles in cells
title Active diffusion and microtubule-based transport oppose myosin forces to position organelles in cells
title_full Active diffusion and microtubule-based transport oppose myosin forces to position organelles in cells
title_fullStr Active diffusion and microtubule-based transport oppose myosin forces to position organelles in cells
title_full_unstemmed Active diffusion and microtubule-based transport oppose myosin forces to position organelles in cells
title_short Active diffusion and microtubule-based transport oppose myosin forces to position organelles in cells
title_sort active diffusion and microtubule-based transport oppose myosin forces to position organelles in cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4895713/
https://www.ncbi.nlm.nih.gov/pubmed/27251117
http://dx.doi.org/10.1038/ncomms11814
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