Cargando…
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 ∼...
Autores principales: | , , , , , , , , |
---|---|
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 |
_version_ | 1782435907261956096 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4895713 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT lincongping activediffusionandmicrotubulebasedtransportopposemyosinforcestopositionorganellesincells AT schustermartin activediffusionandmicrotubulebasedtransportopposemyosinforcestopositionorganellesincells AT guimaraessofiacunha activediffusionandmicrotubulebasedtransportopposemyosinforcestopositionorganellesincells AT ashwinpeter activediffusionandmicrotubulebasedtransportopposemyosinforcestopositionorganellesincells AT schradermichael activediffusionandmicrotubulebasedtransportopposemyosinforcestopositionorganellesincells AT metzjeremy activediffusionandmicrotubulebasedtransportopposemyosinforcestopositionorganellesincells AT hackerchristian activediffusionandmicrotubulebasedtransportopposemyosinforcestopositionorganellesincells AT gurrsarahjane activediffusionandmicrotubulebasedtransportopposemyosinforcestopositionorganellesincells AT steinberggero activediffusionandmicrotubulebasedtransportopposemyosinforcestopositionorganellesincells |