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Mobile late endosomes modulate peripheral endoplasmic reticulum network architecture
The endoplasmic reticulum (ER) is the largest organelle contacting virtually every other organelle for information exchange and control of processes such as transport, fusion, and fission. Here, we studied the role of the other organelles on ER network architecture in the cell periphery. We show tha...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926257/ https://www.ncbi.nlm.nih.gov/pubmed/33554435 http://dx.doi.org/10.15252/embr.202050815 |
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author | Spits, Menno Heesterbeek, Iris T Voortman, Lennard M Akkermans, Jimmy J Wijdeven, Ruud H Cabukusta, Birol Neefjes, Jacques |
author_facet | Spits, Menno Heesterbeek, Iris T Voortman, Lennard M Akkermans, Jimmy J Wijdeven, Ruud H Cabukusta, Birol Neefjes, Jacques |
author_sort | Spits, Menno |
collection | PubMed |
description | The endoplasmic reticulum (ER) is the largest organelle contacting virtually every other organelle for information exchange and control of processes such as transport, fusion, and fission. Here, we studied the role of the other organelles on ER network architecture in the cell periphery. We show that the co‐migration of the ER with other organelles, called ER hitchhiking facilitated by late endosomes and lysosomes is a major mechanism controlling ER network architecture. When hitchhiking occurs, emerging ER structures may fuse with the existing ER tubules to alter the local ER architecture. This couples late endosomal/lysosomal positioning and mobility to ER network architecture. Conditions restricting late endosomal movement—including cell starvation—or the depletion of tether proteins that link the ER to late endosomes reduce ER dynamics and limit the complexity of the peripheral ER network architecture. This indicates that among many factors, the ER is controlled by late endosomal movement resulting in an alteration of the ER network architecture. |
format | Online Article Text |
id | pubmed-7926257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79262572021-03-12 Mobile late endosomes modulate peripheral endoplasmic reticulum network architecture Spits, Menno Heesterbeek, Iris T Voortman, Lennard M Akkermans, Jimmy J Wijdeven, Ruud H Cabukusta, Birol Neefjes, Jacques EMBO Rep Articles The endoplasmic reticulum (ER) is the largest organelle contacting virtually every other organelle for information exchange and control of processes such as transport, fusion, and fission. Here, we studied the role of the other organelles on ER network architecture in the cell periphery. We show that the co‐migration of the ER with other organelles, called ER hitchhiking facilitated by late endosomes and lysosomes is a major mechanism controlling ER network architecture. When hitchhiking occurs, emerging ER structures may fuse with the existing ER tubules to alter the local ER architecture. This couples late endosomal/lysosomal positioning and mobility to ER network architecture. Conditions restricting late endosomal movement—including cell starvation—or the depletion of tether proteins that link the ER to late endosomes reduce ER dynamics and limit the complexity of the peripheral ER network architecture. This indicates that among many factors, the ER is controlled by late endosomal movement resulting in an alteration of the ER network architecture. John Wiley and Sons Inc. 2021-02-08 2021-03-03 /pmc/articles/PMC7926257/ /pubmed/33554435 http://dx.doi.org/10.15252/embr.202050815 Text en © 2021 The Authors. Published under the terms of the CC BY NC ND 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Articles Spits, Menno Heesterbeek, Iris T Voortman, Lennard M Akkermans, Jimmy J Wijdeven, Ruud H Cabukusta, Birol Neefjes, Jacques Mobile late endosomes modulate peripheral endoplasmic reticulum network architecture |
title | Mobile late endosomes modulate peripheral endoplasmic reticulum network architecture |
title_full | Mobile late endosomes modulate peripheral endoplasmic reticulum network architecture |
title_fullStr | Mobile late endosomes modulate peripheral endoplasmic reticulum network architecture |
title_full_unstemmed | Mobile late endosomes modulate peripheral endoplasmic reticulum network architecture |
title_short | Mobile late endosomes modulate peripheral endoplasmic reticulum network architecture |
title_sort | mobile late endosomes modulate peripheral endoplasmic reticulum network architecture |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7926257/ https://www.ncbi.nlm.nih.gov/pubmed/33554435 http://dx.doi.org/10.15252/embr.202050815 |
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