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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...

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Autores principales: Spits, Menno, Heesterbeek, Iris T, Voortman, Lennard M, Akkermans, Jimmy J, Wijdeven, Ruud H, Cabukusta, Birol, Neefjes, Jacques
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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