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The structure and global distribution of the endoplasmic reticulum network are actively regulated by lysosomes

The endoplasmic reticulum (ER) comprises morphologically and functionally distinct domains: sheets and interconnected tubules. These domains undergo dynamic reshaping in response to changes in the cellular environment. However, the mechanisms behind this rapid remodeling are largely unknown. Here, w...

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Autores principales: Lu, Meng, van Tartwijk, Francesca W., Lin, Julie Qiaojin, Nijenhuis, Wilco, Parutto, Pierre, Fantham, Marcus, Christensen, Charles N., Avezov, Edward, Holt, Christine E., Tunnacliffe, Alan, Holcman, David, Kapitein, Lukas, Schierle, Gabriele S. Kaminski, Kaminski, Clemens F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744115/
https://www.ncbi.nlm.nih.gov/pubmed/33328230
http://dx.doi.org/10.1126/sciadv.abc7209
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author Lu, Meng
van Tartwijk, Francesca W.
Lin, Julie Qiaojin
Nijenhuis, Wilco
Parutto, Pierre
Fantham, Marcus
Christensen, Charles N.
Avezov, Edward
Holt, Christine E.
Tunnacliffe, Alan
Holcman, David
Kapitein, Lukas
Schierle, Gabriele S. Kaminski
Kaminski, Clemens F.
author_facet Lu, Meng
van Tartwijk, Francesca W.
Lin, Julie Qiaojin
Nijenhuis, Wilco
Parutto, Pierre
Fantham, Marcus
Christensen, Charles N.
Avezov, Edward
Holt, Christine E.
Tunnacliffe, Alan
Holcman, David
Kapitein, Lukas
Schierle, Gabriele S. Kaminski
Kaminski, Clemens F.
author_sort Lu, Meng
collection PubMed
description The endoplasmic reticulum (ER) comprises morphologically and functionally distinct domains: sheets and interconnected tubules. These domains undergo dynamic reshaping in response to changes in the cellular environment. However, the mechanisms behind this rapid remodeling are largely unknown. Here, we report that ER remodeling is actively driven by lysosomes, following lysosome repositioning in response to changes in nutritional status: The anchorage of lysosomes to ER growth tips is critical for ER tubule elongation and connection. We validate this causal link via the chemo- and optogenetically driven repositioning of lysosomes, which leads to both a redistribution of the ER tubules and a change of its global morphology. Therefore, lysosomes sense metabolic change in the cell and regulate ER tubule distribution accordingly. Dysfunction in this mechanism during axonal extension may lead to axonal growth defects. Our results demonstrate a critical role of lysosome-regulated ER dynamics and reshaping in nutrient responses and neuronal development.
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spelling pubmed-77441152021-01-04 The structure and global distribution of the endoplasmic reticulum network are actively regulated by lysosomes Lu, Meng van Tartwijk, Francesca W. Lin, Julie Qiaojin Nijenhuis, Wilco Parutto, Pierre Fantham, Marcus Christensen, Charles N. Avezov, Edward Holt, Christine E. Tunnacliffe, Alan Holcman, David Kapitein, Lukas Schierle, Gabriele S. Kaminski Kaminski, Clemens F. Sci Adv Research Articles The endoplasmic reticulum (ER) comprises morphologically and functionally distinct domains: sheets and interconnected tubules. These domains undergo dynamic reshaping in response to changes in the cellular environment. However, the mechanisms behind this rapid remodeling are largely unknown. Here, we report that ER remodeling is actively driven by lysosomes, following lysosome repositioning in response to changes in nutritional status: The anchorage of lysosomes to ER growth tips is critical for ER tubule elongation and connection. We validate this causal link via the chemo- and optogenetically driven repositioning of lysosomes, which leads to both a redistribution of the ER tubules and a change of its global morphology. Therefore, lysosomes sense metabolic change in the cell and regulate ER tubule distribution accordingly. Dysfunction in this mechanism during axonal extension may lead to axonal growth defects. Our results demonstrate a critical role of lysosome-regulated ER dynamics and reshaping in nutrient responses and neuronal development. American Association for the Advancement of Science 2020-12-16 /pmc/articles/PMC7744115/ /pubmed/33328230 http://dx.doi.org/10.1126/sciadv.abc7209 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Lu, Meng
van Tartwijk, Francesca W.
Lin, Julie Qiaojin
Nijenhuis, Wilco
Parutto, Pierre
Fantham, Marcus
Christensen, Charles N.
Avezov, Edward
Holt, Christine E.
Tunnacliffe, Alan
Holcman, David
Kapitein, Lukas
Schierle, Gabriele S. Kaminski
Kaminski, Clemens F.
The structure and global distribution of the endoplasmic reticulum network are actively regulated by lysosomes
title The structure and global distribution of the endoplasmic reticulum network are actively regulated by lysosomes
title_full The structure and global distribution of the endoplasmic reticulum network are actively regulated by lysosomes
title_fullStr The structure and global distribution of the endoplasmic reticulum network are actively regulated by lysosomes
title_full_unstemmed The structure and global distribution of the endoplasmic reticulum network are actively regulated by lysosomes
title_short The structure and global distribution of the endoplasmic reticulum network are actively regulated by lysosomes
title_sort structure and global distribution of the endoplasmic reticulum network are actively regulated by lysosomes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744115/
https://www.ncbi.nlm.nih.gov/pubmed/33328230
http://dx.doi.org/10.1126/sciadv.abc7209
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