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Early Endosomes Act as Local Exocytosis Hubs to Repair Endothelial Membrane Damage
The plasma membrane of a cell is subject to stresses causing ruptures that must be repaired immediately to preserve membrane integrity and ensure cell survival. Yet, the spatio‐temporal membrane dynamics at the wound site and the source of the membrane required for wound repair are poorly understood...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161044/ https://www.ncbi.nlm.nih.gov/pubmed/36938863 http://dx.doi.org/10.1002/advs.202300244 |
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author | Raj, Nikita Greune, Lilo Kahms, Martin Mildner, Karina Franzkoch, Rico Psathaki, Olympia Ekaterini Zobel, Thomas Zeuschner, Dagmar Klingauf, Jürgen Gerke, Volker |
author_facet | Raj, Nikita Greune, Lilo Kahms, Martin Mildner, Karina Franzkoch, Rico Psathaki, Olympia Ekaterini Zobel, Thomas Zeuschner, Dagmar Klingauf, Jürgen Gerke, Volker |
author_sort | Raj, Nikita |
collection | PubMed |
description | The plasma membrane of a cell is subject to stresses causing ruptures that must be repaired immediately to preserve membrane integrity and ensure cell survival. Yet, the spatio‐temporal membrane dynamics at the wound site and the source of the membrane required for wound repair are poorly understood. Here, it is shown that early endosomes, previously only known to function in the uptake of extracellular material and its endocytic transport, are involved in plasma membrane repair in human endothelial cells. Using live‐cell imaging and correlative light and electron microscopy, it is demonstrated that membrane injury triggers a previously unknown exocytosis of early endosomes that is induced by Ca(2+) entering through the wound. This exocytosis is restricted to the vicinity of the wound site and mediated by the endosomal soluble N‐ethylmaleimide sensitive factor attachment protein receptor (SNARE) VAMP2, which is crucial for efficient membrane repair. Thus, the newly identified Ca(2+)‐evoked and localized exocytosis of early endosomes supplies the membrane material required for rapid resealing of a damaged plasma membrane, thereby providing the first line of defense against damage in mechanically challenged endothelial cells. |
format | Online Article Text |
id | pubmed-10161044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101610442023-05-06 Early Endosomes Act as Local Exocytosis Hubs to Repair Endothelial Membrane Damage Raj, Nikita Greune, Lilo Kahms, Martin Mildner, Karina Franzkoch, Rico Psathaki, Olympia Ekaterini Zobel, Thomas Zeuschner, Dagmar Klingauf, Jürgen Gerke, Volker Adv Sci (Weinh) Research Article The plasma membrane of a cell is subject to stresses causing ruptures that must be repaired immediately to preserve membrane integrity and ensure cell survival. Yet, the spatio‐temporal membrane dynamics at the wound site and the source of the membrane required for wound repair are poorly understood. Here, it is shown that early endosomes, previously only known to function in the uptake of extracellular material and its endocytic transport, are involved in plasma membrane repair in human endothelial cells. Using live‐cell imaging and correlative light and electron microscopy, it is demonstrated that membrane injury triggers a previously unknown exocytosis of early endosomes that is induced by Ca(2+) entering through the wound. This exocytosis is restricted to the vicinity of the wound site and mediated by the endosomal soluble N‐ethylmaleimide sensitive factor attachment protein receptor (SNARE) VAMP2, which is crucial for efficient membrane repair. Thus, the newly identified Ca(2+)‐evoked and localized exocytosis of early endosomes supplies the membrane material required for rapid resealing of a damaged plasma membrane, thereby providing the first line of defense against damage in mechanically challenged endothelial cells. John Wiley and Sons Inc. 2023-03-20 /pmc/articles/PMC10161044/ /pubmed/36938863 http://dx.doi.org/10.1002/advs.202300244 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Raj, Nikita Greune, Lilo Kahms, Martin Mildner, Karina Franzkoch, Rico Psathaki, Olympia Ekaterini Zobel, Thomas Zeuschner, Dagmar Klingauf, Jürgen Gerke, Volker Early Endosomes Act as Local Exocytosis Hubs to Repair Endothelial Membrane Damage |
title | Early Endosomes Act as Local Exocytosis Hubs to Repair Endothelial Membrane Damage |
title_full | Early Endosomes Act as Local Exocytosis Hubs to Repair Endothelial Membrane Damage |
title_fullStr | Early Endosomes Act as Local Exocytosis Hubs to Repair Endothelial Membrane Damage |
title_full_unstemmed | Early Endosomes Act as Local Exocytosis Hubs to Repair Endothelial Membrane Damage |
title_short | Early Endosomes Act as Local Exocytosis Hubs to Repair Endothelial Membrane Damage |
title_sort | early endosomes act as local exocytosis hubs to repair endothelial membrane damage |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161044/ https://www.ncbi.nlm.nih.gov/pubmed/36938863 http://dx.doi.org/10.1002/advs.202300244 |
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