Cargando…

Annexin A4 and A6 induce membrane curvature and constriction during cell membrane repair

Efficient cell membrane repair mechanisms are essential for maintaining membrane integrity and thus for cell life. Here we show that the Ca(2+)- and phospholipid-binding proteins annexin A4 and A6 are involved in plasma membrane repair and needed for rapid closure of micron-size holes. We demonstrat...

Descripción completa

Detalles Bibliográficos
Autores principales: Boye, Theresa Louise, Maeda, Kenji, Pezeshkian, Weria, Sønder, Stine Lauritzen, Haeger, Swantje Christin, Gerke, Volker, Simonsen, Adam Cohen, Nylandsted, Jesper
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696365/
https://www.ncbi.nlm.nih.gov/pubmed/29158488
http://dx.doi.org/10.1038/s41467-017-01743-6
_version_ 1783280433638670336
author Boye, Theresa Louise
Maeda, Kenji
Pezeshkian, Weria
Sønder, Stine Lauritzen
Haeger, Swantje Christin
Gerke, Volker
Simonsen, Adam Cohen
Nylandsted, Jesper
author_facet Boye, Theresa Louise
Maeda, Kenji
Pezeshkian, Weria
Sønder, Stine Lauritzen
Haeger, Swantje Christin
Gerke, Volker
Simonsen, Adam Cohen
Nylandsted, Jesper
author_sort Boye, Theresa Louise
collection PubMed
description Efficient cell membrane repair mechanisms are essential for maintaining membrane integrity and thus for cell life. Here we show that the Ca(2+)- and phospholipid-binding proteins annexin A4 and A6 are involved in plasma membrane repair and needed for rapid closure of micron-size holes. We demonstrate that annexin A4 binds to artificial membranes and generates curvature force initiated from free edges, whereas annexin A6 induces constriction force. In cells, plasma membrane injury and Ca(2+) influx recruit annexin A4 to the vicinity of membrane wound edges where its homo-trimerization leads to membrane curvature near the edges. We propose that curvature force is utilized together with annexin A6-mediated constriction force to pull the wound edges together for eventual fusion. We show that annexin A4 can counteract various plasma membrane disruptions including holes of several micrometers indicating that induction of curvature force around wound edges is an early key event in cell membrane repair.
format Online
Article
Text
id pubmed-5696365
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-56963652017-11-22 Annexin A4 and A6 induce membrane curvature and constriction during cell membrane repair Boye, Theresa Louise Maeda, Kenji Pezeshkian, Weria Sønder, Stine Lauritzen Haeger, Swantje Christin Gerke, Volker Simonsen, Adam Cohen Nylandsted, Jesper Nat Commun Article Efficient cell membrane repair mechanisms are essential for maintaining membrane integrity and thus for cell life. Here we show that the Ca(2+)- and phospholipid-binding proteins annexin A4 and A6 are involved in plasma membrane repair and needed for rapid closure of micron-size holes. We demonstrate that annexin A4 binds to artificial membranes and generates curvature force initiated from free edges, whereas annexin A6 induces constriction force. In cells, plasma membrane injury and Ca(2+) influx recruit annexin A4 to the vicinity of membrane wound edges where its homo-trimerization leads to membrane curvature near the edges. We propose that curvature force is utilized together with annexin A6-mediated constriction force to pull the wound edges together for eventual fusion. We show that annexin A4 can counteract various plasma membrane disruptions including holes of several micrometers indicating that induction of curvature force around wound edges is an early key event in cell membrane repair. Nature Publishing Group UK 2017-11-20 /pmc/articles/PMC5696365/ /pubmed/29158488 http://dx.doi.org/10.1038/s41467-017-01743-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Boye, Theresa Louise
Maeda, Kenji
Pezeshkian, Weria
Sønder, Stine Lauritzen
Haeger, Swantje Christin
Gerke, Volker
Simonsen, Adam Cohen
Nylandsted, Jesper
Annexin A4 and A6 induce membrane curvature and constriction during cell membrane repair
title Annexin A4 and A6 induce membrane curvature and constriction during cell membrane repair
title_full Annexin A4 and A6 induce membrane curvature and constriction during cell membrane repair
title_fullStr Annexin A4 and A6 induce membrane curvature and constriction during cell membrane repair
title_full_unstemmed Annexin A4 and A6 induce membrane curvature and constriction during cell membrane repair
title_short Annexin A4 and A6 induce membrane curvature and constriction during cell membrane repair
title_sort annexin a4 and a6 induce membrane curvature and constriction during cell membrane repair
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5696365/
https://www.ncbi.nlm.nih.gov/pubmed/29158488
http://dx.doi.org/10.1038/s41467-017-01743-6
work_keys_str_mv AT boyetheresalouise annexina4anda6inducemembranecurvatureandconstrictionduringcellmembranerepair
AT maedakenji annexina4anda6inducemembranecurvatureandconstrictionduringcellmembranerepair
AT pezeshkianweria annexina4anda6inducemembranecurvatureandconstrictionduringcellmembranerepair
AT sønderstinelauritzen annexina4anda6inducemembranecurvatureandconstrictionduringcellmembranerepair
AT haegerswantjechristin annexina4anda6inducemembranecurvatureandconstrictionduringcellmembranerepair
AT gerkevolker annexina4anda6inducemembranecurvatureandconstrictionduringcellmembranerepair
AT simonsenadamcohen annexina4anda6inducemembranecurvatureandconstrictionduringcellmembranerepair
AT nylandstedjesper annexina4anda6inducemembranecurvatureandconstrictionduringcellmembranerepair