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Tetraspanin 4 stabilizes membrane swellings and facilitates their maturation into migrasomes

Migrasomes are newly discovered cell organelles forming by local swelling of retraction fibers. The migrasome formation critically depends on tetraspanin proteins present in the retraction fiber membranes and is modulated by the membrane tension and bending rigidity. It remained unknown how and in w...

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Autores principales: Dharan, Raviv, Huang, Yuwei, Cheppali, Sudheer Kumar, Goren, Shahar, Shendrik, Petr, Wang, Weisi, Qiao, Jiamei, Kozlov, Michael M., Yu, Li, Sorkin, Raya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950420/
https://www.ncbi.nlm.nih.gov/pubmed/36823145
http://dx.doi.org/10.1038/s41467-023-36596-9
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author Dharan, Raviv
Huang, Yuwei
Cheppali, Sudheer Kumar
Goren, Shahar
Shendrik, Petr
Wang, Weisi
Qiao, Jiamei
Kozlov, Michael M.
Yu, Li
Sorkin, Raya
author_facet Dharan, Raviv
Huang, Yuwei
Cheppali, Sudheer Kumar
Goren, Shahar
Shendrik, Petr
Wang, Weisi
Qiao, Jiamei
Kozlov, Michael M.
Yu, Li
Sorkin, Raya
author_sort Dharan, Raviv
collection PubMed
description Migrasomes are newly discovered cell organelles forming by local swelling of retraction fibers. The migrasome formation critically depends on tetraspanin proteins present in the retraction fiber membranes and is modulated by the membrane tension and bending rigidity. It remained unknown how and in which time sequence these factors are involved in migrasome nucleation, growth, and stabilization, and what are the possible intermediate stages of migrasome biogenesis. Here using live cell imaging and a biomimetic system for migrasomes and retraction fibers, we reveal that migrasome formation is a two-stage process. At the first stage, which in biomimetic system is mediated by membrane tension, local swellings largely devoid of tetraspanin 4 form on the retraction fibers. At the second stage, tetraspanin 4 molecules migrate toward and onto these swellings, which grow up to several microns in size and transform into migrasomes. This tetraspanin 4 recruitment to the swellings is essential for migrasome growth and stabilization. Based on these findings we propose that the major role of tetraspanin proteins is in stabilizing the migrasome structure, while the migrasome nucleation and initial growth stages can be driven by membrane mechanical stresses.
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spelling pubmed-99504202023-02-25 Tetraspanin 4 stabilizes membrane swellings and facilitates their maturation into migrasomes Dharan, Raviv Huang, Yuwei Cheppali, Sudheer Kumar Goren, Shahar Shendrik, Petr Wang, Weisi Qiao, Jiamei Kozlov, Michael M. Yu, Li Sorkin, Raya Nat Commun Article Migrasomes are newly discovered cell organelles forming by local swelling of retraction fibers. The migrasome formation critically depends on tetraspanin proteins present in the retraction fiber membranes and is modulated by the membrane tension and bending rigidity. It remained unknown how and in which time sequence these factors are involved in migrasome nucleation, growth, and stabilization, and what are the possible intermediate stages of migrasome biogenesis. Here using live cell imaging and a biomimetic system for migrasomes and retraction fibers, we reveal that migrasome formation is a two-stage process. At the first stage, which in biomimetic system is mediated by membrane tension, local swellings largely devoid of tetraspanin 4 form on the retraction fibers. At the second stage, tetraspanin 4 molecules migrate toward and onto these swellings, which grow up to several microns in size and transform into migrasomes. This tetraspanin 4 recruitment to the swellings is essential for migrasome growth and stabilization. Based on these findings we propose that the major role of tetraspanin proteins is in stabilizing the migrasome structure, while the migrasome nucleation and initial growth stages can be driven by membrane mechanical stresses. Nature Publishing Group UK 2023-02-23 /pmc/articles/PMC9950420/ /pubmed/36823145 http://dx.doi.org/10.1038/s41467-023-36596-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Dharan, Raviv
Huang, Yuwei
Cheppali, Sudheer Kumar
Goren, Shahar
Shendrik, Petr
Wang, Weisi
Qiao, Jiamei
Kozlov, Michael M.
Yu, Li
Sorkin, Raya
Tetraspanin 4 stabilizes membrane swellings and facilitates their maturation into migrasomes
title Tetraspanin 4 stabilizes membrane swellings and facilitates their maturation into migrasomes
title_full Tetraspanin 4 stabilizes membrane swellings and facilitates their maturation into migrasomes
title_fullStr Tetraspanin 4 stabilizes membrane swellings and facilitates their maturation into migrasomes
title_full_unstemmed Tetraspanin 4 stabilizes membrane swellings and facilitates their maturation into migrasomes
title_short Tetraspanin 4 stabilizes membrane swellings and facilitates their maturation into migrasomes
title_sort tetraspanin 4 stabilizes membrane swellings and facilitates their maturation into migrasomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950420/
https://www.ncbi.nlm.nih.gov/pubmed/36823145
http://dx.doi.org/10.1038/s41467-023-36596-9
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