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The phosphatidylinositol (4,5)-bisphosphate-Rab35 axis regulates migrasome formation

Migrasomes are recently discovered organelles, which are formed on the ends or branch points of retraction fibers at the trailing edge of migrating cells. Previously, we showed that recruitment of integrins to the site of migrasome formation is essential for migrasome biogenesis. In this study, we f...

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Autores principales: Ding, Tianlun, Ji, Jinyao, Zhang, Weiying, Liu, Yuheng, Liu, Boqi, Han, Yiyang, Chen, Chunlai, Yu, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397319/
https://www.ncbi.nlm.nih.gov/pubmed/37142675
http://dx.doi.org/10.1038/s41422-023-00811-5
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author Ding, Tianlun
Ji, Jinyao
Zhang, Weiying
Liu, Yuheng
Liu, Boqi
Han, Yiyang
Chen, Chunlai
Yu, Li
author_facet Ding, Tianlun
Ji, Jinyao
Zhang, Weiying
Liu, Yuheng
Liu, Boqi
Han, Yiyang
Chen, Chunlai
Yu, Li
author_sort Ding, Tianlun
collection PubMed
description Migrasomes are recently discovered organelles, which are formed on the ends or branch points of retraction fibers at the trailing edge of migrating cells. Previously, we showed that recruitment of integrins to the site of migrasome formation is essential for migrasome biogenesis. In this study, we found that prior to migrasome formation, PIP5K1A, a PI4P kinase which converts PI4P into PI(4,5)P(2), is recruited to migrasome formation sites. The recruitment of PIP5K1A results in generation of PI(4,5)P(2) at the migrasome formation site. Once accumulated, PI(4,5)P(2) recruits Rab35 to the migrasome formation site by interacting with the C-terminal polybasic cluster of Rab35. We further demonstrated that active Rab35 promotes migrasome formation by recruiting and concentrating integrin α5 at migrasome formation sites, which is likely mediated by the interaction between integrin α5 and Rab35. Our study identifies the upstream signaling events orchestrating migrasome biogenesis.
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spelling pubmed-103973192023-08-04 The phosphatidylinositol (4,5)-bisphosphate-Rab35 axis regulates migrasome formation Ding, Tianlun Ji, Jinyao Zhang, Weiying Liu, Yuheng Liu, Boqi Han, Yiyang Chen, Chunlai Yu, Li Cell Res Article Migrasomes are recently discovered organelles, which are formed on the ends or branch points of retraction fibers at the trailing edge of migrating cells. Previously, we showed that recruitment of integrins to the site of migrasome formation is essential for migrasome biogenesis. In this study, we found that prior to migrasome formation, PIP5K1A, a PI4P kinase which converts PI4P into PI(4,5)P(2), is recruited to migrasome formation sites. The recruitment of PIP5K1A results in generation of PI(4,5)P(2) at the migrasome formation site. Once accumulated, PI(4,5)P(2) recruits Rab35 to the migrasome formation site by interacting with the C-terminal polybasic cluster of Rab35. We further demonstrated that active Rab35 promotes migrasome formation by recruiting and concentrating integrin α5 at migrasome formation sites, which is likely mediated by the interaction between integrin α5 and Rab35. Our study identifies the upstream signaling events orchestrating migrasome biogenesis. Springer Nature Singapore 2023-05-04 2023-08 /pmc/articles/PMC10397319/ /pubmed/37142675 http://dx.doi.org/10.1038/s41422-023-00811-5 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
Ding, Tianlun
Ji, Jinyao
Zhang, Weiying
Liu, Yuheng
Liu, Boqi
Han, Yiyang
Chen, Chunlai
Yu, Li
The phosphatidylinositol (4,5)-bisphosphate-Rab35 axis regulates migrasome formation
title The phosphatidylinositol (4,5)-bisphosphate-Rab35 axis regulates migrasome formation
title_full The phosphatidylinositol (4,5)-bisphosphate-Rab35 axis regulates migrasome formation
title_fullStr The phosphatidylinositol (4,5)-bisphosphate-Rab35 axis regulates migrasome formation
title_full_unstemmed The phosphatidylinositol (4,5)-bisphosphate-Rab35 axis regulates migrasome formation
title_short The phosphatidylinositol (4,5)-bisphosphate-Rab35 axis regulates migrasome formation
title_sort phosphatidylinositol (4,5)-bisphosphate-rab35 axis regulates migrasome formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397319/
https://www.ncbi.nlm.nih.gov/pubmed/37142675
http://dx.doi.org/10.1038/s41422-023-00811-5
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