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Coordinated regulation of Cdc42ep1, actin, and septin filaments during neural crest cell migration
The septin cytoskeleton has been demonstrated to interact with other cytoskeletal components to regulate various cellular processes, including cell migration. However, the mechanisms of how septin regulates cell migration are not fully understood. In this study, we use the highly migratory neural cr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009165/ https://www.ncbi.nlm.nih.gov/pubmed/36923257 http://dx.doi.org/10.3389/fcell.2023.1106595 |
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author | Kho, Mary Hladyshau, Siarhei Tsygankov, Denis Nie, Shuyi |
author_facet | Kho, Mary Hladyshau, Siarhei Tsygankov, Denis Nie, Shuyi |
author_sort | Kho, Mary |
collection | PubMed |
description | The septin cytoskeleton has been demonstrated to interact with other cytoskeletal components to regulate various cellular processes, including cell migration. However, the mechanisms of how septin regulates cell migration are not fully understood. In this study, we use the highly migratory neural crest cells of frog embryos to examine the role of septin filaments in cell migration. We found that septin filaments are required for the proper migration of neural crest cells by controlling both the speed and the direction of cell migration. We further determined that septin filaments regulate these features of cell migration by interacting with actin stress fibers. In neural crest cells, septin filaments co-align with actin stress fibers, and the loss of septin filaments leads to impaired stability and contractility of actin stress fibers. In addition, we showed that a partial loss of septin filaments leads to drastic changes in the orientations of newly formed actin stress fibers, suggesting that septin filaments help maintain the persistent orientation of actin stress fibers during directed cell migration. Lastly, our study revealed that these activities of septin filaments depend on Cdc42ep1, which colocalizes with septin filaments in the center of neural crest cells. Cdc42ep1 interacts with septin filaments in a reciprocal manner, with septin filaments recruiting Cdc42ep1 to the cell center and Cdc42ep1 supporting the formation of septin filaments. |
format | Online Article Text |
id | pubmed-10009165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100091652023-03-14 Coordinated regulation of Cdc42ep1, actin, and septin filaments during neural crest cell migration Kho, Mary Hladyshau, Siarhei Tsygankov, Denis Nie, Shuyi Front Cell Dev Biol Cell and Developmental Biology The septin cytoskeleton has been demonstrated to interact with other cytoskeletal components to regulate various cellular processes, including cell migration. However, the mechanisms of how septin regulates cell migration are not fully understood. In this study, we use the highly migratory neural crest cells of frog embryos to examine the role of septin filaments in cell migration. We found that septin filaments are required for the proper migration of neural crest cells by controlling both the speed and the direction of cell migration. We further determined that septin filaments regulate these features of cell migration by interacting with actin stress fibers. In neural crest cells, septin filaments co-align with actin stress fibers, and the loss of septin filaments leads to impaired stability and contractility of actin stress fibers. In addition, we showed that a partial loss of septin filaments leads to drastic changes in the orientations of newly formed actin stress fibers, suggesting that septin filaments help maintain the persistent orientation of actin stress fibers during directed cell migration. Lastly, our study revealed that these activities of septin filaments depend on Cdc42ep1, which colocalizes with septin filaments in the center of neural crest cells. Cdc42ep1 interacts with septin filaments in a reciprocal manner, with septin filaments recruiting Cdc42ep1 to the cell center and Cdc42ep1 supporting the formation of septin filaments. Frontiers Media S.A. 2023-02-27 /pmc/articles/PMC10009165/ /pubmed/36923257 http://dx.doi.org/10.3389/fcell.2023.1106595 Text en Copyright © 2023 Kho, Hladyshau, Tsygankov and Nie. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Kho, Mary Hladyshau, Siarhei Tsygankov, Denis Nie, Shuyi Coordinated regulation of Cdc42ep1, actin, and septin filaments during neural crest cell migration |
title | Coordinated regulation of Cdc42ep1, actin, and septin filaments during neural crest cell migration |
title_full | Coordinated regulation of Cdc42ep1, actin, and septin filaments during neural crest cell migration |
title_fullStr | Coordinated regulation of Cdc42ep1, actin, and septin filaments during neural crest cell migration |
title_full_unstemmed | Coordinated regulation of Cdc42ep1, actin, and septin filaments during neural crest cell migration |
title_short | Coordinated regulation of Cdc42ep1, actin, and septin filaments during neural crest cell migration |
title_sort | coordinated regulation of cdc42ep1, actin, and septin filaments during neural crest cell migration |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10009165/ https://www.ncbi.nlm.nih.gov/pubmed/36923257 http://dx.doi.org/10.3389/fcell.2023.1106595 |
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