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Spatiotemporal Regulation of Rho GTPases in Neuronal Migration
Neuronal migration is essential for the orchestration of brain development and involves several contiguous steps: interkinetic nuclear movement (INM), multipolar–bipolar transition, locomotion, and translocation. Growing evidence suggests that Rho GTPases, including RhoA, Rac, Cdc42, and the atypica...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627650/ https://www.ncbi.nlm.nih.gov/pubmed/31185627 http://dx.doi.org/10.3390/cells8060568 |
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author | Xu, Zhenyan Chen, Yuewen Chen, Yu |
author_facet | Xu, Zhenyan Chen, Yuewen Chen, Yu |
author_sort | Xu, Zhenyan |
collection | PubMed |
description | Neuronal migration is essential for the orchestration of brain development and involves several contiguous steps: interkinetic nuclear movement (INM), multipolar–bipolar transition, locomotion, and translocation. Growing evidence suggests that Rho GTPases, including RhoA, Rac, Cdc42, and the atypical Rnd members, play critical roles in neuronal migration by regulating both actin and microtubule cytoskeletal components. This review focuses on the spatiotemporal-specific regulation of Rho GTPases as well as their regulators and effectors in distinct steps during the neuronal migration process. Their roles in bridging extracellular signals and cytoskeletal dynamics to provide optimal structural support to the migrating neurons will also be discussed. |
format | Online Article Text |
id | pubmed-6627650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66276502019-07-23 Spatiotemporal Regulation of Rho GTPases in Neuronal Migration Xu, Zhenyan Chen, Yuewen Chen, Yu Cells Review Neuronal migration is essential for the orchestration of brain development and involves several contiguous steps: interkinetic nuclear movement (INM), multipolar–bipolar transition, locomotion, and translocation. Growing evidence suggests that Rho GTPases, including RhoA, Rac, Cdc42, and the atypical Rnd members, play critical roles in neuronal migration by regulating both actin and microtubule cytoskeletal components. This review focuses on the spatiotemporal-specific regulation of Rho GTPases as well as their regulators and effectors in distinct steps during the neuronal migration process. Their roles in bridging extracellular signals and cytoskeletal dynamics to provide optimal structural support to the migrating neurons will also be discussed. MDPI 2019-06-10 /pmc/articles/PMC6627650/ /pubmed/31185627 http://dx.doi.org/10.3390/cells8060568 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Xu, Zhenyan Chen, Yuewen Chen, Yu Spatiotemporal Regulation of Rho GTPases in Neuronal Migration |
title | Spatiotemporal Regulation of Rho GTPases in Neuronal Migration |
title_full | Spatiotemporal Regulation of Rho GTPases in Neuronal Migration |
title_fullStr | Spatiotemporal Regulation of Rho GTPases in Neuronal Migration |
title_full_unstemmed | Spatiotemporal Regulation of Rho GTPases in Neuronal Migration |
title_short | Spatiotemporal Regulation of Rho GTPases in Neuronal Migration |
title_sort | spatiotemporal regulation of rho gtpases in neuronal migration |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627650/ https://www.ncbi.nlm.nih.gov/pubmed/31185627 http://dx.doi.org/10.3390/cells8060568 |
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