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Geometric Control of Cell Migration

Morphological polarization involving changes in cell shape and redistribution of cellular signaling machinery, initiate the migration of mammalian cells. Golgi complex typically localizes in front of the nucleus, and this frontwards polarization has been proposed to be involved in directional migrat...

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Detalles Bibliográficos
Autores principales: Chen, Bo, Kumar, Girish, Co, Carlos C., Ho, Chia-Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789147/
https://www.ncbi.nlm.nih.gov/pubmed/24089214
http://dx.doi.org/10.1038/srep02827
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author Chen, Bo
Kumar, Girish
Co, Carlos C.
Ho, Chia-Chi
author_facet Chen, Bo
Kumar, Girish
Co, Carlos C.
Ho, Chia-Chi
author_sort Chen, Bo
collection PubMed
description Morphological polarization involving changes in cell shape and redistribution of cellular signaling machinery, initiate the migration of mammalian cells. Golgi complex typically localizes in front of the nucleus, and this frontwards polarization has been proposed to be involved in directional migration. However, the sequence of events remains unresolved. Does Golgi polarization precede directional migration or vice-versa? We address this question by constraining cells to specific areas and shapes then tracking their motile behavior and the spatio-temporal distribution of Golgi apparatus upon release. Results show that while the position of the Golgi complex depends on the cell geometry, the subcellular localization of the Golgi complex does not define the cell's leading edge. Cells constrained within elongated geometries exhibit polarized extension of lamellipodia and upon release, migrate preferentially along the long axis of the cell. Minimally constrained cells released from larger areas however, exhibit retarded migration regardless of lamellipodia protrusion activity.
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spelling pubmed-37891472013-10-18 Geometric Control of Cell Migration Chen, Bo Kumar, Girish Co, Carlos C. Ho, Chia-Chi Sci Rep Article Morphological polarization involving changes in cell shape and redistribution of cellular signaling machinery, initiate the migration of mammalian cells. Golgi complex typically localizes in front of the nucleus, and this frontwards polarization has been proposed to be involved in directional migration. However, the sequence of events remains unresolved. Does Golgi polarization precede directional migration or vice-versa? We address this question by constraining cells to specific areas and shapes then tracking their motile behavior and the spatio-temporal distribution of Golgi apparatus upon release. Results show that while the position of the Golgi complex depends on the cell geometry, the subcellular localization of the Golgi complex does not define the cell's leading edge. Cells constrained within elongated geometries exhibit polarized extension of lamellipodia and upon release, migrate preferentially along the long axis of the cell. Minimally constrained cells released from larger areas however, exhibit retarded migration regardless of lamellipodia protrusion activity. Nature Publishing Group 2013-10-03 /pmc/articles/PMC3789147/ /pubmed/24089214 http://dx.doi.org/10.1038/srep02827 Text en Copyright © 2013, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Article
Chen, Bo
Kumar, Girish
Co, Carlos C.
Ho, Chia-Chi
Geometric Control of Cell Migration
title Geometric Control of Cell Migration
title_full Geometric Control of Cell Migration
title_fullStr Geometric Control of Cell Migration
title_full_unstemmed Geometric Control of Cell Migration
title_short Geometric Control of Cell Migration
title_sort geometric control of cell migration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789147/
https://www.ncbi.nlm.nih.gov/pubmed/24089214
http://dx.doi.org/10.1038/srep02827
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