Cargando…
Spatial distribution of filament elasticity determines the migratory behaviors of a cell
Any cellular response leading to morphological changes is highly tuned to balance the force generated from structural reorganization, provided by actin cytoskeleton. Actin filaments serve as the backbone of intracellular force, and transduce external mechanical signal via focal adhesion complex into...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986705/ https://www.ncbi.nlm.nih.gov/pubmed/26919488 http://dx.doi.org/10.1080/19336918.2016.1156825 |
_version_ | 1782448223798951936 |
---|---|
author | Harn, Hans I-Chen Hsu, Chao-Kai Wang, Yang-Kao Huang, Yi-Wei Chiu, Wen-Tai Lin, Hsi-Hui Cheng, Chao-Min Tang, Ming-Jer |
author_facet | Harn, Hans I-Chen Hsu, Chao-Kai Wang, Yang-Kao Huang, Yi-Wei Chiu, Wen-Tai Lin, Hsi-Hui Cheng, Chao-Min Tang, Ming-Jer |
author_sort | Harn, Hans I-Chen |
collection | PubMed |
description | Any cellular response leading to morphological changes is highly tuned to balance the force generated from structural reorganization, provided by actin cytoskeleton. Actin filaments serve as the backbone of intracellular force, and transduce external mechanical signal via focal adhesion complex into the cell. During migration, cells not only undergo molecular changes but also rapid mechanical modulation. Here we focus on determining, the role of spatial distribution of mechanical changes of actin filaments in epithelial, mesenchymal, fibrotic and cancer cells with non-migration, directional migration, and non-directional migration behaviors using the atomic force microscopy. We found 1) non-migratory cells only generated one type of filament elasticity, 2) cells generating spatially distributed two types of filament elasticity showed directional migration, and 3) pathologic cells that autonomously generated two types of filament elasticity without spatial distribution were actively migrating non-directionally. The demonstration of spatial regulation of filament elasticity of different cell types at the nano-scale highlights the coupling of cytoskeletal function with physical characters at the sub-cellular level, and provides new research directions for migration related disease. |
format | Online Article Text |
id | pubmed-4986705 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-49867052016-08-29 Spatial distribution of filament elasticity determines the migratory behaviors of a cell Harn, Hans I-Chen Hsu, Chao-Kai Wang, Yang-Kao Huang, Yi-Wei Chiu, Wen-Tai Lin, Hsi-Hui Cheng, Chao-Min Tang, Ming-Jer Cell Adh Migr Research Paper Any cellular response leading to morphological changes is highly tuned to balance the force generated from structural reorganization, provided by actin cytoskeleton. Actin filaments serve as the backbone of intracellular force, and transduce external mechanical signal via focal adhesion complex into the cell. During migration, cells not only undergo molecular changes but also rapid mechanical modulation. Here we focus on determining, the role of spatial distribution of mechanical changes of actin filaments in epithelial, mesenchymal, fibrotic and cancer cells with non-migration, directional migration, and non-directional migration behaviors using the atomic force microscopy. We found 1) non-migratory cells only generated one type of filament elasticity, 2) cells generating spatially distributed two types of filament elasticity showed directional migration, and 3) pathologic cells that autonomously generated two types of filament elasticity without spatial distribution were actively migrating non-directionally. The demonstration of spatial regulation of filament elasticity of different cell types at the nano-scale highlights the coupling of cytoskeletal function with physical characters at the sub-cellular level, and provides new research directions for migration related disease. Taylor & Francis 2016-02-26 /pmc/articles/PMC4986705/ /pubmed/26919488 http://dx.doi.org/10.1080/19336918.2016.1156825 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Research Paper Harn, Hans I-Chen Hsu, Chao-Kai Wang, Yang-Kao Huang, Yi-Wei Chiu, Wen-Tai Lin, Hsi-Hui Cheng, Chao-Min Tang, Ming-Jer Spatial distribution of filament elasticity determines the migratory behaviors of a cell |
title | Spatial distribution of filament elasticity determines the migratory behaviors of a cell |
title_full | Spatial distribution of filament elasticity determines the migratory behaviors of a cell |
title_fullStr | Spatial distribution of filament elasticity determines the migratory behaviors of a cell |
title_full_unstemmed | Spatial distribution of filament elasticity determines the migratory behaviors of a cell |
title_short | Spatial distribution of filament elasticity determines the migratory behaviors of a cell |
title_sort | spatial distribution of filament elasticity determines the migratory behaviors of a cell |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986705/ https://www.ncbi.nlm.nih.gov/pubmed/26919488 http://dx.doi.org/10.1080/19336918.2016.1156825 |
work_keys_str_mv | AT harnhansichen spatialdistributionoffilamentelasticitydeterminesthemigratorybehaviorsofacell AT hsuchaokai spatialdistributionoffilamentelasticitydeterminesthemigratorybehaviorsofacell AT wangyangkao spatialdistributionoffilamentelasticitydeterminesthemigratorybehaviorsofacell AT huangyiwei spatialdistributionoffilamentelasticitydeterminesthemigratorybehaviorsofacell AT chiuwentai spatialdistributionoffilamentelasticitydeterminesthemigratorybehaviorsofacell AT linhsihui spatialdistributionoffilamentelasticitydeterminesthemigratorybehaviorsofacell AT chengchaomin spatialdistributionoffilamentelasticitydeterminesthemigratorybehaviorsofacell AT tangmingjer spatialdistributionoffilamentelasticitydeterminesthemigratorybehaviorsofacell |