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Actin cytoskeleton self-organization in single epithelial cells and fibroblasts under isotropic confinement
Actin cytoskeleton self-organization in two cell types, fibroblasts and epitheliocytes, was studied in cells confined to isotropic adhesive islands. In fibroblasts plated onto islands of optimal size, an initially circular actin pattern evolves into a radial pattern of actin bundles that undergo asy...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432717/ https://www.ncbi.nlm.nih.gov/pubmed/30787030 http://dx.doi.org/10.1242/jcs.220780 |
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author | Jalal, Salma Shi, Shidong Acharya, Vidhyalakshmi Huang, Ruby Yun-Ju Viasnoff, Virgile Bershadsky, Alexander D. Tee, Yee Han |
author_facet | Jalal, Salma Shi, Shidong Acharya, Vidhyalakshmi Huang, Ruby Yun-Ju Viasnoff, Virgile Bershadsky, Alexander D. Tee, Yee Han |
author_sort | Jalal, Salma |
collection | PubMed |
description | Actin cytoskeleton self-organization in two cell types, fibroblasts and epitheliocytes, was studied in cells confined to isotropic adhesive islands. In fibroblasts plated onto islands of optimal size, an initially circular actin pattern evolves into a radial pattern of actin bundles that undergo asymmetric chiral swirling before finally producing parallel linear stress fibers. Epitheliocytes, however, did not exhibit succession through all the actin patterns described above. Upon confinement, the actin cytoskeleton in non-keratinocyte epitheliocytes was arrested at the circular stage, while in keratinocytes it progressed as far as the radial pattern but still could not break symmetry. Epithelial–mesenchymal transition pushed actin cytoskeleton development from circular towards radial patterns but remained insufficient to cause chirality. Knockout of cytokeratins also did not promote actin chirality development in keratinocytes. Left–right asymmetric cytoskeleton swirling could, however, be induced in keratinocytes by treatment with small doses of the G-actin sequestering drug, latrunculin A in a transcription-independent manner. Both the nucleus and the cytokeratin network followed the induced chiral swirling. Development of chirality in keratinocytes was controlled by DIAPH1 (mDia1) and VASP, proteins involved in regulation of actin polymerization. This article has an associated First Person interview with the first author of the paper. |
format | Online Article Text |
id | pubmed-6432717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-64327172019-03-27 Actin cytoskeleton self-organization in single epithelial cells and fibroblasts under isotropic confinement Jalal, Salma Shi, Shidong Acharya, Vidhyalakshmi Huang, Ruby Yun-Ju Viasnoff, Virgile Bershadsky, Alexander D. Tee, Yee Han J Cell Sci Research Article Actin cytoskeleton self-organization in two cell types, fibroblasts and epitheliocytes, was studied in cells confined to isotropic adhesive islands. In fibroblasts plated onto islands of optimal size, an initially circular actin pattern evolves into a radial pattern of actin bundles that undergo asymmetric chiral swirling before finally producing parallel linear stress fibers. Epitheliocytes, however, did not exhibit succession through all the actin patterns described above. Upon confinement, the actin cytoskeleton in non-keratinocyte epitheliocytes was arrested at the circular stage, while in keratinocytes it progressed as far as the radial pattern but still could not break symmetry. Epithelial–mesenchymal transition pushed actin cytoskeleton development from circular towards radial patterns but remained insufficient to cause chirality. Knockout of cytokeratins also did not promote actin chirality development in keratinocytes. Left–right asymmetric cytoskeleton swirling could, however, be induced in keratinocytes by treatment with small doses of the G-actin sequestering drug, latrunculin A in a transcription-independent manner. Both the nucleus and the cytokeratin network followed the induced chiral swirling. Development of chirality in keratinocytes was controlled by DIAPH1 (mDia1) and VASP, proteins involved in regulation of actin polymerization. This article has an associated First Person interview with the first author of the paper. The Company of Biologists Ltd 2019-03-01 2019-03-07 /pmc/articles/PMC6432717/ /pubmed/30787030 http://dx.doi.org/10.1242/jcs.220780 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Jalal, Salma Shi, Shidong Acharya, Vidhyalakshmi Huang, Ruby Yun-Ju Viasnoff, Virgile Bershadsky, Alexander D. Tee, Yee Han Actin cytoskeleton self-organization in single epithelial cells and fibroblasts under isotropic confinement |
title | Actin cytoskeleton self-organization in single epithelial cells and fibroblasts under isotropic confinement |
title_full | Actin cytoskeleton self-organization in single epithelial cells and fibroblasts under isotropic confinement |
title_fullStr | Actin cytoskeleton self-organization in single epithelial cells and fibroblasts under isotropic confinement |
title_full_unstemmed | Actin cytoskeleton self-organization in single epithelial cells and fibroblasts under isotropic confinement |
title_short | Actin cytoskeleton self-organization in single epithelial cells and fibroblasts under isotropic confinement |
title_sort | actin cytoskeleton self-organization in single epithelial cells and fibroblasts under isotropic confinement |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6432717/ https://www.ncbi.nlm.nih.gov/pubmed/30787030 http://dx.doi.org/10.1242/jcs.220780 |
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