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Cell-type-specific mechanical response and myosin dynamics during retinal lens development in Drosophila
During organogenesis, different cell types need to work together to generate functional multicellular structures. To study this process, we made use of the genetically tractable fly retina, with a focus on the mechanisms that coordinate morphogenesis between the different epithelial cell types that...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353141/ https://www.ncbi.nlm.nih.gov/pubmed/32320320 http://dx.doi.org/10.1091/mbc.E19-09-0523 |
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author | Blackie, Laura Walther, Rhian F. Staddon, Michael F. Banerjee, Shiladitya Pichaud, Franck |
author_facet | Blackie, Laura Walther, Rhian F. Staddon, Michael F. Banerjee, Shiladitya Pichaud, Franck |
author_sort | Blackie, Laura |
collection | PubMed |
description | During organogenesis, different cell types need to work together to generate functional multicellular structures. To study this process, we made use of the genetically tractable fly retina, with a focus on the mechanisms that coordinate morphogenesis between the different epithelial cell types that make up the optical lens. Our work shows that these epithelial cells present contractile apical-medial MyosinII meshworks, which control the apical area and junctional geometry of these cells during lens development. Our study also suggests that these MyosinII meshworks drive cell shape changes in response to external forces, and thus they mediate part of the biomechanical coupling that takes place between these cells. Importantly, our work, including mathematical modeling of forces and material stiffness during lens development, raises the possibility that increased cell stiffness acts as a mechanism for limiting this mechanical coupling. We propose this might be required in complex tissues, where different cell types undergo concurrent morphogenesis and where averaging out of forces across cells could compromise individual cell apical geometry and thereby organ function. |
format | Online Article Text |
id | pubmed-7353141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73531412020-08-30 Cell-type-specific mechanical response and myosin dynamics during retinal lens development in Drosophila Blackie, Laura Walther, Rhian F. Staddon, Michael F. Banerjee, Shiladitya Pichaud, Franck Mol Biol Cell Articles During organogenesis, different cell types need to work together to generate functional multicellular structures. To study this process, we made use of the genetically tractable fly retina, with a focus on the mechanisms that coordinate morphogenesis between the different epithelial cell types that make up the optical lens. Our work shows that these epithelial cells present contractile apical-medial MyosinII meshworks, which control the apical area and junctional geometry of these cells during lens development. Our study also suggests that these MyosinII meshworks drive cell shape changes in response to external forces, and thus they mediate part of the biomechanical coupling that takes place between these cells. Importantly, our work, including mathematical modeling of forces and material stiffness during lens development, raises the possibility that increased cell stiffness acts as a mechanism for limiting this mechanical coupling. We propose this might be required in complex tissues, where different cell types undergo concurrent morphogenesis and where averaging out of forces across cells could compromise individual cell apical geometry and thereby organ function. The American Society for Cell Biology 2020-06-15 /pmc/articles/PMC7353141/ /pubmed/32320320 http://dx.doi.org/10.1091/mbc.E19-09-0523 Text en © 2020 Blackie et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License. |
spellingShingle | Articles Blackie, Laura Walther, Rhian F. Staddon, Michael F. Banerjee, Shiladitya Pichaud, Franck Cell-type-specific mechanical response and myosin dynamics during retinal lens development in Drosophila |
title | Cell-type-specific mechanical response and myosin dynamics during retinal lens development in Drosophila |
title_full | Cell-type-specific mechanical response and myosin dynamics during retinal lens development in Drosophila |
title_fullStr | Cell-type-specific mechanical response and myosin dynamics during retinal lens development in Drosophila |
title_full_unstemmed | Cell-type-specific mechanical response and myosin dynamics during retinal lens development in Drosophila |
title_short | Cell-type-specific mechanical response and myosin dynamics during retinal lens development in Drosophila |
title_sort | cell-type-specific mechanical response and myosin dynamics during retinal lens development in drosophila |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7353141/ https://www.ncbi.nlm.nih.gov/pubmed/32320320 http://dx.doi.org/10.1091/mbc.E19-09-0523 |
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