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Epithelial organ shape is generated by patterned actomyosin contractility and maintained by the extracellular matrix
Epithelial sheets define organ architecture during development. Here, we employed an iterative multiscale computational modeling and quantitative experimental approach to decouple direct and indirect effects of actomyosin-generated forces, nuclear positioning, extracellular matrix, and cell-cell adh...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480841/ https://www.ncbi.nlm.nih.gov/pubmed/32817654 http://dx.doi.org/10.1371/journal.pcbi.1008105 |
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author | Nematbakhsh, Ali Levis, Megan Kumar, Nilay Chen, Weitao Zartman, Jeremiah J. Alber, Mark |
author_facet | Nematbakhsh, Ali Levis, Megan Kumar, Nilay Chen, Weitao Zartman, Jeremiah J. Alber, Mark |
author_sort | Nematbakhsh, Ali |
collection | PubMed |
description | Epithelial sheets define organ architecture during development. Here, we employed an iterative multiscale computational modeling and quantitative experimental approach to decouple direct and indirect effects of actomyosin-generated forces, nuclear positioning, extracellular matrix, and cell-cell adhesion in shaping Drosophila wing imaginal discs. Basally generated actomyosin forces generate epithelial bending of the wing disc pouch. Surprisingly, acute pharmacological inhibition of ROCK-driven actomyosin contractility does not impact the maintenance of tissue height or curved shape. Computational simulations show that ECM tautness provides only a minor contribution to modulating tissue shape. Instead, passive ECM pre-strain serves to maintain the shape independent from actomyosin contractility. These results provide general insight into how the subcellular forces are generated and maintained within individual cells to induce tissue curvature. Thus, the results suggest an important design principle of separable contributions from ECM prestrain and actomyosin tension during epithelial organogenesis and homeostasis. |
format | Online Article Text |
id | pubmed-7480841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74808412020-09-18 Epithelial organ shape is generated by patterned actomyosin contractility and maintained by the extracellular matrix Nematbakhsh, Ali Levis, Megan Kumar, Nilay Chen, Weitao Zartman, Jeremiah J. Alber, Mark PLoS Comput Biol Research Article Epithelial sheets define organ architecture during development. Here, we employed an iterative multiscale computational modeling and quantitative experimental approach to decouple direct and indirect effects of actomyosin-generated forces, nuclear positioning, extracellular matrix, and cell-cell adhesion in shaping Drosophila wing imaginal discs. Basally generated actomyosin forces generate epithelial bending of the wing disc pouch. Surprisingly, acute pharmacological inhibition of ROCK-driven actomyosin contractility does not impact the maintenance of tissue height or curved shape. Computational simulations show that ECM tautness provides only a minor contribution to modulating tissue shape. Instead, passive ECM pre-strain serves to maintain the shape independent from actomyosin contractility. These results provide general insight into how the subcellular forces are generated and maintained within individual cells to induce tissue curvature. Thus, the results suggest an important design principle of separable contributions from ECM prestrain and actomyosin tension during epithelial organogenesis and homeostasis. Public Library of Science 2020-08-20 /pmc/articles/PMC7480841/ /pubmed/32817654 http://dx.doi.org/10.1371/journal.pcbi.1008105 Text en © 2020 Nematbakhsh et al http://creativecommons.org/licenses/by/4.0/ This 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 the original author and source are credited. |
spellingShingle | Research Article Nematbakhsh, Ali Levis, Megan Kumar, Nilay Chen, Weitao Zartman, Jeremiah J. Alber, Mark Epithelial organ shape is generated by patterned actomyosin contractility and maintained by the extracellular matrix |
title | Epithelial organ shape is generated by patterned actomyosin contractility and maintained by the extracellular matrix |
title_full | Epithelial organ shape is generated by patterned actomyosin contractility and maintained by the extracellular matrix |
title_fullStr | Epithelial organ shape is generated by patterned actomyosin contractility and maintained by the extracellular matrix |
title_full_unstemmed | Epithelial organ shape is generated by patterned actomyosin contractility and maintained by the extracellular matrix |
title_short | Epithelial organ shape is generated by patterned actomyosin contractility and maintained by the extracellular matrix |
title_sort | epithelial organ shape is generated by patterned actomyosin contractility and maintained by the extracellular matrix |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480841/ https://www.ncbi.nlm.nih.gov/pubmed/32817654 http://dx.doi.org/10.1371/journal.pcbi.1008105 |
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