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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...

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Autores principales: Nematbakhsh, Ali, Levis, Megan, Kumar, Nilay, Chen, Weitao, Zartman, Jeremiah J., Alber, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
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.
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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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