Cargando…

Growth anisotropy of the extracellular matrix shapes a developing organ

Final organ size and shape result from volume expansion by growth and shape changes by contractility. Complex morphologies can also arise from differences in growth rate between tissues. We address here how differential growth guides the morphogenesis of the growing Drosophila wing imaginal disc. We...

Descripción completa

Detalles Bibliográficos
Autores principales: Harmansa, Stefan, Erlich, Alexander, Eloy, Christophe, Zurlo, Giuseppe, Lecuit, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984492/
https://www.ncbi.nlm.nih.gov/pubmed/36869053
http://dx.doi.org/10.1038/s41467-023-36739-y
_version_ 1784900757263220736
author Harmansa, Stefan
Erlich, Alexander
Eloy, Christophe
Zurlo, Giuseppe
Lecuit, Thomas
author_facet Harmansa, Stefan
Erlich, Alexander
Eloy, Christophe
Zurlo, Giuseppe
Lecuit, Thomas
author_sort Harmansa, Stefan
collection PubMed
description Final organ size and shape result from volume expansion by growth and shape changes by contractility. Complex morphologies can also arise from differences in growth rate between tissues. We address here how differential growth guides the morphogenesis of the growing Drosophila wing imaginal disc. We report that 3D morphology results from elastic deformation due to differential growth anisotropy between the epithelial cell layer and its enveloping extracellular matrix (ECM). While the tissue layer grows in plane, growth of the bottom ECM occurs in 3D and is reduced in magnitude, thereby causing geometric frustration and tissue bending. The elasticity, growth anisotropy and morphogenesis of the organ are fully captured by a mechanical bilayer model. Moreover, differential expression of the Matrix metalloproteinase MMP2 controls growth anisotropy of the ECM envelope. This study shows that the ECM is a controllable mechanical constraint whose intrinsic growth anisotropy directs tissue morphogenesis in a developing organ.
format Online
Article
Text
id pubmed-9984492
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-99844922023-03-05 Growth anisotropy of the extracellular matrix shapes a developing organ Harmansa, Stefan Erlich, Alexander Eloy, Christophe Zurlo, Giuseppe Lecuit, Thomas Nat Commun Article Final organ size and shape result from volume expansion by growth and shape changes by contractility. Complex morphologies can also arise from differences in growth rate between tissues. We address here how differential growth guides the morphogenesis of the growing Drosophila wing imaginal disc. We report that 3D morphology results from elastic deformation due to differential growth anisotropy between the epithelial cell layer and its enveloping extracellular matrix (ECM). While the tissue layer grows in plane, growth of the bottom ECM occurs in 3D and is reduced in magnitude, thereby causing geometric frustration and tissue bending. The elasticity, growth anisotropy and morphogenesis of the organ are fully captured by a mechanical bilayer model. Moreover, differential expression of the Matrix metalloproteinase MMP2 controls growth anisotropy of the ECM envelope. This study shows that the ECM is a controllable mechanical constraint whose intrinsic growth anisotropy directs tissue morphogenesis in a developing organ. Nature Publishing Group UK 2023-03-03 /pmc/articles/PMC9984492/ /pubmed/36869053 http://dx.doi.org/10.1038/s41467-023-36739-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Harmansa, Stefan
Erlich, Alexander
Eloy, Christophe
Zurlo, Giuseppe
Lecuit, Thomas
Growth anisotropy of the extracellular matrix shapes a developing organ
title Growth anisotropy of the extracellular matrix shapes a developing organ
title_full Growth anisotropy of the extracellular matrix shapes a developing organ
title_fullStr Growth anisotropy of the extracellular matrix shapes a developing organ
title_full_unstemmed Growth anisotropy of the extracellular matrix shapes a developing organ
title_short Growth anisotropy of the extracellular matrix shapes a developing organ
title_sort growth anisotropy of the extracellular matrix shapes a developing organ
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984492/
https://www.ncbi.nlm.nih.gov/pubmed/36869053
http://dx.doi.org/10.1038/s41467-023-36739-y
work_keys_str_mv AT harmansastefan growthanisotropyoftheextracellularmatrixshapesadevelopingorgan
AT erlichalexander growthanisotropyoftheextracellularmatrixshapesadevelopingorgan
AT eloychristophe growthanisotropyoftheextracellularmatrixshapesadevelopingorgan
AT zurlogiuseppe growthanisotropyoftheextracellularmatrixshapesadevelopingorgan
AT lecuitthomas growthanisotropyoftheextracellularmatrixshapesadevelopingorgan