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Biophysical principles of choanoflagellate self-organization

Inspired by the patterns of multicellularity in choanoflagellates, the closest living relatives of animals, we quantify the biophysical processes underlying the morphogenesis of rosette colonies in the choanoflagellate Salpingoeca rosetta. We find that rosettes reproducibly transition from an early...

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Autores principales: Larson, Ben T., Ruiz-Herrero, Teresa, Lee, Stacey, Kumar, Sanjay, Mahadevan, L., King, Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6983409/
https://www.ncbi.nlm.nih.gov/pubmed/31896587
http://dx.doi.org/10.1073/pnas.1909447117
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author Larson, Ben T.
Ruiz-Herrero, Teresa
Lee, Stacey
Kumar, Sanjay
Mahadevan, L.
King, Nicole
author_facet Larson, Ben T.
Ruiz-Herrero, Teresa
Lee, Stacey
Kumar, Sanjay
Mahadevan, L.
King, Nicole
author_sort Larson, Ben T.
collection PubMed
description Inspired by the patterns of multicellularity in choanoflagellates, the closest living relatives of animals, we quantify the biophysical processes underlying the morphogenesis of rosette colonies in the choanoflagellate Salpingoeca rosetta. We find that rosettes reproducibly transition from an early stage of 2-dimensional (2D) growth to a later stage of 3D growth, despite the underlying variability of the cell lineages. Our perturbative experiments demonstrate the fundamental importance of a basally secreted extracellular matrix (ECM) for rosette morphogenesis and show that the interaction of the ECM with cells in the colony physically constrains the packing of proliferating cells and, thus, controls colony shape. Simulations of a biophysically inspired model that accounts for the size and shape of the individual cells, the fraction of ECM, and its stiffness relative to that of the cells suffices to explain our observations and yields a morphospace consistent with observations across a range of multicellular choanoflagellate colonies. Overall, our biophysical perspective on rosette development complements previous genetic perspectives and, thus, helps illuminate the interplay between cell biology and physics in regulating morphogenesis.
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spelling pubmed-69834092020-01-30 Biophysical principles of choanoflagellate self-organization Larson, Ben T. Ruiz-Herrero, Teresa Lee, Stacey Kumar, Sanjay Mahadevan, L. King, Nicole Proc Natl Acad Sci U S A PNAS Plus Inspired by the patterns of multicellularity in choanoflagellates, the closest living relatives of animals, we quantify the biophysical processes underlying the morphogenesis of rosette colonies in the choanoflagellate Salpingoeca rosetta. We find that rosettes reproducibly transition from an early stage of 2-dimensional (2D) growth to a later stage of 3D growth, despite the underlying variability of the cell lineages. Our perturbative experiments demonstrate the fundamental importance of a basally secreted extracellular matrix (ECM) for rosette morphogenesis and show that the interaction of the ECM with cells in the colony physically constrains the packing of proliferating cells and, thus, controls colony shape. Simulations of a biophysically inspired model that accounts for the size and shape of the individual cells, the fraction of ECM, and its stiffness relative to that of the cells suffices to explain our observations and yields a morphospace consistent with observations across a range of multicellular choanoflagellate colonies. Overall, our biophysical perspective on rosette development complements previous genetic perspectives and, thus, helps illuminate the interplay between cell biology and physics in regulating morphogenesis. National Academy of Sciences 2020-01-21 2020-01-02 /pmc/articles/PMC6983409/ /pubmed/31896587 http://dx.doi.org/10.1073/pnas.1909447117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle PNAS Plus
Larson, Ben T.
Ruiz-Herrero, Teresa
Lee, Stacey
Kumar, Sanjay
Mahadevan, L.
King, Nicole
Biophysical principles of choanoflagellate self-organization
title Biophysical principles of choanoflagellate self-organization
title_full Biophysical principles of choanoflagellate self-organization
title_fullStr Biophysical principles of choanoflagellate self-organization
title_full_unstemmed Biophysical principles of choanoflagellate self-organization
title_short Biophysical principles of choanoflagellate self-organization
title_sort biophysical principles of choanoflagellate self-organization
topic PNAS Plus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6983409/
https://www.ncbi.nlm.nih.gov/pubmed/31896587
http://dx.doi.org/10.1073/pnas.1909447117
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