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Stress ball morphogenesis: How the lizard builds its lung

The function of the lung is closely coupled to its structural anatomy, which varies greatly across vertebrates. Although architecturally simple, a complex pattern of airflow is thought to be achieved in the lizard lung due to its cavernous central lumen and honeycomb-shaped wall. We find that the wa...

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Autores principales: Palmer, Michael A., Nerger, Bryan A., Goodwin, Katharine, Sudhakar, Anvitha, Lemke, Sandra B., Ravindran, Pavithran T., Toettcher, Jared E., Košmrlj, Andrej, Nelson, Celeste M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694616/
https://www.ncbi.nlm.nih.gov/pubmed/34936466
http://dx.doi.org/10.1126/sciadv.abk0161
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author Palmer, Michael A.
Nerger, Bryan A.
Goodwin, Katharine
Sudhakar, Anvitha
Lemke, Sandra B.
Ravindran, Pavithran T.
Toettcher, Jared E.
Košmrlj, Andrej
Nelson, Celeste M.
author_facet Palmer, Michael A.
Nerger, Bryan A.
Goodwin, Katharine
Sudhakar, Anvitha
Lemke, Sandra B.
Ravindran, Pavithran T.
Toettcher, Jared E.
Košmrlj, Andrej
Nelson, Celeste M.
author_sort Palmer, Michael A.
collection PubMed
description The function of the lung is closely coupled to its structural anatomy, which varies greatly across vertebrates. Although architecturally simple, a complex pattern of airflow is thought to be achieved in the lizard lung due to its cavernous central lumen and honeycomb-shaped wall. We find that the wall of the lizard lung is generated from an initially smooth epithelial sheet, which is pushed through holes in a hexagonal smooth muscle meshwork by forces from fluid pressure, similar to a stress ball. Combining transcriptomics with time-lapse imaging reveals that the hexagonal meshwork self-assembles in response to circumferential and axial stresses downstream of pressure. A computational model predicts the pressure-driven changes in epithelial topology, which we probe using optogenetically driven contraction of 3D-printed engineered muscle. These results reveal the physical principles used to sculpt the unusual architecture of the lizard lung, which could be exploited as a novel strategy to engineer tissues.
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spelling pubmed-86946162022-01-03 Stress ball morphogenesis: How the lizard builds its lung Palmer, Michael A. Nerger, Bryan A. Goodwin, Katharine Sudhakar, Anvitha Lemke, Sandra B. Ravindran, Pavithran T. Toettcher, Jared E. Košmrlj, Andrej Nelson, Celeste M. Sci Adv Physical and Materials Sciences The function of the lung is closely coupled to its structural anatomy, which varies greatly across vertebrates. Although architecturally simple, a complex pattern of airflow is thought to be achieved in the lizard lung due to its cavernous central lumen and honeycomb-shaped wall. We find that the wall of the lizard lung is generated from an initially smooth epithelial sheet, which is pushed through holes in a hexagonal smooth muscle meshwork by forces from fluid pressure, similar to a stress ball. Combining transcriptomics with time-lapse imaging reveals that the hexagonal meshwork self-assembles in response to circumferential and axial stresses downstream of pressure. A computational model predicts the pressure-driven changes in epithelial topology, which we probe using optogenetically driven contraction of 3D-printed engineered muscle. These results reveal the physical principles used to sculpt the unusual architecture of the lizard lung, which could be exploited as a novel strategy to engineer tissues. American Association for the Advancement of Science 2021-12-22 /pmc/articles/PMC8694616/ /pubmed/34936466 http://dx.doi.org/10.1126/sciadv.abk0161 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Physical and Materials Sciences
Palmer, Michael A.
Nerger, Bryan A.
Goodwin, Katharine
Sudhakar, Anvitha
Lemke, Sandra B.
Ravindran, Pavithran T.
Toettcher, Jared E.
Košmrlj, Andrej
Nelson, Celeste M.
Stress ball morphogenesis: How the lizard builds its lung
title Stress ball morphogenesis: How the lizard builds its lung
title_full Stress ball morphogenesis: How the lizard builds its lung
title_fullStr Stress ball morphogenesis: How the lizard builds its lung
title_full_unstemmed Stress ball morphogenesis: How the lizard builds its lung
title_short Stress ball morphogenesis: How the lizard builds its lung
title_sort stress ball morphogenesis: how the lizard builds its lung
topic Physical and Materials Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8694616/
https://www.ncbi.nlm.nih.gov/pubmed/34936466
http://dx.doi.org/10.1126/sciadv.abk0161
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