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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2021
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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. |
format | Online Article Text |
id | pubmed-8694616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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