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Turing mechanism underlying a branching model for lung morphogenesis

The mammalian lung develops through branching morphogenesis. Two primary forms of branching, which occur in order, in the lung have been identified: tip bifurcation and side branching. However, the mechanisms of lung branching morphogenesis remain to be explored. In our previous study, a biological...

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Detalles Bibliográficos
Autores principales: Xu, Hui, Sun, Mingzhu, Zhao, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380321/
https://www.ncbi.nlm.nih.gov/pubmed/28376090
http://dx.doi.org/10.1371/journal.pone.0174946
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author Xu, Hui
Sun, Mingzhu
Zhao, Xin
author_facet Xu, Hui
Sun, Mingzhu
Zhao, Xin
author_sort Xu, Hui
collection PubMed
description The mammalian lung develops through branching morphogenesis. Two primary forms of branching, which occur in order, in the lung have been identified: tip bifurcation and side branching. However, the mechanisms of lung branching morphogenesis remain to be explored. In our previous study, a biological mechanism was presented for lung branching pattern formation through a branching model. Here, we provide a mathematical mechanism underlying the branching patterns. By decoupling the branching model, we demonstrated the existence of Turing instability. We performed Turing instability analysis to reveal the mathematical mechanism of the branching patterns. Our simulation results show that the Turing patterns underlying the branching patterns are spot patterns that exhibit high local morphogen concentration. The high local morphogen concentration induces the growth of branching. Furthermore, we found that the sparse spot patterns underlie the tip bifurcation patterns, while the dense spot patterns underlies the side branching patterns. The dispersion relation analysis shows that the Turing wavelength affects the branching structure. As the wavelength decreases, the spot patterns change from sparse to dense, the rate of tip bifurcation decreases and side branching eventually occurs instead. In the process of transformation, there may exists hybrid branching that mixes tip bifurcation and side branching. Since experimental studies have reported that branching mode switching from side branching to tip bifurcation in the lung is under genetic control, our simulation results suggest that genes control the switch of the branching mode by regulating the Turing wavelength. Our results provide a novel insight into and understanding of the formation of branching patterns in the lung and other biological systems.
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spelling pubmed-53803212017-04-19 Turing mechanism underlying a branching model for lung morphogenesis Xu, Hui Sun, Mingzhu Zhao, Xin PLoS One Research Article The mammalian lung develops through branching morphogenesis. Two primary forms of branching, which occur in order, in the lung have been identified: tip bifurcation and side branching. However, the mechanisms of lung branching morphogenesis remain to be explored. In our previous study, a biological mechanism was presented for lung branching pattern formation through a branching model. Here, we provide a mathematical mechanism underlying the branching patterns. By decoupling the branching model, we demonstrated the existence of Turing instability. We performed Turing instability analysis to reveal the mathematical mechanism of the branching patterns. Our simulation results show that the Turing patterns underlying the branching patterns are spot patterns that exhibit high local morphogen concentration. The high local morphogen concentration induces the growth of branching. Furthermore, we found that the sparse spot patterns underlie the tip bifurcation patterns, while the dense spot patterns underlies the side branching patterns. The dispersion relation analysis shows that the Turing wavelength affects the branching structure. As the wavelength decreases, the spot patterns change from sparse to dense, the rate of tip bifurcation decreases and side branching eventually occurs instead. In the process of transformation, there may exists hybrid branching that mixes tip bifurcation and side branching. Since experimental studies have reported that branching mode switching from side branching to tip bifurcation in the lung is under genetic control, our simulation results suggest that genes control the switch of the branching mode by regulating the Turing wavelength. Our results provide a novel insight into and understanding of the formation of branching patterns in the lung and other biological systems. Public Library of Science 2017-04-04 /pmc/articles/PMC5380321/ /pubmed/28376090 http://dx.doi.org/10.1371/journal.pone.0174946 Text en © 2017 Xu 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
Xu, Hui
Sun, Mingzhu
Zhao, Xin
Turing mechanism underlying a branching model for lung morphogenesis
title Turing mechanism underlying a branching model for lung morphogenesis
title_full Turing mechanism underlying a branching model for lung morphogenesis
title_fullStr Turing mechanism underlying a branching model for lung morphogenesis
title_full_unstemmed Turing mechanism underlying a branching model for lung morphogenesis
title_short Turing mechanism underlying a branching model for lung morphogenesis
title_sort turing mechanism underlying a branching model for lung morphogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380321/
https://www.ncbi.nlm.nih.gov/pubmed/28376090
http://dx.doi.org/10.1371/journal.pone.0174946
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