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Closing the loop on morphogenesis: a mathematical model of morphogenesis by closed-loop reaction-diffusion
Morphogenesis, the establishment and repair of emergent complex anatomy by groups of cells, is a fascinating and biomedically-relevant problem. One of its most fascinating aspects is that a developing embryo can reliably recover from disturbances, such as splitting into twins. While this reliability...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10461482/ https://www.ncbi.nlm.nih.gov/pubmed/37645245 http://dx.doi.org/10.3389/fcell.2023.1087650 |
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author | Grodstein, Joel McMillen, Patrick Levin, Michael |
author_facet | Grodstein, Joel McMillen, Patrick Levin, Michael |
author_sort | Grodstein, Joel |
collection | PubMed |
description | Morphogenesis, the establishment and repair of emergent complex anatomy by groups of cells, is a fascinating and biomedically-relevant problem. One of its most fascinating aspects is that a developing embryo can reliably recover from disturbances, such as splitting into twins. While this reliability implies some type of goal-seeking error minimization over a morphogenic field, there are many gaps with respect to detailed, constructive models of such a process. A common way to achieve reliability is negative feedback, which requires characterizing the existing body shape to create an error signal–but measuring properties of a shape may not be simple. We show how cells communicating in a wave-like pattern could analyze properties of the current body shape. We then describe a closed-loop negative-feedback system for creating reaction-diffusion (RD) patterns with high reliability. Specifically, we use a wave to count the number of peaks in a RD pattern, letting us use a negative-feedback controller to create a pattern with N repetitions, where N can be altered over a wide range. Furthermore, the individual repetitions of the RD pattern can be easily stretched or shrunk under genetic control to create, e.g., some morphological features larger than others. This work contributes to the exciting effort of understanding design principles of morphological computation, which can be used to understand evolved developmental mechanisms, manipulate them in regenerative-medicine settings, or engineer novel synthetic morphology constructs with desired robust behavior. |
format | Online Article Text |
id | pubmed-10461482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104614822023-08-29 Closing the loop on morphogenesis: a mathematical model of morphogenesis by closed-loop reaction-diffusion Grodstein, Joel McMillen, Patrick Levin, Michael Front Cell Dev Biol Cell and Developmental Biology Morphogenesis, the establishment and repair of emergent complex anatomy by groups of cells, is a fascinating and biomedically-relevant problem. One of its most fascinating aspects is that a developing embryo can reliably recover from disturbances, such as splitting into twins. While this reliability implies some type of goal-seeking error minimization over a morphogenic field, there are many gaps with respect to detailed, constructive models of such a process. A common way to achieve reliability is negative feedback, which requires characterizing the existing body shape to create an error signal–but measuring properties of a shape may not be simple. We show how cells communicating in a wave-like pattern could analyze properties of the current body shape. We then describe a closed-loop negative-feedback system for creating reaction-diffusion (RD) patterns with high reliability. Specifically, we use a wave to count the number of peaks in a RD pattern, letting us use a negative-feedback controller to create a pattern with N repetitions, where N can be altered over a wide range. Furthermore, the individual repetitions of the RD pattern can be easily stretched or shrunk under genetic control to create, e.g., some morphological features larger than others. This work contributes to the exciting effort of understanding design principles of morphological computation, which can be used to understand evolved developmental mechanisms, manipulate them in regenerative-medicine settings, or engineer novel synthetic morphology constructs with desired robust behavior. Frontiers Media S.A. 2023-08-14 /pmc/articles/PMC10461482/ /pubmed/37645245 http://dx.doi.org/10.3389/fcell.2023.1087650 Text en Copyright © 2023 Grodstein, McMillen and Levin. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Grodstein, Joel McMillen, Patrick Levin, Michael Closing the loop on morphogenesis: a mathematical model of morphogenesis by closed-loop reaction-diffusion |
title | Closing the loop on morphogenesis: a mathematical model of morphogenesis by closed-loop reaction-diffusion |
title_full | Closing the loop on morphogenesis: a mathematical model of morphogenesis by closed-loop reaction-diffusion |
title_fullStr | Closing the loop on morphogenesis: a mathematical model of morphogenesis by closed-loop reaction-diffusion |
title_full_unstemmed | Closing the loop on morphogenesis: a mathematical model of morphogenesis by closed-loop reaction-diffusion |
title_short | Closing the loop on morphogenesis: a mathematical model of morphogenesis by closed-loop reaction-diffusion |
title_sort | closing the loop on morphogenesis: a mathematical model of morphogenesis by closed-loop reaction-diffusion |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10461482/ https://www.ncbi.nlm.nih.gov/pubmed/37645245 http://dx.doi.org/10.3389/fcell.2023.1087650 |
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