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Cell-in-the-loop pattern formation with optogenetically emulated cell-to-cell signaling
Designing and implementing synthetic biological pattern formation remains challenging due to underlying theoretical complexity as well as the difficulty of engineering multicellular networks biochemically. Here, we introduce a cell-in-the-loop approach where living cells interact through in silico s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069979/ https://www.ncbi.nlm.nih.gov/pubmed/32170129 http://dx.doi.org/10.1038/s41467-020-15166-3 |
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author | Perkins, Melinda Liu Benzinger, Dirk Arcak, Murat Khammash, Mustafa |
author_facet | Perkins, Melinda Liu Benzinger, Dirk Arcak, Murat Khammash, Mustafa |
author_sort | Perkins, Melinda Liu |
collection | PubMed |
description | Designing and implementing synthetic biological pattern formation remains challenging due to underlying theoretical complexity as well as the difficulty of engineering multicellular networks biochemically. Here, we introduce a cell-in-the-loop approach where living cells interact through in silico signaling, establishing a new testbed to interrogate theoretical principles when internal cell dynamics are incorporated rather than modeled. We present an easy-to-use theoretical test to predict the emergence of contrasting patterns in gene expression among laterally inhibiting cells. Guided by the theory, we experimentally demonstrate spontaneous checkerboard patterning in an optogenetic setup, where cell-to-cell signaling is emulated with light inputs calculated in silico from real-time gene expression measurements. The scheme successfully produces spontaneous, persistent checkerboard patterns for systems of sixteen patches, in quantitative agreement with theoretical predictions. Our research highlights how tools from dynamical systems theory may inform our understanding of patterning, and illustrates the potential of cell-in-the-loop for engineering synthetic multicellular systems. |
format | Online Article Text |
id | pubmed-7069979 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70699792020-03-18 Cell-in-the-loop pattern formation with optogenetically emulated cell-to-cell signaling Perkins, Melinda Liu Benzinger, Dirk Arcak, Murat Khammash, Mustafa Nat Commun Article Designing and implementing synthetic biological pattern formation remains challenging due to underlying theoretical complexity as well as the difficulty of engineering multicellular networks biochemically. Here, we introduce a cell-in-the-loop approach where living cells interact through in silico signaling, establishing a new testbed to interrogate theoretical principles when internal cell dynamics are incorporated rather than modeled. We present an easy-to-use theoretical test to predict the emergence of contrasting patterns in gene expression among laterally inhibiting cells. Guided by the theory, we experimentally demonstrate spontaneous checkerboard patterning in an optogenetic setup, where cell-to-cell signaling is emulated with light inputs calculated in silico from real-time gene expression measurements. The scheme successfully produces spontaneous, persistent checkerboard patterns for systems of sixteen patches, in quantitative agreement with theoretical predictions. Our research highlights how tools from dynamical systems theory may inform our understanding of patterning, and illustrates the potential of cell-in-the-loop for engineering synthetic multicellular systems. Nature Publishing Group UK 2020-03-13 /pmc/articles/PMC7069979/ /pubmed/32170129 http://dx.doi.org/10.1038/s41467-020-15166-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Perkins, Melinda Liu Benzinger, Dirk Arcak, Murat Khammash, Mustafa Cell-in-the-loop pattern formation with optogenetically emulated cell-to-cell signaling |
title | Cell-in-the-loop pattern formation with optogenetically emulated cell-to-cell signaling |
title_full | Cell-in-the-loop pattern formation with optogenetically emulated cell-to-cell signaling |
title_fullStr | Cell-in-the-loop pattern formation with optogenetically emulated cell-to-cell signaling |
title_full_unstemmed | Cell-in-the-loop pattern formation with optogenetically emulated cell-to-cell signaling |
title_short | Cell-in-the-loop pattern formation with optogenetically emulated cell-to-cell signaling |
title_sort | cell-in-the-loop pattern formation with optogenetically emulated cell-to-cell signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069979/ https://www.ncbi.nlm.nih.gov/pubmed/32170129 http://dx.doi.org/10.1038/s41467-020-15166-3 |
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