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Synthetic Notch Activation Patterns in a Proliferating Tissue

Cell-cell communication through direct contact is essential during fundamental biological processes such as tissue repair and morphogenesis. Synthetic forms of contact-mediated cell-cell communication can generate custom gene expression outputs, making them valuable for tissue engineering and regene...

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Autores principales: Dawson, Jonathan E., Bryant, Abby, Jordan, Trevor, Bhikot, Simran, Macon, Shawn, Walton, Breana, Ajamu-Johnson, Amber, Langridge, Paul D., Malmi-Kakkada, Abdul N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370035/
https://www.ncbi.nlm.nih.gov/pubmed/37503188
http://dx.doi.org/10.1101/2023.07.12.548752
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author Dawson, Jonathan E.
Bryant, Abby
Jordan, Trevor
Bhikot, Simran
Macon, Shawn
Walton, Breana
Ajamu-Johnson, Amber
Langridge, Paul D.
Malmi-Kakkada, Abdul N.
author_facet Dawson, Jonathan E.
Bryant, Abby
Jordan, Trevor
Bhikot, Simran
Macon, Shawn
Walton, Breana
Ajamu-Johnson, Amber
Langridge, Paul D.
Malmi-Kakkada, Abdul N.
author_sort Dawson, Jonathan E.
collection PubMed
description Cell-cell communication through direct contact is essential during fundamental biological processes such as tissue repair and morphogenesis. Synthetic forms of contact-mediated cell-cell communication can generate custom gene expression outputs, making them valuable for tissue engineering and regenerative medicine. To precisely control the location and timing of synthetic signal outputs in growing tissues, it is necessary to understand the mechanisms underlying its spatiotemporal patterns. Towards this goal, we combine theory and experiments to study patterns of synthetic Notch (synNotch) activation - a custom synthetic gene circuit that we implement within Drosophila wing imaginal discs. We show that output synthesis and degradation rates together with cell division are the key minimal parameters that predict the heterogeneous spatiotemporal patterns of synNotch activation. Notably, synNotch output forms a graded exponential spatial profile that extends several cell diameters from the signal source, establishing evidence for signal propagation without diffusion or long range cell-cell communication. Furthermore, we discover that the shape of the interface between ligand and receptor cells is important in determining the synNotch output. Overall, we elucidate key biophysical principles that underlie complex emergent spatiotemporal patterns of synNotch output in a growing tissue.
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spelling pubmed-103700352023-11-14 Synthetic Notch Activation Patterns in a Proliferating Tissue Dawson, Jonathan E. Bryant, Abby Jordan, Trevor Bhikot, Simran Macon, Shawn Walton, Breana Ajamu-Johnson, Amber Langridge, Paul D. Malmi-Kakkada, Abdul N. bioRxiv Article Cell-cell communication through direct contact is essential during fundamental biological processes such as tissue repair and morphogenesis. Synthetic forms of contact-mediated cell-cell communication can generate custom gene expression outputs, making them valuable for tissue engineering and regenerative medicine. To precisely control the location and timing of synthetic signal outputs in growing tissues, it is necessary to understand the mechanisms underlying its spatiotemporal patterns. Towards this goal, we combine theory and experiments to study patterns of synthetic Notch (synNotch) activation - a custom synthetic gene circuit that we implement within Drosophila wing imaginal discs. We show that output synthesis and degradation rates together with cell division are the key minimal parameters that predict the heterogeneous spatiotemporal patterns of synNotch activation. Notably, synNotch output forms a graded exponential spatial profile that extends several cell diameters from the signal source, establishing evidence for signal propagation without diffusion or long range cell-cell communication. Furthermore, we discover that the shape of the interface between ligand and receptor cells is important in determining the synNotch output. Overall, we elucidate key biophysical principles that underlie complex emergent spatiotemporal patterns of synNotch output in a growing tissue. Cold Spring Harbor Laboratory 2023-11-08 /pmc/articles/PMC10370035/ /pubmed/37503188 http://dx.doi.org/10.1101/2023.07.12.548752 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Dawson, Jonathan E.
Bryant, Abby
Jordan, Trevor
Bhikot, Simran
Macon, Shawn
Walton, Breana
Ajamu-Johnson, Amber
Langridge, Paul D.
Malmi-Kakkada, Abdul N.
Synthetic Notch Activation Patterns in a Proliferating Tissue
title Synthetic Notch Activation Patterns in a Proliferating Tissue
title_full Synthetic Notch Activation Patterns in a Proliferating Tissue
title_fullStr Synthetic Notch Activation Patterns in a Proliferating Tissue
title_full_unstemmed Synthetic Notch Activation Patterns in a Proliferating Tissue
title_short Synthetic Notch Activation Patterns in a Proliferating Tissue
title_sort synthetic notch activation patterns in a proliferating tissue
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370035/
https://www.ncbi.nlm.nih.gov/pubmed/37503188
http://dx.doi.org/10.1101/2023.07.12.548752
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