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A library of mammalian effector modules for synthetic morphology
BACKGROUND: In mammalian development, the formation of most tissues is achieved by a relatively small repertoire of basic morphogenetic events (e.g. cell adhesion, locomotion, apoptosis, etc.), permutated in various sequences to form different tissues. Together with cell differentiation, these mecha...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255936/ https://www.ncbi.nlm.nih.gov/pubmed/25478005 http://dx.doi.org/10.1186/1754-1611-8-26 |
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author | Cachat, Elise Liu, Weijia Hohenstein, Peter Davies, Jamie A |
author_facet | Cachat, Elise Liu, Weijia Hohenstein, Peter Davies, Jamie A |
author_sort | Cachat, Elise |
collection | PubMed |
description | BACKGROUND: In mammalian development, the formation of most tissues is achieved by a relatively small repertoire of basic morphogenetic events (e.g. cell adhesion, locomotion, apoptosis, etc.), permutated in various sequences to form different tissues. Together with cell differentiation, these mechanisms allow populations of cells to organize themselves into defined geometries and structures, as simple embryos develop into complex organisms. The control of tissue morphogenesis by populations of engineered cells is a potentially very powerful but neglected aspect of synthetic biology. RESULTS: We have assembled a modular library of synthetic morphogenetic driver genes to control (separately) mammalian cell adhesion, locomotion, fusion, proliferation and elective cell death. Here we describe this library and demonstrate its use in the T-REx-293 human cell line to induce each of these desired morphological behaviours on command. CONCLUSIONS: Building on from the simple test systems described here, we want to extend engineered control of morphogenetic cell behaviour to more complex 3D structures that can inform embryologists and may, in the future, be used in surgery and regenerative medicine, making synthetic morphology a powerful tool for developmental biology and tissue engineering. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1754-1611-8-26) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4255936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42559362014-12-05 A library of mammalian effector modules for synthetic morphology Cachat, Elise Liu, Weijia Hohenstein, Peter Davies, Jamie A J Biol Eng Research BACKGROUND: In mammalian development, the formation of most tissues is achieved by a relatively small repertoire of basic morphogenetic events (e.g. cell adhesion, locomotion, apoptosis, etc.), permutated in various sequences to form different tissues. Together with cell differentiation, these mechanisms allow populations of cells to organize themselves into defined geometries and structures, as simple embryos develop into complex organisms. The control of tissue morphogenesis by populations of engineered cells is a potentially very powerful but neglected aspect of synthetic biology. RESULTS: We have assembled a modular library of synthetic morphogenetic driver genes to control (separately) mammalian cell adhesion, locomotion, fusion, proliferation and elective cell death. Here we describe this library and demonstrate its use in the T-REx-293 human cell line to induce each of these desired morphological behaviours on command. CONCLUSIONS: Building on from the simple test systems described here, we want to extend engineered control of morphogenetic cell behaviour to more complex 3D structures that can inform embryologists and may, in the future, be used in surgery and regenerative medicine, making synthetic morphology a powerful tool for developmental biology and tissue engineering. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1754-1611-8-26) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-19 /pmc/articles/PMC4255936/ /pubmed/25478005 http://dx.doi.org/10.1186/1754-1611-8-26 Text en © Cachat et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Cachat, Elise Liu, Weijia Hohenstein, Peter Davies, Jamie A A library of mammalian effector modules for synthetic morphology |
title | A library of mammalian effector modules for synthetic morphology |
title_full | A library of mammalian effector modules for synthetic morphology |
title_fullStr | A library of mammalian effector modules for synthetic morphology |
title_full_unstemmed | A library of mammalian effector modules for synthetic morphology |
title_short | A library of mammalian effector modules for synthetic morphology |
title_sort | library of mammalian effector modules for synthetic morphology |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4255936/ https://www.ncbi.nlm.nih.gov/pubmed/25478005 http://dx.doi.org/10.1186/1754-1611-8-26 |
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