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A red/far-red light-responsive bi-stable toggle switch to control gene expression in mammalian cells
Growth and differentiation of multicellular systems is orchestrated by spatially restricted gene expression programs in specialized subpopulations. The targeted manipulation of such processes by synthetic tools with high-spatiotemporal resolution could, therefore, enable a deepened understanding of...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3627562/ https://www.ncbi.nlm.nih.gov/pubmed/23355611 http://dx.doi.org/10.1093/nar/gkt002 |
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author | Müller, Konrad Engesser, Raphael Metzger, Stéphanie Schulz, Simon Kämpf, Michael M. Busacker, Moritz Steinberg, Thorsten Tomakidi, Pascal Ehrbar, Martin Nagy, Ferenc Timmer, Jens Zubriggen, Matias D. Weber, Wilfried |
author_facet | Müller, Konrad Engesser, Raphael Metzger, Stéphanie Schulz, Simon Kämpf, Michael M. Busacker, Moritz Steinberg, Thorsten Tomakidi, Pascal Ehrbar, Martin Nagy, Ferenc Timmer, Jens Zubriggen, Matias D. Weber, Wilfried |
author_sort | Müller, Konrad |
collection | PubMed |
description | Growth and differentiation of multicellular systems is orchestrated by spatially restricted gene expression programs in specialized subpopulations. The targeted manipulation of such processes by synthetic tools with high-spatiotemporal resolution could, therefore, enable a deepened understanding of developmental processes and open new opportunities in tissue engineering. Here, we describe the first red/far-red light-triggered gene switch for mammalian cells for achieving gene expression control in time and space. We show that the system can reversibly be toggled between stable on- and off-states using short light pulses at 660 or 740 nm. Red light-induced gene expression was shown to correlate with the applied photon number and was compatible with different mammalian cell lines, including human primary cells. The light-induced expression kinetics were quantitatively analyzed by a mathematical model. We apply the system for the spatially controlled engineering of angiogenesis in chicken embryos. The system’s performance combined with cell- and tissue-compatible regulating red light will enable unprecedented spatiotemporally controlled molecular interventions in mammalian cells, tissues and organisms. |
format | Online Article Text |
id | pubmed-3627562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36275622013-04-17 A red/far-red light-responsive bi-stable toggle switch to control gene expression in mammalian cells Müller, Konrad Engesser, Raphael Metzger, Stéphanie Schulz, Simon Kämpf, Michael M. Busacker, Moritz Steinberg, Thorsten Tomakidi, Pascal Ehrbar, Martin Nagy, Ferenc Timmer, Jens Zubriggen, Matias D. Weber, Wilfried Nucleic Acids Res Methods Online Growth and differentiation of multicellular systems is orchestrated by spatially restricted gene expression programs in specialized subpopulations. The targeted manipulation of such processes by synthetic tools with high-spatiotemporal resolution could, therefore, enable a deepened understanding of developmental processes and open new opportunities in tissue engineering. Here, we describe the first red/far-red light-triggered gene switch for mammalian cells for achieving gene expression control in time and space. We show that the system can reversibly be toggled between stable on- and off-states using short light pulses at 660 or 740 nm. Red light-induced gene expression was shown to correlate with the applied photon number and was compatible with different mammalian cell lines, including human primary cells. The light-induced expression kinetics were quantitatively analyzed by a mathematical model. We apply the system for the spatially controlled engineering of angiogenesis in chicken embryos. The system’s performance combined with cell- and tissue-compatible regulating red light will enable unprecedented spatiotemporally controlled molecular interventions in mammalian cells, tissues and organisms. Oxford University Press 2013-04 2013-01-25 /pmc/articles/PMC3627562/ /pubmed/23355611 http://dx.doi.org/10.1093/nar/gkt002 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Müller, Konrad Engesser, Raphael Metzger, Stéphanie Schulz, Simon Kämpf, Michael M. Busacker, Moritz Steinberg, Thorsten Tomakidi, Pascal Ehrbar, Martin Nagy, Ferenc Timmer, Jens Zubriggen, Matias D. Weber, Wilfried A red/far-red light-responsive bi-stable toggle switch to control gene expression in mammalian cells |
title | A red/far-red light-responsive bi-stable toggle switch to control gene expression in mammalian cells |
title_full | A red/far-red light-responsive bi-stable toggle switch to control gene expression in mammalian cells |
title_fullStr | A red/far-red light-responsive bi-stable toggle switch to control gene expression in mammalian cells |
title_full_unstemmed | A red/far-red light-responsive bi-stable toggle switch to control gene expression in mammalian cells |
title_short | A red/far-red light-responsive bi-stable toggle switch to control gene expression in mammalian cells |
title_sort | red/far-red light-responsive bi-stable toggle switch to control gene expression in mammalian cells |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3627562/ https://www.ncbi.nlm.nih.gov/pubmed/23355611 http://dx.doi.org/10.1093/nar/gkt002 |
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