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Genetically Encoded Protein Thermometer Enables Precise Electrothermal Control of Transgene Expression
Body temperature is maintained at around 37 °C in humans, but may rise to 40 °C or more during high‐grade fever, which occurs in most adults who are seriously ill. However, endogenous temperature sensors, such as ion channels and heat‐shock promoters, are fully activated only at noxious temperatures...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8564464/ https://www.ncbi.nlm.nih.gov/pubmed/34496151 http://dx.doi.org/10.1002/advs.202101813 |
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author | Stefanov, Bozhidar‐Adrian Teixeira, Ana P. Mansouri, Maysam Bertschi, Adrian Krawczyk, Krzysztof Hamri, Ghislaine Charpin‐El Xue, Shuai Fussenegger, Martin |
author_facet | Stefanov, Bozhidar‐Adrian Teixeira, Ana P. Mansouri, Maysam Bertschi, Adrian Krawczyk, Krzysztof Hamri, Ghislaine Charpin‐El Xue, Shuai Fussenegger, Martin |
author_sort | Stefanov, Bozhidar‐Adrian |
collection | PubMed |
description | Body temperature is maintained at around 37 °C in humans, but may rise to 40 °C or more during high‐grade fever, which occurs in most adults who are seriously ill. However, endogenous temperature sensors, such as ion channels and heat‐shock promoters, are fully activated only at noxious temperatures above this range, making them unsuitable for medical applications. Here, a genetically encoded protein thermometer (human enhanced gene activation thermometer; HEAT) is designed that can trigger transgene expression in the range of 37–40 °C by linking a mutant coiled‐coil temperature‐responsive protein sensor to a synthetic transcription factor. To validate the construct, a HEAT‐transgenic monoclonal human cell line, FeverSense, is generated and it is confirmed that it works as a fever sensor that can temperature‐ and exposure‐time‐dependently trigger reporter gene expression in vitro and in vivo. For translational proof of concept, microencapsulated designer cells stably expressing a HEAT‐controlled insulin production cassette in a mouse model of type‐1 diabetes are subcutaneously implanted and topical heating patches are used to apply heat corresponding to a warm sensation in humans. Insulin release is induced, restoring normoglycemia. Thus, HEAT appears to be suitable for practical electrothermal control of cell‐based therapy, and may also have potential for next‐generation treatment of fever‐associated medical conditions. |
format | Online Article Text |
id | pubmed-8564464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85644642021-11-09 Genetically Encoded Protein Thermometer Enables Precise Electrothermal Control of Transgene Expression Stefanov, Bozhidar‐Adrian Teixeira, Ana P. Mansouri, Maysam Bertschi, Adrian Krawczyk, Krzysztof Hamri, Ghislaine Charpin‐El Xue, Shuai Fussenegger, Martin Adv Sci (Weinh) Research Articles Body temperature is maintained at around 37 °C in humans, but may rise to 40 °C or more during high‐grade fever, which occurs in most adults who are seriously ill. However, endogenous temperature sensors, such as ion channels and heat‐shock promoters, are fully activated only at noxious temperatures above this range, making them unsuitable for medical applications. Here, a genetically encoded protein thermometer (human enhanced gene activation thermometer; HEAT) is designed that can trigger transgene expression in the range of 37–40 °C by linking a mutant coiled‐coil temperature‐responsive protein sensor to a synthetic transcription factor. To validate the construct, a HEAT‐transgenic monoclonal human cell line, FeverSense, is generated and it is confirmed that it works as a fever sensor that can temperature‐ and exposure‐time‐dependently trigger reporter gene expression in vitro and in vivo. For translational proof of concept, microencapsulated designer cells stably expressing a HEAT‐controlled insulin production cassette in a mouse model of type‐1 diabetes are subcutaneously implanted and topical heating patches are used to apply heat corresponding to a warm sensation in humans. Insulin release is induced, restoring normoglycemia. Thus, HEAT appears to be suitable for practical electrothermal control of cell‐based therapy, and may also have potential for next‐generation treatment of fever‐associated medical conditions. John Wiley and Sons Inc. 2021-09-08 /pmc/articles/PMC8564464/ /pubmed/34496151 http://dx.doi.org/10.1002/advs.202101813 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Stefanov, Bozhidar‐Adrian Teixeira, Ana P. Mansouri, Maysam Bertschi, Adrian Krawczyk, Krzysztof Hamri, Ghislaine Charpin‐El Xue, Shuai Fussenegger, Martin Genetically Encoded Protein Thermometer Enables Precise Electrothermal Control of Transgene Expression |
title | Genetically Encoded Protein Thermometer Enables Precise Electrothermal Control of Transgene Expression |
title_full | Genetically Encoded Protein Thermometer Enables Precise Electrothermal Control of Transgene Expression |
title_fullStr | Genetically Encoded Protein Thermometer Enables Precise Electrothermal Control of Transgene Expression |
title_full_unstemmed | Genetically Encoded Protein Thermometer Enables Precise Electrothermal Control of Transgene Expression |
title_short | Genetically Encoded Protein Thermometer Enables Precise Electrothermal Control of Transgene Expression |
title_sort | genetically encoded protein thermometer enables precise electrothermal control of transgene expression |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8564464/ https://www.ncbi.nlm.nih.gov/pubmed/34496151 http://dx.doi.org/10.1002/advs.202101813 |
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