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Artificial cells eavesdropping on HepG2 cells
Cellular communication is a fundamental feature to ensure the survival of cellular assemblies, such as multicellular tissue, via coordinated adaption to changes in their surroundings. Consequently, the development of integrated semi-synthetic systems consisting of artificial cells (ACs) and mammalia...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415741/ https://www.ncbi.nlm.nih.gov/pubmed/37577001 http://dx.doi.org/10.1098/rsfs.2023.0007 |
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author | Westensee, Isabella Nymann Städler, Brigitte |
author_facet | Westensee, Isabella Nymann Städler, Brigitte |
author_sort | Westensee, Isabella Nymann |
collection | PubMed |
description | Cellular communication is a fundamental feature to ensure the survival of cellular assemblies, such as multicellular tissue, via coordinated adaption to changes in their surroundings. Consequently, the development of integrated semi-synthetic systems consisting of artificial cells (ACs) and mammalian cells requires feedback-based interactions. Here, we illustrate that ACs can eavesdrop on HepG2 cells focusing on the activity of cytochrome P450 1A2 (CYP1A2), an enzyme from the cytochrome P450 enzyme family. Specifically, d-cysteine is sent as a signal from the ACs via the triggered reduction of disulfide bonds. Simultaneously, HepG2 cells enzymatically convert 2-cyano-6-methoxybenzothiazole into 2-cyano-6-hydroxybenzothiazole that is released in the extracellular space. d-Cysteine and 2-cyano-6-hydroxybenzothiazole react to form d-luciferin. The ACs respond to this signal by converting d-luciferin into luminescence due to the presence of encapsulated luciferase in the ACs. As a result, the ACs can eavesdrop on the mammalian cells to evaluate the level of hepatic CYP1A2 function. |
format | Online Article Text |
id | pubmed-10415741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104157412023-08-12 Artificial cells eavesdropping on HepG2 cells Westensee, Isabella Nymann Städler, Brigitte Interface Focus Articles Cellular communication is a fundamental feature to ensure the survival of cellular assemblies, such as multicellular tissue, via coordinated adaption to changes in their surroundings. Consequently, the development of integrated semi-synthetic systems consisting of artificial cells (ACs) and mammalian cells requires feedback-based interactions. Here, we illustrate that ACs can eavesdrop on HepG2 cells focusing on the activity of cytochrome P450 1A2 (CYP1A2), an enzyme from the cytochrome P450 enzyme family. Specifically, d-cysteine is sent as a signal from the ACs via the triggered reduction of disulfide bonds. Simultaneously, HepG2 cells enzymatically convert 2-cyano-6-methoxybenzothiazole into 2-cyano-6-hydroxybenzothiazole that is released in the extracellular space. d-Cysteine and 2-cyano-6-hydroxybenzothiazole react to form d-luciferin. The ACs respond to this signal by converting d-luciferin into luminescence due to the presence of encapsulated luciferase in the ACs. As a result, the ACs can eavesdrop on the mammalian cells to evaluate the level of hepatic CYP1A2 function. The Royal Society 2023-08-11 /pmc/articles/PMC10415741/ /pubmed/37577001 http://dx.doi.org/10.1098/rsfs.2023.0007 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Articles Westensee, Isabella Nymann Städler, Brigitte Artificial cells eavesdropping on HepG2 cells |
title | Artificial cells eavesdropping on HepG2 cells |
title_full | Artificial cells eavesdropping on HepG2 cells |
title_fullStr | Artificial cells eavesdropping on HepG2 cells |
title_full_unstemmed | Artificial cells eavesdropping on HepG2 cells |
title_short | Artificial cells eavesdropping on HepG2 cells |
title_sort | artificial cells eavesdropping on hepg2 cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415741/ https://www.ncbi.nlm.nih.gov/pubmed/37577001 http://dx.doi.org/10.1098/rsfs.2023.0007 |
work_keys_str_mv | AT westenseeisabellanymann artificialcellseavesdroppingonhepg2cells AT stadlerbrigitte artificialcellseavesdroppingonhepg2cells |