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Engineering Whole Mammalian Cells for Target‐Cell‐Specific Invasion/Fusion

Live mammalian cells are equipped with a synthetic cell invasion system that enables their target‐specific insertion into other live mammalian cells. By conjugating RhoA activator to a transmembrane protein that is segregated from cell–cell interface when specific cell contact occurs, polarization o...

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Detalles Bibliográficos
Autores principales: Kojima, Ryosuke, Fussenegger, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051388/
https://www.ncbi.nlm.nih.gov/pubmed/30027033
http://dx.doi.org/10.1002/advs.201700971
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author Kojima, Ryosuke
Fussenegger, Martin
author_facet Kojima, Ryosuke
Fussenegger, Martin
author_sort Kojima, Ryosuke
collection PubMed
description Live mammalian cells are equipped with a synthetic cell invasion system that enables their target‐specific insertion into other live mammalian cells. By conjugating RhoA activator to a transmembrane protein that is segregated from cell–cell interface when specific cell contact occurs, polarization of RhoA activity is synthetically induced inside the cells in response to specific cell contact. This polarization is a sufficient condition for invader cells to selectively penetrate cells expressing a target antigen. Further, when an acid‐responsive fusogenic protein is expressed on invader cells, invader/receiver cell fusion occurs after invasion, and the invader's intracellular contents are released into the recipient's cytosol. It is shown that this system can be used for specific cell ablation. This synthetic‐biology‐inspired cell invasion/fusion system might open the door to using whole mammalian cells for cargo delivery purposes or for ablation of a specific cell type.
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spelling pubmed-60513882018-07-19 Engineering Whole Mammalian Cells for Target‐Cell‐Specific Invasion/Fusion Kojima, Ryosuke Fussenegger, Martin Adv Sci (Weinh) Communications Live mammalian cells are equipped with a synthetic cell invasion system that enables their target‐specific insertion into other live mammalian cells. By conjugating RhoA activator to a transmembrane protein that is segregated from cell–cell interface when specific cell contact occurs, polarization of RhoA activity is synthetically induced inside the cells in response to specific cell contact. This polarization is a sufficient condition for invader cells to selectively penetrate cells expressing a target antigen. Further, when an acid‐responsive fusogenic protein is expressed on invader cells, invader/receiver cell fusion occurs after invasion, and the invader's intracellular contents are released into the recipient's cytosol. It is shown that this system can be used for specific cell ablation. This synthetic‐biology‐inspired cell invasion/fusion system might open the door to using whole mammalian cells for cargo delivery purposes or for ablation of a specific cell type. John Wiley and Sons Inc. 2018-05-08 /pmc/articles/PMC6051388/ /pubmed/30027033 http://dx.doi.org/10.1002/advs.201700971 Text en © 2018 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Kojima, Ryosuke
Fussenegger, Martin
Engineering Whole Mammalian Cells for Target‐Cell‐Specific Invasion/Fusion
title Engineering Whole Mammalian Cells for Target‐Cell‐Specific Invasion/Fusion
title_full Engineering Whole Mammalian Cells for Target‐Cell‐Specific Invasion/Fusion
title_fullStr Engineering Whole Mammalian Cells for Target‐Cell‐Specific Invasion/Fusion
title_full_unstemmed Engineering Whole Mammalian Cells for Target‐Cell‐Specific Invasion/Fusion
title_short Engineering Whole Mammalian Cells for Target‐Cell‐Specific Invasion/Fusion
title_sort engineering whole mammalian cells for target‐cell‐specific invasion/fusion
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6051388/
https://www.ncbi.nlm.nih.gov/pubmed/30027033
http://dx.doi.org/10.1002/advs.201700971
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