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Genetic dissection of intercellular interactions in vivo by membrane-permeable protein

Unraveling cell–cell interaction is fundamental to understanding many biological processes. To date, genetic tools for labeling neighboring cells in mammals are not available. Here, we developed a labeling strategy based on the Cre-induced intercellular labeling protein (CILP). Cre-expressing donor...

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Detalles Bibliográficos
Autores principales: Zhang, Shaohua, Zhang, Qianyu, Liu, Zixin, Liu, Kuo, He, Lingjuan, Lui, Kathy O., Wang, Lixin, Zhou, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910597/
https://www.ncbi.nlm.nih.gov/pubmed/36574652
http://dx.doi.org/10.1073/pnas.2120582120
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author Zhang, Shaohua
Zhang, Qianyu
Liu, Zixin
Liu, Kuo
He, Lingjuan
Lui, Kathy O.
Wang, Lixin
Zhou, Bin
author_facet Zhang, Shaohua
Zhang, Qianyu
Liu, Zixin
Liu, Kuo
He, Lingjuan
Lui, Kathy O.
Wang, Lixin
Zhou, Bin
author_sort Zhang, Shaohua
collection PubMed
description Unraveling cell–cell interaction is fundamental to understanding many biological processes. To date, genetic tools for labeling neighboring cells in mammals are not available. Here, we developed a labeling strategy based on the Cre-induced intercellular labeling protein (CILP). Cre-expressing donor cells release a lipid-soluble and membrane-permeable fluorescent protein that is then taken up by recipient cells, enabling fluorescent labeling of neighboring cells. Using CILP, we specifically labeled endothelial cells surrounding a special population of hepatocytes in adult mice and revealed their distinct gene signatures. Our results highlight the potential of CILP as a platform to reveal cell–cell interactions and communications in vivo.
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spelling pubmed-99105972023-02-10 Genetic dissection of intercellular interactions in vivo by membrane-permeable protein Zhang, Shaohua Zhang, Qianyu Liu, Zixin Liu, Kuo He, Lingjuan Lui, Kathy O. Wang, Lixin Zhou, Bin Proc Natl Acad Sci U S A Biological Sciences Unraveling cell–cell interaction is fundamental to understanding many biological processes. To date, genetic tools for labeling neighboring cells in mammals are not available. Here, we developed a labeling strategy based on the Cre-induced intercellular labeling protein (CILP). Cre-expressing donor cells release a lipid-soluble and membrane-permeable fluorescent protein that is then taken up by recipient cells, enabling fluorescent labeling of neighboring cells. Using CILP, we specifically labeled endothelial cells surrounding a special population of hepatocytes in adult mice and revealed their distinct gene signatures. Our results highlight the potential of CILP as a platform to reveal cell–cell interactions and communications in vivo. National Academy of Sciences 2022-12-27 2023-01-03 /pmc/articles/PMC9910597/ /pubmed/36574652 http://dx.doi.org/10.1073/pnas.2120582120 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Zhang, Shaohua
Zhang, Qianyu
Liu, Zixin
Liu, Kuo
He, Lingjuan
Lui, Kathy O.
Wang, Lixin
Zhou, Bin
Genetic dissection of intercellular interactions in vivo by membrane-permeable protein
title Genetic dissection of intercellular interactions in vivo by membrane-permeable protein
title_full Genetic dissection of intercellular interactions in vivo by membrane-permeable protein
title_fullStr Genetic dissection of intercellular interactions in vivo by membrane-permeable protein
title_full_unstemmed Genetic dissection of intercellular interactions in vivo by membrane-permeable protein
title_short Genetic dissection of intercellular interactions in vivo by membrane-permeable protein
title_sort genetic dissection of intercellular interactions in vivo by membrane-permeable protein
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910597/
https://www.ncbi.nlm.nih.gov/pubmed/36574652
http://dx.doi.org/10.1073/pnas.2120582120
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