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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
Descripción
Sumario: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.