Laboratory of Synthetic Immunology, Department of Surgery Oncology and Gastroenterology, University of Padova, Padova, Italy.
Veneto Institute of Oncology IOV-IRCCS, Padova, Italy.
Methods Mol Biol. 2023;2618:71-80. doi: 10.1007/978-1-0716-2938-3_5.
Interactions between different cell types are key for immune function. Traditionally, interactions have been investigated in vivo by intravital two-photon microscopy, but the molecular characterization of the cells participating in a specific interaction is limited by the inability to retrieve the cells for downstream analysis. We recently developed an approach to label cells undergoing specific interactions in vivo, which we called LIPSTIC (Labeling Immune Partnership by Sortagging Intercellular Contacts). Here, we provide detailed instructions on how to track CD40-CD40L interactions between dendritic cells (DCs) and CD4 T cells using genetically engineered LIPSTIC mice. This protocol requires expertise in animal experimentation and multicolor flow cytometry. Once mouse crossing has been achieved, it takes 3 days or more to complete, depending on the kinetics of the interactions that the researcher wishes to investigate.
不同细胞类型之间的相互作用是免疫功能的关键。传统上,通过活体双光子显微镜在体内研究这些相互作用,但由于无法回收参与特定相互作用的细胞,对参与特定相互作用的细胞的分子特征的研究受到限制。我们最近开发了一种在体内标记发生特定相互作用的细胞的方法,我们称之为 LIPSTIC(通过分选标记细胞间接触来标记免疫伙伴关系)。在这里,我们提供了使用基因工程 LIPSTIC 小鼠跟踪树突状细胞 (DC) 和 CD4 T 细胞之间的 CD40-CD40L 相互作用的详细说明。该方案需要动物实验和多色流式细胞术方面的专业知识。一旦实现了小鼠杂交,根据研究人员希望研究的相互作用的动力学,完成该实验需要 3 天或更长时间。