Microbiology & Immunology Department and Immunology Program, Stanford University School of Medicine, Stanford, CA, USA.
Nat Protoc. 2021 Oct;16(10):4855-4877. doi: 10.1038/s41596-021-00599-x. Epub 2021 Sep 3.
The immune system comprises distinct functionally specialized cell populations, which can be characterized in depth by mass cytometry protein profiling. Unfortunately, the low-throughput nature of mass cytometry has made it challenging to analyze minor cell populations. This is the case for dendritic cells, which represent 0.2-2% of all immune cells in tissues and yet perform the critical task of initiating and modulating immune responses. Here, we provide an optimized step-by-step protocol for the characterization of well-known and emerging human dendritic cell populations in blood and tissues using mass cytometry. We provide detailed instructions for the generation of single-cell suspensions, sample enrichment, staining, acquisition and data analysis. We also include a barcoding option that reduces acquisition variability and allows the analysis of low numbers of dendritic cells, i.e., ~20,000. In contrast to other protocols, we emphasize the use of negative selection approaches to enrich for minor populations of immune cells while avoiding their activation. The entire procedure can be completed in 2-3 d and can be conveniently paused at several stages. The procedure described in this robust and reliable protocol allows the analysis of human dendritic cells in health and disease and during vaccination.
免疫系统由功能上专门化的不同细胞群体组成,可以通过质谱流式细胞术蛋白分析进行深入的特征描述。不幸的是,质谱流式细胞术的低通量特性使其难以分析少量细胞群体。树突状细胞就是这种情况,它们在组织中仅占所有免疫细胞的 0.2-2%,但却执行着启动和调节免疫反应的关键任务。在这里,我们提供了一个优化的分步协议,用于使用质谱流式细胞术对血液和组织中的已知和新兴人类树突状细胞群体进行特征描述。我们提供了详细的单细胞悬浮液制备、样品富集、染色、采集和数据分析说明。我们还包括一种条形码选项,可以减少采集的变异性,并允许分析少量的树突状细胞,即约 20,000 个细胞。与其他方案相比,我们强调使用阴性选择方法来富集少量免疫细胞,同时避免其激活。整个过程可以在 2-3 天内完成,并可以在几个阶段方便地暂停。本方案中描述的稳健可靠的程序允许在健康和疾病以及疫苗接种期间分析人类树突状细胞。