Baxter Laboratory in Stem Cell Biology, Department of Microbiology and Immunology, Stanford University, Stanford, CA 94305, USA.
Trends Immunol. 2012 Jul;33(7):323-32. doi: 10.1016/j.it.2012.02.010. Epub 2012 Apr 2.
In recent years, advances in technology have provided us with tools to quantify the expression of multiple genes in individual cells. The ability to measure simultaneously multiple genes in the same cell is necessary to resolve the great diversity of cell subsets, as well as to define their function in the host. Fluorescence-based flow cytometry is the benchmark for this; with it, we can quantify 18 proteins per cell, at >10 000 cells/s. Mass cytometry is a new technology that promises to extend these capabilities significantly. Immunophenotyping by mass spectrometry provides the ability to measure >36 proteins at a rate of 1000 cells/s. We review these cytometric technologies, capable of high-content, high-throughput single-cell assays.
近年来,技术的进步为我们提供了工具,可用于定量测定单个细胞中多个基因的表达。能够同时测量同一细胞中的多个基因,对于解析细胞亚群的巨大多样性以及确定它们在宿主中的功能是必要的。基于荧光的流式细胞术是这方面的基准;通过它,我们可以每细胞定量 18 种蛋白质,速度超过 10000 个细胞/秒。质谱流式细胞术是一种新技术,有望显著扩展这些能力。通过质谱进行免疫表型分析可以以 1000 个细胞/秒的速度测量超过 36 种蛋白质。我们综述了这些可进行高通量、高内涵单细胞分析的细胞测量技术。