Freen-van Heeren Julian J, Nicolet Benoit P, Wolkers Monika C
Department of Hematopoiesis, Sanquin Research-AMC Landsteiner Laboratory, Amsterdam, The Netherlands.
Crit Rev Immunol. 2018;38(2):131-143. doi: 10.1615/CritRevImmunol.2018025938.
T cells produce a wide variety of effector molecules in response to infections, such as cytokines, chemokines, granzymes, and perforins. Because different stimuli promote the production of specific effector molecules, T cell responses come in different flavors. In addition, single-cell analysis of protein production revealed that T cells respond heterogeneously to activation. To unravel the regulatory mechanisms that determine T cell effector function, novel methods were developed that simultaneously measure protein levels with the corresponding mRNA. These flow cytometry-based fluorescence in situ hybridization (Flow-FISH) technologies allow for multiparameter analysis with single-cell resolution of both nucleic acids and proteins. Here, we review the currently available methods of Flow-FISH and describe the possible applications thereof, with a specific focus on T cells.
T细胞在应对感染时会产生多种效应分子,如细胞因子、趋化因子、颗粒酶和穿孔素。由于不同的刺激会促进特定效应分子的产生,T细胞反应具有不同的类型。此外,对蛋白质产生的单细胞分析表明,T细胞对激活的反应具有异质性。为了阐明决定T细胞效应功能的调控机制,人们开发了新的方法,能够同时测量蛋白质水平和相应的mRNA。这些基于流式细胞术的荧光原位杂交(Flow-FISH)技术允许对核酸和蛋白质进行单细胞分辨率的多参数分析。在这里,我们综述了目前可用的Flow-FISH方法,并描述了其可能的应用,特别关注T细胞。