Wiemer Andrew J, Wernimont Sarah, Huttenlocher Anna
Department of Medical Microbiology and Immunology, University of Wisconsin, Madison, WI, USA.
Methods Mol Biol. 2012;757:191-204. doi: 10.1007/978-1-61779-166-6_13.
T-cell motility is critical for leukocyte trafficking both in normal host defense and in pathologic conditions including chronic inflammatory disease. Despite progress in understanding the mechanisms of T-cell polarity and motility, we have limited understanding of the mechanisms that contribute to antigen-induced T cell arrest. Here, we describe methods to analyze leukocyte function antigen-1-mediated T-cell motility and T-cell receptor-induced stop signals using in vitro assays on two-dimensional surfaces. Specifically, methods for live time-lapse imaging of T cell random migration and arrest on ICAM-1-coated surfaces are described. Additionally, we detail methods for live imaging of T-cell motility within 3D substrates to analyze T cell-antigen-presenting cell (APC) interactions and APC-mediated stop signals.
T细胞运动性对于正常宿主防御以及包括慢性炎症性疾病在内的病理状况下的白细胞迁移至关重要。尽管在理解T细胞极性和运动性机制方面取得了进展,但我们对抗原诱导的T细胞停滞机制的了解仍然有限。在此,我们描述了使用二维表面的体外测定法来分析白细胞功能抗原-1介导的T细胞运动性和T细胞受体诱导的停止信号的方法。具体而言,描述了T细胞在ICAM-1包被表面上随机迁移和停滞的实时延时成像方法。此外,我们详细介绍了在三维基质内对T细胞运动性进行实时成像以分析T细胞-抗原呈递细胞(APC)相互作用和APC介导的停止信号的方法。