Fernández-García Juan, Fendt Sarah-Maria
Laboratory of Cellular Metabolism and Metabolic Regulation, VIB Center for Cancer Biology, VIB, Leuven, Belgium.
Laboratory of Cellular Metabolism and Metabolic Regulation, Department of Oncology, Leuven Cancer Institute (LKI), KU Leuven, Leuven, Belgium.
Methods Mol Biol. 2019;1862:187-216. doi: 10.1007/978-1-4939-8769-6_14.
Immune cell function is tightly regulated by cellular metabolism, which in turn is strongly linked to the nutrient availability in the microenvironment surrounding the cells. This link is critical for effector CD8 T cells which, after activation, must migrate from nutrient-rich environments into nutrient-scarce regions such as the tumor microenvironment. Assessing how nutrient availability modulates the metabolism of effector CD8 T cells is thus key for understanding how harsh environments may impair their proliferation and effector function. Here, we describe an approach to systematically study the impact of the nutrient microenvironment on the metabolism of effector CD8 T cells, based on performing stable C isotope labeling measurements on in vitro-differentiated murine effector CD8 T cells.
免疫细胞功能受到细胞代谢的严格调控,而细胞代谢又与细胞周围微环境中的营养物质可用性密切相关。这种联系对于效应性CD8 T细胞至关重要,因为激活后的效应性CD8 T细胞必须从营养丰富的环境迁移到营养匮乏的区域,如肿瘤微环境。因此,评估营养物质可用性如何调节效应性CD8 T细胞的代谢,是理解恶劣环境如何损害其增殖和效应功能的关键。在此,我们描述了一种系统研究营养微环境对效应性CD8 T细胞代谢影响的方法,该方法基于对体外分化的小鼠效应性CD8 T细胞进行稳定碳同位素标记测量。