Pham Duy
Department of Pathology, University of Alabama at Birmingham, BBRB 870, 845 19th St South, Birmingham, AL, 35294, USA.
Methods Mol Biol. 2017;1585:51-57. doi: 10.1007/978-1-4939-6877-0_4.
CD4 T helper cells with the ability to produce effector cytokines provide host protection by regulating immune responses against pathogens. In contrast, these cells are responsible for the development of various inflammatory disease if not regulated properly. Previous studies using naïve CD4 T cell activation in vitro have shown the requirement of various cytokine combinations in addition to TCR activation to differentiate naïve CD4 T cells into various effector T helper lineages. The recently discovered CD4 T helper subset is IL-9-producing Th9 cells. Since Th9 cell differentiation in vitro is essential in understanding the molecular mechanism in regulating Th9 cell development, it is critical to develop a basic protocol in polarizing naïve CD4 T cells to Th9 cells in vitro. Here we describe a simple method for Th9 cell culture conditions in vitro that can be used for other molecular analyses.
具有产生效应细胞因子能力的CD4辅助性T细胞通过调节针对病原体的免疫反应为宿主提供保护。相比之下,如果调节不当,这些细胞会导致各种炎症性疾病的发生。先前在体外使用初始CD4 T细胞激活的研究表明,除了TCR激活外,还需要各种细胞因子组合才能将初始CD4 T细胞分化为各种效应性辅助性T细胞谱系。最近发现的CD4辅助性T细胞亚群是产生IL-9的Th9细胞。由于体外Th9细胞分化对于理解调节Th9细胞发育的分子机制至关重要,因此制定一个将初始CD4 T细胞体外极化为Th9细胞的基本方案至关重要。在此,我们描述了一种用于体外Th9细胞培养条件的简单方法,该方法可用于其他分子分析。