Jabeen Rukhsana
HB Wells Center for Pediatric Research, Indiana School of Medicine, 1044 W Walnut St., Indianapolis, IN, 46202, USA.
Methods Mol Biol. 2017;1585:155-166. doi: 10.1007/978-1-4939-6877-0_12.
Naïve CD4+ T cells differentiate into different T helper subsets in response to specific cytokine environment and transcription factors. Th9 cells are induced in response to signals from cytokines, TGF-β and IL-4. Transcription factors that are downstream of these cytokines converge to drive the development of Th9 cells. Retroviral transduction allows the genetic modification in T cells thereby helping us to better understand the molecular mechanisms that control their development as well as function. In this chapter, an optimized protocol for retroviral transduction of murine Th9 cells as well as transient transfection of Th9 cells with luciferase reporter constructs is described.
初始CD4+ T细胞会根据特定的细胞因子环境和转录因子分化为不同的辅助性T细胞亚群。Th9细胞是在细胞因子、转化生长因子-β(TGF-β)和白细胞介素-4(IL-4)的信号作用下诱导产生的。这些细胞因子下游的转录因子共同作用驱动Th9细胞的发育。逆转录病毒转导可实现T细胞的基因改造,从而帮助我们更好地理解控制其发育和功能的分子机制。在本章中,将描述一种用于小鼠Th9细胞逆转录病毒转导以及用荧光素酶报告基因构建体对Th9细胞进行瞬时转染的优化方案。