效应器
生物
T辅助细胞
细胞生物学
免疫系统
细胞分化
T细胞
体外
免疫学
获得性免疫系统
遗传学
基因
作者
Kaitlin A. Read,Michael D. Powell,Bharath Sreekumar,Kenneth J. Oestreich
出处
期刊:Methods in molecular biology
日期:2019-01-01
卷期号:: 75-84
被引量:36
标识
DOI:10.1007/978-1-4939-9167-9_6
摘要
CD4+ T “helper” cells are key orchestrators of adaptive immune responses. Upon activation, naïve CD4+ T cells are capable of differentiating into a number of effector subsets that perform distinct immune functions. These subsets include T helper 1 (TH1), TH2, TH9, TH17, TH22, T follicular helper (TFH), and regulatory T cell (TREG) populations. The differentiation of these subsets is dependent, in large part, on the coordinated interplay between signals from the extracellular cytokine environment and downstream transcriptional networks. The use of in vitro T helper cell culture systems has been extensively employed to aid in the elucidation of the molecular mechanisms that govern the differentiation of each effector subset. Here, we provide a detailed summary of the differentiation conditions that are utilized to generate effector CD4+ T cell populations in vitro.
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