Fralin Biomedical Research Institute, Virginia Tech Carilion, Roanoke, VA, United States.
Translational Biology, Medicine, and Health Graduate Program, Virginia Tech, Blacksburg, VA, United States.
Front Immunol. 2019 Jun 6;10:1299. doi: 10.3389/fimmu.2019.01299. eCollection 2019.
CD4 T helper cells are capable of differentiating into a number of effector subsets that perform diverse functions during adaptive immune responses. The differentiation of each of these subsets is governed, in large part, by environmental cytokine signals and the subsequent activation of downstream, cell-intrinsic transcription factor networks. Ikaros zinc finger (IkZF) transcription factors are known regulators of immune cell development, including that of CD4 T cell subsets. Over the past decade, members of the IkZF family have also been implicated in the differentiation and function of individual T helper cell subsets, including T helper 1 (T1), T2, T17, T follicular (T), and T regulatory (T) cells. Now, an increasing body of literature suggests that the distinct cell-specific cytokine environments responsible for the development of each subset result in differential expression of IkZF factors across T helper populations. Intriguingly, recent studies suggest that IkZF members influence T helper subset differentiation in a feed-forward fashion through the regulation of these same cytokine-signaling pathways. Here, we review the increasingly prominent role for IkZF transcription factors in the differentiation of effector CD4 T helper cell subsets.
CD4 T 辅助细胞能够分化为许多效应亚群,在适应性免疫反应中发挥不同的功能。这些亚群的分化在很大程度上受到环境细胞因子信号和随后的下游细胞内转录因子网络的激活的控制。Ikaros 锌指 (IkZF) 转录因子是免疫细胞发育的已知调节剂,包括 CD4 T 细胞亚群的发育。在过去的十年中,IkZF 家族的成员也被牵连到个别 T 辅助细胞亚群的分化和功能中,包括 T 辅助 1(T1)、T2、T17、滤泡 T(T)和 T 调节(T)细胞。现在,越来越多的文献表明,负责每个亚群发育的不同细胞特异性细胞因子环境导致 IkZF 因子在 T 辅助群体中的差异表达。有趣的是,最近的研究表明,IkZF 成员通过调节这些相同的细胞因子信号通路以正反馈的方式影响 T 辅助亚群分化。在这里,我们回顾了 IkZF 转录因子在效应 CD4 T 辅助细胞亚群分化中的作用越来越突出。