State Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural University, Beijing, China.
Central Laboratory, School of Stomatology, Peking University, Beijing, China.
Front Immunol. 2021 Nov 30;12:791220. doi: 10.3389/fimmu.2021.791220. eCollection 2021.
T cell factor 1 (Tcf1) is known as a critical mediator for natural killer (NK) cell development and terminal maturation. However, its essential targets and precise mechanisms involved in early NK progenitors (NKP) are not well clarified. To investigate the role of Tcf1 in NK cells at distinct developmental phases, we employed three kinds of genetic mouse models, namely, , and mice, respectively. Similar to Tcf1 germline knockout mice, we found notably diminished cell number and defective development in BM NK cells from all strains. In contrast, mice exhibited modest defects in splenic NK cells compared with those in the other two strains. By analyzing the published ATAC-seq and ChIP-seq data, we found that Tcf1 directly targeted 110 NK cell-related genes which displayed differential accessibility in the absence of Tcf1. Along with this clue, we further confirmed that a series of essential regulators were expressed aberrantly in distinct BM NK subsets with conditional ablating Tcf1 at NKP stage. , , , , , , , , , , , and were downregulated, whereas and were upregulated in distinct NK subsets due to Tcf1 deficiency. The dysregulation of these genes jointly caused severe defects in NK cells lacking Tcf1. Thus, our study identified essential targets of Tcf1 in NK cells, providing new insights into Tcf1-dependent regulatory programs in step-wise governing NK cell development.
T 细胞因子 1(Tcf1)是自然杀伤(NK)细胞发育和终末成熟的关键介质。然而,其在早期 NK 祖细胞(NKP)中涉及的关键靶标和精确机制尚不清楚。为了研究 Tcf1 在不同发育阶段 NK 细胞中的作用,我们分别使用了三种遗传小鼠模型,即 、 和 小鼠。与 Tcf1 生殖系敲除小鼠相似,我们发现所有三种品系的 BM NK 细胞数量明显减少,发育缺陷。相比之下,与其他两种品系相比, 小鼠的脾 NK 细胞缺陷程度较小。通过分析已发表的 ATAC-seq 和 ChIP-seq 数据,我们发现 Tcf1 直接靶向 110 个与 NK 细胞相关的基因,这些基因在缺乏 Tcf1 时显示出不同的可及性。根据这一线索,我们进一步证实,在 NKP 阶段条件性敲除 Tcf1 后,一系列必需的调节因子在不同的 BM NK 亚群中表达异常。由于 Tcf1 缺乏, 、 、 、 、 、 、 、 、 、 和 下调,而 和 上调。由于缺乏 Tcf1,这些基因的失调共同导致 NK 细胞严重缺陷。因此,我们的研究鉴定了 Tcf1 在 NK 细胞中的关键靶标,为 Tcf1 依赖性调控程序在逐步调控 NK 细胞发育方面提供了新的见解。