İzmir International Biomedicine and Genome Institute (iBG-izmir), Dokuz Eylül University (DEU), İzmir, Turkey.
İzmir Biomedicine and Genome Center (IBG), İzmir, Turkey.
J Leukoc Biol. 2021 May;109(5):901-914. doi: 10.1002/JLB.2A0520-321RR. Epub 2020 Nov 4.
IL2 receptor signaling is crucial for human NK cell activation and gain of effector functions. The molecular mechanisms involved in termination of IL2 activation are largely unknown in human NK cells. PR/SET domain 1 was previously reported to decrease cell growth and increase apoptosis in an IL2-dependent manner in malignant NK cell lines, suggesting the possibility of down-regulation of IL2 signaling pathway gene(s) through direct transcriptional repression. Using ChIP-Seq, we identified a PRDM1 binding site on the first intron of CD25 (IL2RA), which codes for the IL2 receptor subunit regulating sensitivity to IL2 signaling, in primary NK cells activated with engineered K562 cells or IL2. Ectopic expression of PRDM1 down-regulated CD25 expression at transcript and protein levels in two PRDM1 nonexpressing NK cell lines. shRNA-mediated knockdown of CD25 in two malignant NK cell lines led to progressive depletion of NK cells in low IL2 concentrations. By contrast, ectopic CD25 expression in primary human NK cells led to progressive increase in cell number in CD25-transduced cells in low IL2 concentrations. Altogether these results reveal a pivotal role of PRDM1 in inhibition of IL2-induced NK cell expansion through direct repression of CD25 in activated human NK cells. These observations provide additional support for the role of PRDM1 in attenuation of NK cell activation and growth, with implications on neoplastic transformation or NK cell function when it is deregulated.
IL2 受体信号对于人类自然杀伤 (NK) 细胞的激活和获得效应功能至关重要。在人类 NK 细胞中,终止 IL2 激活的分子机制在很大程度上尚不清楚。先前有报道称,PR/SET 结构域蛋白 1(PRDM1)以 IL2 依赖的方式降低恶性 NK 细胞系中的细胞生长并增加细胞凋亡,这表明通过直接转录抑制下调 IL2 信号通路基因的可能性。使用 ChIP-Seq,我们在原发性 NK 细胞中鉴定到一个位于 CD25(IL2RA)第一个内含子上的 PRDM1 结合位点,CD25 编码调节对 IL2 信号敏感性的 IL2 受体亚基,该结合位点在经工程化 K562 细胞或 IL2 激活的 NK 细胞中被识别到。在两个不表达 PRDM1 的 NK 细胞系中,异位表达 PRDM1 可在转录和蛋白水平下调 CD25 的表达。在两种恶性 NK 细胞系中,通过 shRNA 介导的 CD25 敲低导致在低 IL2 浓度下 NK 细胞逐渐耗竭。相比之下,在原发性人 NK 细胞中异位表达 CD25 导致在低 IL2 浓度下转导细胞的细胞数量逐渐增加。综上所述,这些结果揭示了 PRDM1 通过直接抑制激活的人类 NK 细胞中的 CD25 在抑制 IL2 诱导的 NK 细胞扩增中的关键作用。这些观察结果为 PRDM1 在衰减 NK 细胞激活和生长中的作用提供了额外的支持,当它失调时,这可能对 NK 细胞的肿瘤转化或功能产生影响。