Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Los Angeles, CA 91010, USA.
Hematologic Malignancies Research Institute, City of Hope National Medical Center, Los Angeles, CA 91010, USA.
Sci Immunol. 2023 Mar 17;8(81):eabn7993. doi: 10.1126/sciimmunol.abn7993. Epub 2023 Mar 10.
Spliced X-box-binding protein 1 (XBP1s) is an essential transcription factor downstream of interleukin-15 (IL-15) and AKT signaling, which controls cell survival and effector functions of human natural killer (NK) cells. However, the precise mechanisms, especially the downstream targets of XBP1s, remain unknown. In this study, by using XBP1 conditional knockout mice, we found that XBP1s is critical for IL-15-mediated NK cell survival but not proliferation in vitro and in vivo. Mechanistically, XBP1s regulates homeostatic NK cell survival by targeting PIM-2, a critical anti-apoptotic gene, which in turn stabilizes XBP1s protein by phosphorylating it at Thr. In addition, XBP1s enhances the effector functions and antitumor immunity of NK cells by recruiting T-bet to the promoter region of . Collectively, our findings identify a previously unknown mechanism by which IL-15-XBP1s signaling regulates the survival and effector functions of NK cells.
spliced X-box-binding protein 1 (XBP1s) 是白细胞介素-15 (IL-15) 和 AKT 信号下游的一个重要转录因子,它控制着人类自然杀伤 (NK) 细胞的存活和效应功能。然而,确切的机制,特别是 XBP1s 的下游靶点,仍然未知。在这项研究中,我们通过使用 XBP1 条件性敲除小鼠发现,XBP1s 对于 IL-15 介导的 NK 细胞存活是至关重要的,但对于体外和体内的 NK 细胞增殖则不是。从机制上讲,XBP1s 通过靶向 PIM-2(一种关键的抗凋亡基因)来调节 NK 细胞的稳态存活,PIM-2 通过在 Thr 位点对其进行磷酸化来稳定 XBP1s 蛋白。此外,XBP1s 通过将 T-bet 招募到 的启动子区域,增强 NK 细胞的效应功能和抗肿瘤免疫。总之,我们的研究结果确定了一个以前未知的机制,即 IL-15-XBP1s 信号通路调节 NK 细胞的存活和效应功能。