效应器
斯达
细胞生物学
鉴定(生物学)
JAK-STAT信号通路
免疫学
生物
信号转导
车站3
酪氨酸激酶
植物
作者
Songyang Li,Yongjie Liu,Xiaofeng Yin,Yang Yao,Xinjia Liu,Jingyi Qiu,Qinglan Yang,Yana Li,Zhiguo Tan,Hongyan Peng,Peiwen Xiong,Shuting Wu,Lanlan Huang,Xiangyu Wang,Sulai Liu,Yuxing Gong,Yuan Gao,Lingling Zhang,Junping Wang,Yafei Deng
标识
DOI:10.1016/j.apsb.2025.02.034
摘要
The Janus kinase/signal transducers and activators of transcription (JAK-STAT) control natural killer (NK) cells development and cytotoxic functions, however, whether long non-coding RNAs (lncRNAs) are involved in this pathway remains unknown. We found that miR155HG was elevated in activated NK cells and promoted their proliferation and effector functions in both NK92 and induced-pluripotent stem cells (iPSCs)-derived NK (iPSC-NK) cells, without reliance on its derived miR-155 and micropeptide P155. Mechanistically, miR155HG bound to miR-6756 and relieved its repression of JAK3 expression, thereby promoting the JAK-STAT pathway and enhancing NK cell proliferation and function. Further investigations disclosed that upon cytokine stimulation, STAT3 directly interacts with miR155HG promoter and induces miR155HG transcription. Collectively, we identify a miR155HG-mediated positive feedback loop of the JAK-STAT signaling. Our study will also provide a power target regarding miR155HG for improving NK cell generation and effector function in the field of NK cell adoptive transfer therapy against cancer, especially iPSC-derived NK cells.
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