LGR5型
干细胞
生物
细胞生物学
Wnt信号通路
地穴
转录因子
潘尼斯电池
免疫系统
肠上皮
造血
免疫学
信号转导
上皮
癌症干细胞
基因
遗传学
小肠
生物化学
内分泌学
作者
Pingping Zhu,Xiaoxiao Zhu,Jiayi Wu,Luyun He,Tiankun Lu,Yanying Wang,Benyu Liu,Buqing Ye,Lei Sun,Dongdong Fan,Jing Wang,Liuliu Yang,Xiwen Qin,Ying Du,Chong Li,Lei He,Weizheng Ren,Xin Wu,Yong Tian,Zusen Fan
标识
DOI:10.1038/s41590-018-0297-6
摘要
Intestinal stem cells (ISCs) are maintained by stemness signaling for precise modulation of self-renewal and differentiation under homeostasis. However, the way in which intestinal immune cells regulate the self-renewal of ISCs remains elusive. Here we found that mouse and human Lgr5+ ISCs showed high expression of the immune cell-associated circular RNA circPan3 (originating from the Pan3 gene transcript). Deletion of circPan3 in Lgr5+ ISCs impaired their self-renewal capacity and the regeneration of gut epithelium in a manner dependent on immune cells. circPan3 bound mRNA encoding the cytokine IL-13 receptor subunit IL-13Rα1 (Il13ra1) in ISCs to increase its stability, which led to the expression of IL-13Rα1 in ISCs. IL-13 produced by group 2 innate lymphoid cells in the crypt niche engaged IL-13Rα1 on crypt ISCs and activated signaling mediated by IL-13‒IL-13R, which in turn initiated expression of the transcription factor Foxp1. Foxp1 is associated with β-catenin in rendering its nuclear translocation, which caused activation of the β-catenin pathway and the maintenance of Lgr5+ ISCs.
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