IL-13 secreted by ILC2s promotes the self-renewal of intestinal stem cells through circular RNA circPan3

被引:175
|
作者
Zhu, Pingping [1 ]
Zhu, Xiaoxiao [2 ]
Wu, Jiayi [1 ,3 ]
He, Luyun [1 ,3 ]
Lu, Tiankun [1 ,3 ]
Wang, Yanying [1 ]
Liu, Benyu [1 ]
Ye, Buqing [1 ]
Sun, Lei [4 ]
Fan, Dongdong [2 ]
Wang, Jing [1 ,3 ]
Yang, Liuliu [1 ,3 ]
Qin, Xiwen [1 ,3 ]
Du, Ying [1 ]
Li, Chong [1 ]
He, Lei [5 ]
Ren, Weizheng [5 ]
Wu, Xin [6 ]
Tian, Yong [2 ,3 ]
Fan, Zusen [1 ,3 ]
机构
[1] Chinese Acad Sci, Inst Biophys, CAS Ctr Excellence Biomacromol, CAS Key Lab Infect & Immun, Beijing, Peoples R China
[2] Chinese Acad Sci, Inst Biophys, CAS Key Lab RNA Biol, Beijing, Peoples R China
[3] Univ Chinese Acad Sci, Beijing, Peoples R China
[4] Chinese Acad Sci, Inst Biophys, Ctr Biol Imaging, Beijing, Peoples R China
[5] Peoples Liberat Army Gen Hosp, Dept Hepatobiliary Surg, Beijing, Peoples R China
[6] Peoples Liberat Army Gen Hosp, Dept Gen Surg, Beijing, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
IN-VITRO; RECEPTOR; TRANSLATION; BIOGENESIS; EXPANSION; MARKER; ROLES; COLON; CRYPT;
D O I
10.1038/s41590-018-0297-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
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-13R alpha 1 (Il13r alpha 1) in ISCs to increase its stability, which led to the expression of IL-13R alpha 1 in ISCs. IL-13 produced by group 2 innate lymphoid cells in the crypt niche engaged IL-13R alpha 1 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 beta-catenin in rendering its nuclear translocation, which caused activation of the beta-catenin pathway and the maintenance of Lgr5(+) ISCs.
引用
收藏
页码:183 / +
页数:18
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