| Literature DB >> 30643264 |
Pingping Zhu1, Xiaoxiao Zhu2, Jiayi Wu1,3, Luyun He1,3, Tiankun Lu1,3, Yanying Wang1, Benyu Liu1, Buqing Ye1, Lei Sun4, Dongdong Fan2, Jing Wang1,3, Liuliu Yang1,3, Xiwen Qin1,3, Ying Du1, Chong Li1, Lei He5, Weizheng Ren5, Xin Wu6, Yong Tian7,8, Zusen Fan9,10.
Abstract
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.Entities:
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Year: 2019 PMID: 30643264 DOI: 10.1038/s41590-018-0297-6
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606