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分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

Lepr+间充质细胞通过Leptin-Igf1轴感知饮食调控肠道干细胞/祖细胞的研究

Lepr+ mesenchymal cells sense diet to modulate intestinal stem/progenitor cells via Leptin–Igf1 axis

Deng Min, Guerrero-Juarez Christian F., Sheng Xiaole, Xu Jiuzhi, Wu Xi, Yao Kai, Li Mengzhen, Yang Xu, Li Guilin, Xiao Jintao, Liu Xiaowei, Wu Kaichun, Ren Fazheng, Nie Qing, Plikus Maksim V., Yu Zhe

Journal:CELL RESEARCH

IF:46.3

DOI:10.1038/s41422-022-00643-9

PMID:35296796

Published:2022-03-16

research field:分子生物学药理学内分泌学自身免疫性疾病

Abstract

Diet can impact on gut health and disease by modulating intestinal stem cells (ISCs). However, it is largely unknown if and how the ISC niche responds to diet and influences ISC function. Here, we demonstrate that Lepr + mesenchymal cells (MCs) surrounding intestinal crypts sense diet change and provide a novel niche signal to maintain ISC and progenitor cell proliferation. The abundance of these MCs increases upon administration of a high-fat diet (HFD) but dramatically decreases upon fasting. Depletion of Lepr + MCs resulted in fewer intestinal stem/progenitor cells, compromised the architecture of crypt–villus axis and impaired intestinal regeneration. Furthermore, we showed that IGF1 secreted by Lepr + MCs is an important effector that promotes proliferation of ISCs and progenitor cells in the intestinal crypt. We conclude that Lepr + MCs sense diet alterations and, in turn, modulate intestinal stem/progenitor cell function via a stromal IGF1–epithelial IGF1R axis. These findings reveal that Lepr + MCs are important mediators linking systemic diet changes to local ISC function and might serve as a novel therapeutic target for gut diseases.

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