细胞生物学
再生(生物学)
生物
免疫学
信号转导
上皮
肠粘膜
医学
内科学
遗传学
作者
Christian Cox,Elaine E. Storm,Varun N. Kapoor,Joseph Chavarría‐Smith,David L. Lin,Lifen Wang,Yun Li,Noelyn M. Kljavin,Naruhisa Ota,Travis W. Bainbridge,Keith R. Anderson,Merone Roose‐Girma,Søren Warming,Joseph R. Arron,Shannon J. Turley,Frédéric J. de Sauvage,Menno van Lookeren Campagne
出处
期刊:Science immunology
[American Association for the Advancement of Science (AAAS)]
日期:2021-05-07
卷期号:6 (59)
被引量:37
标识
DOI:10.1126/sciimmunol.abe8856
摘要
Repair of the intestinal epithelium is tightly regulated to maintain homeostasis. The response after epithelial damage needs to be local and proportional to the insult. How different types of damage are coupled to repair remains incompletely understood. We report that after distinct types of intestinal epithelial damage, IL-1R1 signaling in GREM1+ mesenchymal cells increases production of R-spondin 3 (RSPO3), a Wnt agonist required for intestinal stem cell self-renewal. In parallel, IL-1R1 signaling regulates IL-22 production by innate lymphoid cells and promotes epithelial hyperplasia and regeneration. Although the regulation of both RSPO3 and IL-22 is critical for epithelial recovery from Citrobacter rodentium infection, IL-1R1-dependent RSPO3 production by GREM1+ mesenchymal cells alone is sufficient and required for recovery after dextran sulfate sodium-induced colitis. These data demonstrate how IL-1R1-dependent signaling orchestrates distinct repair programs tailored to the type of injury sustained that are required to restore intestinal epithelial barrier function.
科研通智能强力驱动
Strongly Powered by AbleSci AI