Lactobacillus accelerates ISCs regeneration to protect the integrity of intestinal mucosa through activation of STAT3 signaling pathway induced by LPLs secretion of IL-22

被引:331
作者
Hou, Qihang [1 ]
Ye, Lulu [1 ]
Liu, Haofei [1 ]
Huang, Lulu [1 ]
Yang, Qian [1 ]
Turner, J. R. [2 ,3 ,4 ]
Yu, Qinghua [1 ]
机构
[1] Nanjing Agr Univ, Coll Vet Med, MOE Joint Int Res Lab Anim Hlth & Food Safety, Weigang 1, Nanjing 210095, Jiangsu, Peoples R China
[2] Univ Chicago, Dept Pathol, 5841 S Maryland Ave, Chicago, IL 60637 USA
[3] Brigham & Womens Hosp, Dept Pathol, 75 Francis St, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Dept Med, Div Gastroenterol Hepatol & Endoscopy, 75 Francis St, Boston, MA 02115 USA
基金
中国国家自然科学基金;
关键词
INFLAMMATORY-BOWEL-DISEASE; STEM-CELLS; GUT MICROBIOTA; ORGANOIDS; RECEPTOR; HEALTH; STRAIN; COLON;
D O I
10.1038/s41418-018-0070-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The regeneration of intestinal epithelial are maintained by continuous differentiation and proliferation of intestinal stem cells (ISCs) under physiological and pathological conditions. However, little is known about the regulatory effect of intestinal microbiota on its recovery ability to repair damaged mucosal barrier. In this study, we established intestinal organoids and lamina propria lymphocytes (LPLs) co-cultured system, plus mice experiments, to explore the protective effect of Lactobacillus reuteri D8 on integrity of intestinal mucosa. We found that only live L. reuteri D8 was effective in protecting the morphology of intestinal organoids and normal proliferation of epithelial stained with EdU under TNF-alpha treatment, which was also further verified in mice experiments. L. reuteri D8 colonized in the intestinal mucosa and ameliorated intestinal mucosa damage caused by DSS treatment, including improvement of body weight, colon length, pathological change, and proliferation level. The repair process stimulated by L. reuteri D8 was also accompanied with increased numbers of Lgr5(+) and lysozyme(+) cells both in intestinal organoids and mice intestine. Furthermore, we demonstrated that D8 metabolite indole-3-aldehyde stimulated LPLs to secret IL-22 through aryl hydrocarbon receptor (AhR) and then induced phosphorylation of STAT3 to accelerate proliferation of intestinal epithelial, thus recovering damaged intestinal mucosa. Our findings indicate L. reuteri protects intestinal barrier and activates intestinal epithelial proliferation, which sheds light on treatment approaches for intestinal inflammation based on ISCs with probiotics Lactobacillus and daily probiotic consumption in heath foods.
引用
收藏
页码:1657 / 1670
页数:14
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