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Gut Microbial Metabolite Pravastatin Attenuates Intestinal Ischemia/Reperfusion Injury Through Promoting IL-13 Release From Type II Innate Lymphoid Cells via IL-33/ST2 Signaling.
- Source :
-
Frontiers in immunology [Front Immunol] 2021 Sep 28; Vol. 12, pp. 704836. Date of Electronic Publication: 2021 Sep 28 (Print Publication: 2021). - Publication Year :
- 2021
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Abstract
- Intestinal ischemia/reperfusion (I/R) injury is a grave condition with high morbidity and mortality. We previously confirmed that intestinal I/R induces intestinal flora disorders and changes in metabolites, but the role of different metabolites in intestinal I/R injury is currently unclear. Based on targeted metabolic sequencing, pravastatin (PA) was determined to be a metabolite of the gut microbiota. Further, intestinal I/R model mice were established through superior mesenteric artery obstruction. In addition, a co-culture model of small intestinal organoids and type II innate lymphoid cells (ILC2s) was subjected to hypoxia/reoxygenation (H/R) to simulate an intestinal I/R model. Moreover, correlation analysis between the PA level in preoperative feces of patients undergoing cardiopulmonary bypass and the indices of postoperative intestinal I/R injury was carried out. IL-33-deficient mice, ILC2-deleted mice, and anti-IL-13 neutralizing antibodies were also used to explore the potential mechanism through which PA attenuates intestinal I/R injury. We demonstrated that PA levels in the preoperative stool of patients undergoing cardiopulmonary bypass were negatively correlated with the indices of postoperative intestinal I/R injury. Furthermore, PA alleviated intestinal I/R injury and improved the survival of mice. We further showed that PA promotes IL-13 release from ILC2s by activating IL-33/ST2 signaling to attenuate intestinal I/R injury. In addition, IL-13 promoted the self-renewal of intestinal stem cells by activating Notch1 and Wnt signals. Overall, results indicated that the gut microbial metabolite PA can attenuate intestinal I/R injury by promoting the release of IL-13 from ILC2s via IL-33/ST2 signaling, revealing a novel mechanism of and therapeutic strategy for intestinal I/R injury.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Deng, Hu, Yang, Sun, Lin, Zhao, Yao, Luo, Chen, Liu, Yan, Li, Liu and Liu.)
- Subjects :
- Animals
Disease Models, Animal
Humans
Interleukin-1 Receptor-Like 1 Protein genetics
Interleukin-13 genetics
Interleukin-33 genetics
Intestinal Diseases genetics
Male
Mice
Mice, Knockout
Reperfusion Injury
Gastrointestinal Microbiome immunology
Immunity, Innate
Interleukin-1 Receptor-Like 1 Protein immunology
Interleukin-13 immunology
Interleukin-33 immunology
Intestinal Diseases immunology
Lymphocytes immunology
Pravastatin immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1664-3224
- Volume :
- 12
- Database :
- MEDLINE
- Journal :
- Frontiers in immunology
- Publication Type :
- Academic Journal
- Accession number :
- 34650552
- Full Text :
- https://doi.org/10.3389/fimmu.2021.704836