Paneth Cells Protect against Acute Pancreatitis via Modulating Gut Microbiota Dysbiosis

• Published in: mSystems Vol. 7; no. 3; p. e0150721
• Main Authors: Fu, Yang, Mei, Qixiang, Yin, Nuoming, Huang, Zehua, Li, Baiwen, Luo, Shengzheng, Xu, Binqiang, Fan, Junjie, Huang, Chunlan, Zeng, Yue
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 28.06.2022
• Subjects: Acute Disease; acute pancreatitis; Animals; Clinical Microbiology; Dysbiosis - metabolism; Gastrointestinal Microbiome - physiology; gut microbiota; intestinal enteroid; lysozyme; Mice; Muramidase - metabolism; Pancreatitis - metabolism; Paneth cell; Paneth Cells - metabolism; Research Article; RNA, Ribosomal, 16S - metabolism; Paneth cell; lysozyme; gut microbiota; intestinal enteroid; acute pancreatitis
• ISSN: 2379-5077; 2379-5077
• DOI: 10.1128/msystems.01507-21

Acute pancreatitis (AP) is usually accompanied by intestinal failure, but its mechanism is still unclear. In AP patients, the functions of Paneth cells (lysozyme, HD5, Reg3γ, and Wnt3a) decreased. Compared with AP mice, injuries and inflammation of the pancreas and ileum were aggravated in AP mice treated with dithizone (Dith) (Dith+AP mice). Intestinal permeability and bacterial translocation were also increased. 16S rRNA sequencing showed that the gut microbiota of Dith mice and Dith+AP mice exhibited a marked increase in the pathogenic bacterium and a significant decrease in the probiotic bacterium . Lysozyme gavage in Dith+AP mice effectively alleviated injuries of the pancreas and small intestine. The beneficial effect of lysozyme was associated with a significant increase in the probiotic bacterium and a virtual absence of the pathogenic bacterium . The severity of AP in antibiotic-treated mice (ABX mice) was significantly aggravated when receiving feces from Dith mice and was markedly alleviated when receiving feces from lysozyme-gavaged mice. , lysozyme increased the proliferation of enteroids by promoting the activation of the Wnt pathway and Lgr5 expression in intestinal stem cells. We demonstrate that AP patients and experimental AP mice exhibited a dysfunction of Paneth cells. Our research showed that the severity of AP was exacerbated by the long-term dysfunction of Paneth cells, which was associated with gut microbiota disorder. Restoring part of Paneth cell functions through lysozyme supplementation alleviated the severity of AP and gut microbiota dysbiosis. This study provides novel insight into the link of pancreas-gut interactions in the pathogenesis of AP, providing a new direction for the clinical treatment of intestinal complications during AP.