| Literature DB >> 28273482 |
Malini Ahuja1, Daniella M Schwartz2, Mayank Tandon1, Aran Son1, Mei Zeng1, William Swaim1, Michael Eckhaus3, Victoria Hoffman3, Yiyuan Cui4, Bo Xiao4, Paul F Worley5, Shmuel Muallem6.
Abstract
The gut microbiome participates in numerous physiologic functions and communicates intimately with the host immune system. Antimicrobial peptides are critical components of intestinal innate immunity. We report a prominent role for antimicrobials secreted by pancreatic acini in shaping the gut microbiome that is essential for intestinal innate immunity, barrier function, and survival. Deletion of the Ca2+ channel Orai1 in pancreatic acini of adult mice resulted in 60%-70% mortality within 3 weeks. Despite robust activation of the intestinal innate immune response, mice lacking acinar Orai1 exhibited intestinal bacterial outgrowth and dysbiosis, ultimately causing systemic translocation, inflammation, and death. While digestive enzyme supplementation was ineffective, treatments constraining bacterial outgrowth (purified liquid diet, broad-spectrum antibiotics) rescued survival, feeding, and weight gain. Pancreatic levels of cathelicidin-related antimicrobial peptide (CRAMP) were reduced, and supplement of synthetic CRAMP prevented intestinal disease. These findings reveal a critical role for antimicrobial pancreatic secretion in gut innate immunity. Published by Elsevier Inc.Entities:
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Year: 2017 PMID: 28273482 PMCID: PMC5345693 DOI: 10.1016/j.cmet.2017.02.007
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287