Abstract

Paneth cells at the base of small intestinal crypts secrete granules containing α-defensins in response to bacteria and maintain the intestinal environment by clearing enteric pathogens and regulating the composition of the intestinal microbiota. However, Paneth cell secretory responses remain debatable and the mechanisms that regulate the secretion are not well understood. Although enteroids, three-dimensional cultures of small intestinal epithelial cells, have proven useful for analyzing intestinal epithelial cell functions including ion transport, their closed structures have imposed limitations to investigating interactions between Paneth cells and the intestinal microbiota. Here, we report that microinjection of bacteria or lipopolysaccharide (LPS) into the enteroid lumen provides an ex vivo system for studying Paneth cell secretion in real-time. The results show that Paneth cells released granules immediately when the apical surfaces of enteroid epithelial cells were exposed to LPS or live bacteria by microinjection. However, Paneth cells did not respond to LPS delivered in culture media to enteroid exterior basolateral surface, although they responded to basolateral carbamyl choline. In addition, Paneth cells replenished their granules after secretion, enabling responses to second stimulation. These findings provide new insight for apically-induced Paneth cell secretory responses in regulating the intestinal environment.

Highlights

  • Paneth cells at the base of small intestinal crypts secrete granules containing α-defensins in response to bacteria and maintain the intestinal environment by clearing enteric pathogens and regulating the composition of the intestinal microbiota

  • Epithelial cells that line the small intestine form a barrier consisting of intestinal epithelial stem cells (ISCs) and four major lineages of differentiated cells, including absorptive enterocytes, enteroendocrine cells, goblet cells, and Paneth cells that are oriented along the villus-crypt axis[5]

  • The ileal microbiota of matrix metalloproteinase 7-null (Mmp7−/−) mice, which are deficient in activated luminal α-defensins, had a significantly greater percentage of Firmicutes and fewer Bacteroidetes compared to wild-type control mice20. α-Defensins secreted into the small intestinal lumen have been recovered as intact, functional forms in the lumen of large intestine[21,22]

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Summary

Introduction

Paneth cells at the base of small intestinal crypts secrete granules containing α-defensins in response to bacteria and maintain the intestinal environment by clearing enteric pathogens and regulating the composition of the intestinal microbiota. The results show that Paneth cells released granules immediately when the apical surfaces of enteroid epithelial cells were exposed to LPS or live bacteria by microinjection. Paneth cells, which occupy the base of small intestinal crypts with Lgr5+ ISCs, contribute to innate enteric immunity by releasing secretory granules rich in varied host defense peptides, e.g., α-defensins, in response to bacteria and bacterial antigens such as lipopolysaccharide (LPS)[6,7,8,9].

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