Innate Immunity Laboratory, Graduate School of Life Science, Hokkaido University, Kita-21, Nishi-11, Kita-ku, Sapporo, Hokkaido, 001-0021, Japan.
Department of Cell Biological Science, Faculty of Advanced Life Science, Hokkaido University, Kita-21, Nishi-11, Kita-ku, Sapporo, Hokkaido, 001-0021, Japan.
Sci Rep. 2019 Feb 25;9(1):2710. doi: 10.1038/s41598-019-39610-7.
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.
潘氏细胞位于小肠隐窝的底部,在受到细菌刺激时会分泌含有α-防御素的颗粒,通过清除肠道病原体和调节肠道微生物群落组成来维持肠道环境。然而,潘氏细胞分泌反应仍然存在争议,其分泌的调节机制也尚未完全阐明。尽管类器官——小肠上皮细胞的三维培养物——已被证明可用于分析包括离子转运在内的肠上皮细胞功能,但它们的封闭结构限制了对潘氏细胞与肠道微生物群之间相互作用的研究。在这里,我们报告了将细菌或脂多糖(LPS)微注射到类器官腔中为实时研究潘氏细胞分泌提供了一个体外系统。结果表明,当通过微注射将 LPS 或活菌暴露于类器官上皮细胞的顶端表面时,潘氏细胞会立即释放颗粒。然而,潘氏细胞对培养基中递送到类器官外侧面基底外侧表面的 LPS 没有反应,尽管它们对基底外侧的氨甲酰胆碱有反应。此外,潘氏细胞在分泌后会补充其颗粒,从而能够对第二次刺激做出反应。这些发现为调节肠道环境的顶端诱导潘氏细胞分泌反应提供了新的见解。