Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario L8S 4K1, Canada.
Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario L8S 4K1, Canada.
J Immunol. 2019 May 15;202(10):3041-3052. doi: 10.4049/jimmunol.1801034. Epub 2019 Apr 5.
Serotonin (5-hydroxytryptamine [5-HT]) is a key enteric signaling molecule that mediates various physiological processes in the gut. Enterochromaffin (EC) cells in the mucosal layer of the gut are the main source of 5-HT in the body and are situated in close proximity to the gut microbiota. In this study, we identify a pivotal role of TLR2 in 5-HT production in the gut. Antibiotic treatment reduces EC cell numbers and 5-HT levels in naive C57BL/6 mice, which is associated with downregulation of TLR2 expression but not TLR1 or TLR4. TLR2-deficient ( ) and mice express lower EC cell numbers and 5-HT levels, whereas treatment with TLR2/1 agonist upregulates 5-HT production in irradiated C57BL/6 mice, which are reconstituted with bone marrow cells, and in germ-free mice. Human EC cell line (BON-1 cells) release higher 5-HT upon TLR2/1 agonist via NF-κB pathway. mice and anti-TLR2 Ab-treated mice infected with enteric parasite, , exhibited attenuated 5-HT production, compared with infected wild-type mice. Moreover, excretory-secretory products from induce higher 5-HT production in BON-1 cells via TLR2 in a dose-dependent manner, whereby the effect of excretory-secretory products is abrogated by TLR2 antagonist. These findings not only suggest an important role of TLR2 in mucosal 5-HT production in the gut by resident microbiota as well as by a nematode parasite but also provide, to our knowledge, novel information on the potential benefits of targeting TLR2 in various gut disorders that exhibit aberrant 5-HT signaling.
血清素(5-羟色胺[5-HT])是一种关键的肠内信号分子,介导肠道中的各种生理过程。肠道黏膜层中的肠嗜铬细胞(EC)是体内 5-HT的主要来源,并且与肠道微生物群密切相关。在这项研究中,我们确定了 TLR2 在肠道 5-HT 产生中的关键作用。抗生素治疗可减少未处理的 C57BL/6 小鼠中的 EC 细胞数量和 5-HT 水平,这与 TLR2 表达的下调有关,但与 TLR1 或 TLR4 无关。TLR2 缺陷()和小鼠表达较低的 EC 细胞数量和 5-HT 水平,而 TLR2/1 激动剂可上调辐射处理的 C57BL/6 小鼠(用骨髓细胞重建)和无菌小鼠中 5-HT 的产生。人 EC 细胞系(BON-1 细胞)通过 NF-κB 途径释放更高的 5-HT 对 TLR2/1 激动剂。与感染野生型小鼠相比,感染肠道寄生虫的小鼠和抗 TLR2 Ab 处理的小鼠表现出 5-HT 产生的减弱。此外,寄生虫的排泄分泌产物以剂量依赖的方式通过 TLR2 在 BON-1 细胞中诱导更高的 5-HT 产生,TLR2 拮抗剂可阻断排泄分泌产物的作用。这些发现不仅表明 TLR2 在肠道固有微生物群和线虫寄生虫诱导的黏膜 5-HT 产生中具有重要作用,而且还提供了关于针对 TLR2 治疗各种表现出异常 5-HT 信号的肠道疾病的潜在益处的新信息。