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TLR2 在介导肠道黏膜中 5-羟色胺的产生中发挥关键作用。

TLR2 Plays a Pivotal Role in Mediating Mucosal Serotonin Production in the Gut.

机构信息

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.

出版信息

J Immunol. 2019 May 15;202(10):3041-3052. doi: 10.4049/jimmunol.1801034. Epub 2019 Apr 5.

Abstract

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.

摘要

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。

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