通过肠道微生物群和化学吸引剂受体GPR43调节炎症反应
Kendle M Maslowski1, Angelica T Vieira, Aylwin Ng
1Garvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, New South Wales 2010, Australia.
Nature
|October 30, 2009
概括
由肠道细菌产生的短链脂肪酸 (SCFA) 对于解决炎症至关重要. 它们与G蛋白结合受体43 (GPR43) 的相互作用对于正常的免疫反应和预防炎症性疾病至关重要.
科学领域:
- 免疫学 免疫学 免疫学
- 微生物学 微生物学
- 胃肠病学 胃肠病学
背景情况:
- 免疫系统通过托尔类受体 (TLR) 识别病原体.
- 肠道微生物群及其代谢物,如短链脂肪酸 (SCFA),影响免疫反应,并可能防止炎症性疾病.
- 结肠病与改变的微生物群和减少的SCFA有关,SCFA摄入显示出临床益处.
研究的目的:
- 研究SCFA-G蛋白结合受体43 (GPR43) 相互作用在调节炎症反应中的作用.
- 在各种疾病模型中确定GPR43信号传递对于炎症解决的必要性.
主要方法:
- 使用了缺乏GPR43 (Gpr43(-/-)) 的小鼠和没有细菌的小鼠.
- 在大肠炎,关节炎和喘模型中检查了炎症反应.
- 评估了免疫细胞对炎症媒介的产生和免疫细胞的招募.
主要成果:
- 在大肠炎,关节炎和喘模型中,缺乏GPR43的小鼠表现出恶化的或未解决的炎症.
- Gpr43(-/-) 免疫细胞显示炎症媒介体的产生增加,免疫细胞的招募增强.
- 没有细菌和SCFA的无细菌小鼠表现出类似的炎症失调.
结论:
- SCFA-GPR43相互作用对于炎症反应的正常解决至关重要.
- GPR43信号传递对于预防失调的炎症,连接饮食,肠道微生物群和免疫功能至关重要.
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