Department of Microbiology and Immunology, Stony Brook University, Stony Brook, NY.
Department of Microbiology and Immunology, Stony Brook University, Stony Brook, NY
J Immunol. 2021 Oct 15;207(8):1959-1963. doi: 10.4049/jimmunol.2000986. Epub 2021 Sep 20.
Previous studies indicate that IL-17A plays an important role in mediating the intestinal microbiota and systemic metabolic functions. However, it is not known where IL-17RA signaling occurs to mediate these effects. To investigate this question, we used intestinal epithelial-specific ( ) and liver-specific ( ) IL-17RA knockout mice as well as littermate control mice. Our results indicate that intestinal IL-17RA signaling helps mediate systemic metabolic functions upon exposure to prolonged high-fat diet. mice display impaired glucose metabolism, altered hormone and adipokine levels, increased visceral adiposity, and greater hepatic lipid deposition when compared with their littermate controls. We show that IL-17RA-driven changes in microbiota composition are responsible for regulating systemic glucose metabolism. Altogether, our data elucidate the importance of intestinal IL-17RA signaling in regulating high-fat diet-mediated systemic glucose and lipid metabolism.
先前的研究表明,IL-17A 在调节肠道微生物群和全身代谢功能方面发挥着重要作用。然而,尚不清楚 IL-17RA 信号发生的位置以介导这些作用。为了研究这个问题,我们使用了肠道上皮细胞特异性()和肝特异性()IL-17RA 敲除小鼠以及同窝对照小鼠。我们的结果表明,肠道 IL-17RA 信号有助于在暴露于长期高脂肪饮食时介导全身代谢功能。与同窝对照相比,小鼠表现出葡萄糖代谢受损、激素和脂肪因子水平改变、内脏脂肪增加和肝脏脂质沉积增加。我们表明,IL-17RA 驱动的微生物群落组成变化负责调节全身葡萄糖代谢。总的来说,我们的数据阐明了肠道 IL-17RA 信号在调节高脂肪饮食介导的全身葡萄糖和脂质代谢中的重要性。