Institute of Biochemistry I, Faculty of Medicine, Goethe-University Frankfurt, 60590, Frankfurt, Germany.
Branch for Translational Medicine and Pharmacology TMP of the Fraunhofer Institute for Molecular Biology and Applied Ecology IME, 60590, Frankfurt, Germany.
Eur J Immunol. 2020 Jun;50(6):839-845. doi: 10.1002/eji.201948349. Epub 2020 Feb 18.
The sphingolipid sphingosine-1-phosphate (S1P) fulfills distinct functions in immune cell biology via binding to five G protein-coupled receptors. The immune cell-specific sphingosine-1-phosphate receptor 4 (S1pr4) was connected to the generation of IL-17-producing T cells through regulation of cytokine production in innate immune cells. Therefore, we explored whether S1pr4 affected imiquimod-induced murine psoriasis via regulation of IL-17 production. We did not observe altered IL-17 production, although psoriasis severity was reduced in S1pr4-deficient mice. Instead, ablation of S1pr4 attenuated the production of CCL2, IL-6, and CXCL1 and subsequently reduced the number of infiltrating monocytes and granulocytes. A connection between S1pr4, CCL2, and Mϕ infiltration was also observed in Zymosan-A induced peritonitis. Boyden chamber migration assays functionally linked reduced CCL2 production in murine skin and attenuated monocyte migration when S1pr4 was lacking. Mechanistically, S1pr4 signaling synergized with TLR signaling in resident Mϕs to produce CCL2, likely via the NF-κB pathway. We propose that S1pr4 activation enhances TLR response of resident Mϕs to increase CCL2 production, which attracts further Mϕs. Thus, S1pr4 may be a target to reduce perpetuating inflammatory responses.
鞘氨醇-1-磷酸(S1P)通过与五个 G 蛋白偶联受体结合,在免疫细胞生物学中发挥着不同的功能。免疫细胞特异性鞘氨醇-1-磷酸受体 4(S1pr4)通过调节先天免疫细胞中的细胞因子产生,与产生 IL-17 的 T 细胞的产生有关。因此,我们探讨了 S1pr4 是否通过调节 IL-17 的产生来影响咪喹莫特诱导的小鼠银屑病。虽然 S1pr4 缺陷小鼠的银屑病严重程度降低,但我们没有观察到 IL-17 产生的改变。相反,S1pr4 的缺失减弱了 CCL2、IL-6 和 CXCL1 的产生,随后减少了浸润的单核细胞和粒细胞的数量。在酵母聚糖 A 诱导的腹膜炎中也观察到了 S1pr4、CCL2 和 Mϕ 浸润之间的联系。Boyden 室迁移测定功能上连接了 S1pr4 缺失时小鼠皮肤中 CCL2 产生的减少和单核细胞迁移的减弱。从机制上讲,S1pr4 信号与 TLR 信号在驻留 Mϕ 中协同作用以产生 CCL2,可能通过 NF-κB 途径。我们提出,S1pr4 的激活增强了驻留 Mϕ 对 TLR 反应以增加 CCL2 的产生,从而吸引更多的 Mϕ。因此,S1pr4 可能是减少持续炎症反应的靶点。