Division of Cardiovascular Medicine, Center for Molecular Medicine, Department of Medicine Solna, Karolinska Institute, and.
Theme Heart and Vessels, Division of Valvular and Coronary Disease, Karolinska University Hospital, Stockholm, Sweden.
J Clin Invest. 2021 Dec 15;131(24). doi: 10.1172/JCI142883.
Chronic inflammation is a hallmark of atherosclerosis and results from an imbalance between proinflammatory and proresolving signaling. The human GPR32 receptor, together with the ALX/FPR2 receptor, transduces biological actions of several proresolving mediators that stimulate resolution of inflammation. However, since no murine homologs of the human GPR32 receptor exist, comprehensive in vivo studies are lacking. Using human atherosclerotic lesions from carotid endarterectomies and creating a transgenic mouse model expressing human GPR32 on a Fpr2×ApoE double-KO background (hGPR32myc×Fpr2-/-×Apoe-/-), we investigated the role of GPR32 in atherosclerosis and self-limiting acute inflammation. GPR32 mRNA was reduced in human atherosclerotic lesions and correlated with the immune cell markers ARG1, NOS2, and FOXP3. Atherosclerotic lesions, necrotic core, and aortic inflammation were reduced in hGPR32mycTg×Fpr2-/-×Apoe-/- transgenic mice as compared with Fpr2-/-×Apoe-/- nontransgenic littermates. In a zymosan-induced peritonitis model, the hGPR32mycTg×Fpr2-/-×Apoe-/- transgenic mice had reduced inflammation at 4 hours and enhanced proresolving macrophage responses at 24 hours compared with nontransgenic littermates. The GPR32 agonist aspirin-triggered resolvin D1 (AT-RvD1) regulated leukocyte responses, including enhancing macrophage phagocytosis and intracellular signaling in hGPR32mycTg×Fpr2-/-×Apoe-/- transgenic mice, but not in Fpr2-/-×Apoe-/- nontransgenic littermates. Together, these results provide evidence that GPR32 regulates resolution of inflammation and is atheroprotective in vivo.
慢性炎症是动脉粥样硬化的一个标志,源于促炎信号和促解决信号之间的失衡。人类 GPR32 受体与 ALX/FPR2 受体一起转导几种促解决介质的生物学作用,这些介质刺激炎症的解决。然而,由于人类 GPR32 受体没有相应的鼠类同源物,因此缺乏全面的体内研究。我们使用颈动脉内膜切除术的人动脉粥样硬化病变,并创建了一种在 Fpr2×ApoE 双 KO 背景下表达人 GPR32 的转基因小鼠模型(hGPR32myc×Fpr2-/-×Apoe-/-),研究了 GPR32 在动脉粥样硬化和自限性急性炎症中的作用。人动脉粥样硬化病变中的 GPR32 mRNA 减少,并与免疫细胞标志物 ARG1、NOS2 和 FOXP3 相关。与 Fpr2-/-×Apoe-/-非转基因同窝仔相比,hGPR32mycTg×Fpr2-/-×Apoe-/-转基因小鼠的动脉粥样硬化病变、坏死核心和主动脉炎症减少。在酵母聚糖诱导的腹膜炎模型中,与非转基因同窝仔相比,hGPR32mycTg×Fpr2-/-×Apoe-/-转基因小鼠在 4 小时时炎症减少,在 24 小时时促解决巨噬细胞反应增强。GPR32 激动剂阿司匹林触发的 resolvin D1(AT-RvD1)调节白细胞反应,包括增强 hGPR32mycTg×Fpr2-/-×Apoe-/-转基因小鼠的巨噬细胞吞噬作用和细胞内信号转导,但在 Fpr2-/-×Apoe-/-非转基因同窝仔中没有。这些结果共同证明,GPR32 调节炎症的解决,并且在体内具有抗动脉粥样硬化作用。