Potì Francesco, Scalera Enrica, Feuerborn Renata, Fischer Josephine, Arndt Lilli, Varga Georg, Pardali Evangelia, Seidl Matthias D, Fobker Manfred, Liebisch Gerhard, Hesse Bettina, Lukasz Alexander H, Rossaint Jan, Kehrel Beate E, Rosenbauer Frank, Renné Thomas, Christoffersen Christina, Simoni Manuela, Burkhardt Ralph, Nofer Jerzy-Roch
Unit of Neuroscience, Department of Medicine and Surgery, University of Parma, Parma, Italy.
Unit of Endocrinology, Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Italy.
JCI Insight. 2024 Dec 20;9(24):e158127. doi: 10.1172/jci.insight.158127.
Sphingosine 1-phosphate (S1P) is a lysosphingolipid with antiatherogenic properties, but mechanisms underlying its effects remain unclear. We here investigated atherosclerosis development in cholesterol-rich diet-fed LDL receptor-deficient mice with high or low overexpression levels of S1P receptor 1 (S1P1) in macrophages. S1P1-overexpressing macrophages showed increased activity of transcription factors PU.1, interferon regulatory factor 8 (IRF8), and liver X receptor (LXR) and were skewed toward an M2-distinct phenotype characterized by enhanced production of IL-10, IL-1RA, and IL-5; increased ATP-binding cassette transporter A1- and G1-dependent cholesterol efflux; increased expression of MerTK and efferocytosis; and reduced apoptosis due to elevated B cell lymphoma 6 and Maf bZIP B. A similar macrophage phenotype was observed in mice administered S1P1-selective agonist KRP203. Mechanistically, the enhanced PU.1, IRF8, and LXR activity in S1P1-overexpressing macrophages led to downregulation of the cAMP-dependent PKA and activation of the signaling cascade encompassing protein kinases AKT and mTOR complex 1 as well as the late endosomal/lysosomal adaptor MAPK and mTOR activator 1. Atherosclerotic lesions in aortic roots and brachiocephalic arteries were profoundly or moderately reduced in mice with high and low S1P1 overexpression in macrophages, respectively. We conclude that S1P1 signaling polarizes macrophages toward an antiatherogenic functional phenotype and countervails the development of atherosclerosis in mice.
鞘氨醇-1-磷酸(S1P)是一种具有抗动脉粥样硬化特性的溶血鞘脂,但其作用机制尚不清楚。我们在此研究了富含胆固醇饮食喂养的低密度脂蛋白受体缺陷小鼠中,巨噬细胞中S1P受体1(S1P1)高表达或低表达时动脉粥样硬化的发展情况。过表达S1P1的巨噬细胞显示转录因子PU.1、干扰素调节因子8(IRF8)和肝X受体(LXR)的活性增加,并偏向于一种独特的M2表型,其特征为IL-10、IL-1RA和IL-5的产生增加;ATP结合盒转运蛋白A1和G1依赖性胆固醇外流增加;MerTK表达增加和噬菌作用增强;以及由于B细胞淋巴瘤6和Maf bZIP B升高导致的细胞凋亡减少。在给予S1P1选择性激动剂KRP203的小鼠中也观察到了类似的巨噬细胞表型。从机制上讲,过表达S1P1的巨噬细胞中PU.1、IRF8和LXR活性的增强导致cAMP依赖性蛋白激酶A的下调以及包括蛋白激酶AKT和mTOR复合物1以及晚期内体/溶酶体衔接蛋白MAPK和mTOR激活剂1的信号级联的激活。巨噬细胞中S1P1高表达和低表达的小鼠,其主动脉根部和头臂动脉的动脉粥样硬化病变分别显著或中度减少。我们得出结论,S1P1信号使巨噬细胞向抗动脉粥样硬化功能表型极化,并对抗小鼠动脉粥样硬化的发展。