Division of Nephrology, Endocrinology, and Vascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan;
Division of Nephrology, Endocrinology, and Vascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan; Center for Interdisciplinary Research in Biology (CIRB), College de France, and CNRS UMR 7241 and INSERM U1050, Paris, France;
Am J Physiol Renal Physiol. 2015 Mar 1;308(5):F487-99. doi: 10.1152/ajprenal.00206.2014. Epub 2014 Dec 10.
The renin-angiotensin system (RAS) is involved in inflammation. The signaling via the ANG II type 1 receptor in human lymphocytes and monocytes, which play key roles in pathophysiology of glomerulonephritis (GN), can enhance inflammation. However, the role of the (pro)renin receptor [(P)RR], a component of the RAS, in inflammatory reactions is unknown. We assessed whether (P)RR is expressed in human lymphocytes and monocytes by RT-PCR, Western blotting, flow cytometry, and immunohistochemistry, and whether (P)RR functions in inflammation. (P)RR mRNA and protein were expressed in human peripheral blood mononuclear cells (PBMCs). Flow cytometric analysis revealed high expression of (P)RR on monocytes. (P)RR was present on PBMCs, infiltrating lymphocytes, and macrophages around glomeruli with a crescent in anti-neutrophil cytoplasmic antibody (ANCA)-associated GN. Renin stimulation of PBMCs from healthy subjects in the presence of the ANG II type 1 receptor and ANG II type 2 receptor blockers induced ERK1/2 phosphorylation and release of IL-6 and expression of cyclooxygenase-2 (COX-2). The increases in cytokine release and COX-2 expression were inhibited in the presence of an ERK1/2 inhibitor. (P)RR knockdown by small interfering RNA in U937 cells, a human leukemic monocyte lymphoma cell line, significantly decreased ERK1/2 phosphorylation after renin stimulation. Thus (P)RR expressed in human inflammatory cells might contribute to inflammation in ANCA-associated GN.
肾素-血管紧张素系统(RAS)参与炎症反应。在人淋巴细胞和单核细胞中,血管紧张素 II 型 1 受体(ANG II type 1 receptor)的信号传导作用至关重要,它在肾小球肾炎(GN)的病理生理学中发挥作用,可增强炎症反应。然而,(前)肾素受体((P)RR)作为 RAS 的一个组成部分,其在炎症反应中的作用尚不清楚。我们通过 RT-PCR、Western blot、流式细胞术和免疫组织化学评估了(P)RR 是否在人淋巴细胞和单核细胞中表达,并研究了(P)RR 在炎症中的作用。(P)RR mRNA 和蛋白在人外周血单核细胞(PBMC)中表达。流式细胞术分析显示,(P)RR 在单核细胞上高表达。(P)RR 存在于 PBMC、浸润淋巴细胞和新月体肾炎中肾小球周围的巨噬细胞上。在存在血管紧张素 II 型 1 受体和血管紧张素 II 型 2 受体阻滞剂的情况下,肾素刺激健康受试者的 PBMC 可诱导 ERK1/2 磷酸化以及白细胞介素-6(IL-6)的释放和环氧化酶-2(COX-2)的表达。ERK1/2 抑制剂的存在可抑制细胞因子释放和 COX-2 表达的增加。在人白血病单核细胞淋巴瘤细胞系 U937 细胞中,用小干扰 RNA 敲低(P)RR,可显著降低肾素刺激后的 ERK1/2 磷酸化。因此,在抗中性粒细胞胞质抗体(ANCA)相关性 GN 中,表达于人炎症细胞中的(P)RR 可能有助于炎症反应。