A functional (pro)renin receptor is expressed in human lymphocytes and monocytes

Author:

Narumi Kaori1,Hirose Takuo12,Sato Emiko13,Mori Takefumi14,Kisu Kiyomi1,Ishikawa Mayuko1,Totsune Kazuhito56,Ishii Tomonori7,Ichihara Atsuhiro8,Nguyen Genevieve2,Sato Hiroshi13,Ito Sadayoshi14

Affiliation:

1. Division of Nephrology, Endocrinology, and Vascular Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan;

2. Center for Interdisciplinary Research in Biology (CIRB), College de France, and CNRS UMR 7241 and INSERM U1050, Paris, France;

3. Department of Clinical Pharmacology and Therapeutics, Tohoku University Graduate School of Pharmaceutical Science, Sendai, Japan;

4. Division of Integrative Renal Replacement Therapy, Tohoku University Graduate School of Medicine, Sendai, Japan;

5. Department of Social Welfare, Faculty of Synthetic Welfare, Tohoku Fukushi University, Sendai, Japan;

6. Department of Planning for Drug Development and Clinical Evaluation, Tohoku University Graduate School of Pharmaceutical Science and Medicine, Sendai, Japan;

7. Department of Hematology and Rheumatology, Department of Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan; and

8. Department of Endocrinology and Hypertension, Tokyo Women's Medical University, Tokyo, Japan

Abstract

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.

Funder

Ministry of Education, Culture, Sports, Science, and Technology (MEXT)

Publisher

American Physiological Society

Subject

Physiology

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