Journal Article

Ablation of Myeloid Cell MRP8 Ameliorates Nephrotoxic Serum-induced Glomerulonephritis by Affecting Macrophage Characterization through Intraglomerular Crosstalk

Yokoi, Hideki, Nishiguchi, Yoshihiko, Fujimoto, Daisuke, Yanagita, Motoko, Hata, Yusuke, Kakizoe, Yutaka, Sato, Yuki, Umemoto, Shuro, Mukoyama, Masashi, Kuwabara, Takashige, Kanki, Tomoko, Kan, Youngna, Izumi, Yuichiro, Mori, Kiyoshi

2020

Overview

Toll-like receptor 4 (TLR4) and one of its endogenous ligands myeloid-related protein 8 (MRP8 or S100A8), especially expressed in macrophages, play an important role in diabetic nephropathy and autoimmune disorders. However, detailed mechanisms and consequence of MRP8 expression remain unknown, partly due to embryonic lethality of MRP8 knockout mice. In this study, Myeloid lineage cell-specific MRP8 knockout mice were generated, and nephrotoxic serum-induced glomerulonephritis was developed. Mice with conditional ablation of MRP8 gene in myeloid cells exhibited less severe histological damage, proteinuria and inflammatory changes compared to control mice. Mechanism of MRP8 upregulation was investigated using cultured cells. Co-culture of macrophages with mesangial cells or mesangial cell-conditioned media, but not with proximal tubules, markedly upregulated MRP8 gene expression and inflammatory M1 phenotype in macrophages, which was attenuated in MRP8-deleted bone marrow-derived macrophages. Effects of MRP8 deletion was further studied in the context of macrophage-inducible C-type lectin (Mincle), which is critically involved in maintenance of M1 phenotype of macrophages. MRP8 ablation in myeloid cells suppressed the induction of Mincle expression on macrophages in glomerulonephritis. Thus, we propose that intraglomerular crosstalk between mesangial cells and macrophages plays a role in inflammatory changes in glomerulonephritis, and MRP8-dependent Mincle expression in macrophage may be involved in the process.

• Publisher: Nature Publishing Group UK,Nature Publishing Group
• Subject: 692/4022 / 692/699 / Animals / Autoimmune diseases / Bone marrow / Calgranulin A - deficiency / Calgranulin A - metabolism / Cell culture / Cell Lineage / Clonal deletion / Culture media / Diabetes mellitus / Diabetic nephropathy / Disease Models, Animal / Embryos / Gene Deletion / Gene expression / Glomerulonephritis / Glomerulonephritis - metabolism / Glomerulonephritis - pathology / Humanities and Social Sciences / Inflammation / Integrases - metabolism / Kidney Glomerulus - pathology / Lectins, C-Type - metabolism / Lethality / Macrophages / Macrophages - metabolism / Macrophages - pathology / Membrane Proteins - metabolism / Mesangial cells / Mesangial Cells - metabolism / Mice / Mice, Knockout / multidisciplinary / Myeloid cells / Myeloid Progenitor Cells - metabolism / Nephropathy / Phenotypes / Proteinuria / Proximal tubules / RAW 264.7 Cells / Recombination, Genetic - genetics / Rodents / Science / Science (multidisciplinary) / Serum - metabolism / Stress Fibers - metabolism / TLR4 protein / Toll-Like Receptor 4 - metabolism / Toll-like receptors / Up-Regulation