髓系细胞系中Rac1 GTP酶的缺失可保护小鼠免受炎症介导的肾损伤。
Deletion of Rac1GTPase in the Myeloid Lineage Protects against Inflammation-Mediated Kidney Injury in Mice.
作者信息
Nagase Miki, Kurihara Hidetake, Aiba Atsu, Young Morag J, Sakai Tatsuo
机构信息
Department of Anatomy and Life Structure, Juntendo University School of Medicine, Tokyo, Japan.
Laboratory of Animal Resources, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
出版信息
PLoS One. 2016 Mar 3;11(3):e0150886. doi: 10.1371/journal.pone.0150886. eCollection 2016.
Macrophage-mediated inflammation has been implicated in various kidney diseases. We previously reported that Rac1, a Rho family small GTP-binding protein, was overactivated in several chronic kidney disease models, and that Rac1 inhibitors ameliorated renal injury, in part via inhibition of inflammation, but the detailed mechanisms have not been clarified. In the present study, we examined whether Rac1 in macrophages effects cytokine production and the inflammatory mechanisms contributing to kidney derangement. Myeloid-selective Rac1 flox control (M-Rac1 FC) and knockout (M-Rac1 KO) mice were generated using the cre-loxP system. Renal function under basal conditions did not differ between M-Rac1 FC and KO mice. Accordingly, lipopolysaccharide (LPS)-evoked kidney injury model was created. LPS elevated blood urea nitrogen and serum creatinine, enhanced expressions of kidney injury biomarkers, Kim-1 and Ngal, and promoted tubular injury in M-Rac1 FC mice. By contrast, deletion of myeloid Rac1 almost completely prevented the LPS-mediated renal impairment. LPS triggered a marked induction of macrophage-derived inflammatory cytokines, IL-6 and TNFα, in M-Rac1 FC mice, which was accompanied by Rac1 activation, stimulation of reduced nicotinamide-adenine dinucleotide phosphate (NADPH) oxidase, and reactive oxygen species overproduction. These changes were inhibited in M-Rac1 KO mice. LPS evoked F4/80-positive macrophages accumulation in the kidney, which was not affected by myeloid Rac1 deficiency. We further tested the role of Rac1 signaling in cytokine production using macrophage cell line, RAW264.7. Exposure to LPS increased IL-6 and TNFα mRNA expression. The LPS-driven cytokine induction was dose-dependently blocked by the Rac1 inhibitor EHT1864, NADPH oxidase inhibitor diphenyleneiodonium, and NF-κB inhibitor BAY11-7082. In conclusion, genetic ablation of Rac1 in the myeloid lineage protected against LPS-induced renal inflammation and injury, by suppressing macrophage-derived cytokines, IL-6 and TNFα, without blocking recruitment. Our data suggest that Rac1 in macrophage is a novel target for the treatment of kidney disease through inhibition of cytokine production.
巨噬细胞介导的炎症与多种肾脏疾病有关。我们之前报道过,Rho家族小GTP结合蛋白Rac1在几种慢性肾脏病模型中过度激活,并且Rac1抑制剂可部分通过抑制炎症来改善肾损伤,但具体机制尚未阐明。在本研究中,我们研究了巨噬细胞中的Rac1是否影响细胞因子产生以及导致肾脏紊乱的炎症机制。使用cre-loxP系统构建了髓系选择性Rac1基因敲除对照(M-Rac1 FC)和敲除(M-Rac1 KO)小鼠。在基础条件下,M-Rac1 FC和KO小鼠的肾功能没有差异。因此,构建了脂多糖(LPS)诱发的肾损伤模型。LPS升高了M-Rac1 FC小鼠的血尿素氮和血清肌酐,增强了肾损伤生物标志物Kim-1和Ngal的表达,并促进了肾小管损伤。相比之下,髓系Rac1的缺失几乎完全阻止了LPS介导的肾功能损害。LPS在M-Rac1 FC小鼠中引发了巨噬细胞衍生的炎症细胞因子IL-6和TNFα的显著诱导,这伴随着Rac1激活、还原型烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶的刺激和活性氧的过量产生。这些变化在M-Rac1 KO小鼠中受到抑制。LPS诱发了F4/80阳性巨噬细胞在肾脏中的积聚,而髓系Rac1缺乏对此没有影响。我们进一步使用巨噬细胞系RAW264.7测试了Rac1信号在细胞因子产生中的作用。暴露于LPS会增加IL-6和TNFα mRNA的表达。Rac1抑制剂EHT1864、NADPH氧化酶抑制剂二苯碘鎓和NF-κB抑制剂BAY11-7082可剂量依赖性地阻断LPS驱动的细胞因子诱导。总之,髓系谱系中Rac1的基因缺失通过抑制巨噬细胞衍生的细胞因子IL-6和TNFα,在不阻断募集的情况下,保护小鼠免受LPS诱导的肾脏炎症和损伤。我们的数据表明,巨噬细胞中的Rac1是通过抑制细胞因子产生来治疗肾脏疾病的新靶点。