Hoshino Yuya, Sonoda Hiroko, Nishimura Ryuji, Mori Kazuya, Ishibashi Kenichi, Ikeda Masahiro
Department of Veterinary Pharmacology, University of Miyazaki, Miyazaki 889-2192, Japan.
Department of Medical Physiology, Meiji Pharmaceutical University, Tokyo 204-8588, Japan.
Biochem Biophys Rep. 2019 Jan 11;17:169-176. doi: 10.1016/j.bbrep.2019.01.003. eCollection 2019 Mar.
Aquaporin-11 (AQP11) is an intracellular AQP. Several studies with mice have shown that AQP11 has a role in normal development of the kidney after birth. Our previous studies have suggested that alteration of oxygen homeostasis may be involved in the kidney injury caused by AQP11 deficiency, although the underlying mechanism is largely unknown. To clarify this issue, we examined genes that are related to oxygen homeostasis in mice. Among 62 genes that are involved in oxygen homeostasis, 35 were upregulated by more than 2-fold in mice in comparison with wild-type mice. Pathway analysis using these genes extracted the pathway responsible for production of reactive oxygen species in macrophages. As expression of the genes involved in the NADPH oxidase 2 (NOX2) complex was dramatically increased by more than 14-fold, we further analyzed NOX2 at the protein level. Immunoblotting analysis demonstrated a dramatic increase of NOX2 protein in the kidney of mice, and immunohistochemistry showed that NOX2 protein and a marker protein for macrophages were increased in the renal interstitium. These results indicate that NOX2-induced oxidative stress accompanied by macrophage infiltration plays an important role in alteration of oxygen homeostasis in mice.
水通道蛋白11(AQP11)是一种细胞内水通道蛋白。多项针对小鼠的研究表明,AQP11在出生后肾脏的正常发育中发挥作用。我们之前的研究表明,氧稳态的改变可能与AQP11缺乏导致的肾损伤有关,尽管其潜在机制在很大程度上尚不清楚。为了阐明这个问题,我们研究了与小鼠氧稳态相关的基因。在62个参与氧稳态的基因中,与野生型小鼠相比,35个基因在[具体基因缺失型]小鼠中上调了2倍以上。使用这些基因进行的通路分析提取出了巨噬细胞中负责活性氧产生的通路。由于参与NADPH氧化酶2(NOX2)复合体的基因表达显著增加了14倍以上,我们进一步在蛋白质水平分析了NOX2。免疫印迹分析表明,[具体基因缺失型]小鼠肾脏中NOX2蛋白显著增加,免疫组织化学显示肾间质中NOX2蛋白和巨噬细胞标记蛋白增加。这些结果表明,伴随着巨噬细胞浸润的NOX2诱导的氧化应激在[具体基因缺失型]小鼠氧稳态改变中起重要作用。