Department of Rheumatology, University of Yamanashi, Yamanashi, Japan.
Third Department of Internal Medicine, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Yamanashi, Japan.
Int J Exp Pathol. 2024 Oct;105(5):193-201. doi: 10.1111/iep.12516. Epub 2024 Aug 20.
Matrix metalloproteinase (MMP)-12 has been reported to have diverse functions, including regulation of immune reactions and anti-inflammatory effects, but the potential roles of MMP-12 in kidney injury have not been fully elucidated. This study aimed to determine whether MMP-12 contributes to tubulointerstitial injury in a unilateral ureteric obstruction (UUO) model. MMP-12-deficient (MMP-12) mice and C57BL/6J mice as controls (MMP-12) were subjected to UUO and analysed 7 days after UUO. To analyse the functions of MMP-12 on monocytes/macrophages, we generated MMP-12-deficient, irradiated, chimeric mice (BM-MMP-12) and performed UUO. Bone marrow-derived macrophages (BMDMs) were isolated from both groups of mice and used for investigations. MMP-12 mice showed exacerbation of macrophage accumulation and interstitial fibrosis in the UUO-kidney compared with control mice. BM-MMP-12 mice also showed exacerbation of kidney injury. UUO induced accumulation of Ly6C macrophages in MMP-12 mice compared with control mice. Increases in inflammatory cytokine (tumour necrosis factor α, interleukin [IL]-1β, IL-6) levels from BMDMs after lipopolysaccharide stimulation were higher in MMP-12 mice than in MMP-12 mice. MMP-12 may play protective roles against kidney injury by UUO in mice, decreasing inflammatory cytokines from BMDMs and macrophage accumulation.
基质金属蛋白酶-12(MMP-12)具有多种功能,包括调节免疫反应和抗炎作用,但 MMP-12 在肾损伤中的潜在作用尚未完全阐明。本研究旨在确定 MMP-12 是否参与单侧输尿管梗阻(UUO)模型中的肾小管间质损伤。MMP-12 缺陷(MMP-12)小鼠和 C57BL/6J 小鼠作为对照(MMP-12)接受 UUO,并在 UUO 后 7 天进行分析。为了分析 MMP-12 对单核细胞/巨噬细胞的功能,我们生成了 MMP-12 缺陷、照射、嵌合小鼠(BM-MMP-12)并进行 UUO。从两组小鼠中分离出骨髓来源的巨噬细胞(BMDM)并进行研究。与对照组相比,MMP-12 小鼠在 UUO 肾脏中表现出巨噬细胞积聚和间质纤维化的加重。BM-MMP-12 小鼠也表现出肾脏损伤的加重。与对照组相比,UUO 诱导 MMP-12 小鼠中 Ly6C 巨噬细胞的积聚增加。与 MMP-12 小鼠相比,BMDM 经脂多糖刺激后炎症细胞因子(肿瘤坏死因子-α、白细胞介素[IL]-1β、IL-6)水平升高。MMP-12 可能通过减少 BMDM 中的炎症细胞因子和巨噬细胞积聚,在小鼠中发挥对 UUO 肾损伤的保护作用。