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本文引用的文献

1
MMP12 Inhibits Corneal Neovascularization and Inflammation through Regulation of CCL2.MMP12 通过调节 CCL2 抑制角膜新生血管和炎症。
Sci Rep. 2019 Aug 9;9(1):11579. doi: 10.1038/s41598-019-47831-z.
2
Renal Inflammation and Fibrosis: A Double-edged Sword.肾脏炎症与纤维化:一把双刃剑。
J Histochem Cytochem. 2019 Sep;67(9):663-681. doi: 10.1369/0022155419852932. Epub 2019 May 22.
3
Matrix metalloproteinase-12 produced by Ly6C macrophages prolongs the survival after myocardial infarction by preventing neutrophil influx.Ly6C 巨噬细胞产生的基质金属蛋白酶-12 通过防止中性粒细胞浸润延长心肌梗死后的存活时间。
J Mol Cell Cardiol. 2019 Jun;131:41-52. doi: 10.1016/j.yjmcc.2019.04.007. Epub 2019 Apr 19.
4
Macrophages: versatile players in renal inflammation and fibrosis.巨噬细胞:肾脏炎症和纤维化中的多面手。
Nat Rev Nephrol. 2019 Mar;15(3):144-158. doi: 10.1038/s41581-019-0110-2. Epub 2019 Jan 28.
5
Matrix metalloproteinase-12 as an endogenous resolution promoting factor following myocardial infarction.基质金属蛋白酶-12 作为心肌梗死后的内源性促解决因子。
Pharmacol Res. 2018 Nov;137:252-258. doi: 10.1016/j.phrs.2018.10.026. Epub 2018 Oct 28.
6
Inflammation and renal fibrosis: Recent developments on key signaling molecules as potential therapeutic targets.炎症与肾纤维化:关键信号分子作为潜在治疗靶点的最新研究进展。
Eur J Pharmacol. 2018 Feb 5;820:65-76. doi: 10.1016/j.ejphar.2017.12.016. Epub 2017 Dec 8.
7
F4/80 as a Major Macrophage Marker: The Case of the Peritoneum and Spleen.作为主要巨噬细胞标志物的F4/80:以腹膜和脾脏为例
Results Probl Cell Differ. 2017;62:161-179. doi: 10.1007/978-3-319-54090-0_7.
8
The ligand-bound thyroid hormone receptor in macrophages ameliorates kidney injury via inhibition of nuclear factor-κB activities.巨噬细胞中配体结合的甲状腺激素受体通过抑制核因子-κB 活性改善肾脏损伤。
Sci Rep. 2017 Mar 8;7:43960. doi: 10.1038/srep43960.
9
Matrix metalloproteinase-12 deficiency attenuates experimental crescentic anti-glomerular basement membrane glomerulonephritis.基质金属蛋白酶-12缺乏可减轻实验性新月体性抗肾小球基底膜肾小球肾炎。
Nephrology (Carlton). 2018 Feb;23(2):183-189. doi: 10.1111/nep.12964.
10
GM-CSF Grown Bone Marrow Derived Cells Are Composed of Phenotypically Different Dendritic Cells and Macrophages.粒细胞-巨噬细胞集落刺激因子培养的骨髓来源细胞由表型不同的树突状细胞和巨噬细胞组成。
Mol Cells. 2016 Oct;39(10):734-741. doi: 10.14348/molcells.2016.0160. Epub 2016 Oct 28.

巨噬细胞基质金属蛋白酶-12 在梗阻性肾病小鼠中的肾脏保护作用。

Renal protective roles of macrophage matrix metalloproteinase-12 in mice with obstructed kidneys.

机构信息

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.

出版信息

Int J Exp Pathol. 2024 Oct;105(5):193-201. doi: 10.1111/iep.12516. Epub 2024 Aug 20.

DOI:10.1111/iep.12516
PMID:39164934
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11574677/
Abstract

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.

摘要

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。