CCR2拮抗剂通过调节巨噬细胞活化减轻草酸钙诱导的肾脏氧化应激和炎症。

IF 2.2 4区 农林科学 Q1 VETERINARY SCIENCES Experimental Animals Pub Date : 2024-05-03 Epub Date: 2024-01-11 DOI:10.1538/expanim.23-0113
Xinpeng Wang, Linguo Xie, Chunyu Liu
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引用次数: 0

摘要

CCR2(C-C 趋化因子受体 2 型)是一种与氧化应激和炎症有关的单核细胞趋化因子。肾结石(KS)由草酸钙(CaOx)组成,会引发肾氧化应激和炎症。本研究旨在评估 CCR2 在体内和体外对 KS 的影响。八周大的雄性 C57BL/6J 小鼠每天腹腔注射乙二酸甘油酯(GOX)以建立 KS 模型,并在第 2、4 和 6 天进行 CCR2 拮抗剂(INCB3344)治疗。结果显示,CCR2拮抗剂降低了肾损伤指标(血尿素氮和血清肌酐),减轻了肾小管损伤和 CaOx 晶体沉积。CCR2 拮抗剂还能降低 GOX 处理诱导的 CCR2 表达,增加 Nrf2 表达。GOX 处理会促进丙二醛(MDA)的产生,降低谷胱甘肽(GSH)的含量,抑制过氧化氢酶(CAT)和超氧化物歧化酶(SOD)的活性。CCR2 拮抗剂对 GOX 诱导的炎性细胞因子(IL1B、IL6 和 MCP1)的表达有抑制作用,并通过增加 Bcl-2 的表达、降低 Bax 和裂解-天冬酶 3 的表达来抑制细胞凋亡。体外实验采用 CaOx 诱导的受损 HK-2 细胞和巨噬细胞样 THP-1 细胞共培养模型。CCR2拮抗剂通过降低TNF-α、IL6和iNOS水平抑制了CaOx诱导的THP-1细胞M1极化,并进一步减轻了CaOx诱导的氧化应激损伤、炎症反应和HK-2细胞凋亡。该研究表明,CCR2 拮抗剂可通过抑制巨噬细胞 M1 极化来抵抗 CaOx 晶体诱导的氧化应激和炎症反应。
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CCR2 antagonist attenuates calcium oxalate-induced kidney oxidative stress and inflammation by regulating macrophage activation.

C-C chemokine receptor type 2 (CCR2) is a monocyte chemokine associated with oxidative stress and inflammation. Kidney stones (KS) are composed of calcium oxalate (CaOx), which trigger renal oxidative stress and inflammatory. This study aims to evaluate the effects of CCR2 on KS in vivo and in vitro. Eight-week-old male C57BL/6J mice were intraperitoneally injected with glyoxylate (GOX) daily to establish a KS model, and along with CCR2 antagonist (INCB3344) treatment on days 2, 4, and 6. The results showed that CCR2 antagonist reduced renal injury markers (blood urea nitrogen and serum creatinine), alleviated renal tubular injury and CaOx crystal deposition. CCR2 antagonist also decreased CCR2 expression induced by GOX treatment and increased Nrf2 expression. GOX treatment promoted malondialdehyde (MDA) production, decreased glutathione (GSH) content, and inhibited catalase (CAT) and superoxide dismutase (SOD) activity, however, CCR2 antagonist attenuated the above effects of GOX. CCR2 antagonist had inhibitory effects on GOX-induced inflammatory cytokine expression (IL1B, IL6 and MCP1), and inhibited apoptosis by increasing Bcl-2 expression and decreasing Bax and cleaved-caspase 3 expression. In vitro experiments were performed by co-culture model of CaOx-induced damaged HK-2 cells and macrophage-like THP-1 cells. CCR2 antagonist inhibited CaOx-induced THP-1 cell M1 polarization by decreasing the TNF-α, IL6 and iNOS levels, and further alleviated CaOx-induced oxidative stress damage, inflammatory response and apoptosis of HK-2 cells. The study suggests that CCR2 antagonist may be resistant to CaOx crystals-induced oxidative stress and inflammation by inhibiting macrophage M1 polarization.

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来源期刊
Experimental Animals
Experimental Animals 生物-动物学
CiteScore
2.80
自引率
4.20%
发文量
2
审稿时长
3 months
期刊介绍: The aim of this international journal is to accelerate progress in laboratory animal experimentation and disseminate relevant information in related areas through publication of peer reviewed Original papers and Review articles. The journal covers basic to applied biomedical research centering around use of experimental animals and also covers topics related to experimental animals such as technology, management, and animal welfare.
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