Department of Urology, Tianjin Institute of Urology, The Second Hospital of Tianjin Medical University, 23 Pingjiang Road, Hexi District, Tianjin 300211, P.R. China.
Exp Anim. 2024 May 3;73(2):211-222. doi: 10.1538/expanim.23-0113. Epub 2024 Jan 11.
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.
C-C 趋化因子受体 2(CCR2)是一种与氧化应激和炎症相关的单核细胞趋化因子。肾结石(KS)由草酸钙(CaOx)组成,可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。将 8 周龄雄性 C57BL/6J 小鼠每天腹腔注射乙醛酸(GOX)建立 KS 模型,并在第 2、4 和 6 天进行 CCR2 拮抗剂(INCB3344)治疗。结果表明,CCR2 拮抗剂降低了肾损伤标志物(血尿素氮和血清肌酐),减轻了肾小管损伤和 CaOx 晶体沉积。CCR2 拮抗剂还降低了 GOX 处理诱导的 CCR2 表达,并增加了 Nrf2 表达。GOX 处理促进了丙二醛(MDA)的产生,降低了谷胱甘肽(GSH)的含量,并抑制了过氧化氢酶(CAT)和超氧化物歧化酶(SOD)的活性,但 CCR2 拮抗剂减弱了 GOX 的上述作用。CCR2 拮抗剂对 GOX 诱导的炎症细胞因子表达(IL1B、IL6 和 MCP1)具有抑制作用,并通过增加 Bcl-2 表达和降低 Bax 和 cleaved-caspase 3 表达抑制细胞凋亡。通过 CaOx 诱导损伤的 HK-2 细胞和巨噬细胞样 THP-1 细胞共培养模型进行体外实验。CCR2 拮抗剂通过降低 TNF-α、IL6 和 iNOS 水平抑制 CaOx 诱导的 THP-1 细胞 M1 极化,进一步减轻 CaOx 诱导的 HK-2 细胞氧化应激损伤、炎症反应和细胞凋亡。研究表明,CCR2 拮抗剂可能通过抑制巨噬细胞 M1 极化来抵抗 CaOx 晶体诱导的氧化应激和炎症。