Zhu Dongju, Wu Xiang
Department of Nephrology, Affiliated Hospital of Panzhihua University, No. Taoyuan street, Bingcaogang in East region, Panzhihua, Sichuan, 617000, China.
Department of Pediatrics, Panzhihua Central Hospital, Panzhihua, Sichuan, China.
Biochem Genet. 2024 Jun;62(3):1779-1794. doi: 10.1007/s10528-023-10517-3. Epub 2023 Sep 20.
Resveratrol has a protective effect on sepsis-induced acute kidney injury (AKI). Circ_0074371 has been confirmed to inhibit sepsis-induced AKI process, but whether resveratrol inhibits sepsis-induced AKI by regulating circ_0074371-related pathway remains unclear. In this study, lipopolysaccharide (LPS)-induced renal tubular epithelial cells (HK2) were used to mimic AKI cell models. Quantitative real-time PCR was used to detect relative expression of circ_0074371, microRNA (miR)-145-5p and inositol polyphosphate multikinase (IPMK). Cell proliferation and apoptosis were detected by cell counting kit 8 assay, EdU assay and flow cytometry. The levels of inflammation factors were measured by ELISA assay, and MDA level and SOD activity were examined to assess oxidative stress. Protein expression of IPMK was evaluated by western bolt analysis. The relationship between miR-145-5p and circ_0074371 or IPMK was confirmed by dual-luciferase reporter assay. It was showed that circ_0074371 was upregulated in AKI patients and LPS-induced HK2 cells, and silencing of circ_0074371 promoted proliferation and inhibited apoptosis, inflammation and oxidative stress in LPS-induced HK2 cells. In terms of mechanism, circ_0074371 sponged miR-145-5p to positively regulate IPMK. IPMK overexpression could reverse the relieving effect of circ_0074371 knockdown on LPS-induced HK2 cell injury. Moreover, resveratrol suppressed LPS-induced apoptosis, inflammation and oxidative stress in HK2 cells, and circ_0074371 overexpression also reversed the protective effect of resveratrol against LPS-induced cell injury. Our data suggested that resveratrol alleviated LPS-induced HK2 cell injury by inactivating the circ_0074371/miR-145-5p/IPMK axis.
白藜芦醇对脓毒症诱导的急性肾损伤(AKI)具有保护作用。Circ_0074371已被证实可抑制脓毒症诱导的AKI进程,但白藜芦醇是否通过调节与circ_0074371相关的信号通路来抑制脓毒症诱导的AKI仍不清楚。在本研究中,使用脂多糖(LPS)诱导的肾小管上皮细胞(HK2)来模拟AKI细胞模型。采用定量实时PCR检测circ_0074371、微小RNA(miR)-145-5p和肌醇多磷酸多激酶(IPMK)的相对表达。通过细胞计数试剂盒8检测、EdU检测和流式细胞术检测细胞增殖和凋亡。采用ELISA检测炎症因子水平,检测丙二醛(MDA)水平和超氧化物歧化酶(SOD)活性以评估氧化应激。通过蛋白质免疫印迹分析评估IPMK的蛋白表达。通过双荧光素酶报告基因检测证实miR-145-5p与circ_0074371或IPMK之间的关系。结果显示,circ_0074371在AKI患者和LPS诱导的HK-2细胞中上调,沉默circ_0074371可促进LPS诱导的HK-2细胞增殖并抑制其凋亡、炎症和氧化应激。机制方面,circ_0074371通过吸附miR-145-5p来正向调节IPMK。IPMK过表达可逆转circ_0074371敲低对LPS诱导的HK-2细胞损伤的缓解作用。此外,白藜芦醇可抑制LPS诱导的HK-2细胞凋亡、炎症和氧化应激,circ_0074371过表达也可逆转白藜芦醇对LPS诱导的细胞损伤的保护作用。我们的数据表明,白藜芦醇通过使circ_0074371/miR-145- /IPMK轴失活来减轻LPS诱导的HK-2细胞损伤。