Circ_0001714 knockdown alleviates lipopolysaccharide-induced apoptosis and inflammation in renal tubular epithelial cells via miR-129-5p/TRAF6 axis in septic acute kidney injury.

IF 2.9 4区 生物学 Q2 BIOPHYSICS Journal of Bioenergetics and Biomembranes Pub Date : 2023-08-01 DOI:10.1007/s10863-023-09975-6
Yiqing Tan, Ziying Yu, Pei Li, Yu Liu, Ting You, Feng Kuang, Wei Luo
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Abstract

Background: Circular RNAs (circRNAs) have been shown to play roles in regulating sepsis. Sepsis is a major cause of acute kidney injury (AKI). Herein, we aimed to investigate the role and mechanism of circ_0001714 in the progression of sepsis-induced AKI.

Methods: Human HK-2 cells were exposed to lipopolysaccharide (LPS) for functional experiments. Quantitative real-time polymerase chain reaction and western blotting were used for expression analysis. Functional experiments were performed by using MTT assay, 5-ethynyl-2'-deoxyuridine assay, flow cytometry, and enzyme-linked immunosorbent assay (ELISA). The binding between miR-129-5p and circ_0001714 or TRAF6 (TNF receptor associated factor 6) was validated using dual-luciferase reporter assay.

Results: Circ_0001714 expression was higher in sepsis-AKI patients. HK-2 cells were exposed to LPS to imitate the injury of renal tubular epithelial cells during sepsis-AKI. LPS dose-dependently up-regulated circ_0001714, moreover, circ_0001714 silencing reversed LPS-evoked apoptosis and inflammation in HK-2 cells. Mechanistically, circ_0001714 sequestered miR-129-5p to up-regulate TRAF6 expression, implying the circ_0001714/miR-129-5p/TRAF6 feedback loop. MiR-129-5p was decreased, while TRAF6 was increased in sepsis-AKI patients and LPS-stimulated HK-2 cells. MiR-129-5p re-expression or TRAF6 silencing protected against LPS-induced HK-2 cell apoptosis and inflammation. Additionally, a series of rescue experiments showed that miR-129-5p inhibition reversed the inhibitory action of circ_0001714 knockdown on LPS-induced HK-2 cell injury. Furthermore, TRAF6 overexpression also attenuated the protective effects of miR-129-5p on HK-2 cells under LPS treatment.

Conclusion: Circ_0001714 silencing might alleviate LPS-induced apoptosis and inflammation via targeting miR-129-5p/TRAF6 axis in HK-2 cells.

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Circ_000001714敲低通过miR-129-5p/TRAF6轴减轻脓毒症急性肾损伤中脂多糖诱导的肾小管上皮细胞凋亡和炎症。
背景:环状核糖核酸(circRNAs)已被证明在调节败血症中发挥作用。脓毒症是急性肾损伤(AKI)的主要原因。本文旨在探讨circ_0001714在败血症诱导的AKI进展中的作用和机制。方法:将人HK-2细胞暴露于脂多糖(LPS)中进行功能实验。定量实时聚合酶链反应和蛋白质印迹用于表达分析。采用MTT法、5-乙炔基-2'-脱氧尿苷法、流式细胞术和酶联免疫吸附法(ELISA)进行功能实验。miR-129-5p与circ_0001714或TRAF6(TNF受体相关因子6)之间的结合使用双荧光素酶报告基因测定法进行验证。结果:Circ0001714在脓毒症AKI患者中的表达较高。将HK-2细胞暴露于LPS以模拟败血症AKI期间肾小管上皮细胞的损伤。LPS剂量依赖性上调circ_0001714,此外,circ_00201714沉默逆转了LPS诱导的HK-2细胞凋亡和炎症。从机制上讲,circ_0001714螯合miR-129-5p以上调TRAF6的表达,这意味着circ_0001714/miR-129-5-p/TRAF6的反馈回路。在败血症AKI患者和LPS刺激的HK-2细胞中,MiR-129-5p降低,而TRAF6增加。MiR-129-5p再表达或TRAF6沉默对LPS诱导的HK-2细胞凋亡和炎症具有保护作用。此外,一系列拯救实验表明,miR-129-5p的抑制逆转了circ_0001714敲低对LPS诱导的HK-2细胞损伤的抑制作用。此外,TRAF6过表达也减弱了LPS处理下miR-129-5p对HK-2细胞的保护作用。结论:Circ0001714沉默可能通过靶向miR-129-5p/TRAF6轴来减轻LPS诱导的HK-2细胞凋亡和炎症。
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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
22
审稿时长
6-12 weeks
期刊介绍: The Journal of Bioenergetics and Biomembranes is an international journal devoted to the publication of original research that contributes to fundamental knowledge in the areas of bioenergetics, biomembranes, and transport, including oxidative phosphorylation, photosynthesis, muscle contraction, as well as cellular and systemic metabolism. The timely research in this international journal benefits biophysicists, membrane biologists, cell biologists, biochemists, molecular biologists, physiologists, endocrinologists, and bio-organic chemists.
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