Deng Wenjuan, Wang Xiaoliang, Zhang Jin, Zhao Sainan
Department of Stomatology, Gaoxin Branch of Jinan Stomatological Hospital, Jinan, Shandong, China.
Department of Stomatology, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, China.
J Dent Sci. 2022 Jul;17(3):1125-1134. doi: 10.1016/j.jds.2022.01.010. Epub 2022 Feb 15.
BACKGROUND/PURPOSE: Periodontitis is a chronic inflammatory disease, and periodontal ligament cells (PDLCs) are pivotal for osteogenesis. Circular RNAs (circRNAs) can regulate disease progression via targeting miRNA/mRNA axis. The purposes of this study were to explore the function and mechanism of circ_0138959 in periodontitis.
Periodontitis cell model was established by lipopolysaccharide (LPS) treatment in PDLCs. RNA expression was determined by quantitative reverse transcription-polymerase chain reaction assay. Cell proliferation was detected using 3-(4, 5-dimethylthiazol-2-y1)-2, 5-diphenyl tetrazolium bromide assay. Wound healing and cell apoptosis were examined by wound healing assay and flow cytometry. Inflammatory cytokines were measured via Enzyme-linked immunosorbent assay. Osteogenic differentiation was assessed by Alkaline phosphatase and Alizarin red S staining assays. Western blot was used for protein detection. The target interaction was validated by dual-luciferase reporter assay.
Circ_0138959 was overexpressed in periodontitis tissues and LPS-treated PDLCs. Downregulation of circ_0138959 attenuated LPS-induced inhibition of proliferation, wound healing and osteogenic differentiation but promotion of apoptosis and inflammation. Circ_0138959 acted as a miR-495-3p sponge, and the regulatory role of circ_0138959 in LPS-induced cell injury was achieved by sponging miR-495-3p. Additionally, miR-495-3p targeted TNF Receptor Associated Factor 6 (TRAF6) and miR-495-3p protected against LPS-induced cell dysfunction by targeting TRAF6. Circ_0138959 upregulated TRAF6 level via inhibiting miR-495-3p.
This study suggested that circ_0138959 upregulated the TRAF6 expression by binding to miR-495-3p, consequently aggravating LPS-induced cell damages in PDLCs. Circ_0138959 might be a probable target for treatment of periodontitis.
背景/目的:牙周炎是一种慢性炎症性疾病,牙周膜细胞(PDLCs)在骨生成中起关键作用。环状RNA(circRNAs)可通过靶向miRNA/mRNA轴调节疾病进展。本研究旨在探讨circ_0138959在牙周炎中的作用及其机制。
通过脂多糖(LPS)处理PDLCs建立牙周炎细胞模型。采用定量逆转录-聚合酶链反应检测RNA表达。使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐法检测细胞增殖。通过伤口愈合实验和流式细胞术检测伤口愈合和细胞凋亡情况。采用酶联免疫吸附测定法检测炎症细胞因子。通过碱性磷酸酶和茜素红S染色实验评估成骨分化。采用蛋白质印迹法进行蛋白质检测。通过双荧光素酶报告基因实验验证靶标相互作用。
circ_0138959在牙周炎组织和LPS处理的PDLCs中高表达。circ_0138959表达下调可减轻LPS诱导的细胞增殖抑制、伤口愈合抑制和成骨分化抑制,但可减轻细胞凋亡和炎症。circ_0138959作为miR-495-3p的海绵,通过结合miR-495-3p发挥对LPS诱导的细胞损伤的调控作用。此外,miR-495-3p靶向肿瘤坏死因子受体相关因子6(TRAF6),miR-495-3p通过靶向TRAF6保护细胞免受LPS诱导的功能障碍。circ_0138959通过抑制miR-495-3p上调TRAF6水平。
本研究表明,circ_0138959通过与miR-495-3p结合上调TRAF6表达,从而加重LPS诱导的PDLCs细胞损伤。circ_0138959可能是牙周炎治疗的一个潜在靶点。