Department of Periodontology, Shanghai Ninth People's Hospital Affiliated Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China.
Int J Oral Sci. 2011 Jul;3(3):125-34. doi: 10.4248/IJOS11046.
MicroRNAs (miRNAs) have been demonstrated to play an important role in regulation of the immunoinflammatory response; however, the function of miRNAs in periodontal inflammation has not been investigated. The objective of this study was to explore the properties of miRNAs in periodontal inflammation by comparing miRNA profiles of inflamed and healthy gingival tissues. Gingival tissues were obtained from 10 periodontitis patients and 10 healthy subjects. After RNA extraction, miRNA profiles were analyzed by microarray, and expression levels of selected miRNAs were confirmed by real-time quantitative reverse transcription polymerase chain reaction (RT-PCR). Analyses using two computational methods, Targetscan and MicroRNA.org, were combined to identify common targets of these miRNAs. Finally, the individual miRNA expression levels of three toll-like receptor (TLR)-related miRNAs from inflamed and healthy gingival tissues were evaluated by RT-PCR. Ninety-one miRNAs were found to be upregulated and thirty-four downregulated over two-fold in inflamed gingival tissue compared with those in healthy gingival tissue. Twelve selected inflammatory-related miRNAs, hsa-miR-126*, hsa-miR-20a, hsa-miR-142-3p, hsa-miR-19a, hsa-let-7f, hsa-miR-203, hsa-miR-17, hsa-miR-223, hsa-miR-146b, hsa-miR-146a, hsa-miR-155, and hsa-miR-205 showed comparable expression levels by microarray and real-time quantitative RT-PCR analyses. In addition, the putative inflammation targets of these miRNAs were predicted, and three that were tested (hsa-miRNA-146a, hsa-miRNA-146b, and hsa-miRNA-155), showed significant differences between inflamed and healthy gingiva. This remarkable difference in miRNA profiles between periodontal diseased and healthy gingiva implicates a probable close relationship between miRNAs and periodontal inflammation. The data also suggest that the regulation of TLRs in periodontal inflammation may involve miRNA pathways.
微小 RNA(miRNAs)已被证明在免疫炎症反应的调节中发挥重要作用;然而,miRNAs 在牙周炎症中的功能尚未得到研究。本研究旨在通过比较炎症和健康牙龈组织的 miRNA 谱,探讨 miRNA 在牙周炎症中的特性。从 10 名牙周炎患者和 10 名健康受试者中获取牙龈组织。提取 RNA 后,通过微阵列分析 miRNA 谱,并通过实时定量逆转录聚合酶链反应(RT-PCR)验证选定 miRNA 的表达水平。使用两种计算方法,Targetscan 和 MicroRNA.org,结合分析来识别这些 miRNA 的共同靶标。最后,通过 RT-PCR 评估来自炎症和健康牙龈组织的三个 Toll 样受体(TLR)相关 miRNA 的个体 miRNA 表达水平。与健康牙龈组织相比,在炎症牙龈组织中发现 91 个 miRNA 上调,34 个 miRNA 下调两倍以上。在微阵列和实时定量 RT-PCR 分析中,选择的 12 个炎症相关 miRNA(hsa-miR-126*、hsa-miR-20a、hsa-miR-142-3p、hsa-miR-19a、hsa-let-7f、hsa-miR-203、hsa-miR-17、hsa-miR-223、hsa-miR-146b、hsa-miR-146a、hsa-miR-155 和 hsa-miR-205)表现出可比的表达水平。此外,预测了这些 miRNA 的潜在炎症靶标,并对其中三个进行了测试(hsa-miRNA-146a、hsa-miRNA-146b 和 hsa-miRNA-155),在炎症和健康牙龈之间表现出显著差异。牙周病和健康牙龈之间 miRNA 谱的这种显著差异暗示了 miRNA 与牙周炎症之间可能存在密切关系。该数据还表明,TLR 在牙周炎症中的调节可能涉及 miRNA 途径。