Department of Prosthodontics, Shanghai Key Laboratory of Stomatology, Ninth People's Hospital Affiliated to Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
Department of Prosthodontics, Shanghai Key Laboratory of Stomatology, Ninth People's Hospital Affiliated to Shanghai Jiao Tong University, School of Medicine, Shanghai, China
Biosci Rep. 2017 Oct 11;37(5). doi: 10.1042/BSR20170768. Print 2017 Oct 31.
Peri-implantitis, which is characterized by dense inflammatory infiltrates and increased osteoclast activity, can lead to alveolar bone destruction and implantation failure. miRNAs participate in the regulation of various inflammatory diseases, such as periodontitis and osteoporosis. Therefore, the present study aimed to investigate the differential expression of miRNAs in canine peri-implantitis and to explore the functions of their target genes. An miRNA sequence analysis was used to identify differentially expressed miRNAs in peri-implantitis. Under the criteria of a fold-change >1.5 and <0.01, 8 up-regulated and 30 down-regulated miRNAs were selected for predictions of target genes and their biological functions. Based on the results of Gene Ontology (GO) and KEGG pathway analyses, these miRNAs may fine-tune the inflammatory process in peri-implantitis through an intricate mechanism. The results of quantitative real-time PCR (qRT-PCR) revealed that let-7g, , and may play important roles in peri-implantitis and are worth further investigation. The results of the present study provide insights into the potential biological effects of the differentially expressed miRNAs, and specific enrichment of target genes involved in the mitogen-activated protein kinase (MAPK) signaling pathway was observed. These findings highlight the intricate and specific roles of miRNAs in inflammation and osteoclastogenesis, both of which are key aspects of peri-implantitis, and thus may contribute to future investigations of the etiology, underlying mechanism, and treatment of peri-implantitis.
种植体周围炎的特征是密集的炎症浸润和破骨细胞活性增加,可导致牙槽骨破坏和种植体失败。miRNAs 参与了多种炎症性疾病的调节,如牙周炎和骨质疏松症。因此,本研究旨在探讨犬种植体周围炎中 miRNAs 的差异表达,并探索其靶基因的功能。通过 miRNA 序列分析鉴定种植体周围炎中差异表达的 miRNAs。根据倍数变化 >1.5 和 <0.01 的标准,选择了 8 个上调和 30 个下调的 miRNAs 进行靶基因预测及其生物学功能分析。基于基因本体 (GO) 和 KEGG 通路分析的结果,这些 miRNAs 可能通过复杂的机制微调种植体周围炎的炎症过程。定量实时 PCR (qRT-PCR) 的结果表明,let-7g、miR-146a 和 miR-155 可能在种植体周围炎中发挥重要作用,值得进一步研究。本研究的结果深入了解了差异表达 miRNAs 的潜在生物学效应,并且观察到参与丝裂原活化蛋白激酶 (MAPK) 信号通路的靶基因的特异性富集。这些发现强调了 miRNAs 在炎症和破骨细胞生成中的复杂和特异性作用,这两者都是种植体周围炎的关键方面,因此可能有助于进一步研究种植体周围炎的病因、潜在机制和治疗方法。