Department of Dermatology, Jining First People's Hospital, Jining, Shandong 272011, P.R. China.
Department of Prosthodontics, Jining Hospital of Stomatology, Jining, Shandong 272001, P.R. China.
Mol Med Rep. 2018 Jan;17(1):1919-1925. doi: 10.3892/mmr.2017.8019. Epub 2017 Nov 10.
The present study aimed to investigate the role of miRNAs during the pathogenesis of oral lichen planus (OLP). OLP is a chronic inflammatory disorder, which involves T‑cell mediated autoimmunity and affects the skin, scalp, nails and mucosa. Abundant T lymphocytes have been demonstrated to infiltrate the oral mucosa, in which the activated T cells trigger apoptosis of oral epithelial cells. Overexpression of osteopontin (OPN) and CD44 has been observed in the mucosa of patients with OLP, and it has been confirmed that OPN suppresses the apoptosis of activated CD8+ T cells via CD44. The present study initially detected the protein and mRNA expression of CD44 and OPN in the mucosa of patients with OLP by western blot analysis and reverse transcription‑quantitative polymerase chain reaction (RT‑qPCR), and confirmed the previously reported overexpression of CD44 and OPN in patients with OLP. The current study demonstrated, by RT‑qPCR, that the expression of microRNA‑214 (miR‑214), miR‑216a and miR‑216b was significantly reduced in patients with OLP. By analyzing the association between the protein level of CD44 and the expression of microRNAs (miRNAs), the present study identified a negative correlation between the expression of miR‑214 and CD44 in the mucosa samples of patients with OLP. Subsequently, the present study confirmed that miR‑214 represses endogenous CD44 expression by targeting the 3'untranslated region in HeLa, Raji and Jurkat cells. The current study indicates that reduced miR‑214 may be associated with OLP and, therefore, may be a candidate for drug development.
本研究旨在探讨 microRNAs 在口腔扁平苔藓(OLP)发病机制中的作用。OLP 是一种慢性炎症性疾病,涉及 T 细胞介导的自身免疫,影响皮肤、头皮、指甲和黏膜。大量 T 淋巴细胞已被证明浸润口腔黏膜,其中活化的 T 细胞触发口腔上皮细胞凋亡。在 OLP 患者的黏膜中观察到骨桥蛋白(OPN)和 CD44 的过表达,并且已经证实 OPN 通过 CD44 抑制活化的 CD8+T 细胞的凋亡。本研究通过 Western blot 分析和逆转录-定量聚合酶链反应(RT-qPCR)初步检测了 OLP 患者黏膜中 CD44 和 OPN 的蛋白和 mRNA 表达,并证实了 OLP 患者中 CD44 和 OPN 的过表达。本研究通过 RT-qPCR 证实,miR-214、miR-216a 和 miR-216b 在 OLP 患者中的表达显著降低。通过分析 CD44 蛋白水平与 microRNAs(miRNAs)表达之间的关联,本研究鉴定出 OLP 患者黏膜样本中 miR-214 与 CD44 表达之间存在负相关。随后,本研究证实 miR-214 通过靶向 HeLa、Raji 和 Jurkat 细胞中的 3'非翻译区抑制内源性 CD44 表达。本研究表明,miR-214 的减少可能与 OLP 相关,因此可能是药物开发的候选物。