Orthopedics, First Affiliated Hospital of Kunming Medical University, Kunming, China.
Eur Rev Med Pharmacol Sci. 2019 Nov;23(22):9729-9737. doi: 10.26355/eurrev_201911_19535.
Long noncoding RNAs (lncRNAs) have been indicated to play an important role in many different diseases. Osteoarthritis (OA) is a disease which causes a change of morphology and function in articular cartilage and synovium, leading to cartilage degradation. Synovitis is a common pathological feature of OA, owing to the proliferation of synoviocytes. In this research, we want to verify the role of lncRNA ANRIL in osteoarthritis.
qRT-PCR was used to detect the expression of lncRNA ANRIL in normal synoviocytes and osteoarthritis synoviocytes. The cell proliferation in normal synoviocytes and osteoarthritis synoviocytes after transfection with lncRNA-NC or lncRNA-ANRIL were tested. The apoptosis rate and cell cycle in normal synoviocytes and osteoarthritis synoviocytes were detected by the Flow Cytometry analysis. Western blot was used to analyze the possible mechanism that ANRIL regulated the cells' proliferation in osteoarthritis.
We indicated that the expression of ANRIL was significantly improved in OAS compared to NS. The expression of ANRIL was decreased and the cell proliferation was reduced in OAS after transfected with siRNA. And the cell cycle was suspended in G0/G1 phase and the cell apoptosis was improved in OAS after transfected with siRNA. Moreover, ANRIL could regulate the proliferation and apoptosis of OAS via miR-122-5p/DUSP4 axis.
We suggest that lncRNA ANRIL was closely related to osteoarthritis. ANRIL may be involved in the development and progression of osteoarthritis and become a potential target for diagnosis and treatment in OA.
长链非编码 RNA(lncRNA)在许多不同疾病中发挥着重要作用。骨关节炎(OA)是一种导致关节软骨和滑膜形态和功能改变的疾病,导致软骨降解。滑膜炎是 OA 的常见病理特征,由于滑膜细胞的增殖。在这项研究中,我们旨在验证 lncRNA ANRIL 在骨关节炎中的作用。
qRT-PCR 用于检测正常滑膜细胞和骨关节炎滑膜细胞中 lncRNA ANRIL 的表达。转染 lncRNA-NC 或 lncRNA-ANRIL 后,检测正常滑膜细胞和骨关节炎滑膜细胞的细胞增殖。通过流式细胞术分析检测正常滑膜细胞和骨关节炎滑膜细胞的凋亡率和细胞周期。Western blot 用于分析 ANRIL 调节骨关节炎细胞增殖的可能机制。
我们表明,OAS 中 ANRIL 的表达明显高于 NS。转染 siRNA 后,OAS 中的 ANRIL 表达降低,细胞增殖减少。转染 siRNA 后,OAS 中的细胞周期停滞在 G0/G1 期,细胞凋亡增加。此外,ANRIL 可通过 miR-122-5p/DUSP4 轴调节 OAS 的增殖和凋亡。
我们认为 lncRNA ANRIL 与骨关节炎密切相关。ANRIL 可能参与骨关节炎的发生和发展,并成为 OA 诊断和治疗的潜在靶点。