Department of Pharmacy, Jinan Second People's Hospital (Jinan Eye Hospital), Jinan, China.
Department of Ophthalmology, Jinan Second People's Hospital (Jinan Eye Hospital), Jinan, China and.
Curr Eye Res. 2022 May;47(5):715-726. doi: 10.1080/02713683.2021.2021537. Epub 2022 Mar 27.
Posterior capsule opacification (PCO) is a common complication after cataract surgery, which can lead to secondary loss of vision. Curcumin has been reported to play a suppressive role in PCO progression, and the potential molecular mechanism was explored in this study. Cell viability and proliferation were analyzed by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and 5-Ethynyl-2'-deoxyuridine (EdU) assay. Transwell assay and wound healing assay were performed to assess cell invasion and migration abilities. Western blot assay and reverse transcription-quantitative polymerase chain reaction (RT-qPCR) were conducted to measure the expression of proteins and RNAs. Dual-luciferase reporter assay and RNA immunoprecipitation (RIP) assay were conducted to confirm the interaction between microRNA-377-3p (miR-377-3p) and KCNQ1 opposite strand/antisense transcript 1 (KCNQ1OT1) or collagen type I alpha 2 chain (COL1A2). Curcumin dose-dependently alleviated transforming growth factor-β2 (TGF-β2)-induced proliferation, migration, and invasion in SRA01/04 cells. KCNQ1OT1 was up-regulated in PCO patients and TGF-β2-induced SRA01/04 cells. Curcumin-induced protective effects in TGF-β2-induced SRA01/04 cells were largely overturned by KCNQ1OT1 overexpression. KCNQ1OT1 directly interacted with miR-377-3p and negatively regulated its expression. miR-377-3p silencing overturned Curcumin-mediated protective effects in SRA01/04 cells upon TGF-β2 treatment. miR-377-3p directly interacted with the 3' untranslated region (3'UTR) of COL1A2. COL1A2 overexpression largely counteracted KCNQ1OT1 silencing-induced effects in TGF-β2-stimulated SRA01/04 cells. KCNQ1OT1 could up-regulate COL1A2 expression by sponging miR-377-3p in SRA01/04 cells. In conclusion, Curcumin suppressed TGF-β2-induced malignant changes in lens epithelial cells by targeting KCNQ1OT1/miR-377-3p/COL1A2 axis.
后囊膜混浊 (PCO) 是白内障手术后的一种常见并发症,可导致视力的继发性丧失。姜黄素已被报道在 PCO 进展中发挥抑制作用,本研究探索了其潜在的分子机制。 通过 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐 (MTT) 测定法和 5-乙炔基-2'-脱氧尿苷 (EdU) 测定法分析细胞活力和增殖。Transwell 测定法和划痕愈合测定法用于评估细胞侵袭和迁移能力。Western blot 测定法和逆转录定量聚合酶链反应 (RT-qPCR) 用于测量蛋白质和 RNA 的表达。双荧光素酶报告基因测定法和 RNA 免疫沉淀 (RIP) 测定法用于证实 microRNA-377-3p (miR-377-3p) 与 KCNQ1 反义链/反义转录本 1 (KCNQ1OT1) 或胶原 I 型 α2 链 (COL1A2) 之间的相互作用。 姜黄素剂量依赖性地减轻转化生长因子-β2 (TGF-β2) 诱导的 SRA01/04 细胞增殖、迁移和侵袭。PCO 患者和 TGF-β2 诱导的 SRA01/04 细胞中上调了 KCNQ1OT1。KCNQ1OT1 过表达大大推翻了姜黄素诱导的 TGF-β2 诱导的 SRA01/04 细胞中的保护作用。KCNQ1OT1 与 miR-377-3p 直接相互作用,并负调控其表达。miR-377-3p 沉默推翻了 TGF-β2 处理后 SRA01/04 细胞中姜黄素介导的保护作用。miR-377-3p 直接与 COL1A2 的 3'非翻译区 (3'UTR) 相互作用。COL1A2 的过表达在很大程度上抵消了 KCNQ1OT1 沉默在 TGF-β2 刺激的 SRA01/04 细胞中引起的作用。KCNQ1OT1 可以通过海绵吸附 miR-377-3p 在 SRA01/04 细胞中上调 COL1A2 的表达。 总之,姜黄素通过靶向 KCNQ1OT1/miR-377-3p/COL1A2 轴抑制 TGF-β2 诱导的晶状体上皮细胞恶性变化。