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姜黄素通过靶向后发性白内障中 KCNQ1OT1/miR-377-3p/COL1A2 轴抑制 TGF-β2 诱导的晶状体上皮细胞增殖、迁移和侵袭。

Curcumin Suppresses TGF-β2-Induced Proliferation, Migration, and Invasion in Lens Epithelial Cells by Targeting KCNQ1OT1/miR-377-3p/COL1A2 Axis in Posterior Capsule Opacification.

机构信息

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.

出版信息

Curr Eye Res. 2022 May;47(5):715-726. doi: 10.1080/02713683.2021.2021537. Epub 2022 Mar 27.

Abstract

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.

摘要

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。

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