The Expression of Circ_0000615 in Tenon’s Capsule Fibroblasts and Its Effect on Cell Proliferation and Migration

IF 2.9 4区 医学 Q1 Medicine
Yanxi Wang, Xing Chen, Zhenhua Yang, Xuelin Yu, Manhua Xu, Gangjing Kang
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引用次数: 0

Abstract

To explore the expression of circ_0000615 in HTFs and its effect on cell proliferation and migration. With in vitro culture of HTFs, qRT-PCR was performed to detect the expression of circ_0000615 in HTFs. Cells in logarithmic phase were taken for subsequent experiments, and the following groups were constructed, including HTF blank control group (C group); HTFs+10 ng/mL TGF-β1 group (TGF-β1 group); HTFs+si-NC group (si-NC group); and HTFs+si-circ_0000615 group (si-circ_0000615 group). CCK-8 assay was performed to detect cell proliferation, Cell Monoclonal Assay was used to detect Cell Monoclonal Formationand, Transwell assay was conducted simultaneously to detect cell migration. According to the results of qRT-PCR, compared with C group, after induction of HTFs with TGF-β1 for 24 h and 48 h, TGF-β1 group showed significantly increased expressions of circ_0000615, with statistically significant differences (P < 0.05). After induction of HTFs with TGF-β1, compared with C group, TGF-β1 group had enhanced cell proliferation, monoclonal formation and migration, showing statistically significant differences (P < 0.05). Furthermore, after cell transfections for HTFs, compared with si-NC group, si-circ_0000615 group showed obviously downregulated expression of circ_0000615 in HTFs, accompanied by evidently weakened cell proliferation, monoclonal formation and migration, statistically significant differences (P < 0.05). Circ_0000615 is highly expressed in HTFs. A silenced expression of circ_0000615 may inhibit the proliferation and migration of HTFs.
腱鞘囊成纤维细胞中 Circ_0000615 的表达及其对细胞增殖和迁移的影响
探讨circ_0000615在HTFs中的表达及其对细胞增殖和迁移的影响。体外培养HTFs,采用qRT-PCR检测circ_0000615在HTFs中的表达。取对数期细胞进行后续实验,构建如下组:HTF空白对照组(C组);HTFs+10 ng/mL TGF-β1组(TGF-β1组);HTFs+si-NC组(si-NC组);和html +si-circ_0000615组(si-circ_0000615组)。CCK-8法检测细胞增殖,cell单克隆法检测细胞形成,Transwell法检测细胞迁移。qRT-PCR结果显示,与C组相比,TGF-β1诱导HTFs 24 h和48 h后,TGF-β1组circ_0000615表达显著升高,差异有统计学意义(P < 0.05)。TGF-β1诱导HTFs后,与C组比较,TGF-β1组细胞增殖、单克隆形成和迁移能力增强,差异有统计学意义(P < 0.05)。细胞转染HTFs后,与si-NC组相比,si-circ_0000615组HTFs中circ_0000615的表达明显下调,细胞增殖、单克隆形成和迁移明显减弱,差异有统计学意义(P < 0.05)。Circ_0000615在html中高表达。circ_0000615的沉默表达可能抑制HTFs的增殖和迁移。
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来源期刊
CiteScore
4.30
自引率
17.20%
发文量
145
审稿时长
2.3 months
期刊介绍: Information not localized
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