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靶向结缔组织生长因子的RNA干扰抑制转化生长因子-β2诱导的人眼球筋膜成纤维细胞增殖。

RNA Interference Targeting Connective Tissue Growth Factor Inhibits the Transforming Growth Factor- β 2 Induced Proliferation in Human Tenon Capsule Fibroblasts.

作者信息

Jing Jiaona, Li Ping, Li Tiejun, Sun Yuncheng, Guan Huaijin

机构信息

Eye Institute, Affiliated Hospital of Nantong University, 20 Xisi Road, Nantong, Jiangsu Province 226001, China ; Nanjing Governmental Hospital, 116 Chengxian Street, Nanjing, Jiangsu Province 210018, China.

出版信息

J Ophthalmol. 2013;2013:354798. doi: 10.1155/2013/354798. Epub 2013 Oct 28.

Abstract

Purpose. This study was to determine the effect of CTGF-small interfering RNA (siRNA) on TGF- β 2-induced proliferation in human Tenon capsule fibroblasts (HTFs). Methods. HTFs were transfected with four of CTGF-siRNAs separately for screening of gene silencing efficacy that was determined by transcript level measured by quantitative real-time PCR (qRT-PCR). Recombinant TGF- β 2 was added into the culture to stimulate the proliferation of HTFs. The gene silencing efficacy of the siRNAs was evaluated by qRT-PCR and immunofluorescence of CTGF transcript and protein levels. The viability of HTFs was determined by cell counting kit-8 (CCK-8). FCM was used to assess cell cycle after CTGF-siRNA transfection. Results. The expression of CTGF and proliferation of HTFs were increased significantly by TGF- β 2 stimulation. The transfection of CTGF-siRNA abolished the upregulation of CTGF and cell proliferation induced by TGF- β 2. The analysis of cell cycle indicated that CTGF-siRNA treatment stimulated cells from S phase to G0/G1 phase in comparison with the inverse physiologic function of TGF- β 2. Conclusion. CTGF targeting siRNA could effectively suppress the expression of CTGF and attenuate the proliferation of HTFs. The siRNA approach may provide a therapeutic option for eliminating filtration bleb scarring after glaucoma filtration surgery (GFS).

摘要

目的。本研究旨在确定结缔组织生长因子小干扰RNA(siRNA)对转化生长因子-β2(TGF-β2)诱导的人Tenon囊成纤维细胞(HTF)增殖的影响。方法。将四种CTGF-siRNA分别转染至HTF,通过定量实时聚合酶链反应(qRT-PCR)检测转录水平来筛选基因沉默效果。向培养物中添加重组TGF-β2以刺激HTF增殖。通过qRT-PCR以及CTGF转录本和蛋白水平的免疫荧光评估siRNA的基因沉默效果。使用细胞计数试剂盒-8(CCK-8)测定HTF的活力。采用流式细胞术(FCM)评估CTGF-siRNA转染后的细胞周期。结果。TGF-β2刺激显著增加了CTGF的表达以及HTF的增殖。CTGF-siRNA转染消除了TGF-β2诱导的CTGF上调和细胞增殖。细胞周期分析表明,与TGF-β2的相反生理功能相比,CTGF-siRNA处理使细胞从S期进入G0/G1期。结论。靶向CTGF的siRNA可有效抑制CTGF的表达并减弱HTF的增殖。siRNA方法可能为消除青光眼滤过手术(GFS)后滤过泡瘢痕形成提供一种治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b258/3830853/e80c4b222060/JOP2013-354798.001.jpg

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