Jing Jiaona, Li Ping, Li Tiejun, Sun Yuncheng, Guan Huaijin
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.
J Ophthalmol. 2013;2013:354798. doi: 10.1155/2013/354798. Epub 2013 Oct 28.
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).
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。