首页> 外文期刊>International Journal of Nanomedicine >Protein kinase Cα downregulation via siRNA-PKCα released from foldable capsular vitreous body in cultured human retinal pigment epithelium cells
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Protein kinase Cα downregulation via siRNA-PKCα released from foldable capsular vitreous body in cultured human retinal pigment epithelium cells

机译:通过在培养的人视网膜色素上皮细胞中从可折叠囊玻璃体体释放的SiRNA-PKCα下调蛋白质激酶Cα

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Abstract: We previously found that downregulation of protein kinase Cα (PKCα) can inhibit retinal pigment epithelium (RPE) cell proliferation involved in the development of proliferative vitreoretinopathy (PVR). In this study, we tested whether PKCα could be downregulated via small interfering RNA (siRNA)-PKCα released from foldable capsular vitreous body (FCVB) in cultured human RPE cells. SiRNA-PKCα content, determined by ultraviolet (UV) spectrophotometer, was released from FCVB containing 200, 300, 400, 500, and 600 nm siRNA-PKCα in a time-dependent manner from 1 to 96 hours and a dose-dependent manner at five concentrations. The content (y) had a good linear relationship with time (x), especially in the 600 nm siRNA-PKCα group (y = 16.214x, R2 = 0.9809). After treatment with siRNA-PKCα released from FCVBs, the PKCα was significantly decreased by RT-PCR, Western blot, and immunofluorescence analysis in RPE cells. These results indicate that PKCα was significantly downregulated by siRNA-PKCα released from FCVB in human RPE cells and provide us with a new avenue to prevent PVR.
机译:摘要:我们以前发现蛋白质激酶Cα(PKCα)的下调可以抑制视网膜颜料上皮(RPE)细胞增殖,参与增殖的玻璃体病变(PVR)的发育。在该研究中,我们测试了PKCα是否可以通过在培养的人RPE细胞中从可折叠的荚膜玻璃体(FCVB)中释放的小干扰RNA(siRNA)-pkcα来下调。由紫外(UV)分光光度计测定的siRNA-PKCα含量从含有200,300,400,500和600nm siRNA-PKCα的FCVB释放,以时间依赖于1至96小时和剂量依赖性方式五种浓度。内容(Y)与时间(x)具有良好的线性关系,特别是在600nm siRNA-pKCα组中(Y = 16.214倍,R2 = 0.9809)。在用FCVBS释放的siRNA-PKCα处理后,RT-PCR,Western印迹和RPE细胞中的免疫荧光分析显着降低PKCα。这些结果表明,PKCα通过从FCVB中的SiRNA-PKCα显着下调,在人RPE细胞中释放,并为我们提供新的途径以防止PVR。

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