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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:通过培养的人视网膜色素上皮细胞中可折叠荚膜玻璃体释放的siRNA-PKCα引起的蛋白激酶Cα下调

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摘要

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:我们以前发现,蛋白激酶Cα(PKCα)的下调可以抑制视网膜色素上皮细胞(RPE)的细胞增殖,该细胞参与增殖性玻璃体视网膜病变(PVR)的发展。在这项研究中,我们测试了可培养的人RPE细胞中可折叠荚膜玻璃体(FCVB)释放的小干扰RNA(siRNA)-PKCα是否可以下调PKCα。通过紫外(UV)分光光度计测定的SiRNA-PKCα含量以1到96小时的时间依赖性和剂量依赖性在200到300、400、500和600 nm的FCVB中释放出来。五个浓度。含量(y)与时间(x)具有良好的线性关系,尤其是在600 nmsiRNA-PKCα组中(y = 16.214x,R 2 = 0.9809)。用FCVBs释放的siRNA-PKCα处理后,RT-PCR,Western印迹和RPE细胞的免疫荧光分析显着降低了PKCα。这些结果表明,在人RPE细胞中从FCVB释放的siRNA-PKCα显着下调了PKCα,为我们提供了预防PVR的新途径。

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