State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-Sen University, Guangzhou, People's Republic of China.
Int J Nanomedicine. 2011;6:1303-11. doi: 10.2147/IJN.S19405. Epub 2011 Jun 22.
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, R(2) = 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.
我们之前发现,下调蛋白激酶 Cα(PKCα)可以抑制视网膜色素上皮(RPE)细胞增殖,这涉及到增生性玻璃体视网膜病变(PVR)的发生。在这项研究中,我们测试了折叠式囊玻璃体(FCVB)中释放的小干扰 RNA(siRNA)-PKCα是否可以下调培养的人 RPE 细胞中的 PKCα。通过紫外(UV)分光光度计测定,siRNA-PKCα 含量在 1 至 96 小时内呈时间依赖性,在五个浓度下呈剂量依赖性从 FCVB 中释放出来,其中含有 200、300、400、500 和 600nm 的 siRNA-PKCα。含量(y)与时间(x)呈良好的线性关系,尤其是在 600nm siRNA-PKCα 组中(y=16.214x,R²=0.9809)。在用 FCVB 释放的 siRNA-PKCα 处理后,RPE 细胞中的 RT-PCR、Western blot 和免疫荧光分析均显示 PKCα 显著降低。这些结果表明,siRNA-PKCα 可显著下调人 RPE 细胞中 FCVB 释放的 PKCα,为我们预防 PVR 提供了新途径。