Department of Endocrinology, Fujian Provincial Hospital, Fujian Medical University, Fuzhou 350001, China.
Mol Biol Rep. 2011 Jun;38(5):3089-94. doi: 10.1007/s11033-010-9977-5. Epub 2010 Feb 3.
To construct a recombinant adenovirus vector expressing a RNAi for the Nuclear Factor kappa B (NF-κB)/p65 gene and use it to explore the role of the NF-κB pathway on the regulation of proliferation and apoptosis of vascular endothelial cells. A recombinant adenovirus containing a RNAi cassette targeting the p65 gene was constructed, and its silencing effect on p65 was detected by Western blot analysis in ECV304 cells. Expression of the p65 protein in ECV304 cells was efficiently down-regulated by the RNAi adenovirus for more than 6 days. ECV304 cells proliferation and apoptosis were measured using the MTT assay and flow cytometry, respectively. Blocking the NF-κB pathway with the RNAi adenovirus substantially decreased the proliferation of ECV304 cells, but only slightly affected cell apoptosis. We used a NF-κB/p65-targeting RNAi adenovirus to demonstrate the role of the NF-κB pathway in the regulation of ECV304 cell proliferation. This adenovirus may serve as an important tool to study the NF-κB pathway.
构建靶向核因子 κB(NF-κB)/p65 基因的 RNAi 重组腺病毒载体,并探讨 NF-κB 通路在血管内皮细胞增殖和凋亡调控中的作用。构建了一种包含靶向 p65 基因的 RNAi 盒的重组腺病毒,并用 Western blot 分析检测其在 ECV304 细胞中对 p65 的沉默作用。RNAi 腺病毒能有效下调 ECV304 细胞中 p65 蛋白的表达超过 6 天。分别用 MTT 法和流式细胞术检测 ECV304 细胞的增殖和凋亡。用 RNAi 腺病毒阻断 NF-κB 通路可显著抑制 ECV304 细胞的增殖,但对细胞凋亡影响较小。我们使用靶向 NF-κB/p65 的 RNAi 腺病毒证明了 NF-κB 通路在调节 ECV304 细胞增殖中的作用。该腺病毒可能成为研究 NF-κB 通路的重要工具。