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Adenovirus-mediated delivery of bFGF small interfering RNA increases levels of connexin 43 in the glioma cell line, U251

机译:腺病毒介导的bFGF小干扰RNA的输送增加了神经胶质瘤细胞系U251中连接蛋白43的水平

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Background bFGF is an important growth factor for glioma cell proliferation and invasion, while connexin 43 is implicated in the suppression of glioma growth. Correspondingly, gliomas have been shown to have reduced, or compromised, connexin 43 expression. Methods In this study, a bFGF-targeted siRNA was delivered to the glioma cell line, U251, using adenovirus (Ad-bFGF-siRNA) and the expression of connexin 43 and its phosphorylation state were evaluated. U251 cells were infected with Ad-bFGF-siRNA (100, 50, or 25 MOI), and infection with adenovirus expressing green fluorescent protein (Ad-GFP) at 100 MOI served as a control. Western blotting and immunofluorescence were used to detect the expression levels, phosphorylation, and localization of connexin 43 in U251 cells infected, and not infected, with Ad-bFGF-siRNA. Results Significantly higher levels of connexin 43 were detected in U251 cells infected with Ad-bFGF-siRNA at 100 and 50 MOI than in cells infected with Ad-GFP, and the same amount of connexin 43 was detected in Ad-GFP-infected and uninfected U251 cells. Connexin 43 phosphorylation did not differ between Ad-bFGF-siRNA-infected and uninfected U251 cells. However, the ratio of phosphorylated to unphosphorylated connexin 43 in Ad-bFGF-siRNA cells was lower, and connexin 43 was predominantly localized to the cytoplasm. Using a scrape loading dye transfer assay, more Lucifer Yellow was transferred to neighboring cells in the Ad-bFGF-siRNA treated group than in the control group. Conclusion To our knowledge, this is the first description of a role for connexin 43 in the inhibition of U251 growth using Ad-bFGF-siRNA.
机译:背景bFGF是神经胶质瘤细胞增殖和侵袭的重要生长因子,而连接蛋白43与神经胶质瘤生长的抑制有关。相应地,已经显示神经胶质瘤减少或损害了连接蛋白43的表达。方法在本研究中,使用腺病毒(Ad-bFGF-siRNA)将靶向bFGF的siRNA递送至神经胶质瘤细胞U251,并评估连接蛋白43的表达及其磷酸化状态。将U251细胞用Ad-bFGF-siRNA(100、50或25 MOI)感染,并用表达绿色荧光蛋白(Ad-GFP)的腺病毒以100 MOI感染作为对照。 Western印迹和免疫荧光用于检测感染和未感染Ad-bFGF-siRNA的U251细胞中连接蛋白43的表达水平,磷酸化和定位。结果分别在100和50 MOI下,用Ad-bFGF-siRNA感染的U251细胞中检测到的连接蛋白43水平明显高于用Ad-GFP感染的细胞,并且在感染和未感染Ad-GFP的细胞中检测到了相同量的连接蛋白43 U251细胞。连接蛋白43的磷酸化在Ad-bFGF-siRNA感染和未感染的U251细胞之间没有差异。但是,Ad-bFGF-siRNA细胞中磷酸化与未磷酸化的连接蛋白43的比例较低,并且连接蛋白43主要位于细胞质中。使用刮擦染料转移测定法,与对照组相比,在Ad-bFGF-siRNA处理组中,更多的荧光素黄转移到了相邻细胞中。结论据我们所知,这是连接蛋白43在使用Ad-bFGF-siRNA抑制U251生长中的作用的首次描述。

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