Wu Huarong, Lei Daikun, Zhang Xiaoling, Wang Mengfei, Wang Yuanyuan, Xia Jie, Chen Fan, Chen Bei, Tian Yanming
Department of Ophthalmology, Anqing Municipal Hospital, Anqing, China.
Department of Ophthalmology, Beijing Road Medical District, General Hospital of Xinjiang Military Region, Urumqi, Xinjiang, China.
Stem Cells Int. 2023 Feb 10;2023:2742839. doi: 10.1155/2023/2742839. eCollection 2023.
This study is aimed at discussing the value of RNA interference technology on inhibiting lacrimal gland fibrosis in IgG4-related ocular disease (IgG4-ROD).
Six patients with IgG4-ROD who came to the hospital for surgical treatment from October 2018 to August 2019 were selected, and their diseased lacrimal glands were taken for primary cell culture and fibroblast identification. High efficiency and specificity small interference RNA (siRNA) plasmid vector was constructed, its inhibitory effect on fibroblast proliferation was determined by CCK-8 assay, and the appropriate concentration was selected as the siRNA concentration for subsequent experiments. RT-PCR and Western blot detected the relative expression levels of Fibulin-5 mRNA and protein in the cells 48 hours after transfection. The apoptosis rate of each group of cells at 24 hours, 48 hours, and 72 hours after transfection was detected by flow cytometry, and the proliferation and apoptosis of cells after silencing Fibulin-5 were analyzed and compared.
24 hours after transfection, there was no significant difference in the proliferation rate among the four groups ( > 0.05); 48 hours and 72 hours after Fibulin-5 siRNA transfection, the proliferation activity of the transfected cells was significantly decreased compared with the 0 nM group, and the inhibitory effect of 75 nM siRNA was the strongest. The expression of Fibulin-5 mRNA and protein in the siRNA-transfected cells was significantly decreased compared with the blank and empty vector negative siRNA groups, and the difference was statistically significant ( < 0.05). The apoptosis rate of cells in the Fibulin-5 siRNA transfection group was significantly higher than that of cells in the blank and empty vector negative siRNA groups, and the difference was statistically significant ( < 0.05).
Fibulin-5 siRNA recombinant plasmid can significantly downregulate the mRNA and protein expressions of target gene Fibulin-5 and promote apoptosis after transfection into IgG4-ROD lacrimal gland fibroblasts. It is speculated that Fibulin-5 can be used as a target to effectively inhibit the fibrosis of lacrimal gland tissues by RNAi technique.
探讨RNA干扰技术对抑制IgG4相关性眼病(IgG4-ROD)泪腺纤维化的作用。
选取2018年10月至2019年8月来院接受手术治疗的6例IgG4-ROD患者,取其病变泪腺进行原代细胞培养及成纤维细胞鉴定。构建高效特异性小干扰RNA(siRNA)质粒载体,采用CCK-8法检测其对成纤维细胞增殖的抑制作用,选取合适浓度作为后续实验的siRNA浓度。转染48小时后,采用RT-PCR和Western blot检测细胞中Fibulin-5 mRNA和蛋白的相对表达水平。采用流式细胞术检测转染后24小时、48小时和72小时各组细胞的凋亡率,分析比较沉默Fibulin-5后细胞的增殖与凋亡情况。
转染后24小时,四组细胞增殖率差异无统计学意义(>0.05);Fibulin-5 siRNA转染后48小时和72小时,转染细胞的增殖活性较0 nM组显著降低,75 nM siRNA的抑制作用最强。与空白组和空载体阴性siRNA组相比,siRNA转染细胞中Fibulin-5 mRNA和蛋白的表达显著降低,差异有统计学意义(<0.05)。Fibulin-5 siRNA转染组细胞的凋亡率显著高于空白组和空载体阴性siRNA组,差异有统计学意义(<0.05)。
Fibulin-5 siRNA重组质粒转染IgG4-ROD泪腺成纤维细胞后,可显著下调靶基因Fibulin-5的mRNA和蛋白表达,促进细胞凋亡。推测Fibulin-5可作为靶点,通过RNAi技术有效抑制泪腺组织纤维化。