眼科 ›› 2025, Vol. 34 ›› Issue (2): 110-115.doi: 10.13281/j.cnki.issn.1004-4469.2025.02.004

• 论著 • 上一篇    下一篇

龙胆苦苷对人眼Tenon囊成纤维细胞增生和迁移的抑制效应研究

李亚文 唐艺真2  郭洪涛3 唐广贤  闫晓伟1  耿玉磊 张恒丽    

  1. 1石家庄市人民医院眼科,石家庄050000; 2首都医科大学附属北京同仁医院 北京同仁眼科中心 眼科学与视觉科学北京市重点实验室,北京100730; 3石家庄市人民医院骨科,石家庄 050000
  • 收稿日期:2024-12-06 出版日期:2025-03-25 发布日期:2025-03-13
  • 通讯作者: 张恒丽,Email: simoomy@126.com
  • 基金资助:
    河北省重点研发计划项目(223777110D)

Investigation of the inhibitory effects of gentiopicroside on the proliferation and migration of human Tenon's capsule fibroblasts

Li Yawen1, Tang Yizhen2, Guo Hongtao3, Tang Guangxian1, Yan Xiaowei1, Geng Yulei1, Zhang Hengli1   

  1. 1 Department of Ophthalmology, Shijiazhuang People’s Hospital, Shijiazhuang 050000, China; 2 Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University; Beijing Key Laboratory of Ophthalmology and Visual Science, Beijing 100730, China;  3 Department of Orthopedics, Shijiazhuang People’s Hospital, Shijiazhuang 050000, China 
  • Received:2024-12-06 Online:2025-03-25 Published:2025-03-13
  • Contact: Zhang Hengli, Email: simoomy@126.com
  • Supported by:
    Hebei Province Key Research and Development Program Project(223777110D)

摘要: 目的 观察分析龙胆苦苷(GPS)对体外培养的人眼Tenon囊成纤维细胞(HTCF)增生及迁移能力的抑制效应。设计 实验研究。研究对象 人眼Tenon 囊成纤维细胞。方法 取在本院行斜视矫正术患者的Tenon囊组织进行原代培养,采用免疫荧光染色鉴定HTCF,生长良好的第3~5代HTCF用于实验。设定药物组(GPS浓度依次为5、10、20、35、45和50 μg/mL)和对照组(GPS浓度0 μg/mL,NC组)。采用CCK-8法检测不同实验组HTCF孵育24、48、72及96 h时细胞增生能力,细胞划痕法用于检测不同实验组HTCF孵育6、12、24及48 h时细胞迁移能力。主要指标 细胞鉴定、细胞增生量和细胞迁移量。结果  HTCF原代培养生长良好;免疫荧光染色显示,胞浆中波形蛋白和纤维连接蛋白(FN1)染色均呈阳性,分别表现为均匀的红色和绿色荧光,DAPI核染蓝色荧光。CCK-8检测结果显示,不同浓度GPS孵育HTCF后48、72和96 h,细胞增生能力差异均有统计学意义(F48h=14.947,F72h =25.683,F96h =131.392,P均<0.001)。与NC组相比,35、45及50 μg/mL浓度GPS药物组HTCF孵育48、72和96 h时细胞增生能力均显著降低(P均<0.01)。划痕实验结果显示,与NC组相比,各浓度GPS药物组的细胞在6、12和24 h时迁移能力均无显著差异(P均>0.05)。随着时间延长,NC组,5、10和20 μg/ml浓度GPS药物组的HTCF在30 h划痕已闭合;而35、45和50 μg/mL浓度GPS药物组与NC组相比,30 h时细胞迁移能力显著降低(P均<0.001)。结论 龙胆苦苷浓度达35 μg/mL时可显著抑制HTCF的增生和迁移能力。 (眼科,2025,34: 110-115)

关键词: 龙胆苦苷, 人眼Tenon 囊成纤维细胞

Abstract:  Objective To observe and analyze the inhibitory effects of gentiopicroside (GPS) on the proliferation and migration abilities of human Tenon's capsule fibroblasts (HTCF) cultured in vitro. Design Experiment study. Participants Human Tenon's capsule fibroblasts. Methods Human Tenon's capsular tissue was obtained during the strabismus correction surgery at our hospital. HTCF were identified through immunofluorescence staining, and the well-cultivated third to fifth generation HTCF were utilized in the experiment. The drug groups were established with GPS concentrations of 5, 10, 20, 35, 45 and 50 μg/mL, respectively, and the negative control group with a GPS concentration of 0 μg/mL (NC group) was also set. CCK-8 assay was employed to measure the cell proliferation capabilities of HTCF in the various groups at 24, 48, 72 and 96 h. Cell scratch assay was used to examine the cell migration abilities of HTCF in various groups at 6, 12, 24 and 48 h. Main Outcome Measures The cell identification, cell proliferation amount and cell migration amount. Results Cultured cells grew well. The positive immunoreactivity for Vimentin and fibronectin (FN1) was observed. Specifically, Vimentin manifested as uniform red fluorescence and fibronectin as uniform green fluorescence within the cytoplasm, respectively, while the DAPI stains the nucleus with blue fluorescence. CCK-8 assay showed that significant differences in cell proliferation ability among HTCF incubated for 48, 72 and 96 h with various concentrations of GPS (F48h=14.947, F72h =25.683, F96h =131.392, all P<0.001). The cell proliferation ability of HTCF in the GPS drug groups with concentrations of 35, 45 and 50 μg/mL was significantly reduced at 48, 72 and 96 h, there were significant differences compared with the NC group (all P<0.01). The scratch assay results indicated that, in contrast to the NC group, no significant differences were found in the cell migration abilities of all GPS drug groups at 6, 12 and 24 h (all P>0.05). At 30 h, the HTCF in the NC group, as well as those in the GPS drug groups with concentrations of 5, 10 and 20 μg/mL, had closed. Nevertheless, when compared with the NC group, the cell migration abilities in the GPS drug groups with concentrations of 35, 45 and 50 μg/mL were significantly decreased at 30 h, and all these differences were statistically significant (all P<0.001). Conclusion GPS at a concentration of 35 μg/mL significantly inhibited the proliferation and migration of HTCF. (Ophthalmol CHN, 2025, 34: 110-115)

Key words: gentiopicroside, human Tenon's capsule fibroblasts