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出 处:《山东大学学报(医学版)》2007年第4期376-379,共4页Journal of Shandong University:Health Sciences
基 金:山东省卫生厅科研基金资助课题(2001CA1CJB21)
摘 要:目的:观察全反式维甲酸(ATRA)对体外培养的人Tenon囊成纤维细胞(HTCFs)增殖及凋亡的影响。方法:体外培养HTCFs,采用流式细胞仪检测细胞周期改变、细胞凋亡率、抗凋亡基因bcl-2的水平,琼脂糖凝胶电泳检测细胞DNA,研究不同浓度的ATRA对体外培养的HTCFs增殖及凋亡的影响,同时与丝裂霉素C(MMC)作比较。结果:用ATRA和MMC处理后,HTCFs细胞周期的分布发生了明显的变化,表现为G0/G1期细胞数增多,S期细胞数减少;1×10-9mol/L的ATRA即可诱导细胞的凋亡,随着浓度的增加,凋亡率显著增高;ATRA组bcl-2的水平比空白对照组大约低了一倍;DNA琼脂糖凝胶电泳结果显示:ATRA组为呈一定间隔的DNA梯形条带,MMC组呈现弥漫的片状图谱,无明显的条带。结论:ATRA可有效抑制体外培养的HTCFs的增殖,但与MMC的作用方式不同。MMC主要造成细胞坏死,而ATRA则主要诱导细胞凋亡,无明显细胞毒作用。Objective: To study the effect of all trans-retinoic acid (ATRA) on the proliferation and apoptosis of human Tenon's capsule fibroblasts(HTCFs) in vitro. Methods: Cell cycle distribution, the apoptotic rate and the expression of bcl-2 were determined by flow cytometry. Cell DNA was determined by agarose gel electrophoresis. Mitomycin C was used as a positive control. Results: Cell cycle distribution of HTCFs showed that cells of the G0/G1 phase increased and of the S phase decreased after treatment with ATRA and MMC. Cellular apoptosis was decreased by ATRA at a lower dose ( 1 × 10^-9 mol/L), and the apoptotic rate was significantly increased in a dose-dependent manner. Expression of bcl-2 was significantly decreased by ATRA. A "ladder" strand of DNA was produced from the ATRA groups by DNA agarose gel electrophoresis. Condusion: ATRA can significantly inhibit the proliferation of HTCFs and induce the apoptosis of HTCFs without apparent cytotoxicity.
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