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全反式维甲酸对人视网膜色素上皮细胞增生的抑制作用
引用本文:李中秋,吴雅臻,韩宁.全反式维甲酸对人视网膜色素上皮细胞增生的抑制作用[J].吉林大学学报(医学版),2008,34(2):258-261.
作者姓名:李中秋  吴雅臻  韩宁
作者单位:吉林大学第二医院眼科,吉林 长春130041
基金项目:吉林省科技厅科研项目 , 长春市科技厅基金
摘    要:目的:研究全反式维甲酸(ATRA)对体外培养人视网膜色素上皮(RPE)细胞增生的抑制作用及机制。 方法:采用传代培养的人RPE细胞,分成不同浓度(10-9、10-8、10-7、10-6和10-5 mol?L -1的ATRA)和不同时间点(6、12、24、48、72和96 h)给药组,通过活细胞计数法、MTT比色法和流式细胞术分别检测ATRA对人RPE细胞增生的影响。 结果:ATRA给药组细胞生存率低于非给药组(P<0.01)。细胞增生的抑制率与药物剂量及时间呈正相关 (r1=0.9926,P<0.05; r2=0.9647,P<0.05)。与非给药组比较,ATRA给药组 RPE细胞周期中G1期细胞增加(P<0.05),而G0/G1期细胞数明显减少(P<0.05)。结论:ATRA可能通过阻滞人RPE细胞周期对RPE细胞增生具有剂量依赖和时间依赖的抑制作用。

关 键 词:细胞培养  全反式维甲酸  流式细胞术    
文章编号:1571-587X(2008)02-0258-04
收稿时间:2007-01-19
修稿时间:2007年1月19日

Inhibitory effect of all-trans-retinoic acid on proliferation of human retinal pigment epithelial cells in vitro
LI Zhong-qiu,WU Ya-zhen,HAN Ning.Inhibitory effect of all-trans-retinoic acid on proliferation of human retinal pigment epithelial cells in vitro[J].Journal of Jilin University: Med Ed,2008,34(2):258-261.
Authors:LI Zhong-qiu  WU Ya-zhen  HAN Ning
Affiliation:Department of Ophthalmology,Second Hospital,Jilin University,Changchun 130041,China
Abstract:Objective To investigate the effects of all-trans-retinoic acid(ATRA) on proliferation of cultured human retinal pigment epithelium(RPE) cells and the probable mechanisms.Methods Cultured human RPE cells were treated with various concentrations(10-9,10-8,10-7,10-6 and 10-5 mol·L-1) of ATRA at different time points(6,12,24,48,72 and 96 h).Cell proliferation was evaluated by cell count and MTT colorimetric assay,and cell cycle analysis was performed by flow cytometry.Results The cell viability rates of ATRA treated group were decreased obviously,compared with control groups(P<0.01).The inhibitory rates of RPE cell proliferation had positive correlation with ATRA dose and time of action(r1=0.9926,P<0.05;r2=0.9647,P<0.05).In ATRA groups,compared with non-ATRA treated groups,the cell number in G1 phase was increased(P<0.05),while in G0/G1 phase was decreased(P<0.05).Conclusion ATRA could inhibit the proliferation of human RPE cells in a dose-dependent and time-dependent manner by arresting cell cycle.
Keywords:retinal pigment epithelium  cell culture  all-trans-restinoic acid  flow cytometry
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