首页 | 本学科首页   官方微博 | 高级检索  
检索        

胰岛素样生长因子-1对成骨细胞增殖影响的实验研究
引用本文:郭涛,储诚兵.胰岛素样生长因子-1对成骨细胞增殖影响的实验研究[J].湖北民族学院学报(医学版 ),2001,18(3):1-3.
作者姓名:郭涛  储诚兵
作者单位:1. 湖北民族学院医学院附院外科,
2. 贵阳医学院附属医院骨科,
摘    要:目的:研究不同浓度胰岛素样生长因子-1(IGF-1)对兔成骨细胞增殖的影响。方法:采用组织块细胞培养技术进行兔成骨细胞分离培养,取第2代成骨细胞分别与0.1ng/ml,1ng/ml,10ng/ml,20ng/mlIGF-1培养,培养24、36小时后行四唑盐比色法检测细胞增殖情况。结果:IGF-1与成骨细胞培养24、36小时,经MTT法检测,不同浓度IGF-1与对照组比较,有显著性差异(P<0.01)。IGF-1浓度为0.1、1、10ng/ml,各组之间相比存在显著性差异(P<0.05),结论:IGF-1对成骨细胞有明显促进增殖作用,在0.1-10ng/ml范围,存在浓度的依赖性。

关 键 词:成骨细胞  胰岛素样生长因子-1  细胞增殖
文章编号:1008-8164(2001)03-0001-03
修稿时间:2001年5月10日

Effects of Insulin-like Growth Factor-1 on Proliferation of Rabbit Osteoblast in Vitro.
GUO Tao,CHU Cheng-bing.Effects of Insulin-like Growth Factor-1 on Proliferation of Rabbit Osteoblast in Vitro.[J].Journal of Hubei Institute For Nationalities(Medical Edition),2001,18(3):1-3.
Authors:GUO Tao  CHU Cheng-bing
Abstract:Objective To investigate and compare the effect of insulin-like growth factor-1 on proliferation of rabbit osteoblast in vitro. Methods Osteoblasts were obtained from rabbit costal bone by explant culture technology. The second subculture was exposed to insulin-like growth factor-1 at variant concentrations of 0,0.1,1,10and 20ng/ml for 24 and 36 hours and MTT assay was employed to observe the effects of insulin-like growth factor-1 on osteoblast proliferation. Results Osteoblasts exposed to insulin-like growth factor-l at variant concentrations of 0.1,1,10,20ng/ml were significantly different compared with the control ( P <0.01),and significant differences were found between every two groups when osteoblasts were exposed to insulin-like growth factor-l at range from 0.1 to 10ng/ml ( P <0.05).Conclusions Insulin-like growth factor-l could significantly elevate the proliferation of osteoblasts. At range from 0.1-10ng/ml, It depended on concentration. MTT assay is a good kind of method for determining the proliferation of osteoblasts.
Keywords:Osteoblasts  in vitro insulin-like growth factor-l  proliferation
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号