首页 | 本学科首页   官方微博 | 高级检索  
   检索      

碱性成纤维细胞生长因子对生长板软骨细胞增殖与分化的影响
引用本文:宇丽,吴凤麟,汪卓赟.碱性成纤维细胞生长因子对生长板软骨细胞增殖与分化的影响[J].中国生物工程杂志,2005,25(2):19-21,23-24.
作者姓名:宇丽  吴凤麟  汪卓赟
作者单位:暨南大学医学院生物化学教研室 广州 510632
基金项目:教育部科学技术研究重点项目资助(02190) 广州市科技计划重大科技攻关重点基础项目资助(200221-E0032)
摘    要:目的:探讨碱性成纤维细胞生长因子(bFGF)对生长板软骨细胞增殖和分化的作用。方法:分离并在低血清条件下培养兔生长板软骨细胞。采用改良MTT法检测细胞增殖倍数;羟脯氨酸法测定软骨细胞胶原产量;酶动力学方法测定碱性磷酸酶(ALP)活性。结果:bFGF浓度在5-100ng/ml范围内可以促进软骨细胞增殖,并以25ng/ml刺激时效果最为显著。当bFGF浓度高于25ng/ml时,抑制软骨细胞的胶原合成;当高于1ng/ml时,抑制碱性磷酸酶活性。结论:bFGF刺激生长板软骨细胞增殖,并在较高浓度时抑制生长板软骨细胞的分化。

关 键 词:生长板  软骨细胞  bFGF  增殖  分化  
收稿时间:2005-10-13

The Effect of bFGF on the Proliferation and Diffrentiation of Growth-plate Chondrocytes
YU Li,WU Feng-lin,WANG Zhuo-yun.The Effect of bFGF on the Proliferation and Diffrentiation of Growth-plate Chondrocytes[J].China Biotechnology,2005,25(2):19-21,23-24.
Authors:YU Li  WU Feng-lin  WANG Zhuo-yun
Abstract:Objectives: To study the effect of basic fibroblast growth factor (bFGF) on the proliferation and differentiation in cultured growth-plate chondrocytes. Methods: Growth-plate chondrocytes were isolated from rabbit costal cartilage and cultured under low-serum condition in monolayers. Cell growth was detected by the improved MTT; the production of collagen was estimated according to the hydroxyproline content; ALP activity was measured by modified enzyme dynamical method. Result: The cultured chondrocytes in medium with bFGF at concentrations of 5 -100ng/ml were significantly more than those in control group, which reached the peak at the concentration of 25ng/ml. The synthesis of collagen was inhibited by bFGF at the concentration of above 25ng/ml. The activity of ALP was suppresseded by bFGF at the concentration of above 1ng/ml. Conclusion: bFGF stimulated the proliferation of growth-plate chondrocytes obviously, but inhibited the differentiation of growth-plate chondrocytes at high concentrations.
Keywords:Growth-plate Chondrocyte bFGF Proliferation Differentiation
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《中国生物工程杂志》浏览原始摘要信息
点击此处可从《中国生物工程杂志》下载免费的PDF全文
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