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藻酸钙微载体培养胎儿关节软骨细胞
引用本文:靳小兵,罗卓荆,杨柳,兰丽锋.藻酸钙微载体培养胎儿关节软骨细胞[J].中国组织工程研究与临床康复,2003,7(11):1632-1633.
作者姓名:靳小兵  罗卓荆  杨柳  兰丽锋
作者单位:解放军第四军医大学西京医院全军骨科研究所,陕西省西安市,710032
摘    要:目的观察胎儿关节软骨细胞在藻酸钙微载体培养中的特征,探讨用藻酸钙微载体培养胎儿关节软骨细胞的优缺点。方法用藻酸钙微载体和体外单层培养法培养胎儿关节软骨细胞,观察细胞形态学变化,测定细胞数量变化及其生长曲线,观察细胞增殖;借助免疫组织化学的方法了解细胞II型胶原的合成情况。结果体外单层培养的胎儿关节软骨细胞传至第5代已出现明显的反分化,多数细胞变为成纤维细胞状,合成II型胶原的能力明显减弱;而用藻酸钙微载体培养的软骨细胞3个月后仍保持有旺盛的合成Ⅱ型胶原的能力。结论用藻酸钙微载体培养胎儿关节软骨细胞可较长时间保持其表型及合成基质能力,防止反分化的发生。

关 键 词:藻酸盐  软骨细胞  细胞培养
文章编号:1671-5926(2003)11-1632-02
修稿时间:2002年11月9日

Culture of embryo articular chondrocyte in calcium alginate micro- carrier
Jin Xiaobing,Luo Zhuojing,Yang Liu,Lan Lifeng,Orthopaedic Institute,Xijing Hospital,Fourth Military Medical University,Xi'an ,Shaanxi Province,China.Culture of embryo articular chondrocyte in calcium alginate micro- carrier[J].Journal of Clinical Rehabilitative Tissue Engineering Research,2003,7(11):1632-1633.
Authors:Jin Xiaobing  Luo Zhuojing  Yang Liu  Lan Lifeng  Orthopaedic Institute  Xijing Hospital  Fourth Military Medical University  Xi'an  Shaanxi Province  China
Institution:Jin Xiaobing,Luo Zhuojing,Yang Liu,Lan Lifeng,Orthopaedic Institute,Xijing Hospital,Fourth Military Medical University,Xi'an 710032,Shaanxi Province,China
Abstract:Aim To investigate the advantages and disadvantages of calcium alginate on microcarrier culture of fetus articular chondrocytes. Methods The changes of cell morphology,cell quantity and growth curve were investigated among articular chondrocytes cultured by calcium alginate microcarrier to observe the proliferation of chondrocytes. The biologic synthesis of type II collagen in chondrocytes was comprehended by immunohistochemical method.Results The fifth generation of the mono layer culture chondrocytes appeared obvious de differentiation, and most cells became fibroblast like. The cells cultured in alginate micro carrier gels retained the ability to synthesis the type II collagen.Conclusion Culture of embryo articular chondrocytes in calcium alginate carrier gels can retain the cell phono type and ability to synthesize the type II collagen for 3 months, retarding the happening of de differentiation.
Keywords:alginates  chondrocytes  cell culture  
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