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骨形态发生蛋白对培养胎儿关节软骨细胞代谢的影响及意义
引用本文:余家阔,曲绵域,田得祥.骨形态发生蛋白对培养胎儿关节软骨细胞代谢的影响及意义[J].中国运动医学杂志,1996(1).
作者姓名:余家阔  曲绵域  田得祥
作者单位:北京医科大学运动医学研究所
基金项目:国家教委重点博士点基金
摘    要:为了解骨形态发生蛋白(BMP)在关节软骨损伤与修复及异位化骨中的作用,本研究观察了部分纯化的牛骨形态发生蛋白(bBMP)和高度纯化的人骨形态发生蛋白(hBMP)对体外贴壁培养原代、反分化人胎儿关节软骨细胞及鼠3T3成纤维细胞DNA、胶原和蛋白多糖合成的影响。结果发现:部分纯化的bBMP和高度纯化的hBMP均不促进原代人关节软骨细胞合成DNA和胶原,并显著抑制其蛋白多糖的合成。部分纯化的bBMP对反分化关节软骨细胞和鼠3T3成纤维细胞的DNA合成、胶原合成和蛋白多糖合成却有明显促进作用。因此,本研究认为,BMP诱导下的关节软骨细胞不会发生反分化,而有可能进一步向肥大软骨细胞样细胞或成骨细胞样细胞方向分化,并可能使反分化的软骨细胞重新表达软骨细胞表型。

关 键 词:骨形态发生蛋白,细胞分化,细胞反分化,同位素掺入

Bone Morphogenetic Protein's Influence upon the Metabolism of Human Embryo Articular Chondrocytes Cultured in Vitro
Yu Jiakuo,Qu Mianyu,et al.Bone Morphogenetic Protein's Influence upon the Metabolism of Human Embryo Articular Chondrocytes Cultured in Vitro[J].Chinese Journal of Sports Medicine,1996(1).
Authors:Yu Jiakuo  Qu Mianyu  
Abstract:To understand bone morphogenetic protein(BMP)'s act on the injury and repair of articular cartilage and the formation of ectopic osification, partially purified bovine BMP(bBMP)and highly purified human BMP(hBMP)were used to investigate BMP's influence on the synthesis of DNA,collagen and proteoglycan of cultured primary human embryo articular chondrocytes,dedifferentiated chondrocytes and mouse 3T3 fioroblasts.The results showed that partially purified bBMP and highly purified hBMP couldn't promote the synthesis of DNA and collagen of primary human embryo articular chondrocytes but they inhibit their proteoglycan synthesis remarkably.Partially purified bBMP seriously promoted the synthesis of DNA,collagen and proteoglycan of dedifferentiated chondrocytes and mouse 3T3 fibroblasts.These results indicated that chondrocytes induced by BMP couldn't be dedifferentiated.It was possible for BMP to promote chondrocytes'further differentiation towards hypertrophic chondrocyte-like cells or osteoblast-like cells.It was also possible that BMP could make dedifferentiated chondrocytes express chondrocytes'phenotypes again.
Keywords:bone morphogenetic protein  cell differentiation  cell dedifferentiation  isotope incorporation  
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