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作 者:白秀英[1] 俞文华[1] 李平风[1] 周爱儒[1] 顾文霞[1] 杜国光[1]
机构地区:[1]北京医科大学生物化学与分子生物学系
出 处:《中国生物化学与分子生物学报》1999年第2期300-303,共4页Chinese Journal of Biochemistry and Molecular Biology
基 金:国家自然科学基金
摘 要:为了阐明甲状旁腺素(parathyroidhormone,PTH)、胰岛素样生长因子-Ⅰ(insulin-likegrowthfactor-Ⅰ,IGF-Ⅰ)在促成骨样细胞ROS17/2.8增殖的同时对其分化状况的影响,研究了PTH、IGF-Ⅰ对骨特征性标志蛋白碱性磷酸酶(alkalinephosphatase,ALP)活性、骨钙素(osteocal-cin)mRNA表达及骨胶原蛋白(colagen)合成的影响.结果表明,PTH、IGF-Ⅰ均可抑制ALP活性,PTH的抑制作用强于IGF-Ⅰ,抑制作用具有时间剂量依赖性;PTH、IGF-Ⅰ均可诱导骨钙素mRNA表达增加;PTH能够促进3H-脯氨酸参入新生小鼠颅骨组织,既PTH能够骨胶原蛋白合成增加.这些结果提示,PTH、IGF-Ⅰ在促成骨样细胞ROS17/2.8增殖的同时也促进其分化,表明在成骨细胞的生发成熟过程中,增殖、分化现象相辅相成,相伴而行.Parathyroid hormone(PTH)plays an important role in regulation of calcium and phosphorus homeostasis.Recently it has been demonstrated that PTH can also enhance hone anabolism.In osteoblast like ROS 17/2 8 cells the proliferative effect of PTH has already been observed.This report describes the differentiative effects of PTH(10 -9 and 10 -10 mol/L)that down regulated alkaline phosphates activity,increased the expression of osteocalcin mRNA,and enhanced the incorporation of 3 H proline into collagen.Similar results were also demonstrated in IGF Ⅰ treated ROS 17/2 8 cells.Alkaline phosphatase,osteocalcin and collagen are three main marker proteins of differentiated osteoblast.It means that PTH and IGF Ⅰ can both regulate proliferation and differentiation at different stages of cell growth in osbteoblast like ROS 17/2 8 cells.
分 类 号:R329.26[医药卫生—人体解剖和组织胚胎学] Q573[医药卫生—基础医学]
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