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首页> 外文期刊>Journal of bone and mineral research: the official journal of the American Society for Bone and Mineral Research >Spatiotemporal assessment of fetal bovine osteoblast culture differentiation indicates a role for BSP in promoting differentiation.
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Spatiotemporal assessment of fetal bovine osteoblast culture differentiation indicates a role for BSP in promoting differentiation.

机译:胎牛成骨细胞培养分化的时空评估表明BSP在促进分化中发挥了作用。

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摘要

Fetal bovine mandible-derived osteoblasts were cultured for the purpose of obtaining a spatiotemporal assessment of bone matrix protein expression during in vitro differentiation. The results obtained from electron microscopic, immunohistological, biochemical, and molecular biological analyses indicated that these primary cultured osteoblasts produce an abundant extracellular matrix which mineralizes during a 14-day culture period. During this process, a restricted, spatiotemporal pattern of bone sialoprotein expression was indicated by immunohistological and molecular evaluations. To test the possibility that bone sialoprotein promoted the continued morphodifferentiation of osteoblastic cells, cultures were grown in the presence of anti-bone sialoprotein antibodies known to interfere with cell-bone sialoprotein attachment. Compared with cultures grown in the presence of normal rabbit serum (1:150), cultures grown in the media containing anti-bone sialoprotein antibody (1:150) failed to mineralize as demonstrated by von Kossa staining and failed to express osteocalcin and osteopontin as shown by the reverse transcription polymerase chain reaction. These results contribute to the growing evidence that bone sialoprotein is an important determinant of osteoblast differentiation and bone formation. Matrix protein-cell interactions may be examined using this spatiotemporally defined model.
机译:培养胎儿下颌骨来源的成骨细胞是为了获得体外分化过程中骨基质蛋白表达的时空评估。从电子显微镜,免疫组织学,生物化学和分子生物学分析获得的结果表明,这些原代培养的成骨细胞产生丰富的细胞外基质,该基质在14天的培养期内会矿化。在此过程中,通过免疫组织学和分子评估表明了骨唾液蛋白表达受限制的时空模式。为了测试骨唾液蛋白促进成骨细胞持续形态分化的可能性,在已知会干扰细胞骨骼唾液蛋白附着的抗骨唾液蛋白抗体存在下培养培养物。与在正常兔血清(1:150)存在下培养的培养物相比,在含有抗骨唾液蛋白抗体(1:150)的培养基中培养的培养物无法矿化(如von Kossa染色所示),并且不能表达骨钙蛋白和骨桥蛋白通过逆转录聚合酶链反应显示。这些结果有助于越来越多的证据表明骨唾液蛋白是成骨细胞分化和骨形成的重要决定因素。可以使用该时空定义的模型检查基质蛋白质-细胞相互作用。

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