Kassem M, Risteli L, Mosekilde L, Melsen F, Eriksen E F
University Department of Endocrinology and Metabolism, Aarhus, Amtssygehus, Denmark.
APMIS. 1991 Mar;99(3):269-74. doi: 10.1111/j.1699-0463.1991.tb05149.x.
Osteoblast-like cells are commonly found in the vicinity of osteoclasts formed in long-term human bone marrow cultures, and they are believed to be derived from osteogenic cell precursors belonging to the stromal cell system. This paper describes a new culture method for human osteoblasts from the adherent cell population of long-term human mononuclear bone marrow cultures. The cells obtained exhibited all the classic characteristics of osteoblasts. They contained high intracellular concentrations of alkaline phosphatase and they secreted the osteoblast-specific marker bone Gla protein. Collagen production was mainly (95-98%) procollagen type I propeptide and only minute quantities of procollagen type III propeptide were detectable by radioimmunoassay in the conditioned medium. After eight weeks the cells formed a mineralized matrix on exposure to beta-glycerophosphate and ascorbic acid. This system provides a model for the study of osteoblast differentiation in vitro and may form the basis for the use of defined media in bone cell cultures due to the presence of high concentrations of osteoblast precursors.
在长期培养的人骨髓中形成的破骨细胞附近通常能发现成骨样细胞,据信它们源自属于基质细胞系统的成骨细胞前体。本文描述了一种从长期人单核骨髓培养物的贴壁细胞群体中培养人成骨细胞的新方法。所获得的细胞展现出成骨细胞的所有典型特征。它们细胞内碱性磷酸酶浓度很高,并且分泌成骨细胞特异性标志物骨钙素。胶原蛋白的产生主要是(95 - 98%)I型前胶原原肽,通过放射免疫测定在条件培养基中仅可检测到微量的III型前胶原原肽。八周后,细胞在暴露于β -甘油磷酸酯和抗坏血酸时形成矿化基质。该系统为体外研究成骨细胞分化提供了一个模型,并且由于存在高浓度的成骨细胞前体,可能成为在骨细胞培养中使用限定培养基的基础。