Kassem M, Mosekilde L, Eriksen E F
University Department of Endocrinology and Metabolism, Aarhus amtssygehus, Denmark.
J Bone Miner Res. 1993 Dec;8(12):1453-8. doi: 10.1002/jbmr.5650081207.
In this study we tested the effects of sodium fluoride (NaF) in serum-free cultures of human marrow stromal osteoblast-like [hMS(OB)] cells. NaF (10(-5) M) stimulated hMS(OB) cell proliferation up to 220% of control cultures. NaF alone did not increase type I collagen production, but in the presence of 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3] (10(-9) M), NaF enhanced type I collagen production in a dose-dependent way to 300% of 1,25-(OH)2D3-treated control cultures. The production of alkaline phosphatase (ALP) and osteocalcin (bone gla protein, BGP) was also enhanced in the presence of 1,25-(OH)2D3 to 170 and 200%, respectively, of 1,25-(OH)2D3-treated controls. Our results suggest that 1,25-(OH)2D3 potentiates fluoride-mediated anabolism in hMS(OB) cell cultures and suggest that osteoblast precursors in bone marrow are targets for fluoride action.
在本研究中,我们检测了氟化钠(NaF)对人骨髓基质成骨样[hMS(OB)]细胞无血清培养的影响。NaF(10⁻⁵ M)刺激hMS(OB)细胞增殖,使其达到对照培养物的220%。单独的NaF不会增加I型胶原蛋白的产生,但在存在1,25 - 二羟基维生素D3 [1,25-(OH)2D3](10⁻⁹ M)的情况下,NaF以剂量依赖的方式将I型胶原蛋白的产生提高到1,25-(OH)2D3处理的对照培养物的300%。在存在1,25-(OH)2D3的情况下,碱性磷酸酶(ALP)和骨钙素(骨γ-羧基谷氨酸蛋白,BGP)的产生也分别提高到1,25-(OH)2D3处理对照的170%和200%。我们的结果表明,1,25-(OH)2D3增强了hMS(OB)细胞培养中氟介导的合成代谢,并表明骨髓中的成骨细胞前体是氟作用的靶点。