Kassem M, Kveiborg M, Eriksen E F
Danish Centre for Molecular Gerontology, Aarhus Bone and Mineral Research Group, University Department of Endocrinology and Metabolism, Aarhus, Amtssygehus, DK-8000 Aarhus C, Denmark.
Eur J Clin Invest. 2000 May;30(5):429-37. doi: 10.1046/j.1365-2362.2000.00645.x.
Transforming growth factor beta (TGF-beta) plays an important role in skeletal remodelling. However, few studies have examined its effects on cultured human osteoblasts. Our aim is to characterise the biological effects of TGF-beta1 on human osteoblasts and to examine the interaction between TGF-beta1 and calcitriol.
In vitro study employing two models of normal human osteoblasts: human bone marrow stromal cells [hMS/(OB)] containing osteoprogenitor cells and trabecular bone osteoblasts (hOB), which are mature osteoblasts. A reverse-transcriptase-polymerase-chain-reaction assay was employed to measure steady state mRNA levels of TGF-beta(s) isoforms and receptors. Effects of short-term treatment of TGF-beta1 on osteoblast proliferation and differentiation markers were assessed. The effect of cotreatment of calcitriol (10-8 M) and TGF-beta1 on osteoblast differentiation was also determined.
Both hMS(OB) and hOB cells expressed mRNA transcripts of TGF-beta1, TGF-beta2, TGF-beta 3, TGF-beta type I and type II receptors. TGF-beta 1 stimulated osteoblast proliferation in hMS(OB) and in hOB cultures. In hOB cultures, TGF-beta1 stimulated AP production and cotreatment with calcitriol induced a synergistic increase in AP levels to 250 +/- 61% of calcitriol-treated controls. Effects of TGF-beta1 and calcitriol were less pronounced in hMS(OB) cultures. TGF-beta1 inhibited collagen type I production in hMS(OB) cells and these effects were abolished in presence of calcitriol. In presence of calcitriol, TGF-beta1 increased collagen type I production in hOB cells. In both hOB and hMS(OB) cultures, TGF-beta1 inhibited osteocalcin production.
TGF-beta increases osteoblastic cell proliferation irrespective of the differentiation state. In presence of calcitriol, it initiates osteoblast cell differentiation and matrix formation. As TGF-beta inhibits osteocalcin production, other factors are necessary for inducing terminal differentiation of osteoblasts. The observed effects of TGF-beta on human osteoblasts in vitro may represent important regulatory steps in controlling osteoblast cell proliferation and differentiation in vivo.
转化生长因子β(TGF-β)在骨骼重塑中起重要作用。然而,很少有研究探讨其对培养的人成骨细胞的影响。我们的目的是表征TGF-β1对人成骨细胞的生物学作用,并研究TGF-β1与骨化三醇之间的相互作用。
采用两种正常人成骨细胞模型的体外研究:含有成骨祖细胞的人骨髓基质细胞[hMS/(OB)]和小梁骨成骨细胞(hOB),后者为成熟成骨细胞。采用逆转录聚合酶链反应测定法测量TGF-β亚型和受体的稳态mRNA水平。评估TGF-β1短期处理对成骨细胞增殖和分化标志物的影响。还确定了骨化三醇(10-8 M)与TGF-β1联合处理对成骨细胞分化的影响。
hMS(OB)细胞和hOB细胞均表达TGF-β1、TGF-β2、TGF-β3、TGF-βⅠ型和Ⅱ型受体的mRNA转录本。TGF-β1刺激hMS(OB)细胞和hOB培养物中的成骨细胞增殖。在hOB培养物中,TGF-β1刺激碱性磷酸酶(AP)产生,与骨化三醇联合处理可使AP水平协同增加至骨化三醇处理对照组的250±61%。在hMS(OB)培养物中,TGF-β1和骨化三醇的作用不太明显。TGF-β1抑制hMS(OB)细胞中Ⅰ型胶原的产生,而在骨化三醇存在时这些作用被消除。在骨化三醇存在时,TGF-β1增加hOB细胞中Ⅰ型胶原的产生。在hOB和hMS(OB)培养物中,TGF-β1均抑制骨钙素产生。
TGF-β可增加成骨细胞增殖,而与分化状态无关。在骨化三醇存在时,它可启动成骨细胞分化和基质形成。由于TGF-β抑制骨钙素产生,因此诱导成骨细胞终末分化还需要其他因子。体外观察到的TGF-β对人成骨细胞的作用可能代表体内控制成骨细胞增殖和分化的重要调节步骤。