Li Xudong, Jin Li, Cui Quanjun, Wang Gwo-Jaw, Balian Gary
Department of Orthopaedic Surgery, School of Medicine, University of Virginia, Charlottesville, VA, 22908, USA.
Osteoporos Int. 2005 Jan;16(1):101-8. doi: 10.1007/s00198-004-1649-7. Epub 2004 Jun 15.
We have studied the mechanism of steroid-induced osteonecrosis by examining the effect of dexamethasone on a multipotential cell line, D1, which is derived from bone marrow and is capable of differentiating into either the osteoblast or the adipocyte lineage. The expression of bone cell and fat cell transcription factors Cbfa1/Runx2 and PPARgamma2, were determined. Osteocalcin promoter activity was measured by co-transfecting the cells with the phOC-luc and pSV beta-Gal plasmids. Dexamethasone increased PPARgamma2 gene expression 2-fold, while Cbfa1/Runx2 gene expression and osteocalcin promoter activity decreased by 50-60%, and VEGF protein, measured by ELISA, decreased by 55%. These changes indicate enhanced adipogenesis and decreased osteogenesis by mesenchymal cells in vitro, together with a decrease in VEGF, a potent angiogeneic factor, suggesting that dexamethasone may shunt uncommitted osteoprogenitor cells in marrow from osteoblastic differentiation into the adipocytic pathway, leading to diminished vascularization and eventual osteonecrosis.
我们通过研究地塞米松对一种多能细胞系D1的作用,探讨了类固醇诱导的骨坏死机制。D1细胞系源自骨髓,能够分化为成骨细胞系或脂肪细胞系。我们测定了骨细胞和脂肪细胞转录因子Cbfa1/Runx2和PPARgamma2的表达。通过将细胞与phOC-luc和pSV beta-Gal质粒共转染来测量骨钙素启动子活性。地塞米松使PPARgamma2基因表达增加了2倍,而Cbfa1/Runx2基因表达和骨钙素启动子活性降低了50 - 60%,通过ELISA测定的VEGF蛋白减少了55%。这些变化表明,体外间充质细胞的脂肪生成增强,成骨作用减弱,同时一种强效血管生成因子VEGF减少,这表明地塞米松可能使骨髓中未定向的骨祖细胞从成骨细胞分化转向脂肪细胞途径,导致血管化减少并最终引起骨坏死。