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Antagonistic and synergistic effects of bone morphogenetic protein 2/7 and all-trans retinoic acid on the osteogenic differentiation of rat bone marrow stromal cells

机译:骨形态发生蛋白2/7和全反式维甲酸对大鼠骨髓基质细胞成骨分化的拮抗和协同作用

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摘要

The osteogenesis of bone marrow stromal cells (BMSCs) is of paramount importance for the repair of large-size bone defects, which may be compromised by the dietary-accumulated all-trans retinoic acid (ATRA). We have shown that heterodimeric bone morphogenetic protein 2/7 (BMP2/7) could induce bone regeneration in a significantly higher dose-efficiency in comparison with homodimeric BMPs. In this study, we evaluated the effects of ATRA and BMP2/7 on the proliferation, differentiation, mineralization and osteogenic genes. ATRA and BMP2/7 exhibited both antagonistic and synergistic effects on the osteogenesis of BMSCs. ATRA significantly inhibited proliferation and expression of osteocalcin but enhanced the activity of alkaline phosphatase of BMSCs. On day 21, 50 ng/mL BMP2/7 could antagonize the inhibitive effects of ATRA and significantly enhance osteogenesis of BMSCs. These findings suggested a promising application potential of heterodimeric BMP2/7 in clinic to promote bone regeneration for the cases with dietary accumulated ATRA.
机译:骨髓基质细胞(BMSC)的成骨作用对于修复大型骨缺损至关重要,而这种缺损可能会因饮食中积累的全反式维甲酸(ATRA)受损。我们已经显示,异源二聚体骨形态发生蛋白2/7(BMP2 / 7)与同质二聚体BMPs相比,可以显着更高的剂量效率诱导骨再生。在这项研究中,我们评估了ATRA和BMP2 / 7对增殖,分化,矿化和成骨基因的影响。 ATRA和BMP2 / 7对BMSCs的成骨性均表现出拮抗作用和协同作用。 ATRA显着抑制骨钙素的增殖和表达,但增强了BMSCs碱性磷酸酶的活性。在第21天,50 ng / mL BMP2 / 7可以拮抗ATRA的抑制作用,并显着增强BMSC的成骨作用。这些发现表明,异二聚体BMP2 / 7在临床上具有潜在的应用前景,可用于饮食累积ATRA的病例促进骨再生。

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