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HIF-1α Transgenic Bone Marrow Cells Can Promote Tissue Repair in Cases of Corticosteroid-Induced Osteonecrosis of the Femoral Head in Rabbits

机译:HIF-1α转基因骨髓细胞可促进皮质类固醇诱导的兔股骨头坏死的组织修复

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摘要

Although corticosteroid-induced osteonecrosis of the femoral head (ONFH) is common, the treatment for it remains limited and largely ineffective. We examined whether implantation of hypoxia inducible factor-1α (HIF-1α) transgenic bone marrow cells (BMCs) can promote the repair of the necrotic area of corticosteroid-induced ONFH. In this study, we confirmed that HIF-1α gene transfection could enhance mRNA expression of osteogenic genes in BMCs in vitro. Alkaline phosphatase activity assay and alizarin red-S staining indicated HIF-1α transgenic BMCs had enhanced osteogenic differentiation capacity in vitro. Furthermore, enzyme linked immunosorbent assay (ELISA) for VEGF revealed HIF-1α transgenic BMCs secreted more VEGF as compared to normal BMCs. An experimental rabbit model of early-stage corticosteroid-induced ONFH was established and used for an evaluation of cytotherapy. Transplantation of HIF-1α transgenic BMCs dramatically improved the bone regeneration of the necrotic area of the femoral head. The number and volume of blood vessel were significantly increased in the necrotic area of the femoral head compared to the control groups. These results support HIF-1α transgenic BMCs have enhanced osteogenic and angiogenic activity in vitro and in vivo. Transplantation of HIF-1α transgenic BMCs can potentially promote the repair of the necrotic area of corticosteroid-induced ONFH.
机译:尽管皮质类固醇诱发的股骨头坏死(ONFH)很常见,但对其的治疗仍然有限,并且在很大程度上无效。我们检查了缺氧诱导因子-1α(HIF-1α)转基因骨髓细胞(BMC)的植入是否可以促进皮质类固醇诱导的ONFH坏死区域的修复。在这项研究中,我们证实了HIF-1α基因转染可以增强体外BMC中成骨基因的mRNA表达。碱性磷酸酶活性测定和茜素红-S染色表明HIF-1α转基因BMC具有增强的体外成骨分化能力。此外,VEGF的酶联免疫吸附试验(ELISA)显示,与正常BMC相比,HIF-1α转基因BMC分泌更多的VEGF。建立了早期皮质类固醇激素诱导的ONFH的实验兔模型,并将其用于细胞疗法的评估。 HIF-1α转基因BMC的移植显着改善了股骨头坏死区域的骨再生。与对照组相比,股骨头坏死区域的血管数量和体积明显增加。这些结果支持HIF-1α转基因BMC在体外和体内均具有增强的成骨和血管生成活性。 HIF-1α转基因BMC的移植可能促进皮质类固醇诱导的ONFH坏死区域的修复。

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