首页> 美国卫生研究院文献>International Journal of Molecular Sciences >A Novel Human TGF-β1 Fusion Protein in Combination with rhBMP-2 Increases Chondro-Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells
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A Novel Human TGF-β1 Fusion Protein in Combination with rhBMP-2 Increases Chondro-Osteogenic Differentiation of Bone Marrow Mesenchymal Stem Cells

机译:新型人类TGF-β1融合蛋白与rhBMP-2的结合增加了骨髓间充质干细胞的软骨成骨分化。

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摘要

Transforming growth factor-beta (TGF-β) is involved in processes related to the differentiation and maturation of osteoprogenitor cells into osteoblasts. Rat bone marrow (BM) cells were cultured in a collagen-gel containing 0.5% fetal bovine serum (FBS) for 10 days in the presence of rhTGF (recombinant human TGF)-β1-F2, a fusion protein engineered to include a high-affinity collagen-binding decapeptide derived from von Willebrand factor. Subsequently, cells were moderately expanded in medium with 10% FBS for 4 days and treated with a short pulse of rhBMP (recombinant human bone morphogenetic protein)-2 for 4 h. During the last 2 days, dexamethasone and β-glycerophosphate were added to potentiate osteoinduction. Concomitant with an up-regulation of cell proliferation, DNA synthesis levels were determined. Polymerase chain reaction was performed to reveal the possible stemness of these cells. Osteogenic differentiation was evaluated in terms of alkaline phosphatase activity and mineralized matrix formation as well as by mRNA expression of osteogenic marker genes. Moreover, cells were placed inside diffusion chambers and implanted subcutaneously into the backs of adult rats for 4 weeks. Histological study provided evidence of cartilage and bone-like tissue formation. This experimental procedure is capable of selecting cell populations from BM that, in the presence of rhTGF-β1-F2 and rhBMP-2, achieve skeletogenic potential in vitro and in vivo.
机译:转化生长因子-β(TGF-β)参与与骨祖细胞向成骨细胞分化和成熟有关的过程。将大鼠骨髓(BM)细胞在含有0.5%胎牛血清(FBS)的胶原蛋白凝胶中培养rhTGF(重组人TGF)-β1-F2(一种经工程改造以包含高水平von Willebrand因子衍生的亲和性胶原结合十肽。随后,将细胞在含10%FBS的培养基中适度扩增4天,并用短脉冲rhBMP(重组人骨形态发生蛋白)-2处理4 h。在最后两天内,加入地塞米松和β-甘油磷酸以增强骨诱导作用。伴随细胞增殖的上调,确定DNA合成水平。进行聚合酶链反应以揭示这些细胞的可能干性。根据碱性磷酸酶活性和矿化的基质形成以及成骨标记基因的mRNA表达来评估成骨分化。此外,将细胞放置在扩散室内,并皮下植入成年大鼠的背部4周。组织学研究提供了软骨和骨样组织形成的证据。该实验程序能够从BM中选择在rhTGF-β1-F2和rhBMP-2存在下可在体外和体内实现成骨潜能的细胞群。

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