首页> 美国卫生研究院文献>Tissue Engineering. Part A >Response of Human Embryonic Stem Cell–Derived Mesenchymal Stem Cells to Osteogenic Factors and Architectures of Materials During In Vitro Osteogenesis
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Response of Human Embryonic Stem Cell–Derived Mesenchymal Stem Cells to Osteogenic Factors and Architectures of Materials During In Vitro Osteogenesis

机译:人类胚胎干细胞衍生的间充质干细胞对体外成骨过程中成骨因子和材料结构的反应

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摘要

One of the major challenges to the application of human embryonic stem cells (hESCs) to the repair of defective tissues is the directed differentiation of cells into specific lineages to avoid the formation of inferior heterogeneous tissues. To accomplish this goal, the lineage-specific stem cell population needs to be isolated and optimal differentiation conditions need to be defined. In this study, homogenous hESC-derived mesenchymal stem cells (hESC-MSCs) were generated and used to construct bone tissue. The effect of osteogenic factors, including dexamethasone (Dex) and bone morphogenetic protein-7 (BMP-7), on the osteogenesis of hESC-MSCs was investigated. It was found that BMP-7 itself had little effect on the in vitro osteogenic differentiation of hESC-MSCs; however, there was a synergic effect between BMP-7 and Dex in promoting osteogenesis. The effect of osteoconductive nanofibrous polylactic acid material on osteogenesis of hESC-MSCs was also investigated. It was found that the nanofibrous matrix architecture promoted alkaline phosphatase activity and calcium deposition of cells cultured under osteogenic conditions. Based on these findings, the hESC-MSCs were cultured on three-dimensional nanofibrous scaffolds in combination with Dex and BMP-7 stimulation in vitro to generate bone-like tissues. After 6 weeks of culture, highly mineralized tissues developed with specific bone marker genes expressed. These data illustrate the promise of hESC-MSCs for bone regeneration under optimal conditions.
机译:将人类胚胎干细胞(hESCs)应用于缺损组织修复的主要挑战之一是将细胞定向分化为特定谱系,以避免形成劣质异质组织。为了实现这一目标,需要分离出特定于谱系的干细胞,并需要定义最佳的分化条件。在这项研究中,生成了均质的hESC来源的间充质干细胞(hESC-MSC),并将其用于构建骨组织。研究了地塞米松(Dex)和骨形态发生蛋白7(BMP-7)等成骨因子对hESC-MSCs成骨的影响。已经发现,BMP-7本身对hESC-MSC的体外成骨分化几乎没有影响。然而,BMP-7和Dex在促进成骨方面有协同作用。还研究了骨传导性纳米纤维聚乳酸材料对hESC-MSCs成骨的影响。发现在成骨条件下培养的细胞,纳米纤维基质结构促进碱性磷酸酶活性和钙沉积。基于这些发现,将hESC-MSC与Dex和BMP-7刺激一起在三维纳米纤维支架上培养,以产生骨样组织。培养6周后,高度矿化的组织发育并表达了特定的骨标记基因。这些数据说明了hESC-MSC在最佳条件下具有骨再生的前景。

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