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首页> 外文期刊>Tissue engineering, Part A >Modulation of BMP-2-Induced chondrogenic versus osteogenic differentiation of human mesenchymal stem cells by cell-specific extracellular matrices
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Modulation of BMP-2-Induced chondrogenic versus osteogenic differentiation of human mesenchymal stem cells by cell-specific extracellular matrices

机译:细胞特异性细胞外基质对BMP-2诱导的人间充质干细胞软骨形成和成骨分化的调节

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Bone morphogenetic protein-2 (BMP-2) is known to induce both osteogenic and chondrogenic commitment of human mesenchymal stem cells (hMSCs). However, factors influencing BMP-2-dependent chondrogenic and osteogenic differentiation have not been investigated. In this study, we demonstrated that extracellular microenvironments, in the form of cell-derived matrices, play important roles in determining the specific lineage commitment of hMSCs in the presence of BMP-2. Extracellular matrices (ECMs) derived from osteoblasts and chondrocytes were utilized to regulate cell differentiation. Osteogenic and chondrogenic differentiation of hMSCs cultured on the two different cell-derived ECMs were assessed by quantitative real-time-polymerase chain reaction, immunocytochemistry, and western blot analysis. To minimize the effects of the cell-adhesion proteins contained in serum on the ECMs, hMSCs were cultured in serum-free osteogenic or chondrogenic differentiation medium. Fibronectin-, collagen type I-, or collagen type II-coated substrates were utilized as ECM controls. The ECM specific to each cell type promoted lineage-specific commitment of hMSCs in the presence of BMP-2, that is, osteoblast- and chondrocyte-derived ECM promoted osteogenic and chondrogenic commitment, respectively. Therefore, cell-specific ECMs are capable of modulating the BMP-2-induced osteogenic and chondrogenic differentiation of hMSCs.
机译:已知骨形态发生蛋白2(BMP-2)可以诱导人间充质干细胞(hMSCs)的成骨和成软骨作用。但是,尚未研究影响BMP-2依赖性软骨形成和成骨分化的因素。在这项研究中,我们证明,细胞外基质形式的细胞外微环境在BMP-2存在下确定hMSC的特定谱系承诺中起着重要作用。源自成骨细胞和软骨细胞的细胞外基质(ECM)用于调节细胞分化。通过定量实时聚合酶链反应,免疫细胞化学和蛋白质印迹分析评估了在两种不同的细胞源性ECM上培养的hMSC的成骨和成软骨分化。为了最大程度地降低血清中包含的细胞粘附蛋白对ECM的影响,将hMSCs在无血清的成骨或成软骨分化培养基中培养。纤连蛋白,I型胶原或II型胶原基质被用作ECM对照。在BMP-2存在下,对每种细胞类型特异的ECM促进了hMSC的谱系特异性承诺,也就是说,成骨细胞和软骨细胞衍生的ECM分别促进了成骨和软骨生成承诺。因此,细胞特异性ECM能够调节hMSC的BMP-2诱导的成骨和软骨形成分化。

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