首页> 外文期刊>Cell and Tissue Research >Stromal-cell-derived factor (SDF) 1-alpha in combination with BMP-2 and TGF-β1 induces site-directed cell homing and osteogenic and chondrogenic differentiation for tissue engineering without the requirement for cell seeding
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Stromal-cell-derived factor (SDF) 1-alpha in combination with BMP-2 and TGF-β1 induces site-directed cell homing and osteogenic and chondrogenic differentiation for tissue engineering without the requirement for cell seeding

机译:基质细胞衍生因子(SDF)1-alpha与BMP-2和TGF-β1结合可诱导定点细胞归巢以及组织工程中的成骨和成软骨分化,而无需细胞接种

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The clinical translation of tissue engineering approaches is limited by the requirement of a cell source. Cell guidance is a new concept that provides an alternative approach, obviating a requirement for an external cell source. This relies on site-specific homing and differentiation of the patient’s own cells to an implanted scaffold through controlled delivery of cytokines. In this study, we used stromal-cell-derived factor 1-alpha (SDF-1α) in combination with bone morphogenic protein (BMP)-2 or transforming growth factor (TGF)-β1 to induce cell migration and osteogenic or chondrogenic differentiation, respectively, in implanted scaffolds in a rat model. A customized cytokine microdelivery apparatus was used to ensure the constant rate and concentration of cytokine delivery around the scaffold. The formation of osteoid or early cartilage was observed after 4 weeks in specimens treated with SDF-1α and either BMP-2 or TGF-β1. The density of cellular infiltrate and formation of differentiated tissue were lower in scaffolds treated only with BMP-2 or TGF-β1. Thus, controlled SDF-1α delivery induces cell migration into scaffolds and can result in enhanced osteogenesis and chondrogenesis when used in combination with differentiation cytokines for purposes of tissue engineering.
机译:组织工程方法的临床翻译受到细胞来源的要求的限制。细胞指导是一个新概念,它提供了一种替代方法,从而消除了对外部细胞源的需求。这依赖于特定部位的归巢和通过控制细胞因子的递送将患者自身细胞分化为植入的支架。在这项研究中,我们将基质细胞衍生因子1-alpha(SDF-1α)与骨形态发生蛋白(BMP)-2或转化生长因子(TGF)-β1结合使用,诱导细胞迁移以及成骨或软骨形成分化,分别在大鼠模型的植入支架中。使用定制的细胞因子微递送装置以确保围绕支架的细胞因子递送的恒定速率和浓度。在用SDF-1α和BMP-2或TGF-β1处理的标本中,在4周后观察到了类骨质或早期软骨的形成。仅用BMP-2或TGF-β1处理的支架中细胞浸润的密度和分化组织的形成较低。因此,当与分化细胞因子结合用于组织工程目的时,受控的SDF-1α递送可诱导细胞迁移至支架中,并可以增强成骨作用和软骨形成。

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