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首页> 外文期刊>Tissue engineering, Part A >An Engineered Multiphase Three-Dimensional Microenvironment to Ensure the Controlled Delivery of Cyclic Strain and Human Growth Differentiation Factor 5 for the Tenogenic Commitment of Human Bone Marrow Mesenchymal Stem Cells
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An Engineered Multiphase Three-Dimensional Microenvironment to Ensure the Controlled Delivery of Cyclic Strain and Human Growth Differentiation Factor 5 for the Tenogenic Commitment of Human Bone Marrow Mesenchymal Stem Cells

机译:工程化的多相三维微环境,以确保循环菌株和人生长分化因子5的受控递送,用于人骨髓间充质干细胞的初步承诺

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摘要

At present, injuries or rupture of tendons are treated by surgical repair or conservative approaches with unpredictable clinical outcome. Alternative strategies to repair tendon defects without the undesirable side effects associated with the current options are needed. With this in mind, a tissue engineering approach has gained considerable attention as a promising strategy. Here we investigated a synthetic three-dimensional (3D) microenvironment able to interact with stem cells and inducing, via coupled biochemical and physical signals, their early commitment toward the tenogenic lineage. This multiphase 3D construct consisted of a braided hyaluronate elastic band merged with human bone marrow mesenchymal stem cells (hBMSCs) and poly-lactic-co-glycolic acid microcarriers loaded with human growth differentiation factor 5 (hGDF-5) by means of fibrin hydrogel. The multiphase structure allowed hBMSC culture under cyclic strain within a microenvironment where a controlled amount of hGDF-5 was regularly delivered. The cooperative biochemical and physical stimuli induced significantly increased expression of tenogenic markers, such as collagen type I and III, decorin, scleraxis, and tenascin-C, within only 3 days of dynamic hBMSC culture. This approach opens exciting perspectives for future development of engineered tendon tissue substitutes.
机译:目前,肌腱的伤害或破裂是通过具有不可预测的临床结果的手术修复或保守方法治疗。需要在没有与当前选择相关的不希望的副作用的情况下修复肌腱缺陷的替代策略。考虑到这一点,组织工程方法作为一个有希望的战略获得了相当大的关注。在这里,我们调查了能够与干细胞相互作用的合成三维(3D)微环境,通过耦合的生物化学和物理信号来诱导它们对遗传谱系的早期承诺。该多相3D构建体由编织的透明质酸盐弹性带组成,其与人骨髓间充质干细胞(HBMSCs)和具有人生长分化因子5(HGDF-5)的聚乳酸共甘油酸微载体通过纤维蛋白水凝胶合并。多相结构在微环境内允许HBMSC培养物,其中经常递送受控的HGDF-5。合作生化和物理刺激诱导胎生物标志物的表达显着增加,例如胶原蛋白I和III,Decorin,Scleraxis和Tenascin-C,仅在动态HBMSC培养的3天内。这种方法打开了未来的工程肌腱组织替代品的令人兴奋的观点。

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