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首页> 外文期刊>Advanced Functional Materials >Directing Osteogenesis of Stem Cells with Drug-Laden, Polymer-Microsphere-Based Micropatterns Generated by Teflon Microfluidic Chips
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Directing Osteogenesis of Stem Cells with Drug-Laden, Polymer-Microsphere-Based Micropatterns Generated by Teflon Microfluidic Chips

机译:用铁氟龙微流控芯片生成的载有药物,基于聚合物微球的微模式指导干细胞的成骨

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摘要

Human bone tissue is built in a hierarchical way by assembling various cells of specific functions; the behaviors of these cells in vivo are sophisticatedly regulated. However, the cells in an injured bone caused by tumor or other bone-related diseases cannot properly perform self-regulation behaviors, such as specialized differentiation. To address this challenge, a simple one-step strategy for patterning drug-laden poly(lactic-co-glycolic acid) (PLGA) micro-spheres into grooves by Teflon chips is developed to direct cellular alignment and osteogenic commitment of adipose-derived stem cells (ADSCs) for bone regeneration. A hydrophilic model protein and a hydrophobic model drug are encapsulated into microsphere-based grooved micropatterns to investigate the release of the molecules from the PLGA matrix. Both types of molecules show a sustained release with a small initial burst during the first couple of days. Osteogenic differentiated factors are also encapsulated in the micropatterns and the effect of these factors on inducing the osteogenic differentiation of ADSCs is studied. The ADSCs on the drug-laden micropatterns show stronger osteogenic commitment in culture than those on flat PLGA film or on drug-free grooved micropatterns cultured under the same conditions. The results demonstrate that a combination of chemical and topographical cues is more effective to direct the osteogenic commitment of stem cells than either is alone. The microsphere-based groove micropatterns show potential for stem cell research and bone regenerative therapies.
机译:人体骨骼组织是通过组装具有特定功能的各种细胞以分层的方式构建的。这些细胞在体内的行为受到精密调节。但是,由肿瘤或其他与骨骼相关的疾病引起的受伤骨骼中的细胞无法正确执行自我调节行为,例如专门的分化。为了应对这一挑战,开发了一种简单的一步法,该方法通过特富龙芯片将载有药物的聚乳酸-乙醇酸(PLGA)微球构图成凹槽,以指导细胞排列和脂肪来源的茎的成骨作用细胞(ADSC)用于骨骼再生。将亲水性模型蛋白和疏水性模型药物封装到基于微球的带槽微图案中,以研究分子从PLGA基质中的释放。两种类型的分子均显示出持续释放的方式,并且在最初的几天内初始释放量很小。成骨分化因子也被封装在微模式中,并且研究了这些因子在诱导ADSCs成骨分化中的作用。在相同条件下培养的载药微模式上的ADSC比在平坦的PLGA膜或无药物的沟槽微模式上显示出更强的成骨作用。结果表明,化学和地形学提示的组合比单独使用更有效地指导干细胞的成骨作用。基于微球的凹槽微图案显示了干细胞研究和骨再生疗法的潜力。

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  • 来源
    《Advanced Functional Materials》 |2012年第18期|3799-3807|共9页
  • 作者单位

    WPI-Advanced Institute for Materials Research Tohoku University Sendai 980-8578, Japan;

    WPI-Advanced Institute for Materials Research Tohoku University Sendai 980-8578, Japan;

    WPI-Advanced Institute for Materials Research Tohoku University Sendai 980-8578, Japan,Department of Chemistry Hong Kong University of Science and Technology Hong Kong, China;

    WPI-Advanced Institute for Materials Research Tohoku University Sendai 980-8578, Japan;

    WPI-Advanced Institute for Materials Research Tohoku University Sendai 980-8578, Japan,State Key Laboratory of Integrated Optoelectronics Institute of Semiconductors Chinese Academy of Sciences, Beijing, 100083, China;

    WPI-Advanced Institute for Materials Research Tohoku University Sendai 980-8578, Japan,Department of Chemistry Hong Kong University of Science and Technology Hong Kong, China;

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