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Microfabricated scaffold-guided endothelial morphogenesis in three-dimensional culture

机译:三维支架中的微型支架引导的内皮形态发生

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摘要

Morphogenesis is a fundamental process by which new blood vessels are formed during angiogenesis. The ability to control angiogenesis would lead to improvements in tissue engineering constructions; indeed, the study of angiogenesis has numerous clinical applications, for example, in the investigation of metastatic cancer, peripheral and coronary vascular disease, and wound healing. Conventional in vitro organotypic cell culture approaches to these studies are limited primarily by their reliance on microvascular vessel formation through a random process of morphogenesis that lacks the spatial reproducibility and orientation needed for high-throughput drug testing. We have developed a bioreactor system for scaffold-guided tubulogenesis coupled with 3-D organotypic culture to spatially control vessel formation and its orientation. To create microchannels to guide microvessel formation, we fabricated rigid scaffolds using photolithography and light curing epoxy, and soft scaffolds formed by a polydimethylsiloxane (PDMS) stamp directly into collagen. Scaffolds seeded with dermal microvascular endothelial cells were placed between gelled layers of collagen containing dermal fibroblasts within a Transwell filter system and cultured for up to 2 weeks to allow for vessel maturation. Morphological analysis of thin tissue sections following standard histology and immunohistochemical detection of endothelial cells, fibroblasts, and basement membrane confirmed vessel formation along the microchannel walls with either scaffold. This system may also provide a means to explore revascularization within decellularized extracellular matrices, the culture of micro-vessel networks with controlled geometries, and possibly the spatial guidance of angiogenesis for interfacing with an external microfluidic supply network. As a new tool for guided angiogenesis, our approach introduces new possibilities for identification of anti-angiogenic therapeutics.
机译:形态发生是在血管生成过程中形成新血管的基本过程。控制血管生成的能力将导致组织工程构造的改善。实际上,血管生成的研究具有许多临床应用,例如,在转移癌,周围和冠状血管疾病以及伤口愈合的研究中。用于这些研究的常规体外器官型细胞培养方法主要受到它们通过形态发生的随机过程对微血管血管形成的依赖的限制,而形态形成的随机过程缺乏高通量药物测试所需的空间可再现性和方向。我们已经开发了一种生物反应器系统,用于支架引导的肾小管生成以及3-D器官型培养,以空间控制血管的形成及其方向。为了创建引导微血管形成的微通道,我们使用光刻和光固化环氧树脂制造了刚性支架,并使用聚二甲基硅氧烷(PDMS)将软支架直接压制成胶原蛋白。将装有真皮微血管内皮细胞的支架置于Transwell过滤器系统内的含有胶原的真皮成纤维细胞的胶凝层之间,并培养2周以使血管成熟。按照标准组织学对内皮细胞,成纤维细胞和基底膜进行免疫组织化学检测后,对薄组织切片进行形态学分析,证实了沿任一支架的微通道壁均形成了血管。该系统还可以提供一种手段,以探索脱细胞的细胞外基质内的血运重建,具有受控几何形状的微血管网络的培养,以及可能的血管生成与外部微流体供应网络接口的空间指导。作为指导血管生成的新工具,我们的方法为鉴定抗血管生成疗法带来了新的可能性。

著录项

  • 来源
    《Biomedical Microdevices 》 |2011年第5期| p.837-846| 共10页
  • 作者单位

    Lane Department of Computer Science and Electrical Engineering, and WVNano Initiative, West Virginia University, Morgantown, WV 26506, USA;

    Vanderbilt Institute for Integrative Biosystems Research and Education, Vanderbilt University, Nashville, TN 37235, USA,Department of Biomedical Engineering, Vanderbilt University, Nashville, TN 37235, USA;

    Vanderbilt Institute for Integrative Biosystems Research and Education, Vanderbilt University, Nashville, TN 37235, USA,Departments of Molecular Physiology & Biophysics and Physics & Astronomy, Vanderbilt University, Nashville, TN 37235, USA;

    Vanderbilt Institute for Integrative Biosystems Research and Education, Vanderbilt University, Nashville, TN 37235, USA,Department of Cancer Biology, Vanderbilt University, Nashville, TN 37232, USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    primary endothelial cells; morphogenesis; engineered scaffold; bioreactor- 3-d culture;

    机译:原代内皮细胞;形态发生;工程脚手架;生物反应器3 d培养;

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