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Micropocket hydrogel devices for all-in-one formation, assembly, and analysis of aggregate-based tissues

机译:用于一体化形成,组装和分析的微量电容器水凝胶器件,以及基于总基组织的分析

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Multicellular aggregated tissues have grown critically important in benchtop biomedical research, both as stand-alone spheroids and when assembled into larger bioengineered constructs. However, typical systems for aggregate formation are limited in their capacity to reliably handle such cultures at various experimental stages in a broadly accessible, consistent, and scalable manner. In this work, we develop a broadly versatile all-in-one biofabrication strategy to form uniform, spherical, multicellular aggregates that can be maintained at precisely defined positions for analysis or transfer into a larger tissue. The 3D-printed MicroPocket Culture (MPoC) system consists of an array of simple geometry-based valves in a polyacrylamide hydrogel, and is able to produce hundreds of uniformly-sized aggregates in standard tissue culture well plates, using simple tools that are readily available in all standard biological wet-labs. The model breast cancer aggregates formed in these experiments are retained in defined positions on chip during all liquid handling steps required to stimulate, label, and image the experiment, enabling high-throughput studies on this culture model. Furthermore, MPoCs enable robust formation of aggregates in cell types that do not conventionally form such structures. Finally, we demonstrate that this single platform can also be used to generate complex 3D tissues from the precisely-positioned aggregate building blocks. To highlight the unique and broad versatility of this technique, we develop a simple 3D invasion assay and show that cancer cells preferentially migrate towards nearby model tumors; demonstrating the importance of spatial precision when engineering 3D tissues. Together, this platform presents a broadly accessible and uniquely capable system with which to develop advanced aggregate-based models for tissue engineering, fundamental research, and applied drug discovery.
机译:多细胞聚集组织在Benchtop生物医学研究中生长至关重要,无论是独立的球体和组装成较大的生物工程构建体。然而,用于聚集体的典型系统的能力受到可靠地处理各种实验阶段的这种培养物,以广泛地访问,一致,一致,可扩展的方式。在这项工作中,我们开发了一种广泛多功能的一体化生物破坏策略,形成均匀的球形,多细胞聚集体,其可以在精确定义的位置保持用于分析或转移到更大的组织中。 3D印刷的微囊培养(MPOC)系统由聚丙烯酰胺水凝胶中的简单几何阀阵列组成,并且能够使用易于获得的简单工具在标准组织培养孔板中产生数百种均匀的聚集体在所有标准的生物湿式实验室中。在这些实验中形成的模型乳腺癌聚集体在刺激,标记和图像所需的步骤期间保留在芯片上的定义位置,使其对该培养模型进行高通量研究。此外,MPOCS能够在不常规形成这种结构的细胞类型中稳健地形成聚集体。最后,我们证明,该单一平台还可用于从精确定位的聚合构建块生成复杂的3D组织。为了突出这种技术的独特和广泛的多功能性,我们开发了一种简单的3D侵袭测定,并表明癌细胞优先迁移到附近的模型肿瘤;展示工程3D组织时空间精度的重要性。该平台在一起介绍了广泛的可访问和独特的能力系统,为组织工程,基础研究和应用药物发现开发基于先进的基于聚合的模型。

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