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Three-dimensional spheroid culture targeting versatile tissue bioassays using a PDMS-based hanging drop array

机译:使用基于PDMS的悬挂滴阵列靶向多功能组织生物测定的三维球体培养

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摘要

Biomaterial-based tissue culture platforms have emerged as useful tools to mimic in vivo physiological microenvironments in experimental cell biology and clinical studies. We describe herein a three-dimensional (3D) tissue culture platform using a polydimethylsiloxane (PDMS)-based hanging drop array (PDMS-HDA) methodology. Multicellular spheroids can be achieved within 24 h and further boosted by incorporating collagen fibrils in PDMS-HDA. In addition, the spheroids generated from different human tumor cells exhibited distinct sensitivities toward drug chemotherapeutic agents and radiation as compared with two-dimensional (2D) cultures that often lack in vivo-like biological insights. We also demonstrated that multicellular spheroids may enable key hallmarks of tissue-based bioassays, including drug screening, tumor dissemination, cell co-culture, and tumor invasion. Taken together, these results offer new opportunities not only to achieve the active control of 3D multicellular spheroids on demand, but also to establish a rapid and cost-effective platform to study anti-cancer therapeutics and tumor microenvironments.
机译:基于生物材料的组织培养平台已经成为在实验性细胞生物学和临床研究中模仿体内生理微环境的有用工具。我们在这里描述了使用基于聚二甲基硅氧烷(PDMS)的悬挂滴阵列(PDMS-HDA)方法的三维(3D)组织培养平台。多细胞球体可在24小时内实现,并通过在PDMS-HDA中掺入胶原纤维进一步增强。此外,与通常缺乏体内样生物学见解的二维(2D)培养相比,由不同人类肿瘤细胞产生的球体对药物化学治疗剂和放射线表现出不同的敏感性。我们还证明了多细胞球体可能成为基于组织的生物测定的关键标志,包括药物筛选,肿瘤扩散,细胞共培养和肿瘤侵袭。综上所述,这些结果不仅提供了按需主动控制3D多细胞球体的新机会,而且为建立快速且具有成本效益的平台来研究抗癌疗法和肿瘤微环境提供了新的机会。

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