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Open multi-culture platform for simple and flexible study of multi-cell type interactions

机译:开放式多种文化平台,简单灵活地研究多细胞型相互作用

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The study of multi-cell-type (MCT) interactions has the potential to significantly impact our understanding of tissue and disease biology. Such studies require innovative culture tools for unraveling the contributions of each cell type. Micro- and macro-scale platforms for MCT culture each have different advantages and disadvantages owing to their widely different capabilities, availability, and ease-of-use. However, as evidenced in the literature, there are very few examples of MCT studies and culture platforms, suggesting both biological and technical barriers. We have developed an open multi-culture platform to promote more rapid progress by integrating advantages of both micro- and macro-scale culture devices. The proposed open multi-culture platform addresses technical barriers by allowing easy customization, independent control of basic physical culture parameters, and incorporation of multiple culture modalities ( e.g. , 2D, 3D, transwell, and spheroid). The design also permits the user to obtain independent endpoints for each culture region. We demonstrate use of the platform in two example studies where we evaluated how cell ratio and cell types influence the response of triple negative breast cancer cells to heat damage and Hedgehog signaling. We also show that the platform can improve soluble factor transport between cell types compared to compartmentalized macro- and micro-scale alternatives. Last, we examine current and future challenges of the platform. We envision simple, yet flexible and customizable, platforms such as this will be important for advancing in vitro study of tissue and tumor biology.
机译:多细胞型(MCT)相互作用的研究具有显着影响我们对组织和疾病生物学的理解。这些研究需要创新的文化工具来解除每个细胞类型的贡献。 MCT培养的微型和宏观规模平台,由于其广泛不同的能力,可用性和易用性,因此具有不同的优点和缺点。然而,正如文献所证明的那样,MCT研究和文化平台的例子很少,表明生物和技术障碍。我们开发了一个开放的多种文化平台,通过整合微型和宏观培养设备的优势来促进更快的进展。拟议的开放式多种文化平台通过允许容易定制,对基本物理培养参数的独立控制来解决技术障碍,并纳入多种培养方式(例如,2D,3D,Transwell和Spheroid)。该设计还允许用户获得每个文化区域的独立端点。我们在两个示例研究中展示了该平台的使用,在两个示例研究中,我们评估了细胞比和细胞类型如何影响三重阴性乳腺癌细胞对热损伤和刺猬信号传导的响应。我们还表明,与划分的宏观和微尺度替代方案相比,该平台可以改善细胞类型之间的可溶性因子传输。最后,我们检查平台的当前和未来挑战。我们设想简单,但灵活可自定义,平台,诸如此类方面对于推进组织和肿瘤生物学的体外研究非常重要。

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