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在高密度微流控液滴阵列中对 3D 球体进行个体控制和量化。

Individual Control and Quantification of 3D Spheroids in a High-Density Microfluidic Droplet Array.

机构信息

LadHyX and Department of Mechanics, Ecole Polytechnique, CNRS, 91128 Palaiseau, France; Physical Microfluidics and Bio-Engineering, Department of Genomes and Genetics, Institut Pasteur, 75015 Paris, France.

LadHyX and Department of Mechanics, Ecole Polytechnique, CNRS, 91128 Palaiseau, France.

出版信息

Cell Rep. 2020 May 26;31(8):107670. doi: 10.1016/j.celrep.2020.107670.

Abstract

As three-dimensional cell culture formats gain in popularity, there emerges a need for tools that produce vast amounts of data on individual cells within the spheroids or organoids. Here, we present a microfluidic platform that provides access to such data by parallelizing the manipulation of individual spheroids within anchored droplets. Different conditions can be applied in a single device by triggering the merging of new droplets with the spheroid-containing drops. This allows cell-cell interactions to be initiated for building microtissues, studying stem cells' self-organization, or observing antagonistic interactions. It also allows the spheroids' physical or chemical environment to be modulated, as we show by applying a drug over a large range of concentrations in a single parallelized experiment. This convergence of microfluidics and image acquisition leads to a data-driven approach that allows the heterogeneity of 3D culture behavior to be addressed across the scales, bridging single-cell measurements with population measurements.

摘要

随着三维细胞培养形式的普及,人们需要能够在球体或类器官内的单个细胞上产生大量数据的工具。在这里,我们提出了一种微流控平台,通过在锚定液滴内平行操作单个球体来提供获取此类数据的途径。通过触发与含球体液滴的新液滴融合,可以在单个设备中应用不同的条件。这允许通过建立微组织来启动细胞间相互作用,研究干细胞的自我组织,或观察拮抗相互作用。通过在单个平行实验中施加大范围浓度的药物,我们还可以调节球体的物理或化学环境。这种微流控和图像采集的融合导致了一种数据驱动的方法,允许在多个尺度上解决 3D 培养行为的异质性,将单细胞测量与群体测量联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74c3/7262598/c3a2628a89a2/fx1.jpg

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