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Microfluidically-unified cell culture, sample preparation, imaging and flow cytometry for measurement of cell signaling pathways with single cell resolution

机译:微流控统一的细胞培养,样品制备,成像和流式细胞仪,用于以单细胞分辨率测量细胞信号通路

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摘要

We have developed a microfluidic platform that enables, in one experiment, monitoring of signaling events spanning multiple time-scales and cellular locations through seamless integration of cell culture, stimulation and preparation with downstream analysis. A combination of two single-cell resolution techniques-on-chip multi-color flow cytometry and fluorescence imaging provides multiplexed and orthogonal data on cellular events. Automated, microfluidic operation allows quantitatively- and temporally-precise dosing leading to fine time-resolution and improved reproducibility of measurements. The platform was used to profile the toll-like receptor (TLR4) pathway in macrophages challenged with lipopolysaccharide (LPS)-beginning with TLR4 receptor activation by LPS, through intracellular MAPK signaling, RelA/p65 translocation in real time, to TNF-α cytokine production, all in one small macrophage population (< 5000 cells) while using minute reagent volume (540 nL/condition). The platform is easily adaptable to many cell types including primary cells and provides a generic platform for profiling signaling pathways.
机译:我们已经开发出一种微流体平台,该平台可以在一个实验中通过无缝整合细胞培养,刺激和制备以及下游分析来监控跨越多个时间尺度和细胞位置的信号事件。两种单细胞分辨率技术片上多色流式细胞术和荧光成像相结合,可提供有关细胞事件的多路复用和正交数据。自动化的微流体操作允许定量和时间精确定量,从而实现精细的时间分辨率并提高了测量的可重复性。该平台用于通过细胞内MAPK信号转导,实时RelA / p65易位,通过TNF-α细胞因子对脂多糖(LPS)激发的巨噬细胞中的Toll样受体(TLR4)通路进行分析-通过LPS激活TLR4受体。只需少量试剂体积(540 nL /条件),即可在一个小的巨噬细胞群(<5000个细胞)中进行全部生产。该平台易于适应包括原代细胞在内的多种细胞类型,并提供了用于分析信号传导途径的通用平台。

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