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

被引:25
|
作者
Wu, Meiye [1 ]
Perroud, Thomas D. [1 ]
Srivastava, Nimisha [1 ]
Branda, Catherine S. [1 ]
Sale, Kenneth L. [1 ]
Carson, Bryan D. [1 ]
Patel, Kamlesh D. [1 ]
Branda, Steven S. [1 ]
Singh, Anup K. [1 ]
机构
[1] Sandia Natl Labs, Biotechnol & Bioengn Dept, Livermore, CA 94551 USA
关键词
CHIP-BASED SYSTEM; HIGH-THROUGHPUT; MAMMALIAN-CELLS; TLR4; BACTERIAL; PROTEIN; CD14; LIPOPOLYSACCHARIDE; EXPRESSION; DYNAMICS;
D O I
10.1039/c2lc40344g
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
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-alpha 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.
引用
收藏
页码:2823 / 2831
页数:9
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