Redefining Signaling Pathways with an Expanding Single-Cell Toolbox

被引:27
作者
Gaudet, Suzanne [1 ,2 ,3 ]
Miller-Jensen, Kathryn [4 ,5 ]
机构
[1] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02215 USA
[2] Dana Farber Canc Inst, Ctr Canc Syst Biol, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[4] Yale Univ, Dept Biomed Engn, New Haven, CT 06520 USA
[5] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
NF-KAPPA-B; INDIVIDUAL LIVING CELLS; EPIDERMAL-GROWTH-FACTOR; ERK ACTIVATION; IN-VIVO; INFORMATION-TRANSMISSION; P53; TETRAMERIZATION; KINASE-ACTIVITIES; TEMPORAL CONTROL; FRET BIOSENSORS;
D O I
10.1016/j.tibtech.2016.02.009
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Genetically identical cells respond heterogeneously to uniform environmental stimuli. Consequently, investigating the signaling networks that control these cell responses using 'average' bulk cell measurements can obscure underlying mechanisms and misses information emerging from cell-to-cell variability. Here we review recent technological advances including live-cell fluorescence imaging-based approaches and microfluidic devices that enable measurements of signaling networks, dynamics, and responses in single cells. We discuss how these single-cell tools have uncovered novel mechanistic insights for canonical signaling pathways that control cell proliferation (ERK), DNA-damage responses (p53), and innate immune and stress responses (NF-kappa B). Future improvements in throughput and multiplexing, analytical pipelines, and in vivo applicability will all significantly expand the biological information gained from single-cell measurements of signaling pathways.
引用
收藏
页码:458 / 469
页数:12
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