Novel Systems for Dynamically Assessing Insulin Action in Live Cells Reveals Heterogeneity in the Insulin Response

被引:21
作者
Burchfield, James G. [1 ]
Lu, Jinling [2 ]
Fazakerley, Daniel J. [1 ]
Tan, Shi-Xiong [1 ]
Ng, Yvonne [1 ]
Mele, Katarina [1 ,3 ]
Buckley, Michael J. [1 ,3 ]
Han, Weiping [2 ]
Hughes, William E. [1 ,5 ]
James, David E. [1 ,4 ]
机构
[1] Garvan Inst Med Res, Diabet & Obes Res Program, Sydney, NSW 2010, Australia
[2] ASTAR, Lab Metab Med, Singapore Bioimaging Consortium BMSI, Singapore 138667, Singapore
[3] CSIRO, CSIRO Math Informat & Stat, Sydney, NSW 1670, Australia
[4] Univ New S Wales, Sch Biotechnol & Biomed Sci, Sydney, NSW 2033, Australia
[5] St Vincents Hosp, Dept Med, Sydney, NSW 2010, Australia
关键词
fluorescence; GLUT4; heterogeneity; insulin; microscopy; quantification; single-cell; TIRF; trafficking; GLUCOSE-TRANSPORTER GLUT4; 3T3-L1; ADIPOCYTES; FLUORESCENCE MICROSCOPY; PLASMA-MEMBRANE; RAT ADIPOCYTES; SINGLE-CELL; TRAFFICKING; PROTEIN; VESICLES; FUSION;
D O I
10.1111/tra.12035
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Regulated GLUT4 trafficking is a key action of insulin. Quantitative stepwise analysis of this process provides a powerful tool for pinpointing regulatory nodes that contribute to insulin regulation and insulin resistance. We describe a novel GLUT4 construct and workflow for the streamlined dissection of GLUT4 trafficking; from simple high throughput screens to high resolution analyses of individual vesicles. We reveal single cell heterogeneity in insulin action highlighting the utility of this approach each cell displayed a unique and highly reproducible insulin response, implying that each cell is hard-wired to produce a specific output in response to a given stimulus. These data highlight that the response of a cell population to insulin is underpinned by extensive heterogeneity at the single cell level. This heterogeneity is pre-programmed within each cell and is not the result of intracellular stochastic events.
引用
收藏
页码:259 / 273
页数:15
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