Molecular live cell bioimaging in stem cell research

被引:12
作者
Endele, Max [1 ]
Schroeder, Timm [1 ]
机构
[1] German Res Ctr Environm Hlth, Helmholtz Ctr Munich, Res Unit Stem Cell Dynam, D-85764 Neuherberg, Germany
来源
HEMATOPOIETIC STEM CELLS VIII | 2012年 / 1266卷
关键词
biosensors; cytokines; M-CSF; signaling; lineage choice; stem cell; imaging; time lapse; PROTEIN-KINASE-C; STIMULATING FACTOR-I; HEMATOPOIETIC PROGENITOR CELLS; INFRARED FLUORESCENT PROTEINS; RECEPTOR TYROSINE KINASE; M-CSF RECEPTOR; SELF-RENEWAL; LINEAGE COMMITMENT; LIVING CELLS; SCAFFOLDING PROTEIN;
D O I
10.1111/j.1749-6632.2012.06560.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Functional heterogeneity within stem and progenitor cells has been shown to influence cell fate decisions. Similarly, intracellular signaling activated by external stimuli is highly heterogeneous and its spatiotemporal activity is linked to future cell behavior. To quantify these heterogeneous states and link them to future cell fates, it is important to observe cell populations continuously with single cell resolution. Live cell imaging in combination with fluorescent biosensors for signaling activity serves as a powerful tool to study cellular and molecular heterogeneity and the long-term biological effects of signaling. Here, we describe these methodologies, their advantages over classical approaches, and we illustrate how they could be applied to improve our understanding of the importance of heterogeneous cellular and molecular responses to external signaling cues.
引用
收藏
页码:18 / 27
页数:10
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