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Molecular live cell bioimaging in stem cell research.

Ann. NY Acad. Sci. 1266, 18-27 (2012)
DOI PMC
Open Access Green as soon as Postprint is submitted to ZB.
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.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords 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
ISSN (print) / ISBN 0077-8923
e-ISSN 1749-6632
Quellenangaben Volume: 1266, Issue: 1, Pages: 18-27 Article Number: , Supplement: ,
Publisher New York Academy of Sciences
Non-patent literature Publications
Reviewing status Peer reviewed