4.1 Review

Photomodulatable fluorescent proteins for imaging cell dynamics and cell fate

Journal

ORGANOGENESIS
Volume 5, Issue 4, Pages 217-226

Publisher

TAYLOR & FRANCIS INC
DOI: 10.4161/org.5.4.10939

Keywords

fluorescent protein; photomodulation; photoactivation; photoconversion; mouse; live imaging; embryonic development; organogenesis; GFP; PA-GFP; PS-CFP; Kaede; KikGR

Funding

  1. National Institutes of Health [RO1-HD052115, RO1-DK084391]
  2. NYSTEM
  3. American Heart Association

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An organism arises from the coordinate generation of different cell types and the stereotypical organization of these cells into tissues and organs. Even so, the dynamic behaviors, as well as the ultimate fates, of cells driving the morphogenesis of an organism, or even an individual organ, remain largely unknown. Continued innovations in optical imaging modalities, along with the discovery and evolution of improved genetically-encoded fluorescent protein reporters in combination with model organism, stem cell and tissue engineering paradigms are providing the means to investigate these unresolved questions. The emergence of fluorescent proteins whose spectral properties can be photomodulated is one of the most significant new developments in the field of cell biology where they are primarily used for studying protein dynamics in cells. Likewise, the use of photomodulatable fluorescent proteins holds great promise for use in developmental biology. Photomodulatable fluorescent proteins also represent attractive and emergent tools for studying cell dynamics in complex populations by facilitating the labeling and tracking of individual or defined groups of cells. Here, we review the currently available photomodulatable fluorescent proteins and their application in model organisms. We also discuss prospects for their use in mice, and by extension in embryonic stem cell and tissue engineering paradigms.

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