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Stem Cells 2005;23:10-15 www.StemCells.com
© 2005 AlphaMed Press


RAPID COMMUNICATION

In Vivo and In Vitro Tissue-Specific Expression of Green Fluorescent Protein Using the Cre-Lox System in Mouse Embryonic Stem Cells

Jan Schindehüttea, Hidefumi Fukumitsub, Patrick Collombatc, Gundula Grieselc, Christopher Brinkc, Paul C. Baiera, Mario R. Capecchid, Ahmed Mansouric

a Georg-August University Göttingen, Department of Clinical Neurophysiology, Göttingen, Germany;
b Gifu Pharmaceutical University, Laboratory of Molecular Biology, Gifu, Japan;
c Max-Planck-Institute for Biophysical Chemistry, Department of Molecular Cell Biology, Göttingen, Germany;
d University of Utah School of Medicine, Howard Hughes Medical Institute and Department of Human Genetics, Salt Lake City, Utah, USA

Key Words. Conditional green fluorescent protein expression • Embryonic stem cells • Transplantation • Mouse

Correspondence: Ahmed Mansouri, Ph.D., Max-Planck Institute for Biophysical Chemistry, Department of Molecular Cell Biology, Am Fassberg 11, 37077 Göttingen, Germany. Telephone: 49-551-201-1490; Fax: 49-551-201-1504; e-mail: amansou{at}gwdg.de

Embryonic stem cells (ES) are pluripotent and may therefore serve as a source for the generation of specific cell types required for future therapies based on cell replacement. The isolation of defined cell populations from a certain lineage or tissue is a prerequisite for the analysis of the potential of such ES-derived cells in animal transplantation studies. Here, using the Cre/loxP system, we report the generation of murine ES cells conditionally expressing the hrGFP gene at the cell surface. Such ES cells can be differentiated in vitro into neurons displaying GFP activity in neurites. Transgenic mice derived from these ES cells permit the targeting of GFP-expression to specific tissues and provide material from the three germ layers suitable for molecular and biochemical analysis.




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S. Haupt, F. Edenhofer, M. Peitz, A. Leinhaas, and O. Brustle
Stage-Specific Conditional Mutagenesis in Mouse Embryonic Stem Cell-Derived Neural Cells and Postmitotic Neurons by Direct Delivery of Biologically Active Cre Recombinase
Stem Cells, January 1, 2007; 25(1): 181 - 188.
[Abstract] [Full Text] [PDF]




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