Murine transgenic embryonic stem cell lines for the investigation of sinoatrial node-related molecular pathways

The elucidation of molecular mechanisms that restrict the potential of pluripotent stem cells and promote cardiac lineage differentiation is of crucial relevance, since embryonic stem cells (ESCs) hold great potential for cell based heart therapies. The homeodomain transcription factor Shox2 is esse...

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Hauptverfasser: Mellein, Stefanie (VerfasserIn) , Sumer, Simon (VerfasserIn) , Jauch, Anna (VerfasserIn) , Rolletschek, Alexandra (VerfasserIn) , Niesler, Beate (VerfasserIn) , Rappold, Gudrun (VerfasserIn) , Hoffmann, Sandra (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 11 July 2017
In: Stem cell research
Year: 2017, Jahrgang: 25, Pages: 278-282
ISSN:1876-7753
DOI:10.1016/j.scr.2017.07.011
Online-Zugang:Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1016/j.scr.2017.07.011
Verlag, kostenfrei, Volltext: http://www.sciencedirect.com/science/article/pii/S1873506117301356
Volltext
Verfasserangaben:Stefanie Schmitteckert, Anne Griesbeck, Simon Sumer, Anna Jauch, Alexandra Rolletschek, Beate Niesler, Gudrun A. Rappold, Sandra Hoffmann
Beschreibung
Zusammenfassung:The elucidation of molecular mechanisms that restrict the potential of pluripotent stem cells and promote cardiac lineage differentiation is of crucial relevance, since embryonic stem cells (ESCs) hold great potential for cell based heart therapies. The homeodomain transcription factor Shox2 is essential for the development and proper function of the native cardiac pacemaker, the sinoatrial node. This prompted us to develop a cardiac differentiation model using ESC lines isolated from blastocysts of Shox2-deficient mice. The established cell model provides a fundamental basis for the investigation of molecular pathways under physiological and pathophysiological conditions for evaluating novel therapeutic approaches.
Beschreibung:Gesehen am 21.12.2017
Beschreibung:Online Resource
ISSN:1876-7753
DOI:10.1016/j.scr.2017.07.011