Comparative expression analysis of Shox2-deficient embryonic stem cell-derived sinoatrial node-like cells

• Verfasst von: Hoffmann, Sandra [VerfasserIn]
• Verfasst von: Schmitteckert, Stefanie [VerfasserIn]
• Verfasst von: Griesbeck, Anne [VerfasserIn]
• Verfasst von: Preiss, Hannes [VerfasserIn]
• Verfasst von: Sumer, Simon [VerfasserIn]
• Verfasst von: Granzow, Martin [VerfasserIn]
• Verfasst von: Eckstein, Volker [VerfasserIn]
• Verfasst von: Niesler, Beate [VerfasserIn]
• Verfasst von: Rappold, Gudrun [VerfasserIn]
• Titel: Comparative expression analysis of Shox2-deficient embryonic stem cell-derived sinoatrial node-like cells
• Verf.angabe: Sandra Hoffmann, Stefanie Schmitteckert, Anne Griesbeck, Hannes Preiss, Simon Sumer, Alexandra Rolletschek, Martin Granzow, Volker Eckstein, Beate Niesler, Gudrun A. Rappold
• Umfang: 7 S.
• Fussnoten: Available online 29 March 2017 ; Gesehen am 27.06.2018
• Titel Quelle: Enthalten in: Stem cell research
• Jahr Quelle: 2017
• Band/Heft Quelle: 21(2017), S. 51-57
• ISSN Quelle: 1876-7753
• DOI: doi:10.1016/j.scr.2017.03.018
• Sprache: eng
• K10plus-PPN: 157690556X

Abstract

The homeodomain transcription factor Shox2 controls the development and function of the native cardiac pacemaker, the sinoatrial node (SAN). Moreover, SHOX2 mutations have been associated with cardiac arrhythmias in humans. For detailed examination of Shox2-dependent developmental mechanisms in SAN cells, we established a murine embryonic stem cell (ESC)-based model using Shox2 as a molecular tool. Shox2+/+ and Shox2−/− ESC clones were isolated and differentiated according to five different protocols in order to evaluate the most efficient enrichment of SAN-like cells. Expression analysis of cell subtype-specific marker genes revealed most efficient enrichment after CD166-based cell sorting. Comparative cardiac expression profiles of Shox2+/+ and Shox2−/− ESCs were examined by nCounter technology. Among other genes, we identified Nppb as a novel putative Shox2 target during differentiation in ESCs. Differential expression of Nppb could be confirmed in heart tissue of Shox2−/− embryos. Taken together, we established an ESC-based cardiac differentiation model and successfully purified Shox2+/+ and Shox2−/− SAN-like cells. This now provides an excellent basis for the investigation of molecular mechanisms under physiological and pathophysiological conditions for evaluating novel therapeutic approaches.