SHOX2 overexpression favors differentiation of embryonic stem cells into cardiac pacemaker cells, improving biological pacing ability

Stem Cell Reports. 2015 Jan 13;4(1):129-142. doi: 10.1016/j.stemcr.2014.11.004. Epub 2014 Dec 18.

Abstract

When pluripotency factors are removed, embryonic stem cells (ESCs) undergo spontaneous differentiation, which, among other lineages, also gives rise to cardiac sublineages, including chamber cardiomyocytes and pacemaker cells. Such heterogeneity complicates the use of ESC-derived heart cells in therapeutic and diagnostic applications. We sought to direct ESCs to differentiate specifically into cardiac pacemaker cells by overexpressing a transcription factor critical for embryonic patterning of the native cardiac pacemaker (the sinoatrial node). Overexpression of SHOX2 during ESC differentiation upregulated the pacemaker gene program, resulting in enhanced automaticity in vitro and induced biological pacing upon transplantation in vivo. The accentuated automaticity is accompanied by temporally evolving changes in the effectors and regulators of Wnt signaling. Our findings provide a strategy for enriching the cardiac pacemaker cell population from ESCs.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cardiac Electrophysiology
  • Cell Culture Techniques
  • Cell Differentiation / genetics*
  • Embryo Transfer
  • Embryoid Bodies / cytology
  • Embryoid Bodies / metabolism
  • Embryonic Stem Cells / cytology*
  • Embryonic Stem Cells / metabolism*
  • Gene Expression*
  • Genes, Reporter
  • Homeodomain Proteins / genetics*
  • Humans
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels / genetics
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels / metabolism
  • Mice
  • Myocytes, Cardiac / cytology*
  • Myocytes, Cardiac / metabolism*
  • Single-Cell Analysis
  • Sinoatrial Node / cytology*
  • Sinoatrial Node / metabolism*
  • Transduction, Genetic

Substances

  • Homeodomain Proteins
  • Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels
  • SHOX2 protein, human