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CD13 and ROR2 Permit Isolation of Highly Enriched Cardiac Mesoderm from Differentiating Human Embryonic Stem Cells

  • Rhys J.P. Skelton
  • , Bevin Brady
  • , Suhail Khoja
  • , Debashis Sahoo
  • , James Engel
  • , Deevina Arasaratnam
  • , Kholoud K. Saleh
  • , Oscar J. Abilez
  • , Peng Zhao
  • , Edouard G. Stanley
  • , Andrew G. Elefanty
  • , Murray Kwon
  • , David A. Elliott
  • , Reza Ardehali*
  • *Corresponding author for this work
  • University of California at Los Angeles
  • Royal Children's Hospital Melbourne
  • Stanford University
  • Division of Cardiology
  • Eli and Edythe Broad Stem Cell Research Center

Research output: Contribution to journalArticlepeer-review

Abstract

The generation of tissue-specific cell types from human embryonic stem cells (hESCs) is critical for the development of future stem cell-based regenerative therapies. Here, we identify CD13 and ROR2 as cell-surface markers capable of selecting early cardiac mesoderm emerging during hESC differentiation. We demonstrate that the CD13+/ROR2+ population encompasses pre-cardiac mesoderm, which efficiently differentiates to all major cardiovascular lineages. We determined the engraftment potential of CD13+/ROR2+ in small (murine) and large (porcine) animal models, and demonstrated that CD13+/ROR2+ progenitors have the capacity to differentiate toward cardiomyocytes, fibroblasts, smooth muscle, and endothelial cells in vivo. Collectively, our data show that CD13 and ROR2 identify a cardiac lineage precursor pool that is capable of successful engraftment into the porcine heart. These markers represent valuable tools for further dissection of early human cardiac differentiation, and will enable a detailed assessment of human pluripotent stem cell-derived cardiac lineage cells for potential clinical applications.

Original languageEnglish
Pages (from-to)95-108
Number of pages14
JournalStem Cell Reports
Volume6
Issue number1
DOIs
Publication statusPublished - 12 Jan 2016
Externally publishedYes

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