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Stem Cell Reports ; 6(1): 95-108, 2016 Jan 12.
Article in English | MEDLINE | ID: mdl-26771355

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.


Subject(s)
CD13 Antigens/metabolism , Human Embryonic Stem Cells/metabolism , Mesoderm/metabolism , Myocardium/metabolism , Receptor Tyrosine Kinase-like Orphan Receptors/metabolism , Animals , CD13 Antigens/genetics , Cell Differentiation/genetics , Cell Differentiation/physiology , Cell Line , Cell Lineage/genetics , Cell Lineage/physiology , Endothelial Cells/cytology , Endothelial Cells/metabolism , Fibroblasts/cytology , Fibroblasts/metabolism , Fluorescent Antibody Technique , Gene Expression Profiling/methods , Human Embryonic Stem Cells/cytology , Humans , Mesoderm/cytology , Mice , Muscle, Smooth/cytology , Muscle, Smooth/metabolism , Myocardium/cytology , Myocytes, Cardiac/cytology , Myocytes, Cardiac/metabolism , Pluripotent Stem Cells/cytology , Pluripotent Stem Cells/metabolism , Receptor Tyrosine Kinase-like Orphan Receptors/genetics , Reverse Transcriptase Polymerase Chain Reaction , Stem Cell Transplantation/methods , Swine , Time Factors , Transplantation, Heterologous
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