GFRA2 Identifies Cardiac Progenitors and Mediates Cardiomyocyte Differentiation in a RET-Independent Signaling Pathway
Author(s) -
Hidekazu Ishida,
Rie Saba,
Ioannis Kokkinopoulos,
Masakazu Hashimoto,
Osamu Yamaguchi,
Sonja Nowotschin,
Manabu Shiraishi,
Prashant J. Ruchaya,
Duncan C. Miller,
Stephen C. Harmer,
Ariel Poliandri,
Shigetoyo Kogaki,
Yasushi Sakata,
Leo Dunkel,
Andrew Tinker,
AnnaKaterina Hadjantonakis,
Yoshiki Sawa,
Hiroshi Sasaki,
Keiichi Ozono,
Ken Suzuki,
Kenta Yashiro
Publication year - 2016
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2016.06.050
Subject(s) - microbiology and biotechnology , biology , cell sorting , progenitor cell , signal transduction , cellular differentiation , induced pluripotent stem cell , neurotrophic factors , transplantation , stem cell , receptor , embryonic stem cell , cell , genetics , gene , medicine
A surface marker that distinctly identifies cardiac progenitors (CPs) is essential for the robust isolation of these cells, circumventing the necessity of genetic modification. Here, we demonstrate that a Glycosylphosphatidylinositol-anchor containing neurotrophic factor receptor, Glial cell line-derived neurotrophic factor receptor alpha 2 (Gfra2), specifically marks CPs. GFRA2 expression facilitates the isolation of CPs by fluorescence activated cell sorting from differentiating mouse and human pluripotent stem cells. Gfra2 mutants reveal an important role for GFRA2 in cardiomyocyte differentiation and development both in vitro and in vivo. Mechanistically, the cardiac GFRA2 signaling pathway is distinct from the canonical pathway dependent on the RET tyrosine kinase and its established ligands. Collectively, our findings establish a platform for investigating the biology of CPs as a foundation for future development of CP transplantation for treating heart failure.
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