GFRA2 Identifies Cardiac Progenitors and Mediates Cardiomyocyte Differentiation in a RET-Independent Signaling Pathway
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-de...
Main Authors: | , , , , , , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
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Elsevier
2016-07-01
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Series: | Cell Reports |
Online Access: | http://www.sciencedirect.com/science/article/pii/S221112471630804X |
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doaj-5e85abb0c44e43099e2efbde36699c23 |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hidekazu Ishida Rie Saba Ioannis Kokkinopoulos Masakazu Hashimoto Osamu Yamaguchi Sonja Nowotschin Manabu Shiraishi Prashant Ruchaya Duncan Miller Stephen Harmer Ariel Poliandri Shigetoyo Kogaki Yasushi Sakata Leo Dunkel Andrew Tinker Anna-Katerina Hadjantonakis Yoshiki Sawa Hiroshi Sasaki Keiichi Ozono Ken Suzuki Kenta Yashiro |
spellingShingle |
Hidekazu Ishida Rie Saba Ioannis Kokkinopoulos Masakazu Hashimoto Osamu Yamaguchi Sonja Nowotschin Manabu Shiraishi Prashant Ruchaya Duncan Miller Stephen Harmer Ariel Poliandri Shigetoyo Kogaki Yasushi Sakata Leo Dunkel Andrew Tinker Anna-Katerina Hadjantonakis Yoshiki Sawa Hiroshi Sasaki Keiichi Ozono Ken Suzuki Kenta Yashiro GFRA2 Identifies Cardiac Progenitors and Mediates Cardiomyocyte Differentiation in a RET-Independent Signaling Pathway Cell Reports |
author_facet |
Hidekazu Ishida Rie Saba Ioannis Kokkinopoulos Masakazu Hashimoto Osamu Yamaguchi Sonja Nowotschin Manabu Shiraishi Prashant Ruchaya Duncan Miller Stephen Harmer Ariel Poliandri Shigetoyo Kogaki Yasushi Sakata Leo Dunkel Andrew Tinker Anna-Katerina Hadjantonakis Yoshiki Sawa Hiroshi Sasaki Keiichi Ozono Ken Suzuki Kenta Yashiro |
author_sort |
Hidekazu Ishida |
title |
GFRA2 Identifies Cardiac Progenitors and Mediates Cardiomyocyte Differentiation in a RET-Independent Signaling Pathway |
title_short |
GFRA2 Identifies Cardiac Progenitors and Mediates Cardiomyocyte Differentiation in a RET-Independent Signaling Pathway |
title_full |
GFRA2 Identifies Cardiac Progenitors and Mediates Cardiomyocyte Differentiation in a RET-Independent Signaling Pathway |
title_fullStr |
GFRA2 Identifies Cardiac Progenitors and Mediates Cardiomyocyte Differentiation in a RET-Independent Signaling Pathway |
title_full_unstemmed |
GFRA2 Identifies Cardiac Progenitors and Mediates Cardiomyocyte Differentiation in a RET-Independent Signaling Pathway |
title_sort |
gfra2 identifies cardiac progenitors and mediates cardiomyocyte differentiation in a ret-independent signaling pathway |
publisher |
Elsevier |
series |
Cell Reports |
issn |
2211-1247 |
publishDate |
2016-07-01 |
description |
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. |
url |
http://www.sciencedirect.com/science/article/pii/S221112471630804X |
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doaj-5e85abb0c44e43099e2efbde36699c232020-11-25T01:46:35ZengElsevierCell Reports2211-12472016-07-011641026103810.1016/j.celrep.2016.06.050GFRA2 Identifies Cardiac Progenitors and Mediates Cardiomyocyte Differentiation in a RET-Independent Signaling PathwayHidekazu Ishida0Rie Saba1Ioannis Kokkinopoulos2Masakazu Hashimoto3Osamu Yamaguchi4Sonja Nowotschin5Manabu Shiraishi6Prashant Ruchaya7Duncan Miller8Stephen Harmer9Ariel Poliandri10Shigetoyo Kogaki11Yasushi Sakata12Leo Dunkel13Andrew Tinker14Anna-Katerina Hadjantonakis15Yoshiki Sawa16Hiroshi Sasaki17Keiichi Ozono18Ken Suzuki19Kenta Yashiro20Centre for Endocrinology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UKCentre for Endocrinology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UKCentre for Endocrinology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UKLaboratory for Embryogenesis, Osaka University Graduate School of Frontier Biosciences, Osaka 565-0871, JapanDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, JapanDevelopmental Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USATranslational Medicine and Therapeutics, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UKTranslational Medicine and Therapeutics, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UKCardiac Electrophysiology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UKCardiac Electrophysiology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UKCentre for Endocrinology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UKDepartment of Paediatrics, Osaka University Graduate School of Medicine, Osaka 565-0871, JapanDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka 565-0871, JapanCentre for Endocrinology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UKCardiac Electrophysiology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UKDevelopmental Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USADepartment of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Osaka 565-0871, JapanLaboratory for Embryogenesis, Osaka University Graduate School of Frontier Biosciences, Osaka 565-0871, JapanDepartment of Paediatrics, Osaka University Graduate School of Medicine, Osaka 565-0871, JapanTranslational Medicine and Therapeutics, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UKCentre for Endocrinology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, UKA 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.http://www.sciencedirect.com/science/article/pii/S221112471630804X |