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...

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Main Authors: 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
Format: Article
Language:English
Published: Elsevier 2016-07-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S221112471630804X
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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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spelling 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