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Endothelial cells regulate cardiomyocyte development from embryonic stem cells

The molecules and environment that direct pluripotent stem cell differentiation into cardiomyocytes are largely unknown. Here, we determined a critical role of receptor tyrosine kinase, EphB4, in regulating cardiomyocyte generation from embryonic stem (ES) cells through endothelial cells. The number...

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Published in:Journal of cellular biochemistry 2010-09, Vol.111 (1), p.29-39
Main Authors: Chen, Kang, Bai, Hao, Arzigian, Melanie, Gao, Yong-Xing, Bao, Jing, Wu, Wen-Shu, Shen, Wei-Feng, Wu, Liqun, Wang, Zack Z.
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cited_by cdi_FETCH-LOGICAL-c5500-6cc8bfb0ea6d5618a94eab142ea068fdf93d71324b9599488cc74d03d064f9e63
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creator Chen, Kang
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description The molecules and environment that direct pluripotent stem cell differentiation into cardiomyocytes are largely unknown. Here, we determined a critical role of receptor tyrosine kinase, EphB4, in regulating cardiomyocyte generation from embryonic stem (ES) cells through endothelial cells. The number of spontaneous contracting cardiomyocytes, and the expression of cardiac‐specific genes, including α‐MHC and MLC‐2V, was significantly decreased in EphB4‐null ES cells. EphB4 was expressed in endothelial cells underneath contracting cardiomyocytes, but not in cardiomyocytes. Angiogenic inhibitors, including endostatin and angiostatin, inhibited endothelial cell differentiation and diminished cardiomyogenesis in ES cells. Generation of functional cardiomyocytes and the expression of cardiac‐specific genes were significantly enhanced by co‐culture of ES cells with human endothelial cells. Furthermore, the defects of cardiomyocyte differentiation in EphB4‐deficient ES cells were rescued by human endothelial cells. For the first time, our study demonstrated that endothelial cells play an essential role in facilitating cardiomyocyte differentiation from pluripotent stem cells. EphB4 signaling is a critical component of the endothelial niche to regulate regeneration of cardiomyocytes. J. Cell. Biochem. 111: 29–39, 2010. © 2010 Wiley‐Liss, Inc.
doi_str_mv 10.1002/jcb.22680
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Here, we determined a critical role of receptor tyrosine kinase, EphB4, in regulating cardiomyocyte generation from embryonic stem (ES) cells through endothelial cells. The number of spontaneous contracting cardiomyocytes, and the expression of cardiac‐specific genes, including α‐MHC and MLC‐2V, was significantly decreased in EphB4‐null ES cells. EphB4 was expressed in endothelial cells underneath contracting cardiomyocytes, but not in cardiomyocytes. Angiogenic inhibitors, including endostatin and angiostatin, inhibited endothelial cell differentiation and diminished cardiomyogenesis in ES cells. Generation of functional cardiomyocytes and the expression of cardiac‐specific genes were significantly enhanced by co‐culture of ES cells with human endothelial cells. Furthermore, the defects of cardiomyocyte differentiation in EphB4‐deficient ES cells were rescued by human endothelial cells. 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Cell. Biochem</addtitle><description>The molecules and environment that direct pluripotent stem cell differentiation into cardiomyocytes are largely unknown. Here, we determined a critical role of receptor tyrosine kinase, EphB4, in regulating cardiomyocyte generation from embryonic stem (ES) cells through endothelial cells. The number of spontaneous contracting cardiomyocytes, and the expression of cardiac‐specific genes, including α‐MHC and MLC‐2V, was significantly decreased in EphB4‐null ES cells. EphB4 was expressed in endothelial cells underneath contracting cardiomyocytes, but not in cardiomyocytes. Angiogenic inhibitors, including endostatin and angiostatin, inhibited endothelial cell differentiation and diminished cardiomyogenesis in ES cells. Generation of functional cardiomyocytes and the expression of cardiac‐specific genes were significantly enhanced by co‐culture of ES cells with human endothelial cells. 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Biochem. 111: 29–39, 2010. © 2010 Wiley‐Liss, Inc.</description><subject>Angiogenesis</subject><subject>Angiogenesis Inhibitors - pharmacology</subject><subject>angiostatin</subject><subject>Animals</subject><subject>Biomarkers - metabolism</subject><subject>cardiomyocytes</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Line</subject><subject>Differentiation</subject><subject>Embryo cells</subject><subject>embryonic stem (ES) cells</subject><subject>Embryonic Stem Cells - cytology</subject><subject>Embryonic Stem Cells - drug effects</subject><subject>Embryonic Stem Cells - physiology</subject><subject>endostatin</subject><subject>Endothelial cells</subject><subject>Endothelial Cells - cytology</subject><subject>Endothelial Cells - drug effects</subject><subject>Endothelial Cells - physiology</subject><subject>EphB4</subject><subject>ephrin</subject><subject>Ephrin-B2 - genetics</subject><subject>Ephrin-B2 - metabolism</subject><subject>Humans</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Myocytes, Cardiac - cytology</subject><subject>Myocytes, Cardiac - physiology</subject><subject>Protein-tyrosine kinase receptors</subject><subject>Receptor, EphB4 - genetics</subject><subject>Receptor, EphB4 - metabolism</subject><subject>Signal Transduction</subject><subject>Stem cells</subject><issn>0730-2312</issn><issn>1097-4644</issn><issn>1097-4644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFkU9v1DAQxS1ERZfCgS-AckMc0o7_xI4vSLBqC1VVQCriaDn2pE1x4sXOFvLtSUm7ggPiNBrN7z3N0yPkBYVDCsCOblxzyJis4RFZUdCqFFKIx2QFikPJOGX75GnONwCgNWdPyD6DCiTVakUujgcfx2sMnQ2FwxBykfBqG-yIhbPJd7GfopvmzeMthrjpcRiLNsW-wL5JUxw6V-QR-0X8jOy1NmR8fj8PyJeT48v1-_L84-mH9dvz0lUVQCmdq5u2AbTSV5LWVgu0DRUMLci69a3mXlHORKMrrUVdO6eEB-5Bilaj5AfkzeK72TY9ejc_lWwwm9T1Nk0m2s78fRm6a3MVbw3THCjls8Gre4MUv28xj6bv8l0EO2DcZqNlTSWXlP2XVEIDKMWqmXy9kC7FnBO2u38omLuizFyU-V3UzL78M8COfGhmBo4W4EcXcPq3kzlbv3uwLBdFN_fxc6ew6ZuRiqvKfL04NSf15Zz-09p85r8A8ZutlQ</recordid><startdate>20100901</startdate><enddate>20100901</enddate><creator>Chen, Kang</creator><creator>Bai, Hao</creator><creator>Arzigian, Melanie</creator><creator>Gao, Yong-Xing</creator><creator>Bao, Jing</creator><creator>Wu, Wen-Shu</creator><creator>Shen, Wei-Feng</creator><creator>Wu, Liqun</creator><creator>Wang, Zack Z.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20100901</creationdate><title>Endothelial cells regulate cardiomyocyte development from embryonic stem cells</title><author>Chen, Kang ; 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subjects Angiogenesis
Angiogenesis Inhibitors - pharmacology
angiostatin
Animals
Biomarkers - metabolism
cardiomyocytes
Cell Differentiation - drug effects
Cell Differentiation - physiology
Cell Line
Differentiation
Embryo cells
embryonic stem (ES) cells
Embryonic Stem Cells - cytology
Embryonic Stem Cells - drug effects
Embryonic Stem Cells - physiology
endostatin
Endothelial cells
Endothelial Cells - cytology
Endothelial Cells - drug effects
Endothelial Cells - physiology
EphB4
ephrin
Ephrin-B2 - genetics
Ephrin-B2 - metabolism
Humans
Mice
Mice, Knockout
Myocytes, Cardiac - cytology
Myocytes, Cardiac - physiology
Protein-tyrosine kinase receptors
Receptor, EphB4 - genetics
Receptor, EphB4 - metabolism
Signal Transduction
Stem cells
title Endothelial cells regulate cardiomyocyte development from embryonic stem cells
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