Neuregulin-1 promotes cardiomyocyte differentiation of genetically engineered embryonic stem cell clones
Embryonic stem (ES) cell-derived cardiomyocytes (ESCMs) must be specifically purified in order to prevent teratoma formation, and this confusing issue has hampered their clinical application. We therefore investigated a technique to generate pure labeled ESCMs for possible use in cardiac repair. We...
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Published in | BMB reports Vol. 41; no. 10; pp. 699 - 704 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | Korean |
Published |
생화학분자생물학회
31.10.2008
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Subjects | |
Online Access | Get full text |
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Summary: | Embryonic stem (ES) cell-derived cardiomyocytes (ESCMs) must be specifically purified in order to prevent teratoma formation, and this confusing issue has hampered their clinical application. We therefore investigated a technique to generate pure labeled ESCMs for possible use in cardiac repair. We generated transgenic ES cell lines expressing enhanced green fluorescent protein (EGFP) under the transcriptional control of the $\alpha$-cardiac myosin heavy chain ($\alpha$-MHC) promoter. Differentiated EGFP-positive ES cells displayed characteristics of CMs. Furthermore, neuregulin-1 (NRG-1) upregulated the expression of the cardiac-restricted transcription factors Nkx2.5 and GATA-4, as well as differentiated CM factors ($\alpha$-MHC, $\beta$-MHC). Immunohistochemistry demonstrated that NRG-1 increased expression of cardiac-specific troponin T in the beating foci of the embryoid bodies. This work revealed a potential method for specifically labeling and enriching ESCMs by combining genetically-engineered ES cell clones and exogenous growth factor treatment. |
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Bibliography: | Korean Society for Biochemistry and Molecular Biology KISTI1.1003/JNL.JAKO200810103442671 |
ISSN: | 1976-6696 1976-670X |