Concept
cardiac reprogramming
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Children
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426.7K
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27.1K
Authors
3.4K
Institutions
Transcription Factor Oncogene Cardiogenesis
1990 - 1996
During 1990-1996, research converged on cardiac fate specification via transcription factor networks involving factors such as Csx and GATA-4 and their interplay with proto-oncogenes like c-myc to regulate cardiac gene programs. In vitro models using embryonic stem cells and embryoid bodies recapitulated cardiomyocyte differentiation and chamber-specific gene expression, providing a scalable platform for early reprogramming concepts. Extrinsic modulation through growth factors, peptide signals, and mechanical stretch revealed how nonmyocyte cues and mechanical environments drive hypertrophic and fetal-contractile gene responses; in vivo work demonstrated growth and morphogenesis control through oncogenic pathways and gene regulation.
• Pattern shows molecular networks governing cardiomyocyte fate across development and stem-cell differentiation, integrating transcription factors (Csx, GATA-4) with proto-oncogenes (c-myc) to regulate cardiac gene programs [2], [17], [7], [6].
• In vitro stem cell models recapitulate cardiac differentiation and chamber-specific gene programs, using ES cells/embryoid bodies to express cardiac myosin heavy chain, ventricular markers, and functional properties [5], [8], [10], [12], [11].
• Extrinsic modulation of cardiac growth by factors and mechanical cues: nonmyocyte-derived growth factors, peptide growth factors, and stretch drive hypertrophic and fetal-contractile gene responses [9], [4], [19].
• In vivo manipulation demonstrates growth and morphogenesis control via oncogenic pathways and gene regulation, showing SV40 T antigen proliferation, c-myc-driven development, and gene-trap–induced heart defects [13], [6], [7], [20].
Popular Keywords
BMP-Driven Cardiogenesis
1997 - 2003
Direct Cardiomyocyte Reprogramming
2004 - 2010
Cardiac Regenerative Reprogramming
2011 - 2017
Maturation-Integrated Cardiac Regeneration
2018 - 2024