Abstract
Embryonic Stem Cells not only hold a lot of potential for use in regenerative medicine, but also provide an elegant and efficient way to study specific developmental processes and pathways in mammals when whole animal gene knock out experiments fail. We have investigated a pathway through which HDAC1 affects cardiovascular and more specifically cardiomyocyte differentiation in ES cells by controlling expression of SOX17 and BMP2 during early differentiation. This data explains current discrepancies in the role of HDAC1 in cardiovascular differentiation and sheds light into a new pathway through which ES cells determine cardiovascular cell fate.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Bone Morphogenetic Protein 2 / genetics*
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Bone Morphogenetic Protein 2 / metabolism
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Cell Differentiation / genetics*
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Cell Line
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Embryoid Bodies / cytology
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Embryoid Bodies / metabolism
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Embryonic Stem Cells / cytology
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Embryonic Stem Cells / metabolism
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Fluorescent Antibody Technique
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Gene Expression
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Gene Knockdown Techniques
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HMGB Proteins / genetics*
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HMGB Proteins / metabolism
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Histone Deacetylase 1 / genetics*
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Histone Deacetylase 1 / metabolism
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Mice
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Mice, Inbred C57BL
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Models, Genetic
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Myocytes, Cardiac / cytology
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Myocytes, Cardiac / metabolism*
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Reverse Transcriptase Polymerase Chain Reaction
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SOXF Transcription Factors / genetics*
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SOXF Transcription Factors / metabolism
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Signal Transduction / genetics
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Time Factors
Substances
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Bmp2 protein, mouse
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Bone Morphogenetic Protein 2
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HMGB Proteins
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SOXF Transcription Factors
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Sox17 protein, mouse
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Hdac1 protein, mouse
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Histone Deacetylase 1