دورية أكاديمية

Genome-Wide Transcriptome and Binding Sites Analyses Identify Early FOX Expressions for Enhancing Cardiomyogenesis Efficiency of hESC Cultures.

التفاصيل البيبلوغرافية
العنوان: Genome-Wide Transcriptome and Binding Sites Analyses Identify Early FOX Expressions for Enhancing Cardiomyogenesis Efficiency of hESC Cultures.
المؤلفون: Yeo HC; Bioprocessing Technology Institute, Agency for Science, Technology and Research (A*STAR), 20 Biopolis Way, #06-01, Singapore 138668, Singapore.; Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore 117585, Singapore., Ting S; Bioprocessing Technology Institute, Agency for Science, Technology and Research (A*STAR), 20 Biopolis Way, #06-01, Singapore 138668, Singapore., Brena RM; USC Epigenome Center, University of Southern California, Los Angeles, CA 90033, USA., Koh G; Bioprocessing Technology Institute, Agency for Science, Technology and Research (A*STAR), 20 Biopolis Way, #06-01, Singapore 138668, Singapore., Chen A; Bioprocessing Technology Institute, Agency for Science, Technology and Research (A*STAR), 20 Biopolis Way, #06-01, Singapore 138668, Singapore., Toh SQ; Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore 117585, Singapore., Lim YM; Bioprocessing Technology Institute, Agency for Science, Technology and Research (A*STAR), 20 Biopolis Way, #06-01, Singapore 138668, Singapore., Oh SK; Bioprocessing Technology Institute, Agency for Science, Technology and Research (A*STAR), 20 Biopolis Way, #06-01, Singapore 138668, Singapore., Lee DY; Bioprocessing Technology Institute, Agency for Science, Technology and Research (A*STAR), 20 Biopolis Way, #06-01, Singapore 138668, Singapore.; Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore 117585, Singapore.; NUS Synthetic Biology for Clinical and Technological Innovation (SynCTI), Life Sciences Institute, National University of Singapore, 28 Medical Drive, Singapore 117456, Singapore.
المصدر: Scientific reports [Sci Rep] 2016 Aug 09; Vol. 6, pp. 31068. Date of Electronic Publication: 2016 Aug 09.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE
أسماء مطبوعة: Original Publication: London : Nature Publishing Group, copyright 2011-
مواضيع طبية MeSH: Forkhead Transcription Factors/*genetics , Forkhead Transcription Factors/*metabolism , Human Embryonic Stem Cells/*cytology , Human Embryonic Stem Cells/*metabolism , Myocytes, Cardiac/*cytology , Myocytes, Cardiac/*metabolism, Animals ; Binding Sites ; Cell Culture Techniques/methods ; Cell Differentiation/genetics ; Cell Differentiation/physiology ; Cells, Cultured ; Collagen ; Drug Combinations ; Epigenesis, Genetic ; Feeder Cells/metabolism ; Gene Expression Profiling ; Genome-Wide Association Study ; Humans ; Laminin ; Mesoderm/cytology ; Mesoderm/metabolism ; Mice ; Models, Cardiovascular ; Proteoglycans ; Signal Transduction ; Wnt Proteins/metabolism
مستخلص: The differentiation efficiency of human embryonic stem cells (hESCs) into heart muscle cells (cardiomyocytes) is highly sensitive to culture conditions. To elucidate the regulatory mechanisms involved, we investigated hESCs grown on three distinct culture platforms: feeder-free Matrigel, mouse embryonic fibroblast feeders, and Matrigel replated on feeders. At the outset, we profiled and quantified their differentiation efficiency, transcriptome, transcription factor binding sites and DNA-methylation. Subsequent genome-wide analyses allowed us to reconstruct the relevant interactome, thereby forming the regulatory basis for implicating the contrasting differentiation efficiency of the culture conditions. We hypothesized that the parental expressions of FOXC1, FOXD1 and FOXQ1 transcription factors (TFs) are correlative with eventual cardiomyogenic outcome. Through WNT induction of the FOX TFs, we observed the co-activation of WNT3 and EOMES which are potent inducers of mesoderm differentiation. The result strengthened our hypothesis on the regulatory role of the FOX TFs in enhancing mesoderm differentiation capacity of hESCs. Importantly, the final proportions of cells expressing cardiac markers were directly correlated to the strength of FOX inductions within 72 hours after initiation of differentiation across different cell lines and protocols. Thus, we affirmed the relationship between early FOX TF expressions and cardiomyogenesis efficiency.
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المشرفين على المادة: 0 (Drug Combinations)
0 (Forkhead Transcription Factors)
0 (Laminin)
0 (Proteoglycans)
0 (Wnt Proteins)
119978-18-6 (matrigel)
9007-34-5 (Collagen)
تواريخ الأحداث: Date Created: 20160810 Date Completed: 20180430 Latest Revision: 20181113
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC4977469
DOI: 10.1038/srep31068
PMID: 27501774
قاعدة البيانات: MEDLINE
الوصف
تدمد:2045-2322
DOI:10.1038/srep31068