The bHLH transcription factor Tcf21 is required for lineage-specific EMT of cardiac fibroblast progenitors
Open accessAbstract
The basic helix-loop-helix (bHLH) family of transcription factors orchestrates cell-fate specification, commitment and differentiation in multiple cell lineages during development. Here, we describe the role of a bHLH transcription factor, Tcf21 (epicardin/Pod1/capsulin), in specification of the cardiac fibroblast lineage. In the developing heart, the epicardium constitutes the primary source of progenitor cells that form two cell lineages: coronary vascular smooth muscle cells (cVSMCs) and cardiac fibroblasts. Currently, there is a debate regarding whether the specification of these lineages occurs early in the formation of the epicardium or later after the cells have entered the myocardium. Lineage tracing using a tamoxifen-inducible Cre expressed from the Tcf21 locus demonstrated that the majority of Tcf21-expressing epicardial cells are committed to the cardiac fibroblast lineage prior to initiation of epicardial epithelial-to-mesenchymal transition (EMT). Furthermore, Tcf21 null hearts fail to form cardiac fibroblasts, and lineage tracing of the null cells showed their inability to undergo EMT. This is the first report of a transcription factor essential for the development of cardiac fibroblasts. We demonstrate a unique role for Tcf21 in multipotent epicardial progenitors, prior to the process of EMT that is essential for cardiac fibroblast development.
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In mice lacking Tcf21, chamber EpiMT is impaired.
“Of note, in mice lacking Tcf21, chamber EpiMT is impaired61.”
From Cell diversity and plasticity during atrioventricular heart valve EMTs (2023) · cites this paper as [61]
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- Authors
- Acharya, A., Baek, S. T., Huang, G., Eskiocak, B., Goetsch, S., Sung, C. Y., Banfi, S., Sauer, M. F., Olsen, G. S., Duffield, J. S., Olson, E. N., & Tallquist, M. D.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- University of Washington (US)
- Corresponding author
- Tallquist, Michelle D.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2012-06-15
- Volume
- 139
- Issue
- 12
- Pages
- 2139-2149
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- PMC
- PMC3357908
- OpenAlex
- W2077226203
- Cited by
- 498
- References
- 51
- Citations by year
- 2026: 36 · 2025: 26 · 2024: 42 · 2023: 39 · 2022: 42 · 2021: 41 · 2020: 43 · 2019: 33 · 2018: 34 · 2017: 41 · 2016: 38 · 2015: 34 · 2014: 20 · 2013: 26 · 2012: 3
- FWCI
- 10.66
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Development (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Open Access System for Information Sharing (Pohang University of Science and Technology) (submittedVersion)
- Funders
- National Institutes of Health (5u01hl100401-07)
- National Heart, Lung, and Blood Institute (T32HL007360, R01HL077439, HL100401, U01-HL-100401, HL074257, R01HL093039, K99HL114738, R01HL074257, R01HL77439-05)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK084077)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Fibrosis and Remodeling
- Keywords
- TCF21, bHLH transcription factors, epicardium, epithelial-mesenchymal transition, lineage specification, heart development, lineage tracing
- MeSH terms
- Animals, Coronary Vessels, Embryo, Mammalian, Fibroblasts, Models, Biological, Muscle, Smooth, Vascular, Myocardium, Phenotype, Stem Cells, Time Factors, Cell Lineage, Integrases, Myocytes, Cardiac, Myocytes, Smooth Muscle, Mice, Basic Helix-Loop-Helix Proteins, Epithelial-Mesenchymal Transition
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