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Notch Signaling Plays a Key Role in Cardiac Cell Differentiation

Overview
Journal Mech Dev
Publisher Elsevier
Date 2006 Jul 18
PMID 16843648
Citations 20
Authors
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Abstract

Results from lineage tracing studies indicate that precursor cells in the ventricles give rise to both cardiac muscle and conduction cells. Cardiac conduction cells are specialized cells responsible for orchestrating the rhythmic contractions of the heart. Here, we show that Notch signaling plays an important role in the differentiation of cardiac muscle and conduction cell lineages in the ventricles. Notch1 expression coincides with a conduction marker, HNK-1, at early stages. Misexpression of constitutively active Notch1 (NIC) in early heart tubes in chick exhibited multiple effects on cardiac cell differentiation. Cells expressing NIC had a significant decrease in expression of cardiac muscle markers, but an increase in expression of conduction cell markers, HNK-1, and SNAP-25. However, the expression of the conduction marker connexin 40 was inhibited. Loss-of-function study, using a dominant-negative form of Suppressor-of-Hairless, further supports that Notch1 signaling is important for the differentiation of these cardiac cell types. Functional studies show that the expression of constitutively active Notch1 resulted in abnormalities in ventricular conduction pathway patterns.

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References
1.
Loomes K, Taichman D, Glover C, Williams P, Markowitz J, Piccoli D . Characterization of Notch receptor expression in the developing mammalian heart and liver. Am J Med Genet. 2002; 112(2):181-9. DOI: 10.1002/ajmg.10592. View

2.
Gessler M, Knobeloch K, Helisch A, Amann K, Schumacher N, Rohde E . Mouse gridlock: no aortic coarctation or deficiency, but fatal cardiac defects in Hey2 -/- mice. Curr Biol. 2002; 12(18):1601-4. DOI: 10.1016/s0960-9822(02)01150-8. View

3.
Donovan J, Kordylewska A, Jan Y, Utset M . Tetralogy of fallot and other congenital heart defects in Hey2 mutant mice. Curr Biol. 2002; 12(18):1605-10. DOI: 10.1016/s0960-9822(02)01149-1. View

4.
Sakata Y, Kamei C, Nakagami H, Bronson R, Liao J, Chin M . Ventricular septal defect and cardiomyopathy in mice lacking the transcription factor CHF1/Hey2. Proc Natl Acad Sci U S A. 2002; 99(25):16197-202. PMC: 138588. DOI: 10.1073/pnas.252648999. View

5.
Schroeder T, Fraser S, Ogawa M, Nishikawa S, Oka C, Bornkamm G . Recombination signal sequence-binding protein Jkappa alters mesodermal cell fate decisions by suppressing cardiomyogenesis. Proc Natl Acad Sci U S A. 2003; 100(7):4018-23. PMC: 153040. DOI: 10.1073/pnas.0438008100. View