Molecular regulation of atrioventricular valvuloseptal morphogenesis - PubMed (original) (raw)
Review
Molecular regulation of atrioventricular valvuloseptal morphogenesis
L M Eisenberg et al. Circ Res. 1995 Jul.
Abstract
The majority of congenital heart defects arise from abnormal development of valvuloseptal tissue. The primordia of the valve leaflets and membranous septa of the heart are the cardiac cushions. Remodeling of the cushions is associated with a transitional extracellular matrix that includes sulfated proteoglycans and the microfibrillar proteins fibulin and fibrillin. Cushion formation is restricted to the AV canal and ventricular outflow tract regions of the primary heart tube. The proper placement of the cushions may be the result of the development of the primary heart tube as a segmented organ, as well as the subsequent looping of the heart. Segmentation of the heart tube may be demonstrated by the alternating molecular expression pattern along the longitudinal axis. In support of this hypothesis is the restricted expression of BMP-4 and msx-2 to the AV canal and ventricular outflow tract. The importance of looping for cushion positioning may imply that the iv and inv genes and retinoic acid are important for the proper patterning of the heart. The cells of the cushions evolve from endocardial cells that undergo an epithelial-to-mesenchymal transformation. This developmental event is regulated by the myocardium and is probably due to the production of protein complexes, present within the cardiac jelly of the cushion-forming regions, that consist of fibronectin and the ES proteins. Both the cushion mesenchyme and its endocardial cell antecedents express JB3, an ECM protein. JB3 expression is also featured within the heart-forming fields of the primary mesoderm, from which the endocardial progenitors of the cushion cells originate.(ABSTRACT TRUNCATED AT 250 WORDS)
Similar articles
- Fibulin-1, vitronectin, and fibronectin expression during avian cardiac valve and septa development.
Bouchey D, Argraves WS, Little CD. Bouchey D, et al. Anat Rec. 1996 Apr;244(4):540-51. doi: 10.1002/(SICI)1097-0185(199604)244:4<540::AID-AR12>3.0.CO;2-P. Anat Rec. 1996. PMID: 8694289 - Cell biology of cardiac cushion development.
Person AD, Klewer SE, Runyan RB. Person AD, et al. Int Rev Cytol. 2005;243:287-335. doi: 10.1016/S0074-7696(05)43005-3. Int Rev Cytol. 2005. PMID: 15797462 Review. - Expression of bone morphogenetic protein-5 gene during chick heart development: possible roles in valvuloseptal endocardial cushion formation.
Yamagishi T, Nakajima Y, Nishimatsu S, Nohno T, Ando K, Nakamura H. Yamagishi T, et al. Anat Rec. 2001 Dec 1;264(4):313-6. doi: 10.1002/ar.10013. Anat Rec. 2001. PMID: 11745086 - The Role of Cell Autonomous Signaling by BMP in Endocardial Cushion Cells in AV Valvuloseptal Morphogenesis.
Sugi Y, Zhou B, Inai K, Mishina Y, Burnside JL. Sugi Y, et al. 2016 Jun 25. In: Nakanishi T, Markwald RR, Baldwin HS, Keller BB, Srivastava D, Yamagishi H, editors. Etiology and Morphogenesis of Congenital Heart Disease: From Gene Function and Cellular Interaction to Morphology [Internet]. Tokyo: Springer; 2016. Chapter 22. 2016 Jun 25. In: Nakanishi T, Markwald RR, Baldwin HS, Keller BB, Srivastava D, Yamagishi H, editors. Etiology and Morphogenesis of Congenital Heart Disease: From Gene Function and Cellular Interaction to Morphology [Internet]. Tokyo: Springer; 2016. Chapter 22. PMID: 29787124 Free Books & Documents. Review.
Cited by
- Endocardial to myocardial notch-wnt-bmp axis regulates early heart valve development.
Wang Y, Wu B, Chamberlain AA, Lui W, Koirala P, Susztak K, Klein D, Taylor V, Zhou B. Wang Y, et al. PLoS One. 2013;8(4):e60244. doi: 10.1371/journal.pone.0060244. Epub 2013 Apr 1. PLoS One. 2013. PMID: 23560082 Free PMC article. - Neural crest-derived SEMA3C activates endothelial NRP1 for cardiac outflow tract septation.
Plein A, Calmont A, Fantin A, Denti L, Anderson NA, Scambler PJ, Ruhrberg C. Plein A, et al. J Clin Invest. 2015 Jul 1;125(7):2661-76. doi: 10.1172/JCI79668. Epub 2015 Jun 8. J Clin Invest. 2015. PMID: 26053665 Free PMC article. - The matricellular protein CCN1 is essential for cardiac development.
Mo FE, Lau LF. Mo FE, et al. Circ Res. 2006 Oct 27;99(9):961-9. doi: 10.1161/01.RES.0000248426.35019.89. Epub 2006 Oct 5. Circ Res. 2006. PMID: 17023674 Free PMC article. - Heart valve development: endothelial cell signaling and differentiation.
Armstrong EJ, Bischoff J. Armstrong EJ, et al. Circ Res. 2004 Sep 3;95(5):459-70. doi: 10.1161/01.RES.0000141146.95728.da. Circ Res. 2004. PMID: 15345668 Free PMC article. Review. - Oxidative Stress in Calcific Aortic Valve Stenosis: Protective Role of Natural Antioxidants.
Adhikari R, Shiwakoti S, Ko JY, Dhakal B, Park SH, Choi IJ, Kim HJ, Oak MH. Adhikari R, et al. Antioxidants (Basel). 2022 Jun 14;11(6):1169. doi: 10.3390/antiox11061169. Antioxidants (Basel). 2022. PMID: 35740065 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources