Literature DB >> 10433836

Myocardialization of the cardiac outflow tract.

M J van den Hoff1, A F Moorman, J M Ruijter, W H Lamers, R W Bennington, R R Markwald, A Wessels.   

Abstract

During development, the single-circuited cardiac tube transforms into a double-circuited four-chambered heart by a complex process of remodeling, differential growth, and septation. In this process the endocardial cushion tissues of the atrioventricular junction and outflow tract (OFT) play a crucial role as they contribute to the mesenchymal components of the developing septa and valves in the developing heart. After fusion, the endocardial ridges in the proximal portion of the OFT initially form a mesenchymal outlet septum. In the adult heart, however, this outlet septum is basically a muscular structure. Hence, the mesenchyme of the proximal outlet septum has to be replaced by cardiomyocytes. We have dubbed this process "myocardialization." Our immunohistochemical analysis of staged chicken hearts demonstrates that myocardialization takes place by ingrowth of existing myocardium into the mesenchymal outlet septum. Compared to other events in cardiac septation, it is a relatively late process, being initialized around stage H/H28 and being basically completed around stage H/H38. To unravel the molecular mechanisms that are responsible for the induction and regulation of myocardialization, an in vitro culture system in which myocardialization could be mimicked and manipulated was developed. Using this in vitro myocardialization assay it was observed that under the standard culture conditions (i) whole OFT explants from stage H/H20 and younger did not spontaneously myocardialize the collagen matrix, (ii) explants from stage H/H21 and older spontaneously formed extensive myocardial networks, (iii) the myocardium of the OFT could be induced to myocardialize and was therefore "myocardialization-competent" at all stages tested (H/H16-30), (iv) myocardialization was induced by factors produced by, most likely, the nonmyocardial component of the outflow tract, (v) at none of the embryonic stages analyzed was ventricular myocardium myocardialization-competent, and finally, (vi) ventricular myocardium did not produce factors capable of supporting myocardialization. Copyright 1999 Academic Press.

Entities:  

Keywords:  NASA Discipline Cardiopulmonary; Non-NASA Center

Mesh:

Substances:

Year:  1999        PMID: 10433836     DOI: 10.1006/dbio.1999.9366

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  46 in total

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Authors:  T D Camenisch; A P Spicer; T Brehm-Gibson; J Biesterfeldt; M L Augustine; A Calabro; S Kubalak; S E Klewer; J A McDonald
Journal:  J Clin Invest       Date:  2000-08       Impact factor: 14.808

Review 2.  Development and structure of the atrial septum.

Authors:  Robert H Anderson; Nigel A Brown; Sandra Webb
Journal:  Heart       Date:  2002-07       Impact factor: 5.994

Review 3.  Septation and separation within the outflow tract of the developing heart.

Authors:  Sandra Webb; Sonia R Qayyum; Robert H Anderson; Wouter H Lamers; Michael K Richardson
Journal:  J Anat       Date:  2003-04       Impact factor: 2.610

Review 4.  Form and function of developing heart valves: coordination by extracellular matrix and growth factor signaling.

Authors:  Joyce A Schroeder; Leslie F Jackson; David C Lee; Todd D Camenisch
Journal:  J Mol Med (Berl)       Date:  2003-06-25       Impact factor: 4.599

Review 5.  Combinatorial transcriptional interaction within the cardiac neural crest: a pair of HANDs in heart formation.

Authors:  Anthony B Firulli; Simon J Conway
Journal:  Birth Defects Res C Embryo Today       Date:  2004-06

Review 6.  Cardiogenesis: an embryological perspective.

Authors:  Ramón Muñoz-Chápuli; José M Pérez-Pomares
Journal:  J Cardiovasc Transl Res       Date:  2009-11-04       Impact factor: 4.132

Review 7.  The neural crest in cardiac congenital anomalies.

Authors:  Anna Keyte; Mary Redmond Hutson
Journal:  Differentiation       Date:  2012-05-15       Impact factor: 3.880

8.  FOG-2 attenuates endothelial-to-mesenchymal transformation in the endocardial cushions of the developing heart.

Authors:  Alleda E Flagg; Judy U Earley; Eric C Svensson
Journal:  Dev Biol       Date:  2006-12-21       Impact factor: 3.582

9.  Versican proteolysis mediates myocardial regression during outflow tract development.

Authors:  Christine B Kern; Russell A Norris; Robert P Thompson; W Scott Argraves; Sarah E Fairey; Leticia Reyes; Stanley Hoffman; Roger R Markwald; Corey H Mjaatvedt
Journal:  Dev Dyn       Date:  2007-03       Impact factor: 3.780

Review 10.  The role of vertebrate nonmuscle Myosin II in development and human disease.

Authors:  Xuefei Ma; Robert S Adelstein
Journal:  Bioarchitecture       Date:  2014-08-06
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