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Published on: September 23, 2014
Multiple transcriptional domains, with distinct left and right components, in the atrial chambers of the developing
D Franco1, M Campione, R Kelly
1Experimental and Molecular Cardiology Group, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands. dfranco@ujaen.es
Insights
This study identifies distinct molecular regions within the developing mouse heart's atrial myocardium. These findings help understand congenital heart defects and the inflow tract's contribution to atrial chambers.
Area of Science:
- Developmental Biology
- Cardiovascular Research
- Molecular Cardiology
Background:
- The contribution of the inflow tract to the developing atrial chambers is poorly understood due to a lack of specific molecular markers.
- Understanding myocardial regionalization is crucial for studying congenital heart malformations.
Purpose of the Study:
- To identify molecular markers for distinct myocardial domains within the developing mouse atrial chambers.
- To elucidate the regional contribution of the inflow tract to the definitive atria.
Main Methods:
- Analysis of gene expression patterns for atrial natriuretic factor, myosin light chain (MLC) 3F, MLC2V, and Pitx-2.
- Utilized transgenic mouse lines with nlacZ reporter under MLC1F/3F gene regulatory control.
Main Results:
- Identified four transcriptional domains in the atrial myocardium: atrioventricular canal, atrial appendages, caval vein myocardium (systemic inlet), and mediastinal myocardium (pulmonary inlet).
- Demonstrated distinct left and right components within these domains, particularly revealed by Pitx-2 expression.
- Showcased differential gene expression in systemic and pulmonary inlets, distinct from atrial appendages.
Conclusions:
- The atrial myocardium comprises multiple, molecularly distinct compartments, including the systemic and pulmonary venous inlets.
- This molecular compartmentalization provides a basis for studying congenital heart anomalies, especially those involving abnormal venous return.
Abstract:
During heart development, 2 fast-conducting regions of working myocardium balloon out from the slow-conducting primary myocardium of the tubular heart. Three regions of primary myocardium persist: the outflow tract, atrioventricular canal, and inflow tract, which are contiguous throughout the inner curvature of the heart. The contribution of the inflow tract to the definitive atrial chambers has remained enigmatic largely because of the lack of molecular markers that permit unambiguous identification of this myocardial domain. We now report that the genes encoding atrial natriuretic factor, myosin light chain (MLC) 3F, MLC2V, and Pitx-2, and transgenic mouse lines expressing nlacZ under the control of regulatory sequences of the mouse MLC1F/3F gene, display regionalized patterns of expression in the atrial component of the developing mouse heart. These data distinguish 4 broad transcriptional domains in the atrial myocardium: (1) the atrioventricular canal that will form the smooth-walled lower atrial rim proximal to the ventricles; (2) the atrial appendages; (3) the caval vein myocardium (systemic inlet); and (4) the mediastinal myocardium (pulmonary inlet), including the atrial septa. The pattern of expression of Pitx-2 reveals that each of these transcriptional domains has a distinct left and right component. This study reveals for the first time differential gene expression in the systemic and pulmonary inlets, which is not shared by the contiguous atrial appendages and provides evidence for multiple molecular compartments within the atrial chambers. Furthermore, this work will allow the contribution of each of these myocardial components to be studied in congenitally malformed hearts, such as those with abnormal venous return.
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