Key result
A review of cardiac looping and laterality highlights the crucial morphogenetic roles of the Nodal and Pitx2 signaling pathways, which are also linked to atrial fibrillation.
This review highlights the molecular mechanisms of cardiac laterality, particularly the roles of Nodal and Pitx2, and their implications for cardiac morphogenesis and atrial fibrillation.
Cardiac asymmetry requires precise embryonic regulation for proper topology; leaves open translation from animal models to human congenital defects.
The heart is the first organ to break symmetry in the developing embryo and onset of dextral looping is the first indication of this event. Looping is a complex process that progresses concomitantly to cardiac chamber differentiation and ultimately leads to the alignment of the cardiac regions in their final topology. Generation of cardiac asymmetry is crucial to ensuring proper form and consequent functionality of the heart, and therefore it is a highly regulated process. It has long been known that molecular left/right signals originate far before morphological asymmetry and therefore can direct it. The use of several animal models has led to the characterization of a complex regulatory network, which invariably converges on the Tgf-β signaling molecule Nodal and its downstream target, the homeobox transcription factor Pitx2. Here, we review current data on the cellular and molecular bases of cardiac looping and laterality, and discuss the contribution of Nodal and Pitx2 to these processes. A special emphasis will be given to the morphogenetic role of Pitx2 and to its modulation of transcriptional and functional properties, which have also linked laterality to atrial fibrillation.
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Campione et al. (2016) conducted a review in Cardiac laterality and looping. A review of cardiac looping and laterality highlights the crucial morphogenetic roles of the Nodal and Pitx2 signaling pathways, which are also linked to atrial fibrillation.
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