Distinct mechanisms regulate ventricular and atrial chamber wall formation

Tissues undergo distinct morphogenetic processes to achieve similarly shaped structures. In the heart, cardiomyocytes in both the ventricle and atrium build internal structures for efficient contraction. Ventricular wall formation (trabeculation) is initiated by cardiomyocyte delamination. How cardiomyocytes build the atrial wall is poorly understood. Using longitudinal imaging in zebrafish, we found that at least 25% of the atrial cardiomyocytes elongate along the long axis of the heart. These cell shape changes result in cell intercalation and convergent thickening, leading to the formation of the internal muscle network. We tested factors important for ventricular trabeculation including Nrg/ErbB and Notch signaling and found no evidence for their role in atrial muscle network formation. Instead, our data suggest that atrial cardiomyocyte elongation is regulated by Yap, which has not been implicated in trabeculation. Altogether, these data indicate that distinct cellular and molecular mechanisms build the internal muscle structures in the atrium and ventricle.

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Publication Details

Journal
Nature Communications
Published
2024-09-17
DOI
https://doi.org/10.1038/s41467-024-52340-3
Citations
6
Primary Topic
Congenital heart defects research
Type
article
Field-Weighted Citation Impact
1.40

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article

Distinct mechanisms regulate ventricular and atrial chamber wall formation

Khrievono Kikhi, Sarah P Howard, Rashmi Priya, Felix Gunawan et al.
6 citations
Nature Communications
Congenital heart defects research
1.40
article

Distinct mechanisms regulate ventricular and atrial chamber wall formation

Khrievono Kikhi, Sarah P Howard, Rashmi Priya, Felix Gunawan, Carsten Kuenne, Didier Y. R. Stainier, Marga Albu, Alessandra Gentile, Yanli Xu, Eileen Affolter
article en
6 citations

Abstract

Tissues undergo distinct morphogenetic processes to achieve similarly shaped structures. In the heart, cardiomyocytes in both the ventricle and atrium build internal structures for efficient contraction. Ventricular wall formation (trabeculation) is initiated by cardiomyocyte delamination. How cardiomyocytes build the atrial wall is poorly understood. Using longitudinal imaging in zebrafish, we found that at least 25% of the atrial cardiomyocytes elongate along the long axis of the heart. These cell shape changes result in cell intercalation and convergent thickening, leading to the formation of the internal muscle network. We tested factors important for ventricular trabeculation including Nrg/ErbB and Notch signaling and found no evidence for their role in atrial muscle network formation. Instead, our data suggest that atrial cardiomyocyte elongation is regulated by Yap, which has not been implicated in trabeculation. Altogether, these data indicate that distinct cellular and molecular mechanisms build the internal muscle structures in the atrium and ventricle.

Nature CommunicationsVol. 15(1)
King's College London (GB), University of Münster (DE), The Francis Crick Institute (GB), Max Planck Institute for Heart and Lung Research (DE), German Centre for Cardiovascular Research (DE), Cardio-Pulmonary Institute (DE)
Max-Planck-Gesellschaft
Openalex Percentile: Top 19%
Congenital heart defects research
1.40
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