» Articles » PMID: 20657579

Wnt11 Patterns a Myocardial Electrical Gradient Through Regulation of the L-type Ca(2+) Channel

Overview
Journal Nature
Specialty Science
Date 2010 Jul 27
PMID 20657579
Citations 83
Authors
Affiliations
Soon will be listed here.
Abstract

Electrical gradients are critical for many biological processes, including the normal function of excitable tissues, left-right patterning, organogenesis and wound healing. The fundamental mechanisms that regulate the establishment and maintenance of such electrical polarities are poorly understood. Here we identify a gradient of electrical coupling across the developing ventricular myocardium using high-speed optical mapping of transmembrane potentials and calcium concentrations in the zebrafish heart. We excluded a role for differences in cellular excitability, connexin localization, tissue geometry and mechanical inputs, but in contrast we were able to demonstrate that non-canonical Wnt11 signals are required for the genesis of this myocardial electrical gradient. Although the traditional planar cell polarity pathway is not involved, we obtained evidence that Wnt11 acts to set up this gradient of electrical coupling through effects on transmembrane Ca(2+) conductance mediated by the L-type calcium channel. These data reveal a previously unrecognized role for Wnt/Ca(2+) signalling in establishing an electrical gradient in the plane of the developing cardiac epithelium through modulation of ion-channel function. The regulation of cellular coupling through such mechanisms may be a general property of non-canonical Wnt signals.

Citing Articles

Regionalized regulation of actomyosin organization influences cardiomyocyte cell shape changes during chamber curvature formation.

Leerberg D, Avillion G, Priya R, Stainier D, Yelon D bioRxiv. 2025; .

PMID: 39829878 PMC: 11741281. DOI: 10.1101/2025.01.07.631779.


Zebrafish Models for Skeletal and Extraskeletal Osteogenesis Imperfecta Features: Unveiling Pathophysiology and Paving the Way for Drug Discovery.

Masiero C, Aresi C, Forlino A, Tonelli F Calcif Tissue Int. 2024; 115(6):931-959.

PMID: 39320469 PMC: 11607041. DOI: 10.1007/s00223-024-01282-5.


Outlining cardiac ion channel protein interactors and their signature in the human electrocardiogram.

Maurya S, Mills R, Kahnert K, Chiang D, Bertoli G, Lundegaard P Nat Cardiovasc Res. 2024; 2(7):673-692.

PMID: 38666184 PMC: 11041666. DOI: 10.1038/s44161-023-00294-y.


Differentiation of Pluripotent Stem Cells for Disease Modeling: Learning from Heart Development.

Chi C, Roland T, Song K Pharmaceuticals (Basel). 2024; 17(3).

PMID: 38543122 PMC: 10975450. DOI: 10.3390/ph17030337.


The Role of and Microtubules in Maintaining Normal Ventricular Conduction.

Chiang D, Verkerk A, Victorio R, Shneyer B, van der Vaart B, Jouni M Circ Res. 2023; 134(1):46-59.

PMID: 38095085 PMC: 11889334. DOI: 10.1161/CIRCRESAHA.123.323231.


References
1.
Eisenberg C, Eisenberg L . WNT11 promotes cardiac tissue formation of early mesoderm. Dev Dyn. 1999; 216(1):45-58. DOI: 10.1002/(SICI)1097-0177(199909)216:1<45::AID-DVDY7>3.0.CO;2-L. View

2.
Flaherty M, Dawn B . Noncanonical Wnt11 signaling and cardiomyogenic differentiation. Trends Cardiovasc Med. 2009; 18(7):260-8. PMC: 2673908. DOI: 10.1016/j.tcm.2008.12.001. View

3.
Costantini D, Arruda E, Agarwal P, Kim K, Zhu Y, Zhu W . The homeodomain transcription factor Irx5 establishes the mouse cardiac ventricular repolarization gradient. Cell. 2005; 123(2):347-58. PMC: 1480411. DOI: 10.1016/j.cell.2005.08.004. View

4.
Cohen E, Tian Y, Morrisey E . Wnt signaling: an essential regulator of cardiovascular differentiation, morphogenesis and progenitor self-renewal. Development. 2008; 135(5):789-98. DOI: 10.1242/dev.016865. View

5.
Robu M, Larson J, Nasevicius A, Beiraghi S, Brenner C, Farber S . p53 activation by knockdown technologies. PLoS Genet. 2007; 3(5):e78. PMC: 1877875. DOI: 10.1371/journal.pgen.0030078. View