|ZFIN ID: ZDB-PUB-120105-83|
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Sodium pump activity in the yolk syncytial layer regulates zebrafish heart tube morphogenesis
Langenbacher, A.D., Huang, J., Chen, Y., and Chen, J.N.
|Source:||Developmental Biology 362(2): 263-270 (Journal)|
|Registered Authors:||Chen, Jau-Nian, Chen, Yi, Huang, Jie, Langenbacher, Adam|
|Keywords:||zebrafish, heart development, Na+, K+ ATPase, yolk syncytial layer, fibronectin, extracellular matrix|
|PubMed:||22182522 Full text @ Dev. Biol.|
Langenbacher, A.D., Huang, J., Chen, Y., and Chen, J.N. (2012) Sodium pump activity in the yolk syncytial layer regulates zebrafish heart tube morphogenesis. Developmental Biology. 362(2):263-270.
ABSTRACTNa+,K+ ATPase pumps Na+ out of and K+ into the cytosol, maintaining a resting potential that is essential for the function of excitable tissues like cardiac muscle. In addition to its well-characterized physiological role in the heart, Na+,K+ ATPase also regulates the morphogenesis of the embryonic zebrafish heart via an as yet unknown mechanism. Here, we describe a novel non-cell autonomous function of Na+,K+ ATPase/Atp1a1 in the elongation of the zebrafish heart tube. Embryos lacking Atp1a1 function exhibit abnormal migration behavior of cardiac precursors, defects in the elongation of the heart tube, and a severe reduction in ECM/Fibronectin deposition around the myocardium, despite the presence of normal cell polarity and junctions in the myocardial epithelium prior to the timeframe of heart tube elongation. Interestingly, we found that Atp1a1 is not present in the myocardium at the time when cardiac morphogenesis defects first become apparent, but is expressed in an extra-embryonic tissue, the yolk syncytial layer (YSL), at earlier stages. Knockdown of Atp1a1 activity specifically in the YSL using morpholino oligonucleotides produced heart tube elongation defects like those found in atp1a1 mutants, indicating that Atp1a1 function in the YSL is necessary for heart tube elongation. Furthermore, atp1a1 expression in the YSL was regulated by the homeobox transcription factor mxtx1. Together, these data reveal a new non-cell autonomous role for Atp1a1 in cardiac morphogenesis and establish Na+,K+ ATPase as a major player in the genetic pathway by which the YSL regulates embryonic ECM deposition.