N-cadherin relocalization during cardiac trabeculation
- Cherian, A.V., Fukuda, R., Augustine, S.M., Maischein, H.M., Stainier, D.Y.
- Proceedings of the National Academy of Sciences of the United States of America 113(27): 7569-74 (Journal)
- Registered Authors
- Maischein, Hans-Martin, Stainier, Didier
- Cdh2-EGFP, Erbb2 signaling, N-cadherin, heart development, trabeculation
- MeSH Terms
- Animals, Genetically Modified
- Coronary Circulation
- Green Fluorescent Proteins
- Myocardial Contraction
- Myocytes, Cardiac/metabolism*
- Receptor, ErbB-2/metabolism
- Zebrafish Proteins/metabolism*
- 27339140 Full text @ Proc. Natl. Acad. Sci. USA
Cherian, A.V., Fukuda, R., Augustine, S.M., Maischein, H.M., Stainier, D.Y. (2016) N-cadherin relocalization during cardiac trabeculation. Proceedings of the National Academy of Sciences of the United States of America. 113(27):7569-74.
During cardiac trabeculation, cardiomyocytes delaminate from the outermost (compact) layer to form complex muscular structures known as trabeculae. As these cardiomyocytes delaminate, the remodeling of adhesion junctions must be tightly coordinated so cells can extrude from the compact layer while remaining in tight contact with their neighbors. In this study, we examined the distribution of N-cadherin (Cdh2) during cardiac trabeculation in zebrafish. By analyzing the localization of a Cdh2-EGFP fusion protein expressed under the control of the zebrafish cdh2 promoter, we initially observed Cdh2-EGFP expression along the lateral sides of embryonic cardiomyocytes, in an evenly distributed pattern, and with the occasional appearance of punctae. Within a few hours, Cdh2-EGFP distribution on the lateral sides of cardiomyocytes evolves into a clear punctate pattern as Cdh2-EGFP molecules outside the punctae cluster to increase the size of these aggregates. In addition, Cdh2-EGFP molecules also appear on the basal side of cardiomyocytes that remain in the compact layer. Delaminating cardiomyocytes accumulate Cdh2-EGFP on the surface facing the basal side of compact layer cardiomyocytes, thereby allowing tight adhesion between these layers. Importantly, we find that blood flow/cardiac contractility is required for the transition from an even distribution of Cdh2-EGFP to the formation of punctae. Furthermore, using time-lapse imaging of beating hearts in conjunction with a Cdh2 tandem fluorescent protein timer transgenic line, we observed that Cdh2-EGFP molecules appear to move from the lateral to the basal side of cardiomyocytes along the cell membrane, and that Erb-b2 receptor tyrosine kinase 2 (Erbb2) function is required for this relocalization.
Genes / Markers
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Engineered Foreign Genes