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  4. Endocardial cushion morphogenesis and coronary vessel development require chicken ovalbumin upstream promoter-transcription factor II
 
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Endocardial cushion morphogenesis and coronary vessel development require chicken ovalbumin upstream promoter-transcription factor II

Journal
Arteriosclerosis, Thrombosis, and Vascular Biology
Journal Volume
32
Journal Issue
11
ISSN
1524-4636
Date Issued
2012-09-06
Author(s)
FU-JUNG LIN  
You L.-R.
Yu C.-T.
Hsu W.-H.
Ming-Jer Tsai
Sophia Y. Tsai
DOI
10.1161/ATVBAHA.112.300255
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/461265
https://www.scopus.com/pages/publications/84871862705?origin=resultslist
URL
https://www2.scopus.com/inward/record.uri?eid=2-s2.0-84871862705&doi=10.1161%2fATVBAHA.112.300255&partnerID=40&md5=e672bf6145f45dc7795338f23120ac3e
Abstract
OBJECTIVE: Septal defects and coronary vessel anomalies are common congenital heart defects, yet their ontogeny and the underlying genetic mechanisms are not well understood. Here, we investigated the role of chicken ovalbumin upstream promoter-transcription factor II (COUP-TFII, NR2F2) in cardiac organogenesis. METHODS AND RESULTS: We analyzed embryos deficient in COUP-TFII and observed a spectrum of cardiac defects, including atrioventricular septal defect, thin-walled myocardium, and abnormal coronary morphogenesis. We show by expression analysis that COUP-TFII is expressed in the endocardium and the epicardium but not in the myocardium of the ventricle. Using endothelial-specific COUP-TFII mutants and molecular approaches, we show that COUP-TFII deficiency resulted in endocardial cushion hypoplasia. This was attributed to the reduced growth and survival of atrioventricular cushion mesenchymal cells and defective epithelial-mesenchymal transformation (EMT) in the underlying endocardium. In addition, the endocardial EMT defect was accompanied by downregulation of Snai1, one of the master regulators of EMT, and upregulation of vascular endothelial-cadherin. Furthermore, we show that although COUP-TFII does not play a major role in the formation of epicardial cell cysts, it is critically important for the formation of epicardium. Ablation of COUP-TFII impairs epicardial EMT and coronary plexus formation. CONCLUSIONS: Our results reveal that COUP-TFII plays cell-autonomous roles in the endocardium and the epicardium for endocardial and epicardial EMT, which are required for proper valve and coronary vessel formation during heart development.
Subjects
Atrioventricular septal defect
Cardiac morphogenesis
Chicken ovalbumin upstream promoter-transcription factor II
Epicardium
Epithelial-mesenchymal transformation
Publisher
American Heart Association, Inc.
Type
journal article

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