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Publication : Coronary anomalies in mice with congenital heart defects.

First Author  Tomanek RJ Year  2015
Journal  Anat Rec (Hoboken) Volume  298
Issue  2 Pages  408-17
PubMed ID  25266175 Mgi Jnum  J:217298
Mgi Id  MGI:5613729 Doi  10.1002/ar.23056
Citation  Tomanek RJ, et al. (2015) Coronary anomalies in mice with congenital heart defects. Anat Rec (Hoboken) 298(2):408-17
abstractText  BACKGROUND: Coronary anomalies are frequently associated with congenital cardiac defects. Accordingly, we tested the hypothesis that the development of the tunica media of coronary arteries/arterioles is compromised in mice with cardiac defects of the outflow tract (persistent truncus arteriosus, double outlet right ventricle and transposition of the great arteries) by studying hearts of G7-9 generation mice bred from mutagenized mice caused by N-ethyl-N-nitrosourea. Mice were studied at embryonic days E16.5, E17.5, and postnatal days 1 and 11. Data were based on immunohistochemistry of serial sections. RESULTS: In 21 of 24 mice with outflow tract defects, the development of smooth muscle in arteries and arterioles was retarded; most commonly arterioles had an incomplete layer of smooth muscle or in a few instances, lacked a tunica media. In this model, an absence of a coronary ostium occurred in only 2 mice, indicating that the mechanisms underlying the formation of coronary ostia and the recruitment and differentiation of vascular smooth muscle differ. Coronary fistulas were present in 20% and dilated vessels in 30% of the hearts with cardiac defects. CONCLUSIONS: The data suggest that vascular smooth muscle recruitment and differentiation are not necessarily linked to other coronary anomalies, such as absence of a main coronary artery or branching patterns. Anat Rec, 298:408-417, 2015. (c) 2014 Wiley Periodicals, Inc.
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