NOing the heart: Role of nitric oxide synthase-3 in heart development

被引:58
作者
Liu, Yin [1 ]
Feng, Qingping [1 ]
机构
[1] Univ Western Ontario, Dept Physiol & Pharmacol, London, ON N6A 5C1, Canada
基金
加拿大健康研究院;
关键词
Heart development; Nitric oxide; Endothelial nitric oxide synthase; Congenital heart disease; TRANSCRIPTION FACTORS; GENE-EXPRESSION; MICE LACKING; CARDIOMYOCYTE PROLIFERATION; VASCULAR DEVELOPMENT; VALVE DEVELOPMENT; CARDIAC-MUSCLE; DEFICIENT MICE; CA2+ CHANNEL; GATA4;
D O I
10.1016/j.diff.2012.04.004
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Congenital heart disease is the most common birth defect in humans. Identifying factors that are critical to embryonic heart development could further our understanding of the disease and lead to new strategies of its prevention and treatment. Nitric oxide synthase-3 (NOS3) or endothelial nitric oxide synthase (eNOS) is known for many important biological functions including vasodilation, vascular homeostasis and angiogenesis. Over the past decade, studies from our lab and others have shown that NOS3 is required during heart development. More specifically, deficiency in NOS3 results in congenital septal defects, cardiac hypertrophy and postnatal heart failure. In addition, NOS3 is pivotal to the morphogenesis of major coronary arteries and myocardial capillary development Interestingly, these effects of NOS3 are mediated through induction of transcription and growth factors that are crucial in the formation of coronary arteries. Finally, deficiency in NOS3 results in high incidences of bicuspid aortic valves, a disease in humans that often leads to complications with age including aortic valve stenosis or regurgitation, endocarditis, aortic aneurysm formation, and aortic dissection. In summary, these data suggest NOS3 plays a critical role in embryonic heart development and morphogenesis of coronary arteries and aortic valves. (C) 2012 International Society of Differentiation. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:54 / 61
页数:8
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