Kathiriya I S, Srivastava D
Department of Pediatrics, University of Texas Southwestern Medical Center at Dallas, 75390-9148, USA.
Am J Med Genet. 2000 Winter;97(4):271-9. doi: 10.1002/1096-8628(200024)97:4<271::aid-ajmg1277>3.0.co;2-o.
Proper morphogenesis and positioning of internal organs requires delivery and interpretation of precise signals along the anterior-posterior, dorsal-ventral, and left-right axes. An elegant signaling cascade determines left- versus right-sided identity in visceral organs in a concordant fashion, resulting in a predictable left-right (LR) organ asymmetry in all vertebrates. The complex morphogenesis of the heart and its connections to the vasculature are particularly dependent upon coordinated LR signaling pathways. Disorganization of LR signals can result in myriad congenital heart defects that are a consequence of abnormal looping and remodeling of the primitive heart tube into a multi-chambered organ. A framework for understanding how LR asymmetric signals contribute to normal organogenesis has emerged and begins to explain the basis of many human diseases of LR asymmetry. Here we review the impact of LR signaling pathways on cardiac development and congenital heart disease.
体内器官的正常形态发生和定位需要沿前后轴、背腹轴和左右轴传递并解读精确的信号。一个精妙的信号级联反应以协调一致的方式决定内脏器官的左右特征,在所有脊椎动物中形成可预测的左右(LR)器官不对称性。心脏复杂的形态发生及其与脉管系统的连接尤其依赖于协调的LR信号通路。LR信号紊乱可导致无数先天性心脏缺陷,这些缺陷是原始心管异常环化并重塑为多腔器官的结果。一个理解LR不对称信号如何促进正常器官发生的框架已经出现,并开始解释许多LR不对称性人类疾病的发病基础。在此,我们综述LR信号通路对心脏发育和先天性心脏病的影响。