Mechanical Engineering Department, Koç University, Istanbul, Turkey.
Kosair Charities Pediatric Heart Research Program, Cardiovascular Innovation Institute, University of Louisville, Louisville, KY, United States of America.
Sci Rep. 2018 Nov 16;8(1):16948. doi: 10.1038/s41598-018-35127-7.
Embryonic aortic arches (AA) are initially bilaterally paired, transitional vessels and failures in remodeling based on hemodynamic and growth-related adaptations cause a spectrum of congenital heart disease (CHD) anatomies. Identifying regulatory mechanisms and cross-talk between the genetic elements of these vessels are critical to understand the ethiology of CHD and refine predictive computational models. This study aims to screen expression profiles of fundamental biological pathways in AA at early stages of chick embryo morphogenesis and correlate them with our current understanding of growth and mechanical loading. Reverse transcription-quantitative PCR (RT-qPCR) was followed by correlation and novel peak expression analyses to compare the behaviour and activation period of the genes. Available protein networks were also integrated to investigate the interactions between molecules and highlight major hierarchies. Only wall shear stress (WSS) and growth-correlated expression patterns were investigated. Effect of WSS was seen directly on angiogenesis as well on structural and apoptosis-related genes. Our time-resolved network suggested that WSS-correlated genes coordinate the activity of critical growth factors. Moreover, differential gene expression of left and right AA might be an indicator of subsequent asymmetric morphogenesis. These findings may further our understanding of the complex processes of cardiac morphogenesis and errors resulting in CHD.
胚胎主动脉弓(AA)最初是双侧成对的过渡性血管,如果基于血液动力学和生长相关适应的重塑失败,就会导致一系列先天性心脏病(CHD)的解剖结构。鉴定这些血管的遗传因素的调节机制和串扰对于理解 CHD 的病因学和完善预测性计算模型至关重要。本研究旨在筛选鸡胚形态发生早期 AA 中基本生物学途径的表达谱,并将其与我们目前对生长和机械加载的理解相关联。采用反转录定量 PCR(RT-qPCR)进行相关性和新的峰表达分析,以比较基因的行为和激活期。还整合了现有的蛋白质网络,以研究分子之间的相互作用并突出主要层次结构。仅研究了壁切应力(WSS)和生长相关的表达模式。WSS 对血管生成以及结构和细胞凋亡相关基因的直接影响。我们的时分辨网络表明,WSS 相关基因协调关键生长因子的活性。此外,左右 AA 的差异基因表达可能是随后不对称形态发生的一个指标。这些发现可能进一步加深我们对心脏形态发生的复杂过程以及导致 CHD 的错误的理解。