Yap Choon Hwai, Liu Xiaoqin, Pekkan Kerem
Department of Biomedical Engineering, National University of Singapore, Singapore, Singapore.
Department of Developmental Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
PLoS One. 2014 Jan 27;9(1):e86878. doi: 10.1371/journal.pone.0086878. eCollection 2014.
Abnormal fluid mechanical environment in the pre-natal cardiovascular system is hypothesized to play a significant role in causing structural heart malformations. It is thus important to improve our understanding of the prenatal cardiovascular fluid mechanical environment at multiple developmental time-points and vascular morphologies. We present such a study on fetal great arteries on the wildtype mouse from embryonic day 14.5 (E14.5) to near-term (E18.5).
Ultrasound bio-microscopy (UBM) was used to measure blood velocity of the great arteries. Subsequently, specimens were cryo-embedded and sectioned using episcopic fluorescent image capture (EFIC) to obtain high-resolution 2D serial image stacks, which were used for 3D reconstructions and quantitative measurement of great artery and aortic arch dimensions. EFIC and UBM data were input into subject-specific computational fluid dynamics (CFD) for modeling hemodynamics.
In normal mouse fetuses between E14.5-18.5, ultrasound imaging showed gradual but statistically significant increase in blood velocity in the aorta, pulmonary trunk (with the ductus arteriosus), and descending aorta. Measurement by EFIC imaging displayed a similar increase in cross sectional area of these vessels. However, CFD modeling showed great artery average wall shear stress and wall shear rate remain relatively constant with age and with vessel size, indicating that hemodynamic shear had a relative constancy over gestational period considered here.
Our EFIC-UBM-CFD method allowed reasonably detailed characterization of fetal mouse vascular geometry and fluid mechanics. Our results suggest that a homeostatic mechanism for restoring vascular wall shear magnitudes may exist during normal embryonic development. We speculate that this mechanism regulates the growth of the great vessels.
产前心血管系统中异常的流体力学环境被认为在导致心脏结构畸形方面起着重要作用。因此,增进我们对多个发育时间点和血管形态下的产前心血管流体力学环境的理解非常重要。我们展示了一项针对野生型小鼠从胚胎第14.5天(E14.5)到接近足月(E18.5)的胎儿大动脉的研究。
使用超声生物显微镜(UBM)测量大动脉的血流速度。随后,对标本进行冷冻包埋,并使用落射荧光图像采集(EFIC)进行切片,以获得高分辨率的二维连续图像堆栈,用于大动脉和主动脉弓尺寸的三维重建和定量测量。将EFIC和UBM数据输入特定个体的计算流体动力学(CFD)中以模拟血流动力学。
在E14.5 - 18.5的正常小鼠胎儿中,超声成像显示主动脉、肺动脉干(含动脉导管)和降主动脉的血流速度逐渐增加,但具有统计学意义。通过EFIC成像测量显示这些血管的横截面积也有类似增加。然而,CFD建模显示大动脉的平均壁面剪切应力和壁面剪切速率随年龄和血管大小保持相对恒定,表明在所考虑的妊娠期内血流动力学剪切具有相对稳定性。
我们的EFIC - UBM - CFD方法能够对胎儿小鼠血管几何形状和流体力学进行较为详细的表征。我们的结果表明,在正常胚胎发育过程中可能存在一种恢复血管壁剪切大小的稳态机制。我们推测这种机制调节大血管的生长。