Ghaffari Siavash, Leask Richard L, Jones Elizabeth A V
Lady Davis Institute for Medical Research, McGill University, 3755 Chemin de la Côte-Ste-Catherine, Montréal, Quebec H3T 1E2, Canada Department of Chemical Engineering, McGill University, 3610 University Street, Montréal, Quebec H3A 0C5, Canada.
Department of Chemical Engineering, McGill University, 3610 University Street, Montréal, Quebec H3A 0C5, Canada.
Development. 2015 Dec 1;142(23):4158-67. doi: 10.1242/dev.127019. Epub 2015 Oct 6.
Normal vascular development requires blood flow. Time-lapse imaging techniques have revolutionised our understanding of developmental biology, but measuring changes in blood flow dynamics has met with limited success. Ultrasound biomicroscopy and optical coherence tomography can concurrently image vascular structure and blood flow velocity, but these techniques lack the resolution to accurately calculate fluid forces such as shear stress. This is important because hemodynamic forces are biologically active and induce changes in the expression of genes important for vascular development. Regional variations in shear stress, rather than the overall level, control processes such as vessel enlargement and regression during vascular remodelling. We present a technique to concurrently visualise vascular remodelling and blood flow dynamics. We use an avian embryonic model and inject an endothelial-specific dye and fluorescent microspheres. The motion of the microspheres is captured with a high-speed camera and the velocity of the blood flow in and out of the region of interest is quantified by micro-particle image velocitymetry (µPIV). The vessel geometry and flow are used to numerically solve the flow physics with computational fluid dynamics (CFD). Using this technique, we can analyse changes in shear stress, pressure drops and blood flow velocities over a period of 10 to 16 h. We apply this to study the relationship between shear stress and chronic changes in vessel diameter during embryonic development, both in normal development and after TGFβ stimulation. This technique allows us to study the interaction of biomolecular and biomechanical signals during vascular remodelling using an in vivo developmental model.
正常的血管发育需要血流。延时成像技术彻底改变了我们对发育生物学的理解,但测量血流动力学变化的成效有限。超声生物显微镜和光学相干断层扫描可以同时对血管结构和血流速度进行成像,但这些技术缺乏精确计算诸如剪切应力等流体力的分辨率。这很重要,因为血流动力学力具有生物活性,并能诱导对血管发育至关重要的基因表达发生变化。在血管重塑过程中,剪切应力的区域差异而非总体水平控制着诸如血管扩张和消退等过程。我们提出了一种同时可视化血管重塑和血流动力学的技术。我们使用鸟类胚胎模型,并注射一种内皮特异性染料和荧光微球。用高速相机捕捉微球的运动,并通过微粒子图像测速技术(µPIV)对进出感兴趣区域的血流速度进行量化。利用计算流体动力学(CFD),根据血管几何形状和血流情况对流体物理进行数值求解。使用这种技术,我们可以分析10至16小时内剪切应力、压降和血流速度的变化。我们将此应用于研究胚胎发育过程中,正常发育以及TGFβ刺激后,剪切应力与血管直径慢性变化之间的关系。这项技术使我们能够利用体内发育模型研究血管重塑过程中生物分子信号与生物力学信号的相互作用。