Computational Science and Engineering Laboratory, ETH Zürich, CH-8092, Switzerland.
Integr Biol (Camb). 2013 Dec;5(12):1426-38. doi: 10.1039/c3ib40085a.
The mouse retina has become a prominent model for studying angiogenesis. The easy access and well-known developmental progression have significantly propelled our ability to examine and manipulate blood vessels in vivo. Nonetheless, most studies have restricted their evaluations to the superficial plexus (an upper vascular layer in contact with the vitreous). Here we present experimental data and quantification for the developmental progression of the full retina including the intermediate and deeper plexus that sprouts from the superficial layer. We analyze the origin and advancement of vertical sprouting and present the progression of vascular perfusion within the tissue. Furthermore, we introduce the use of Minkowsky functionals to quantify remodeling in the superficial and deeper plexus. The work expands information on the retina towards a 3D structure. This is of particular interest, as recent data have demonstrated differential effects of gene deletion on the upper and deeper plexus, highlighting the concept of distinct operational pathways during sprouting angiogenesis.
小鼠视网膜已成为研究血管生成的重要模型。其易于获取和明确的发育进程极大地促进了我们在体内检查和操纵血管的能力。尽管如此,大多数研究都将其评估仅限于浅层丛(与玻璃体接触的上层血管层)。在这里,我们提供了包括从中层丛(浅层丛发芽的深层血管层)发育而来的完整视网膜的实验数据和发育进程的定量分析。我们分析了垂直发芽的起源和进展,并展示了组织内血管灌注的进展。此外,我们引入了 Minkowski 函数来定量分析浅层和深层丛的重塑。这项工作扩展了关于 3D 结构的视网膜信息。这一点尤其重要,因为最近的数据表明,基因缺失对上层和深层丛有不同的影响,突出了在发芽性血管生成过程中存在不同操作途径的概念。