Department of Bioengineering, University of Washington, Seattle, WA, 98109, USA.
Center for Cardiovascular Biology, University of Washington, Seattle, WA, 98109, USA.
Nat Commun. 2019 Feb 4;10(1):584. doi: 10.1038/s41467-019-08388-7.
Vascularization and efficient perfusion are long-standing challenges in cardiac tissue engineering. Here we report engineered perfusable microvascular constructs, wherein human embryonic stem cell-derived endothelial cells (hESC-ECs) are seeded both into patterned microchannels and the surrounding collagen matrix. In vitro, the hESC-ECs lining the luminal walls readily sprout and anastomose with de novo-formed endothelial tubes in the matrix under flow. When implanted on infarcted rat hearts, the perfusable microvessel grafts integrate with coronary vasculature to a greater degree than non-perfusable self-assembled constructs at 5 days post-implantation. Optical microangiography imaging reveal that perfusable grafts have 6-fold greater vascular density, 2.5-fold higher vascular velocities and >20-fold higher volumetric perfusion rates. Implantation of perfusable grafts containing additional hESC-derived cardiomyocytes show higher cardiomyocyte and vascular density. Thus, pre-patterned vascular networks enhance vascular remodeling and accelerate coronary perfusion, potentially supporting cardiac tissues after implantation. These findings should facilitate the next generation of cardiac tissue engineering design.
血管生成和有效的灌注是心脏组织工程中的长期挑战。在这里,我们报告了工程化的可灌注微血管构建体,其中将人胚胎干细胞衍生的内皮细胞(hESC-ECs)接种到图案化的微通道和周围的胶原基质中。在体外,在流动条件下,沿着腔壁排列的 hESC-ECs 迅速发芽并与基质中新形成的内皮管吻合。当植入梗死大鼠心脏时,可灌注微血管移植物与冠状动脉血管的整合程度大于非可灌注自组装构建体在植入后 5 天。光学微血管成像显示,可灌注移植物的血管密度增加 6 倍,血管速度增加 2.5 倍,容积灌注率增加 20 倍以上。植入含有额外 hESC 衍生的心肌细胞的可灌注移植物显示出更高的心肌细胞和血管密度。因此,预先图案化的血管网络增强了血管重塑并加速了冠状动脉灌注,这可能为植入后的心脏组织提供支持。这些发现应该有助于下一代心脏组织工程设计。