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Patterned human microvascular grafts enable rapid vascularization and increase perfusion in infarcted rat hearts

机译:图案化的人类微血管移植物能够快速血管化并增加梗死大鼠心脏的灌注

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摘要

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.
机译:血管化和有效灌注是心脏组织工程学中的长期挑战。在这里,我们报道了工程化的可灌注微血管构建体,其中人类胚胎干细胞衍生的内皮细胞(hESC-ECs)既被植入了图案化的微通道,又被植入了周围的胶原蛋白基质。在体外,内腔内壁的hESC-ECs易于在流动的基质中从头形成的内皮管发芽并吻合。当植入梗塞的大鼠心脏时,可植入的微血管移植物在植入后5天比不可灌入的自组装构建体与冠状血管的融合程度更高。光学微血管造影成像显示,可灌注移植物的血管密度高6倍,血管速度高2.5倍,体积灌注率高20倍以上。包含额外的hESC来源的心肌细胞的可灌注移植物的植入显示出更高的心肌细胞和血管密度。因此,预先形成图案的血管网络可增强血管重塑并加速冠状动脉灌注,从而潜在地支持植入后的心脏组织。这些发现应有助于下一代心脏组织工程设计。

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