Endo Yuki, Homma Jun, Sekine Hidekazu, Matsuura Katsuhisa, Shimizu Tatsuya, Niinami Hiroshi
Department of Cardiovascular Surgery, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo, 162-8666, Japan.
Institute of Advanced Biomedical Engineering and Science, Tokyo Women's Medical University, TWIns, 8-1 Kawada-cho, Shinjuku-ku, Tokyo, 162-8666, Japan.
NPJ Regen Med. 2022 Mar 31;7(1):22. doi: 10.1038/s41536-022-00218-7.
There is great interest in the development of techniques to bioengineer pulsatile myocardial tissue as a next-generation regenerative therapy for severe heart failure. However, creation of thick myocardial grafts for regenerative medicine requires the incorporation of blood vessels. In this study, we describe a new method of constructing a vascular network in vivo that allows the construction of thick human myocardial tissue from multi-layered cell sheets. A gelatin sheet pre-loaded with growth factors was transplanted onto the superficial femoral artery and vein of the rat. These structures were encapsulated together within an ethylene vinyl alcohol membrane and incubated in vivo for 3 weeks (with distal superficial femoral artery ligation after 2 weeks to promote blood flow to the vascular bed). Subsequently, six cardiomyocyte sheets were transplanted onto the vascular bed in two stages (three sheets, two times). Incubation of this construct for a further week generated vascularized human myocardial tissue with an independent circulation supplied by an artery and vein suitable for anastomosis to host vessels. Notably, laminating six cell sheets on the vascular bed in two stages rather than one allowed the creation of thicker myocardial tissue while suppressing tissue remodeling and fibrosis. Finally, the pulsatile myocardial tissue was shown to generate auxiliary pressure when wrapped around the common iliac artery of a rat. Further development of this technique might facilitate the generation of circulatory assist devices for patients with heart failure.
作为严重心力衰竭的下一代再生疗法,生物工程化搏动性心肌组织技术的发展引起了人们极大的兴趣。然而,为再生医学创建厚的心肌移植物需要纳入血管。在本研究中,我们描述了一种在体内构建血管网络的新方法,该方法允许从多层细胞片构建厚的人心肌组织。将预先装载生长因子的明胶片移植到大鼠股浅动脉和静脉上。这些结构一起封装在乙烯-乙烯醇膜内,并在体内孵育3周(2周后结扎股浅动脉远端以促进血液流向血管床)。随后,分两个阶段(每次三张)将六张心肌细胞片移植到血管床上。将该构建体再孵育一周,产生具有独立循环的血管化人心肌组织,该循环由适合与宿主血管吻合的动脉和静脉供应。值得注意的是,分两个阶段而不是一个阶段在血管床上层压六张细胞片,能够在抑制组织重塑和纤维化的同时创建更厚的心肌组织。最后,当将搏动性心肌组织包裹在大鼠髂总动脉周围时,显示其能产生辅助压力。该技术的进一步发展可能会促进心力衰竭患者循环辅助装置的产生。