Yang Xue, Li Shuai, Sun Xin, Ren Ya, Qiang Lei, Liu Yihao, Wang Jinwu, Dai Kerong
College of Medicine, Southwest Jiaotong University, No. 144 Jiaoda Road, Chengdu 610031, People's Republic of China.
Department of Orthopedics, The First Affiliated Hospital, Zhejiang University School of Medicine, No. 79 Qingchun Rd, Hangzhou 310003, People's Republic of China.
Int J Bioprint. 2023 May 10;9(5):749. doi: 10.18063/ijb.749. eCollection 2023.
Engineered vasculature is widely employed to maintain the cell viability within tissues. A variety of fabrication techniques for engineered vasculature have been explored, with combination of additive manufacturing with a sacrifice-based technique being the most common approach. However, the size deformation of vasculature caused by the swelling of sacrificial materials remains unaddressed. In this study, Pluronic F-127 (PF-127), the most widely used sacrificial material, was employed to study the deformation of the vasculature. Then, a thermoresponsive hydrogel comprising poly(N-isopropylacrylamide) (PNIPAM) and gelatin methacrylate (GelMA) was used to induce volume shrinkage at 37°C to compensate for the deformation of vasculature caused by the swelling of a three-dimensional (3D)-printed sacrificial template, and to generate vasculature of a smaller size than that after deformation. Our results showed that the vasculature diameter increased after the sacrificial template was removed, whereas it decreased to the designed diameter after the volume shrinkage. Human umbilical vein endothelial cells (HUVECs) formed an endothelial monolayer in the engineered vasculature. Osteosarcoma cells (OCs) were loaded into a hierarchical vasculature within the thermoresponsive hydrogel to investigate the interaction between HUVECs and OCs. New blood vessel infiltration was observed within the lumen of the engineered vasculature after subcutaneous implantation for 4 weeks. In addition, engineered vasculature was implanted in a rat ischemia model to further study the function of engineered vasculature for blood vessel infiltration. This study presents a small method aiming to accurately create engineered vasculature by additive manufacturing and a sacrificebased technique.
工程化血管系统被广泛用于维持组织内细胞的活力。人们探索了多种用于工程化血管系统的制造技术,其中增材制造与牺牲性技术相结合是最常见的方法。然而,牺牲性材料膨胀导致的血管系统尺寸变形问题仍未得到解决。在本研究中,使用了最广泛使用的牺牲性材料普朗尼克F-127(PF-127)来研究血管系统的变形。然后,使用一种由聚(N-异丙基丙烯酰胺)(PNIPAM)和甲基丙烯酸明胶(GelMA)组成的热响应水凝胶在37°C下诱导体积收缩,以补偿三维(3D)打印牺牲模板膨胀引起的血管系统变形,并生成比变形后尺寸更小的血管系统。我们的结果表明,去除牺牲模板后血管直径增加,而体积收缩后直径减小至设计直径。人脐静脉内皮细胞(HUVECs)在工程化血管系统中形成内皮单层。将骨肉瘤细胞(OCs)加载到热响应水凝胶内的分级血管系统中,以研究HUVECs与OCs之间的相互作用。皮下植入4周后,在工程化血管系统的管腔内观察到新的血管浸润。此外,将工程化血管系统植入大鼠缺血模型中,以进一步研究工程化血管系统对血管浸润的功能。本研究提出了一种旨在通过增材制造和牺牲性技术精确创建工程化血管系统的方法。