细胞外基质
细胞生物学
组织工程
焦点粘着
形态发生
分区(防火)
芯片上器官
整合素
化学
材料科学
生物医学工程
细胞
纳米技术
生物
微流控
信号转导
医学
生物化学
基因
酶
作者
Jun Chen,Yuqiong Wu,Jia-Rong Huang,Junjin Jie,Chan Huang,Di Zhang,Yuxin Huang,Rui Mao,Ming Zhao,Linping Wu
标识
DOI:10.1002/adhm.202502347
摘要
Abstract Prevascularization is the key challenge for large‐scale tissue engineering. Nevertheless, none of the engineered vasculature simultaneously recapitulates the multi‐layered heterogeneous characterizations and functions yet. The recent studies reveal that matrix dynamics play an important role in vasculature morphogenesis. In this study, an extracellular matrix‐mimicking bioink is developed by the interpenetrated dynamic‐covalent crosslinking orthogonal design. The dynamic covalent crosslinking network of the bioink allows an adaptable microenvironment contributing to the functional compartmentalization of endothelial cells and smooth muscle cells toward histological vasculature configurations. Focal adhesion kinase pathway participates in the morphogenesis process by coupling the microscopically adaptable environment to the vasculature organization via upregulation of integrin‐mediated adhesion and glycolysis. The engineered vasculature exhibits in vitro contraction in response to angiotensin II and significantly improves blood perfusion in the mouse hind limb ischemia model. In addition, the vascular network successfully prolongs the survival and function of surrounding human dermal fibroblasts postimplantation, which enhances the healing of large full‐thickness wounds. Altogether, this work presents a one‐step bioprinting strategy of prevascularization in predesigned architecture for vascular tissue engineering.
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