细胞外基质
自愈水凝胶
生物医学工程
去细胞化
组织工程
先天免疫系统
免疫原性
免疫系统
材料科学
细胞生物学
生物
医学
免疫学
高分子化学
作者
Dhavan Sharma,Archita Sharma,Linghao Hu,Te-An Chen,Sarah Voon,Kayla J. Bayless,Jeremy Goldman,Alex J. Walsh,Feng Zhao
标识
DOI:10.1016/j.bioactmat.2023.07.023
摘要
Vascularization is a key pre-requisite to engineered anatomical scale three dimensional (3-D) constructs to ensure their nutrient and oxygen supply upon implantation. Presently, engineered pre-vascularized 3-D tissues are limited to only micro-scale hydrogels, which meet neither the anatomical scale needs nor the complexity of natural extracellular matrix (ECM) environments. Anatomical scale perfusable constructs are critically needed for translational applications. To overcome this challenge, we previously developed pre-vascularized ECM sheets with long and oriented dense microvascular networks. The present study further evaluated the patency, perfusability and innate immune response toward these pre-vascularized constructs. Macrophage-co-cultured pre-vascularized constructs were evaluated in vitro to confirm micro-vessel patency and perturbations in macrophage metabolism. Subcutaneously implanted pre-vascularized constructs remained viable and formed a functional anastomosis with host vasculature within 3 days of implantation. This completely biological pre-vascularized construct holds great potential as a building block to engineer perfusable anatomical scale tissues.
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