Sharma Dhavan, Sharma Archita, Hu Linghao, Chen Te-An, Voon Sarah, Bayless Kayla J, Goldman Jeremy, Walsh Alex J, Zhao Feng
Department of Biomedical Engineering, Texas A&M University, College Station, TX, United States.
School of Medicine, Texas A&M University, College Station, TX, United States.
Bioact Mater. 2023 Aug 11;30:184-199. doi: 10.1016/j.bioactmat.2023.07.023. eCollection 2023 Dec.
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 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.
血管化是构建工程化解剖尺度三维(3-D)结构的关键前提条件,以确保植入后其营养和氧气供应。目前,工程化的预血管化3-D组织仅限于微观尺度的水凝胶,既无法满足解剖尺度需求,也不符合天然细胞外基质(ECM)环境的复杂性。转化应用迫切需要解剖尺度的可灌注结构。为了克服这一挑战,我们之前开发了具有长而定向的致密微血管网络的预血管化ECM片。本研究进一步评估了这些预血管化结构的通畅性、可灌注性和固有免疫反应。对巨噬细胞共培养的预血管化结构进行评估,以确认微血管通畅性和巨噬细胞代谢的扰动。皮下植入的预血管化结构在植入后3天内保持存活,并与宿主血管形成功能性吻合。这种完全生物性的预血管化结构作为构建可灌注解剖尺度组织的基本单元具有巨大潜力。