用于生产血管化三维人微组织的自组装和可灌注微血管床的微生理工程。
Microphysiological Engineering of Self-Assembled and Perfusable Microvascular Beds for the Production of Vascularized Three-Dimensional Human Microtissues.
出版信息
ACS Nano. 2019 Jul 23;13(7):7627-7643. doi: 10.1021/acsnano.9b00686. Epub 2019 Jun 18.
The vasculature is an essential component of the circulatory system that plays a vital role in the development, homeostasis, and disease of various organs in the human body. The ability to emulate the architecture and transport function of blood vessels in the integrated context of their associated organs represents an important requirement for studying a wide range of physiological processes. Traditional models of the vasculature, however, largely fail to offer such capabilities. Here we combine microfluidic three-dimensional (3D) cell culture with the principle of vasculogenic self-assembly to engineer perfusable 3D microvascular beds . Our system is created in a micropatterned hydrogel construct housed in an elastomeric microdevice that enables coculture of primary human vascular endothelial cells and fibroblasts to achieve formation, anastomosis, and controlled perfusion of 3D vascular networks. An open-top chamber design adopted in this hybrid platform also makes it possible to integrate the microengineered 3D vasculature with other cell types to recapitulate organ-specific cellular heterogeneity and structural organization of vascularized human tissues. Using these capabilities, we developed stem cell-derived microphysiological models of vascularized human adipose tissue and the blood-retinal barrier. Our approach was also leveraged to construct a 3D organotypic model of vascularized human lung adenocarcinoma as a high-content drug screening platform to simulate intravascular delivery, tumor-killing effects, and vascular toxicity of a clinical chemotherapeutic agent. Furthermore, we demonstrated the potential of our platform for applications in nanomedicine by creating microengineered models of vascular inflammation to evaluate a nanoengineered drug delivery system based on active targeting liposomal nanocarriers. These results represent a significant improvement in our ability to model the complexity of native human tissues and may provide a basis for developing predictive preclinical models for biopharmaceutical applications.
脉管系统是循环系统的重要组成部分,在人体各种器官的发育、稳态和疾病中起着至关重要的作用。在与其相关器官的综合环境中模拟血管的结构和运输功能的能力是研究广泛的生理过程的重要要求。然而,传统的脉管模型在很大程度上无法提供这种能力。在这里,我们将微流控三维(3D)细胞培养与血管生成自组装原理相结合,构建可灌注的 3D 微血管床。我们的系统是在一个弹性微器件中容纳的微图案化水凝胶构建体中创建的,该构建体能够共培养原代人血管内皮细胞和成纤维细胞,以实现 3D 血管网络的形成、吻合和受控灌注。在这个混合平台中采用的开放式顶室设计还使得能够将微工程化的 3D 脉管与其他细胞类型集成,以再现血管化人体组织的特定器官细胞异质性和结构组织。利用这些能力,我们开发了源自干细胞的血管化人体脂肪组织和血视网膜屏障的微生理模型。我们的方法还被用于构建血管化人肺腺癌细胞的 3D 器官样模型,作为高通量药物筛选平台,模拟临床化疗药物的血管内输送、杀伤效果和血管毒性。此外,我们通过创建血管炎症的微工程模型来展示我们平台在纳米医学中的应用潜力,以评估基于主动靶向脂质体纳米载体的纳米工程药物输送系统。这些结果代表了我们模拟天然人体组织复杂性的能力的重大提高,并可能为开发用于生物制药应用的预测性临床前模型提供基础。