School of Biomedical Engineering, University of British Columbia; Life Sciences Institute, University of British Columbia;
School of Biomedical Engineering, University of British Columbia; Life Sciences Institute, University of British Columbia; Department of Medical Genetics, University of British Columbia; Institute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA).
J Vis Exp. 2023 Jan 20(191). doi: 10.3791/64715.
An organoid is defined as an engineered multicellular in vitro tissue that mimics its corresponding in vivo organ such that it can be used to study defined aspects of that organ in a tissue culture dish. The breadth and application of human pluripotent stem cell (hPSC)-derived organoid research have advanced significantly to include the brain, retina, tear duct, heart, lung, intestine, pancreas, kidney, and blood vessels, among several other tissues. The development of methods for the generation of human microvessels, specifically, has opened the way for modeling human blood vessel development and disease in vitro and for the testing and analysis of new drugs or tissue tropism in virus infections, including SARS-CoV-2. Complex and lengthy protocols lacking visual guidance hamper the reproducibility of many stem cell-derived organoids. Additionally, the inherent stochasticity of organoid formation processes and self-organization necessitates the generation of optical protocols to advance the understanding of cell fate acquisition and programming. Here, a visually guided protocol is presented for the generation of 3D human blood vessel organoids (BVOs) engineered from hPSCs. Presenting a continuous basement membrane, vascular endothelial cells, and organized articulation with mural cells, BVOs exhibit the functional, morphological, and molecular features of human microvasculature. BVO formation is initiated through aggregate formation, followed by mesoderm and vascular induction. Vascular maturation and network formation are initiated and supported by embedding aggregates in a 3D collagen and solubilized basement membrane matrix. Human vessel networks form within 2-3 weeks and can be further grown in scalable culture systems. Importantly, BVOs transplanted into immunocompromised mice anastomose with the endogenous mouse circulation and specify into functional arteries, veins, and arterioles. The present visually guided protocol will advance human organoid research, particularly in relation to blood vessels in normal development, tissue vascularization, and disease.
类器官被定义为一种经过工程设计的体外多细胞组织,可模拟其相应的体内器官,从而可在组织培养皿中用于研究该器官的特定方面。人类多能干细胞 (hPSC) 衍生类器官研究的广度和应用已经取得了重大进展,包括大脑、视网膜、泪管、心脏、肺、肠、胰腺、肾脏和血管等多种组织。生成人类微血管的方法的发展,特别是为体外模拟人类血管发育和疾病以及测试和分析新药物或病毒感染中的组织嗜性(包括 SARS-CoV-2)开辟了道路。缺乏视觉指导的复杂而冗长的方案会阻碍许多干细胞衍生类器官的可重复性。此外,类器官形成过程和自组织的固有随机性需要生成光学方案来推进对细胞命运获得和编程的理解。在这里,提出了一种从 hPSC 生成 3D 人类血管类器官 (BVOs) 的可视化指导方案。BVOs 呈现出连续的基底膜、血管内皮细胞和与壁细胞的有组织连接,表现出人类微血管的功能、形态和分子特征。BVOs 的形成是通过聚集体形成开始的,随后是中胚层和血管诱导。通过将聚集体嵌入 3D 胶原和可溶基底膜基质中,开始并支持血管成熟和网络形成。人类血管网络在 2-3 周内形成,并可在可扩展的培养系统中进一步生长。重要的是,移植到免疫功能低下的小鼠中的 BVO 与内源性小鼠循环吻合,并特化为功能性动脉、静脉和小动脉。本可视化指导方案将推进人类类器官研究,特别是在正常发育、组织血管化和疾病方面的研究。