Vascularizing Organoids to Promote Long-Term Organogenesis on a Chip

Organoids Pub Date : 2023-12-07 DOI:10.3390/organoids2040019
Xinhui Wang, Brent M. Bijonowski, N. A. Kurniawan
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Abstract

Organoids have emerged as a powerful tool for studying organ development, disease modeling, and drug discovery due to their ability to mimic the in vivo structure and function of organs in a three-dimensional in vitro model. During in vivo organ maturation, the process of vascularization is crucial for the provision of nutrients and oxygen to cells and the removal of waste products as the organ increases in size. Similarly, organoids can grow to sizes greater than the millimeter scale, yet transport of oxygen and nutrients to the center becomes increasingly difficult, often resulting in the formation of a necrotic core. Herein, we provide a concise summary of the recent development of methods to initiate and maintain vascularization of organoids. Broadly, vascularization of organoids has been achieved primarily by two means: generating organoids that contain endothelial cells or employing the secretion of vascular growth factors to promote vascularization. Growth factors play a fundamental role in regulating blood vessel formation through chemical signals that cause changes in the cell–cell adhesions and ultimately the migration of endothelial cells. Furthermore, models with perfusable systems demonstrate that through the application of growth factors and cells, the vascular network in vascularization-based organoids can administer biological substances to the interior of the organoid, opening up new possibilities for long-term organoid culture in vitro. This goal is being realized through the development of bioengineering tools, such as vascularized organoids on a chip, which are currently tested for various organ systems, including the lung, brain, kidney, and tumors, with applications in cancer angiogenesis and metastasis research. Taken together, our review underlines the vast potential of vascularized organoids to improve the understanding of organ development, while also proposing exciting avenues of organoid-on-a-chip and disease modeling.
血管化器官组织,促进芯片上的长期器官生成
类器官已成为研究器官发育、疾病建模和药物发现的有力工具,因为它们能够在三维体外模型中模拟器官的体内结构和功能。在体内器官成熟过程中,血管化过程对于向细胞提供营养和氧气以及随着器官体积增大而清除废物至关重要。类似地,类器官可以生长到大于毫米的尺寸,然而氧气和营养物质向中心的运输变得越来越困难,经常导致核心坏死的形成。在此,我们提供了一个简明的总结,最近的发展方法,以启动和维持类器官血管化。一般来说,类器官的血管化主要通过两种方式实现:生成含有内皮细胞的类器官或利用血管生长因子的分泌来促进血管化。生长因子通过化学信号调节血管形成,导致细胞间的粘附变化,最终导致内皮细胞的迁移。此外,具有可灌注系统的模型表明,通过生长因子和细胞的应用,基于血管化的类器官中的血管网络可以将生物物质输送到类器官的内部,为体外长期培养类器官开辟了新的可能性。这一目标正在通过生物工程工具的发展来实现,例如芯片上的血管化类器官,目前正在各种器官系统中进行测试,包括肺、脑、肾和肿瘤,并应用于癌症血管生成和转移研究。综上所述,我们的综述强调了血管化类器官的巨大潜力,以提高对器官发育的理解,同时也提出了令人兴奋的类器官芯片和疾病建模的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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