Chen Xi, Lin Weiping, Tortorella Micky Daniel
Cardiovascular Research Institute & Department of Physiology, Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California San Francisco, San Francisco, CA, USA.
Barts and The London School of Medicine and Dentistry, Queen Mary University, London, UK.
Am Heart J Plus. 2025 Mar 1;53:100520. doi: 10.1016/j.ahjo.2025.100520. eCollection 2025 May.
The development of vascularized organoids as novel modelling tools of the human cardio-cerebrovascular system for preclinical research has become an essential platform for studying human vascularized tissues/organs for development of personalized therapeutics during recent decades. Organ-on-chip technology is promising for investigating physiological in vitro responses in drug screening development and advanced disease models. Vascularized tissue/organ-on-a-chip benefits every step of drug discovery pipeline as a screening tool with close human genome relevance to investigate human systems biology. Simultaneously, cardio-cerebrovascular-on-chip-integrated microfluidic system serves as an alternative to preclinical animal research for studying (patho-)physiological processes of human blood vessels during embryonic development and cardio-cerebrovascular disease. Integrated with next-generation techniques, such as three-dimensional bioprinting of both cells and matrix, may enable vascularized organoid-on-chip-based novel drug development as personalized therapeutics.
近几十年来,血管化类器官作为用于临床前研究的新型人类心脑血管系统建模工具得到了发展,已成为研究人类血管化组织/器官以开发个性化疗法的重要平台。芯片器官技术有望用于药物筛选开发和先进疾病模型中的生理体外反应研究。作为一种与人类基因组密切相关的筛选工具,用于研究人类系统生物学,血管化组织/器官芯片有利于药物研发流程的每一步。同时,心脑血管芯片集成微流控系统可替代临床前动物研究,用于研究人类血管在胚胎发育和心脑血管疾病中的(病理)生理过程。与细胞和基质的三维生物打印等下一代技术相结合,可能实现基于芯片上血管化类器官的新型个性化药物开发。