类有机物
血管生成
血管生成
血管
再生医学
生物
胚胎干细胞
神经科学
个性化医疗
表观基因组
疾病
干细胞
医学
病理
生物信息学
计算生物学
细胞生物学
祖细胞
癌症研究
内分泌学
生物化学
基因表达
基因
DNA甲基化
作者
Kirill Salewskij,Josef Penninger
出处
期刊:Circulation Research
[Ovid Technologies (Wolters Kluwer)]
日期:2023-02-16
卷期号:132 (4): 498-510
被引量:26
标识
DOI:10.1161/circresaha.122.321768
摘要
Despite enormous advances, cardiovascular disorders are still a major threat to global health and are responsible for one-third of deaths worldwide. Research for new therapeutics and the investigation of their effects on vascular parameters is often limited by species-specific pathways and a lack of high-throughput methods. The complex 3-dimensional environment of blood vessels, intricate cellular crosstalks, and organ-specific architectures further complicate the quest for a faithful human in vitro model. The development of novel organoid models of various tissues such as brain, gut, and kidney signified a leap for the field of personalized medicine and disease research. By utilizing either embryonic- or patient-derived stem cells, different developmental and pathological mechanisms can be modeled and investigated in a controlled in vitro environment. We have recently developed self-organizing human capillary blood vessel organoids that recapitulate key processes of vasculogenesis, angiogenesis, and diabetic vasculopathy. Since then, this organoid system has been utilized as a model for other disease processes, refined, and adapted for organ specificity. In this review, we will discuss novel and alternative approaches to blood vessel engineering and explore the cellular identity of engineered blood vessels in comparison to in vivo vasculature. Future perspectives and the therapeutic potential of blood vessel organoids will be discussed.
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