Blood Vessel Organoids for Development and Disease

被引:43
作者
Salewskij, Kirill [1 ,2 ,3 ]
Penninger, Josef M. [1 ,4 ]
机构
[1] Austrian Acad Sci, Inst Mol Biotechnol, Vienna, Austria
[2] Univ Vienna, Doctoral Sch, Vienna Bioctr PhD Program, Vienna, Austria
[3] Med Univ Vienna, Vienna, Austria
[4] Univ British Columbia, Life Sci Inst, Dept Med Genet, Vancouver, BC, Canada
关键词
blood-brain barrier; blood vessels; endothelial cell; extracellular matrix; organoids; vascular diseases; SMOOTH-MUSCLE-CELLS; ENDOTHELIAL-CELLS; NITRIC-OXIDE; BASEMENT-MEMBRANE; GUANYLATE-CYCLASE; PROGENITOR CELLS; SHEAR-STRESS; VEGF; DIFFERENTIATION; GROWTH;
D O I
10.1161/CIRCRESAHA.122.321768
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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.
引用
收藏
页码:498 / 510
页数:13
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