Vascularized organoids on a chip: strategies for engineering organoids with functional vasculature

被引:188
作者
Zhang, Shun [1 ]
Wan, Zhengpeng [1 ]
Kamm, Roger D. [1 ]
机构
[1] MIT, Dept Biol Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
关键词
IN-VITRO; STEM-CELLS; ENDOTHELIAL-CELLS; MICROVASCULAR NETWORKS; KIDNEY ORGANOIDS; MODEL; DIFFERENTIATION; MORPHOGENESIS; ANGIOGENESIS; MECHANISMS;
D O I
10.1039/d0lc01186j
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Human organoids, self-organized and differentiated from homogenous pluripotent stem cells (PSC), replicate the key structural and functional characteristics of their in vivo counterparts. Despite the rapid advancement of organoid technology and its diverse applications, major limitations in achieving truly in vivo like functionality have been the lack of matured structural organization and constraints on tissue size, both of which are direct consequences of lacking a functional vasculature. In the absence of perfusable vessels, a core region within organoids quickly becomes necrotic during development due to increased metabolic demands that cannot be met by diffusion alone. Thus, incorporating functional vasculature in organoid models is indispensable for their growth in excess of several hundred microns and maturaturation beyond the embryonic and fetal phase. Here, we review recent advancements in vascularizing organoids and engineering in vitro capillary beds, and further explore strategies to integrate them on a microfluidic based platform, aiming for establishing perfused vasculature throughout organoids in vitro.
引用
收藏
页码:473 / 488
页数:16
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