Kowalski William J, Vatti Shravani, Sakamoto Tyler, Li Wenling, Odutola Sarah Rose, Liu Chengyu, Chen Guibin, Boehm Manfred, Mukouyama Yoh-Suke
Laboratory of Stem Cell and Neuro-Vascular Biology, Cell and Developmental Biology Center, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Weill Cornell Graduate School of Medical Sciences, New York, NY, USA.
Sci Rep. 2025 Feb 28;15(1):7150. doi: 10.1038/s41598-025-91826-y.
The dynamic remodeling of the nascent vascular network into a mature hierarchy is essential for embryo survival. Cell behaviors and signaling mechanisms are often investigated with animal models and perfused microchannels, giving insights into this process. To support these studies and enrich our understanding, we demonstrate a complementary approach using vascular organoids. Organoids initially form a primitive endothelial plexus lined with NG2/PDGFRβ mural cell progenitors containing immature pericytes, but there is no formation of large-diameter vessels covered with αSMA cells containing immature vascular smooth muscle cells (vSMCs). After transplantation to the chick chorioallantoic membrane, the network reorganizes into a branched architecture with large-diameter vessels covered by αSMA cells. We additionally show that blood flow from the host circulation perfuses the organoid. Compared with the developing skin vasculature in mouse embryos, organoids successfully recapitulate vascular morphogenesis, both in vitro and after transplantation. The model described here presents a further approach to enhance the study of vascular remodeling.
新生血管网络动态重塑为成熟层级结构对胚胎存活至关重要。细胞行为和信号传导机制常通过动物模型和灌注微通道进行研究,从而深入了解这一过程。为支持这些研究并丰富我们的认识,我们展示了一种使用血管类器官的补充方法。类器官最初形成一个原始内皮丛,内衬含有未成熟周细胞的NG2/PDGFRβ壁细胞祖细胞,但没有形成覆盖有含有未成熟血管平滑肌细胞(vSMC)的αSMA细胞的大直径血管。移植到鸡胚尿囊膜后,网络重新组织成具有被αSMA细胞覆盖的大直径血管的分支结构。我们还表明,来自宿主循环的血流灌注类器官。与小鼠胚胎中发育的皮肤血管系统相比,类器官在体外和移植后都成功地重现了血管形态发生。这里描述的模型提供了一种进一步加强血管重塑研究的方法。