恒河猴
诱导多能干细胞
干细胞
猕猴
生物
细胞生物学
免疫学
神经科学
胚胎干细胞
遗传学
基因
作者
Jue Zhang,Diana M. Tabima,David Vereide,Weifeng Zeng,Nicholas J. Albano,Sarah Lyon,Peter J. Nicksic,Ellen C. Shaffrey,Robert E. George,Mitchell D. Probasco,Elizabeth Perrin,Yiyang Xu,Matthew E. Brown,Ron Stewart,Naomi C. Chesler,Lih-Sheng Turng,Samuel O. Poore,Igor I. Slukvin,James A. Thomson,John P. Maufort
标识
DOI:10.1016/j.xcrm.2025.102002
摘要
Autologous vascular grafts, the only clinically approved option for small-diameter (<6 mm) revascularizations, require invasive harvesting and have limited availability and variable quality. To address these challenges, we develop a 3-mm-diameter artery graft by using arterial endothelial cells (AECs) derived from pluripotent stem cells (PSCs). After establishing technologies for pure AEC generation and expanded polytetrafluoroethylene (ePTFE) graft coating, we engineer artery grafts by seeding the inner lumen of ePTFE vascular grafts with either major histocompatibility complex (MHC) mismatched unmodified-wild-type (MHC-WT) AECs or MHC class I/II double knockout (MHC-DKO) AECs. Their function is evaluated in a rhesus arterial interposition grafting model. MHC-WT grafts maintained 100% patency for 6 months, significantly better than naked and MHC-DKO grafts. Additionally, the endothelium of MHC-WT grafts is repopulated with host cells, supporting long-term patency. Collectively, our study demonstrates that PSC-derived MHC-WT artery grafts provide an unlimited homogenous resource for allogeneic arterial revascularization.
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