Extracellular vesicles from three dimensional culture of human placental mesenchymal stem cells ameliorated renal ischemia/reperfusion injury

间充质干细胞 肾缺血 肌酐 再灌注损伤 细胞凋亡 细胞培养 急性肾损伤 医学 器官培养 肾功能 炎症 肾 缺血 生物 男科 病理 体外 免疫学 内科学 生物化学 遗传学
作者
Xuefeng Zhang,Nan Wang,Yuhua Huang,Yan Li,Gang� Li,Yuxin Lin,Anthony Atala,Jianquan Hou,Weixin Zhao
出处
期刊:International Journal of Artificial Organs [SAGE Publishing]
卷期号:45 (2): 181-192 被引量:35
标识
DOI:10.1177/0391398820986809
摘要

Three-dimensional (3D) culture has been reported to increase the therapeutic potential of mesenchymal stem cells (MSCs). The present study assessed the therapeutic efficacy of extracellular vesicles (EVs) from 3D cultures of human placental MSCs (hPMSCs) for acute kidney injury (AKI).The supernatants from monolayer culture (2D) and 3D culture of hPMSCs were ultra-centrifuged for EVs isolation. C57BL/6 male mice were submitted to 45 min bilateral ischemia of kidney, followed by renal intra-capsular administration of EVs within a 72 h reperfusion period. Histological, immunohistochemical, and ELISA analyses of kidney samples were performed to evaluate cell death and inflammation. Kidney function was evaluated by measuring serum creatinine and urea nitrogen. The miRNA expression profiles of EVs from 2D and 3D culture of hPMSCs were evaluated using miRNA microarray analysis.The 3D culture of hPMSCs formed spheroids with different diameters depending on the cell density seeded. The hPMSCs produced significantly more EVs in 3D culture than in 2D culture. More importantly, injection of EVs from 3D culture of hPMSCs into mouse kidney with ischemia-reperfusion (I/R)-AKI was more beneficial in protecting from progression of I/R than those from 2D culture. The EVs from 3D culture of hPMSCs were more efficient against apoptosis and inflammation than those from 2D culture, which resulted in a reduction in tissue damage and amelioration of renal function. MicroRNA profiling analysis revealed that a set of microRNAs were significantly changed in EVs from 3D culture of hPMSCs, especially miR-93-5p.The EVs from 3D culture of hPMSCs have therapeutic potential for I/R-AKI.
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