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

被引:26
|
作者
Zhang, Xuefeng [1 ]
Wang, Nan [1 ]
Huang, Yuhua [1 ]
Li, Yan [2 ]
Li, Gang [1 ]
Lin, Yuxin [1 ]
Atala, Anthony J. [3 ]
Hou, Jianquan [1 ]
Zhao, Weixin [3 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Dept Urol, 899 Pinghai St, Suzhou 215006, Peoples R China
[2] Soochow Univ, Childrens Hosp, Dept Infect Dis, Suzhou, Peoples R China
[3] Wake Forest Sch Med, Wake Forest Inst Regenerat Med, 391 Technol Way NE, Winston Salem, NC 27101 USA
来源
基金
中国国家自然科学基金;
关键词
Exosome; placental mesenchymal stem cells; three-dimensional culture; acute kidney injury; ischemia; reperfusion; STROMAL CELLS; MSCS; SPHEROIDS; OUTCOMES;
D O I
10.1177/0391398820986809
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Background: 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). Methods: 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. Results: 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. Conclusion: The EVs from 3D culture of hPMSCs have therapeutic potential for I/R-AKI.
引用
收藏
页码:181 / 192
页数:12
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