Mesenchymal Stem Cell-Derived Exosomes Attenuate Epithelial-Mesenchymal Transition of HK-2 Cells

被引:1
|
作者
Yin, Shuai [1 ]
Zhou, Shilin [2 ]
Ren, Dadui [2 ]
Zhang, Jing [2 ]
Xin, Hong [2 ]
He, Xiaozhou [1 ]
Gao, Hongjian [2 ]
Hou, Jiayun [3 ]
Zeng, Feng [2 ]
Lu, Yunjie [1 ]
Zhang, Xuemei [2 ]
Fan, Min [1 ]
机构
[1] Soochow Univ, Dept Urol, Affiliated Hosp 3, 185 Juqian St, Changzhou 213000, Jiangsu, Peoples R China
[2] Fudan Univ, Sch Pharm, Dept Pharmacol, 826 Zhangheng Rd, Shanghai 201203, Peoples R China
[3] Fudan Univ, Zhongshan Hosp, Inst Clin Sci, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
MSC; exosome; EMT; autophagy; ceria nanoparticles; MICROVESICLES; PROTECT; AUTOPHAGY; DYSFUNCTION; ACTIVATION; INJURY;
D O I
10.1089/ten.tea.2021.0190
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Renal fibrosis (RF) predisposes patients to an increased risk of progressive chronic kidney disease, and effective treatments remain elusive. Mesenchymal stem cell (MSC)-derived exosomes are considered a new treatment for tissue damage. Our study aimed to investigate the in vitro effects of bone marrow MSC-derived exosomes (BM-MSC-Exs) on transforming growth factor-beta 1 (TGF-beta 1)-induced fibrosis in renal tubular epithelial cells (HK-2 cells) and the associated mechanisms. Herein, we found BM-MSC-Exs could inhibit TGF-beta 1-induced epithelial-mesenchymal transition (EMT) in HK-2 cells, and may involve autophagy activation of BM-MSC-Exs. Moreover, we first reported that after ceria nanoparticles (CeNPs) treatment, the improvements induced by BM-MSC-Ex on EMT were significantly enhanced by upregulating the expression of Nedd4Lof MSCs and promoting the secretion of exosomes, which contained Nedd4L. In addition, Nedd4L could activate autophagy in HK-2 cells. In conclusion, BM-MSC-Ex prevents the TGF-beta 1-induced EMT of renal tubular epithelial cells by transporting Nedd4L, which activates autophagy. The results of this in vitro experiment may extend to RF, whereby BM-MSC-Ex may also be used as a novel treatment for improving RF. Impact statementRenal fibrosis (RF) is an important pathological change in chronic kidney disease that ultimately leads to end-stage renal failure, and effective treatments remain elusive. In this study, there are two contributions. First, our results suggest that bone marrow mesenchymal stem cell-derived exosomes (BM-MSC-Exs) can prevent transforming growth factor-beta 1 (TGF-beta 1)-induced epithelial-mesenchymal transition (EMT) of renal tubular epithelial cells through Nedd4L trafficking, which activates autophagy. Second, the improvement effects of BM-MSC-Ex on TGF-beta 1-induced HK-2 EMT can be enhanced by ceria nanoparticles (CeNPs). The findings in this study may be extended to RF: BM-MSC-Exs may be used as a novel treatment to improve RF.
引用
收藏
页码:651 / 659
页数:9
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