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Human umbilical cord mesenchymal stem cell-derived exosomes protect renal tubular epithelial cells against tunicamycin-induced apoptosis

Authors :
Lei Yan, Zhan Shihuai, Shi Xiaohua, Yang Lan, Wang Jiawei, Wang Shuiliang, Zhang Shenghang
Source :
Xin yixue, Vol 54, Iss 6, Pp 397-402 (2023)
Publication Year :
2023
Publisher :
Editorial Office of Journal of New Medicine, 2023.

Abstract

Objective To investigate the role of human umbilical cord mesenchymal stem cell-derived exosomes (hUC-MSC-Exo) in the tunicamycin-induced apoptosis of renal tubular epithelial cells (HKC). Methods Endoplasmic reticulum stress (ERS) was induced by tunicamycin in HKC cells. Cell proliferation was detected by CCK-8 assay. The expression levels of ERS-related proteins of glucose-regulated protein 78 (GRP78),GRP94 and C/EBP homologous protein (CHOP) were determined by Western blot. Cell apoptosis was assessed by flow cytometry. hUC-MSC-Exo were isolated and identified by flow cytometry. The effects of different concentrations of hUC-MSC-Exo (0,40,60,80,100,150 and 200 μg/mL) upon cell activity were evaluated. Cell proliferation and apoptosis after co-treatment with hUC-MSC-Exo and tunicamycin were assessed by resazurin assay and flow cytometry. Results Treatment with 1,2 and 4 μg/mL tunicamycin could inhibit the proliferation of HKC in a concentration-dependent manner. Different concentrations of tunicamycin could induce ERS and cell apoptosis in HKC. Treatment with 100,150 and 200 μg/mL hUC-MSC-Exo could enhance cell proliferation. Compared with the 2 μg/mL tunicamycin group,cell proliferation was significantly increased in the 2 μg/mL tunicamycin and 150 μg/mL hUC-MSC-Exo co-treatment group (P < 0.05). The apoptosis rate in the 2 μg/mL tunicamycin group was (14.16±1.58)%,and (8.18±0.58)% in the 2 μg/mL tunicamycin and 150 μg/mL hUC-MSC-Exo co-treatment group,and the difference was statistically significant (P

Details

Language :
Chinese
ISSN :
02539802
Volume :
54
Issue :
6
Database :
Directory of Open Access Journals
Journal :
Xin yixue
Publication Type :
Academic Journal
Accession number :
edsdoj.8d2bb467b759479ba9de23b51ecae3ac
Document Type :
article
Full Text :
https://doi.org/10.3969/j.issn.0253-9802.2023.06.005