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