Exosomes derived from human umbilical cord mesenchymal stem cells protect against cisplatin-induced ovarian granulosa cell stress and apoptosis in vitro

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作者
Liping Sun
Dong Li
Kun Song
Jianlu Wei
Shu Yao
Zhao Li
Xuantao Su
Xiuli Ju
Lan Chao
Xiaohui Deng
Beihua Kong
Li Li
机构
[1] Shandong University,Department of obstetrics and gynecology, Qilu Hospital
[2] Shandong University,Cryomedicine Laboratory, Qilu Hospital
[3] Shandong University,Department of Orthopedics, Qilu Hospital
[4] Shandong University,Department of obstetrics and gynecology, Qianfoshan Hospital
[5] Shandong University,Institute of Biomedical Engineering, School of Control Science and Engineering
[6] Shandong University,Reproduction Medicine Center, Qilu Hospital
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Scientific Reports | / 7卷
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摘要
Human umbilical cord mesenchymal stem cells (huMSCs) can treat primary ovarian insufficiency (POI) related to ovarian granulosa cell (OGC) apoptosis caused by cisplatin chemotherapy. Exosomes are a class of membranous vesicles with diameters of 30–200 nm that are constitutively released by eukaryotic cells. Exosomes mediate local cell-to-cell communication by transferring microRNAs and proteins. In the present study, we demonstrated the effects of exosomes derived from huMSCs (huMSC-EXOs) on a cisplatin-induced OGC model in vitro and discussed the preliminary mechanisms involved in these effects. We successfully extracted huMSC-EXOs from huMSC culture supernatant and observed the effective uptake of exosomes by cells with fluorescent staining. Using flow cytometry (with annexin-V/PI labelling), we found that huMSC-EXOs increased the number of living cells. Western blotting showed that the expression of Bcl-2 and caspase-3 were upregulated, whilst the expression of Bax, cleaved caspase-3 and cleaved PARP were downregulated to protect OGCs. These results suggest that huMSC-EXOs can be used to prevent and treat chemotherapy-induced OGC apoptosis in vitro. Therefore, this work provides insight and further evidence of stem cell function and indicates that huMSC-EXOs protect OGCs from cisplatin-induced injury in vitro.
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