微泡
间充质干细胞
脐带
细胞凋亡
体外
细胞生物学
顺铂
男科
生物
医学
癌症研究
免疫学
内科学
小RNA
化疗
遗传学
基因
作者
Li‐Ping Sun,Dong Li,Kun Song,Jianlu Wei,Shu Yao,Li Zhao,Xuantao Su,Xiuli Ju,Chao Lan,Xiaohui Deng,Beihua Kong,Li Li
标识
DOI:10.1038/s41598-017-02786-x
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI