间充质干细胞
细胞凋亡
膜联蛋白
脐带
流式细胞术
细胞内
免疫印迹
化学
药理学
男科
MTT法
细胞生物学
分子生物学
生物
免疫学
医学
生物化学
基因
作者
Xiaojuan Wei,Hongchao Zhang,Zi‐Kuan Guo,Haibin Zheng,Leilei Yang,Chaozhong Liu
出处
期刊:PubMed
日期:2015-10-01
卷期号:23 (5): 1422-6
被引量:2
标识
DOI:10.7534/j.issn.1009-2137.2015.05.038
摘要
To investigate the protection of silymarin against the human mesenchymal stem cell (MSC) apoptosis induced by serum deprivation and its underlying mechanism.Human umbilical cord MSCs were cultured in the absence of serum, and the silymain of different concentration (1-10 µg/ml) was added into the medium. MTT test was performed to observe the cell proliferation status. After being cultured for 72 hours, the cells were collected, and flow cytometry with Annexin-V-PI double-staining was used to detect the apoptotic cells from the control and silymarin-treated groups. Furthermore, the intracellular contents of BAX and BCL-2 were detected by Western blot for exploring the potential mechanism.The silymarin promoted the proliferation of human UC-MSCs in a dose-dependent manner, reaching its maximal at a dose of 5 µg/ml. Moreover, silymarin could inhibit the serum deprivation-induced apoptosis of MSCs and, the inhibitory rate reached up to 30% when it was added at a concentration of 5 µg/ml. The content of intracellular BAX was obviously elevated after serum-deprivation treatment, and this increase could be blunted by the addition of silymarin. Meanwhile, the content of BCL-2 was not obviously changed.The silymarin can stimulate MSC growth and inhibit the apoptosis of MSCs probably by the mitochondria pathway.
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