Vanadate Inhibits Dexamethasone-Induced Apoptosis of Rat Bone Marrow-Derived Mesenchymal Stem Cells

被引:3
|
作者
Fan, Qie [1 ]
Zhan, Xinli [1 ]
Li, Xiaofeng [2 ]
Zhao, Jinmin [2 ]
Chen, Yueping [3 ]
机构
[1] Guangxi Med Univ, Affiliated Hosp 1, Dept Spinal Surg, Nanning 530021, Guangxi, Peoples R China
[2] Guangxi Med Univ, Affiliated Hosp 1, Dept Traumat Orthoped & Hand Surg, Nanning 530021, Guangxi, Peoples R China
[3] Affiliated Rui Kang Hosp, Guangxi Tradit Chinese Med Sch, Dept Orthoped, Nanning, Guangxi, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
vanadate; glucocorticoid; caspase; BM-MSCs; apoptosis; GLUCOCORTICOID-INDUCED OSTEOPOROSIS; STROMAL CELLS; IN-VITRO; PHOSPHATASE INHIBITORS; GENE-EXPRESSION; PROLIFERATION; DIFFERENTIATION; OSTEOBLASTS; ORTHOVANADATE; KINASE;
D O I
暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Apoptosis of bone marrow-derived mesenchymal stem cells (BM-MSCs) has been shown to contribute to the development of osteoporosis, which is often the result of long-term use of glucocorticoid drugs such as dexamethasone (Dex). However, it remains unknown whether Dex induces apoptosis of BM-MSCs, and whether a chemical agent like vanadate can block such effects. To investigate these two issues, we isolated BM-MSCs from SD rats and treated the cells with different doses of Dex. We found that Dex induced apoptosis in dose-and time-dependent manners. Pretreating BM-MSCs with vanadate prevented Dex-induced apoptosis. Furthermore, we found that expression of caspases (3, 8, and 9) increased in Dex-treated BM-MSC and was attenuated by vanadate pretreatment. These results not only demonstrate the role of vanadate in the inhibition of Dex-induced apoptosis of BM-MSCs, but also reveal the therapeutic potential of vanadate in glucocorticoid-mediated osteoporosis.
引用
收藏
页码:173 / 180
页数:8
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