去卵巢大鼠
运行x2
间充质干细胞
骨钙素
内分泌学
内科学
碱性磷酸酶
破骨细胞
骨吸收
骨髓
化学
骨质疏松症
生物
细胞生物学
医学
激素
生物化学
受体
酶
作者
Chuang Huang,Rui Ling,Feijiang Li,E.-M. Li,QI-KE HUANG,BAO-GANG LIU,Yin Ding,Si–Wei You
标识
DOI:10.3892/mmr.2016.5342
摘要
Sphingosine-1-phosphate and its structural analog FTY720 (fingolimod) are important in the inhibition of osteoclast differentiation and bone resorption, however, it remains unknown whether they enhance osteogenic differentiation of the bone marrow mesenchymal stem cells (BM‑MSCs). The present study investigated the effect of FTY720 on the osteogenic differentiation of BM‑MSCs from the femurs of the ovariectomized (OVX) rats. Three different concentrations (1, 10 and 100 nM) of FTY720 were demonstrated to markedly upregulate mRNA expression levels of Runt‑related transcription factor 2 (Runx2) and Sp7 transcription factor (Sp7) at 2 weeks, and alkaline phosphatase (ALP) at 3 weeks. The osteocalcin (OCN) expression was similar at weeks 2 and 3. The protein expression levels of Runx2, Sp7, OCN and ALP induced by three different concentrations of FTY720 were higher than those in the control groups at 3 weeks in the OVX and sham groups. The findings of the current study suggested a beneficial effect of FTY720 on bone formation in OVX rats, and provided a potential therapeutic method of FTY720 to prevent alveolar bone resorption in patients with post‑menopausal osteoporosis.
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