Wang Jie, Zhang Wenwen, Yu Chunxiao, Zhang Xu, Zhang Haiqing, Guan Qingbo, Zhao Jiajun, Xu Jin
Department of Endocrinology, Affiliated Hospital of Weifang Medical University, Weifang, Shandong Province, China.
Department of Endocrinology, Shandong Provincial Hospital affiliated to Shandong University, Jinan, Shandong Province, China; Shandong Clinical Medical Center of Endocrinology and Metabolism, Jinan, Shandong Province, China; Institute of Endocrinology and Metabolism, Shandong Academy of Clinical Medicine, Jinan, Shandong Province, China.
PLoS One. 2015 Aug 4;10(8):e0134986. doi: 10.1371/journal.pone.0134986. eCollection 2015.
The objectives of this study were to observe the changes in follicle-stimulating hormone (FSH) and bone mineral density (BMD) in postmenopausal women, to research the relationship between FSH and postmenopausal osteoporosis, and to observe the effects of FSH on osteoclast differentiation in RAW264.7 cells.
We analyzed 248 postmenopausal women with normal bone metabolism. A radioimmunoassay (RIA) was used to detect serum FSH, luteinizing hormone (LH), and estradiol (E2). Dual-energy X-ray absorptiometry was used to measure forearm BMD. Then, we analyzed the age-related changes in serum FSH, LH and E2. Additionally, FSH serum concentrations were compared between a group of postmenopausal women with osteoporosis and a control group. Osteoclasts were induced from RAW264.7 cells in vitro by receptor activator of nuclear factor kappa B ligand (RANKL), and these cells were treated with 0, 5, 10, and 20 ng/ml FSH. After the osteoclasts matured, tartrate-resistant acid phosphatase (TRAP) staining was used to identify osteoclasts, and the mRNA expression levels of genes involved in osteoclastic phenotypes and function, such as receptor activator of NF-κB (Rank), Trap, matrix metalloproteinase-9 (Mmp-9) and Cathepsin K, were detected in different groups using real-time PCR (polymerase chain reaction).
The circulating concentration of FSH may play an important role in the acceleration of bone loss in postmenopausal women. FSH increases osteoclastogenesis in vitro.
本研究旨在观察绝经后女性促卵泡生成素(FSH)和骨密度(BMD)的变化,研究FSH与绝经后骨质疏松症之间的关系,并观察FSH对RAW264.7细胞中破骨细胞分化的影响。
我们分析了248名骨代谢正常的绝经后女性。采用放射免疫分析法(RIA)检测血清FSH、黄体生成素(LH)和雌二醇(E2)。使用双能X线吸收法测量前臂骨密度。然后,我们分析了血清FSH、LH和E2随年龄的变化。此外,比较了一组绝经后骨质疏松症女性和对照组的FSH血清浓度。通过核因子κB受体活化剂配体(RANKL)在体外诱导RAW264.7细胞形成破骨细胞,并用0、5、10和20 ng/ml的FSH处理这些细胞。破骨细胞成熟后,用抗酒石酸酸性磷酸酶(TRAP)染色鉴定破骨细胞,并使用实时聚合酶链反应(PCR)检测不同组中参与破骨细胞表型和功能的基因(如核因子κB受体活化剂(Rank)、TRAP、基质金属蛋白酶-9(Mmp-9)和组织蛋白酶K)的mRNA表达水平。
FSH的循环浓度可能在绝经后女性骨质流失加速过程中起重要作用。FSH在体外增加破骨细胞生成。