Chen Fang-Ping, Hsu Todd, Hu Chin-Hwa, Wang Wen-Der, Wang Kun-Chuang, Teng Li-Fen
Department of Obstetrics and Gynecology, Keelung Chang Gung Memorial Hospital and Chang Gung University, Keelung, Taiwan.
Taiwan J Obstet Gynecol. 2006 Dec;45(4):307-12. doi: 10.1016/S1028-4559(09)60248-5.
To evaluate the expression of estrogen receptors (ER) alpha and beta, and activity of alkaline phosphatase during differentiation of primary osteoblast cells (hOB) from aged postmenopausal women and human osteosarcoma cell lines (HOS, MG63).
Osteoblast cultures were prepared from the upper femur of postmenopausal patients (age, 60-74 years) and HOS. At the indicated times (days 5, 10, 15, 20, and 25), alkaline phosphatase activity and expression of ERalpha and ERbeta mRNA were evaluated.
In both cultures of primary hOB and HOS, alkaline phosphatase activity decreased at the osteoblast proliferation stage, whereas it subsequently increased at the matrix maturation stage. ER beta mRNA was strongly expressed in HOS on day 15 and remained at high levels of transcription through to day 25 (matrix maturation phase), whereas ERalpha mRNA was barely detectable during osteoblast differentiation. In hOB, transcription of ERalpha mRNA was much stronger than that of ERbeta mRNA.
The presence of ERalpha and ERbeta mRNA in osteoblasts supports the involvement of estrogen in human bone formation. The developmental expression of alkaline phosphatase was not correlated to ER mRNA expression during osteoblast differentiation. ER isoforms may have different functions or interact with each other during osteoblast differentiation. Since the expression of ER isoforms is different between postmenopausal women and osteosarcoma cell lines, characteristics of osteosarcoma cell lines may not be suitable as a model for the evaluation of estrogen effects on postmenopausal osteoporosis.
评估绝经后老年女性原代成骨细胞(hOB)和人骨肉瘤细胞系(HOS、MG63)分化过程中雌激素受体(ER)α和β的表达以及碱性磷酸酶的活性。
从绝经后患者(年龄60 - 74岁)的股骨上段和HOS制备成骨细胞培养物。在指定时间(第5、10、15、20和25天),评估碱性磷酸酶活性以及ERα和ERβ mRNA的表达。
在原代hOB和HOS的两种培养物中,碱性磷酸酶活性在成骨细胞增殖阶段降低,而在基质成熟阶段随后升高。ERβ mRNA在第15天在HOS中强烈表达,并一直保持高水平转录直至第25天(基质成熟阶段),而在成骨细胞分化过程中ERα mRNA几乎检测不到。在hOB中,ERα mRNA的转录比ERβ mRNA强得多。
成骨细胞中ERα和ERβ mRNA的存在支持雌激素参与人类骨形成。在成骨细胞分化过程中,碱性磷酸酶的发育表达与ER mRNA表达不相关。ER亚型在成骨细胞分化过程中可能具有不同功能或相互作用。由于绝经后女性和骨肉瘤细胞系中ER亚型的表达不同,骨肉瘤细胞系的特征可能不适合作为评估雌激素对绝经后骨质疏松症影响的模型。