Kubota Tatsuya, Hasuike Akira, Tsukune Naoya, Ozawa Yasumasa, Yamamoto Takanobu, Min Seiko, Naito Masako, Sato Shuichi
Division of Applied Oral Sciences, Nihon University Graduate School of Dentistry, Tokyo, Japan.
Department of Periodontology, Nihon University School of Dentistry, Tokyo, Japan.
Eur J Oral Sci. 2018 Jun;126(3):206-213. doi: 10.1111/eos.12415. Epub 2018 Apr 20.
The effect of estrogen deficiency in bone augmentation, and the mechanisms by which estrogen deficiency impedes osteoblast differentiation and collagen matrix production, were examined. Twenty female Jcl:Wistar rats were divided into two groups: ovariectomized rats; and control rats. Guided bone augmentation was performed by positioning plastic caps in the calvarium of all animals at 8 wk after ovariectomy or sham surgery. Micro-computed tomography and histological sections were used to determine the amount of bone augmentation within the plastic caps. At 8 wk, there was statistically significantly less newly formed bone volume in ovariectomized rats. Immunohistological staining revealed the rare alignment of runt-related transcription factor 2-positive osteoblast-like cells and collagen I-positive bundle fibers in ovariectomized rats. In cell culture experiments, pre-osteoblast-like cells, MC3T3-E1, were treated with the estrogen receptor antagonist, fulvestrant. In treated cells, alkaline phosphatase activity remained high, whereas Alizarin Red staining was completely inhibited. Extracellular staining intensity of collagen I was decreased after fulvestrant treatment. Consistent with these observations, gene-expression analysis confirmed that fulvestrant treatment led to weaker expression of mRNA for osteogenic transcription factors and bone matrix protein-related genes. The results demonstrate that estrogen deficiency suppresses osteoblast differentiation and collagen matrix production in bone augmentation.
研究了雌激素缺乏对骨增量的影响,以及雌激素缺乏阻碍成骨细胞分化和胶原基质产生的机制。将20只雌性Jcl:Wistar大鼠分为两组:去卵巢大鼠;和对照大鼠。在去卵巢或假手术后8周,通过在所有动物的颅骨中放置塑料帽进行引导性骨增量。使用微型计算机断层扫描和组织学切片来确定塑料帽内的骨增量。在8周时,去卵巢大鼠中新形成的骨体积在统计学上显著减少。免疫组织化学染色显示,去卵巢大鼠中与矮小相关转录因子2阳性的成骨细胞样细胞和I型胶原阳性束状纤维排列稀少。在细胞培养实验中,前成骨细胞样细胞MC3T3-E1用雌激素受体拮抗剂氟维司群处理。在处理过的细胞中,碱性磷酸酶活性仍然很高,而茜素红染色被完全抑制。氟维司群处理后I型胶原的细胞外染色强度降低。与这些观察结果一致,基因表达分析证实,氟维司群处理导致成骨转录因子和骨基质蛋白相关基因的mRNA表达减弱。结果表明,雌激素缺乏会抑制骨增量过程中的成骨细胞分化和胶原基质产生。