Department of Oral Biology, Graduate School of Biomedical Sciences, Hiroshima University, Kasumi, Minami-ku, Hiroshima, Japan.
J Exp Zool B Mol Dev Evol. 2012 Jul;318(5):344-52. doi: 10.1002/jez.b.22451.
Medullary bone is formed reticularly in the bone marrow cavity of the long bones of female birds. Although this bone matrix contains fewer collagen fibers and more acid mucopolysaccharides than cortical bone, it is not clear that the expression pattern of osteoblast phenotypic genes during bone remodeling. Therefore, 17β-estradiol (E2)-treated male Japanese quails were used to examine the temporal expression patterns of osteoblast phenotypic genes, and to simultaneously confirm the morphological changes occurring in the bone marrow cavity during medullary bone formation and resorption. After E2 treatment, bone lining cells proliferated and developed into mature osteoblasts that had intense alkaline phosphatase (ALP) activity. These cells began to form medullary bone that contained acid mucopolysaccharides and tartrate-resistantacid phosphatase. Runt-related gene 2 (Runx2) mRNA was stably expressed throughout the process. The expression of both ALP and type I collagen mRNAs increased initially, and then rapidly decreased after day 7, while osteoclasts began to resorb medullary bone at day 5. The expression of bone matrix-related genes peaked at day 5, and suddenly decreased at day 7, except for osteopontin. Taken together with these results, the expression patterns of bone matrix-related genes during the later stages might be related to osteoclast activity. Additionally, the constant expression of Runx2 during bone formation and resorption suggested that osteoprogenitor cells always exist in the bone marrow cavity. Therefore, the expression patterns of these genes and the characteristics of bone matrix might extremely be related to the quick remodeling of medullary bone.
髓质骨在雌性鸟类长骨的骨髓腔中呈网状形成。尽管这种骨基质中的胶原纤维比皮质骨少,酸性黏多糖多,但尚不清楚在骨重建过程中成骨细胞表型基因的表达模式。因此,使用 17β-雌二醇(E2)处理雄性日本鹌鹑来检查成骨细胞表型基因的时间表达模式,并同时确认骨髓腔中在形成和吸收髓质骨过程中发生的形态变化。E2 处理后,衬里细胞增殖并发育成具有强烈碱性磷酸酶(ALP)活性的成熟成骨细胞。这些细胞开始形成含有酸性黏多糖和抗酒石酸酸性磷酸酶的髓质骨。Runt 相关基因 2(Runx2)mRNA 在整个过程中稳定表达。ALP 和 I 型胶原 mRNA 的表达最初增加,然后在第 7 天迅速减少,而破骨细胞在第 5 天开始吸收髓质骨。骨基质相关基因的表达在第 5 天达到峰值,然后在第 7 天突然下降,除了骨桥蛋白。综合这些结果,后期骨基质相关基因的表达模式可能与破骨细胞活性有关。此外,Runx2 在成骨和吸收过程中的持续表达表明成骨祖细胞始终存在于骨髓腔中。因此,这些基因的表达模式和骨基质的特征可能与髓质骨的快速重塑密切相关。