Sato Rei, Fukuoka Hiroki, Yokohama-Tamaki Tamaki, Kaku Masaru, Shibata Shunichi
Maxillofacial Anatomy, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo-Ku, Tokyo, 113-8549, Japan.
Maxillofacial Orthognatics, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Anat Sci Int. 2016 Mar;91(2):196-206. doi: 10.1007/s12565-015-0285-y. Epub 2015 May 9.
We investigated the immunohistochemical localization of tenascin-C in 8-week-old rat periodontal ligaments. Tenascin-C immunoreactivity was detected in zones along with cementum and alveolar bone, and more intensely on the resorption surface of alveolar bone than on the formation surface. On the resorbing surface, tenascin-C immunoreactivity was detected in Howship's lacunae without osteoclasts, and in the interfibrous space of the periodontal ligaments, indicating that this molecule works as an adhesion molecule between bone and fibers of periodontal ligaments. Upon experimental tooth movement by inserting elastic bands (Waldo method), the physiological resorption surface of alveolar bone under compressive force showed enhanced bone resorption and enhanced tenascin-C immunoreactivity. However, on the physiological bone formation surface under compressive force, bone resorption was seen only occasionally, and no enhanced tenascin-C immunoreactivity was noted. In an experiment involving excessive occlusal loading to rat molars, transient bone resorption occurred within interradicular septa, but no enhanced tenascin-C immunoreactivity was seen in the periodontal ligaments. These results indicate that tenascin-C works effectively on the bone resorbing surface of physiological alveolar bone remodeling sites, rather than on the non-physiological transient bone resorbing surface. Fibronectin immunoreactivity was distributed evenly in the periodontal ligaments under experimental conditions. Co-localization of tenascin-C and fibronectin immunoreactivity was observed in many regions, but mutually exclusive expression patterns were also seen in some regions, indicating that fibronectin might not be directly involved in alveolar bone remodeling, but may play a role via interaction with tenascin-C.
我们研究了8周龄大鼠牙周韧带中肌腱蛋白-C的免疫组织化学定位。在与牙骨质和牙槽骨相邻的区域检测到肌腱蛋白-C免疫反应性,且在牙槽骨的吸收表面比形成表面更强烈。在吸收表面,在没有破骨细胞的Howship陷窝以及牙周韧带的纤维间隙中检测到肌腱蛋白-C免疫反应性,表明该分子作为骨与牙周韧带纤维之间的粘附分子发挥作用。通过插入弹性带(Waldo法)进行实验性牙齿移动时,受压下牙槽骨的生理性吸收表面显示出骨吸收增强和肌腱蛋白-C免疫反应性增强。然而,在受压下的生理性骨形成表面,仅偶尔可见骨吸收,且未观察到肌腱蛋白-C免疫反应性增强。在一项对大鼠磨牙施加过度咬合负荷的实验中,根间间隔内出现短暂性骨吸收,但在牙周韧带中未观察到肌腱蛋白-C免疫反应性增强。这些结果表明,肌腱蛋白-C在生理性牙槽骨重塑部位的骨吸收表面有效发挥作用,而非在非生理性短暂性骨吸收表面。在实验条件下,纤连蛋白免疫反应性在牙周韧带中均匀分布。在许多区域观察到肌腱蛋白-C和纤连蛋白免疫反应性的共定位,但在一些区域也观察到相互排斥的表达模式,表明纤连蛋白可能不直接参与牙槽骨重塑,但可能通过与肌腱蛋白-C相互作用发挥作用。