Wang Ziyi, Odagaki Naoya, Tanaka Tomoyo, Hashimoto Mana, Nakamura Masahiro, Hayano Satoru, Ishihara Yoshihito, Kawanabe Noriaki, Kamioka Hiroshi
Department of Orthodontics, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama, Japan.
Department of Orthodontics, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama, Japan.
Bone. 2016 Oct;91:20-9. doi: 10.1016/j.bone.2016.06.016. Epub 2016 Jun 29.
The intercellular network of cell-cell communication among osteocytes is mediated by gap junctions. Gap junctional intercellular communication (GJIC) is thought to play an important role in the integration and synchronization of bone remodeling. To further understand the mechanism of bone development it is important to quantify the difference in the GJIC capacity of young and developmentally mature osteocytes.
We first established an embryonic chick calvaria growth model to show the growth of the calvaria in embryos at 13 to 21days of age. We then applied a fluorescence recovery after photobleaching (FRAP) technique to compare the difference in the GJIC capacity of young osteocytes with that of developmentally mature osteocytes. Finally, we quantified the dye (Calcein) diffusion from the FRAP data using a mathematic model of simple diffusion which was also used to identify simple diffusion GJIC pattern cells (fitted model) and accelerated diffusion GJIC pattern cells (non-fitted model).
The relationship between the longest medial-lateral length of the calvaria (frontal bone) and the embryonic age fit a logarithmic growth model: length=5.144×ln(day)-11.340. The morphometric data during osteocyte differentiation showed that the cellular body becomes more spindle-shaped and that the cell body volume decreased by approximately 22% with an increase in the length of the processes between the cells. However, there were no significant differences in the cellular body surface area or in the distance between the mass centres of the cells. The dye-displacement rate in young osteocytes was significantly higher than that in developmentally mature osteocytes: dye displacement only occurred in 26.88% of the developmentally mature osteocytes, while it occurred in 64.38% of the young osteocytes. Additionally, in all recovered osteocytes, 36% of the developmentally mature osteocytes comprised non-fitted model cells while 53.19% of the young osteocytes were the non-fitted model, which indicates the active transduction of dye molecules. However, there were no statistically significant differences between the young and developmentally mature osteocytes with regard to the diffusion coefficient, permeability coefficient, or permeance of the osteocyte processes, which were 3.93±3.77 (×10(-8)cm(2)/s), 5.12±4.56 (×10(-5)cm(2)/s) and 2.99±2.47 (×10(-13)cm(2)/s) (mean±SD), respectively.
These experiments comprehensively quantified the GJIC capacity in the embryonic chick calvaria and indicated that the cell-cell communication capacity of the osteocytes in the embryonic chick calvaria was related to their development.
骨细胞间的细胞通讯网络由缝隙连接介导。缝隙连接细胞间通讯(GJIC)被认为在骨重塑的整合与同步中发挥重要作用。为进一步了解骨骼发育机制,量化年轻和发育成熟骨细胞的GJIC能力差异很重要。
我们首先建立了一个胚胎鸡颅骨生长模型,以展示13至21日龄胚胎颅骨的生长情况。然后应用光漂白后荧光恢复(FRAP)技术比较年轻骨细胞与发育成熟骨细胞的GJIC能力差异。最后,我们使用简单扩散数学模型从FRAP数据中量化染料(钙黄绿素)扩散情况,该模型还用于识别简单扩散GJIC模式细胞(拟合模型)和加速扩散GJIC模式细胞(非拟合模型)。
颅骨(额骨)最长内外侧长度与胚胎年龄的关系符合对数生长模型:长度 = 5.144×ln(天数) - 11.340。骨细胞分化过程中的形态计量学数据显示,细胞体变得更呈纺锤形,细胞体体积随着细胞间突起长度的增加而减少约22%。然而,细胞体表面积或细胞质心之间的距离没有显著差异。年轻骨细胞中的染料置换率显著高于发育成熟骨细胞:染料置换仅发生在26.88%的发育成熟骨细胞中,而发生在64.38%的年轻骨细胞中。此外,在所有恢复的骨细胞中,36%的发育成熟骨细胞为非拟合模型细胞,而53.19%的年轻骨细胞为非拟合模型,这表明染料分子的活跃转导。然而,年轻和发育成熟骨细胞在骨细胞突起的扩散系数(3.93±3.77(×10(-8)cm(2)/s))、渗透系数(5.12±4.56(×10(-5)cm(2)/s))或通透率(2.99±2.47(×10(-13)cm(2)/s))方面没有统计学显著差异(均值±标准差)。
这些实验全面量化了胚胎鸡颅骨中的GJIC能力,并表明胚胎鸡颅骨中骨细胞的细胞间通讯能力与其发育有关。