Nefussi J R, Casamajor P, Serfaty R, Bolle M, Hugly C, Forest N
Laboratoire de Biologie-Odontologie, Département de Chirurgie, Université Paris VII, France.
Eur J Oral Sci. 1998 Jan;106 Suppl 1:424-8. doi: 10.1111/j.1600-0722.1998.tb02209.x.
Activated adult human alveolar bone cells were isolated from 2-wk-old osteogenic tissue recuperated from dental implant surgeries following a two-step procedure. Osteogenic tissues were cultured as explant for 2 months. Cells began to migrate in the first 3 d and were confluent in 3-4 wk. However, adjacent to the explants, multicellular cell layers began to form in 10 d, and matrix mineralization was observed by 4 wk in these areas. These formations enlarged and by the end of the culture period, large diffuse matrix mineralization areas were observed. Light and electron microscopic observations confirmed the presence of a collagen matrix undergoing a mineralization process but showing important differences with the mineralized matrix tissue formed with a rat embryo calvaria bone cell system. This new model, using activated human alveolar bone cells, may provide a tool to investigate alveolar bone development and physiology and to set up new therapeutic approaches.
通过两步法从牙科植入手术中回收的2周龄成骨组织中分离出活化的成人人类牙槽骨细胞。将成骨组织作为外植体培养2个月。细胞在最初3天开始迁移,并在3至4周内汇合。然而,在外植体附近,多细胞层在10天开始形成,并且在这些区域4周时观察到基质矿化。这些结构不断扩大,到培养期结束时,观察到大面积的弥漫性基质矿化区域。光镜和电镜观察证实存在正在经历矿化过程的胶原基质,但与用大鼠胚胎颅骨骨细胞系统形成的矿化基质组织有重要差异。这种使用活化的人类牙槽骨细胞的新模型可能为研究牙槽骨发育和生理学以及建立新的治疗方法提供一种工具。