Department of Prosthodontics and Periodontics, Division of Periodontics, Piracicaba Dental School, State University of Campinas, São Paulo, Brazil.
Division of Biosciences, College of Dentistry, The Ohio State University, Columbus, OH.
J Periodontol. 2021 Nov;92(11):116-127. doi: 10.1002/JPER.21-0119. Epub 2021 Jun 9.
Cellular cementum, a mineralized tissue covering apical tooth roots, grows by apposition to maintain the tooth in its occlusal position. We hypothesized that resident cementocytes would show morphological changes in response to cementum apposition, possibly implicating a role in cementum biology.
Mandibular first molars were induced to super-erupt (EIA) by extraction of maxillary molars, promoting rapid new cementum formation. Tissue and cell responses were analyzed at 6 and/or 21 days post-procedure (dpp).
High-resolution micro-computed tomography (micro-CT) and confocal laser scanning microscopy showed increased cellular cementum by 21 dpp. Transmission electron microscopy (TEM) revealed that cementocytes under EIA were 50% larger than control cells, supported by larger pore sizes detected by micro-CT. Cementocytes under EIA displayed ultrastructural changes consistent with increased activity, including increased cytoplasm and nuclear size. We applied EIA to Hyp mutant mice, where cementocytes have perilacunar hypomineralization defects, to test cell and tissue responses in an altered mechanoresponsive milieu. Hyp and WT molars displayed similar super-eruption, with Hyp molars exhibiting 28% increased cellular cementum area versus 22% in WT mice at 21 dpp. Compared to control, Hyp cementocytes featured well-defined, disperse euchromatin and a thick layer of peripherally condensed heterochromatin in nuclei, indicating cellular activity. Immunohistochemistry (IHC) for cementum markers revealed intense dentin matrix protein-1 expression and abnormal osteopontin deposition in Hyp mice. Both WT and Hyp cementocytes expressed gap junction protein, connexin 43.
This study provides new insights into the EIA model and cementocyte activity in association with new cementum formation.
覆盖牙根部的矿化组织细胞牙骨质,通过形成新的牙骨质来维持牙齿的咬合位置。我们假设固有牙骨质细胞在牙骨质形成过程中会发生形态变化,这可能暗示着它们在牙骨质生物学中的作用。
通过拔除上颌磨牙来诱导下颌第一磨牙过度萌出(EIA),以促进快速形成新的牙骨质。在术后 6 天和/或 21 天(dpp)分析组织和细胞反应。
高分辨率微计算机断层扫描(micro-CT)和共聚焦激光扫描显微镜显示,21 dpp 时细胞牙骨质增加。透射电子显微镜(TEM)显示,EIA 下的牙骨质细胞比对照细胞大 50%,这与 micro-CT 检测到的较大的孔尺寸相符。EIA 下的牙骨质细胞表现出与活性增加一致的超微结构变化,包括细胞质和核大小增加。我们将 EIA 应用于 Hyp 突变小鼠中,这些小鼠的牙骨质细胞在牙骨质陷窝周围存在矿化缺陷,以测试在改变的机械反应环境中细胞和组织的反应。Hyp 和 WT 磨牙表现出相似的过度萌出,与 WT 小鼠相比,Hyp 磨牙在 21 dpp 时细胞牙骨质面积增加 28%,而 WT 小鼠增加 22%。与对照相比,Hyp 牙骨质细胞的常染色质边界清晰,弥散,核内异染色质层厚,表明细胞活性。牙骨质标志物的免疫组织化学(IHC)显示 Hyp 小鼠中牙本质基质蛋白 1 表达强烈,骨桥蛋白异常沉积。WT 和 Hyp 牙骨质细胞均表达缝隙连接蛋白,连接蛋白 43。
本研究为 EIA 模型和与新牙骨质形成相关的牙骨质细胞活性提供了新的见解。