An Seo-Young, Lee Ye-Ji, Neupane Sanjiv, Jun Jong-Hwa, Kim Ji-Youn, Lee Youngkyun, Choi Karp-Shik, An Chang-Hyeon, Suh Jo-Young, Shin Hong-In, Sohn Wern-Joo, Kim Jae-Young
Department of Oral and Maxillofacial Radiology, School of Dentistry, IHBR, Kyungpook National University, Daegu, Korea.
Department of Biochemistry, School of Dentistry, IHBR, Kyungpook National University, 2177 Dalgubeol-daero, Joong-gu, Daegu, 41940, Korea.
Histochem Cell Biol. 2017 Oct;148(4):435-443. doi: 10.1007/s00418-017-1584-2. Epub 2017 Jun 13.
The alveolar bone process is the thickened ridge of bone that bears the teeth and is known to have dynamic functional interactions with surrounding tissues. However, the detailed morphological changes that occur during alveolar bone process development and the underlying molecular mechanisms behind this morphogenesis have not been elucidated. In this study, we examined the detailed morphological changes of the alveolar bone process during mouse development using HE and MTC staining. In addition, we evaluated the precise localization pattern of various signaling molecules involved in blood vessel formation including CD31, α-SMA, VEGF, periostin, and TGF-β. Innervation of the alveolar bone process was examined following injection of the nerve terminal dye AM1-43. The morphological and immunohistochemical data suggested that there is an intimate relationship between alveolar bone process development and blood vessel formation. To more closely examine the role of blood vessels in alveolar bone process formation, we microinjected mice with a clinically available anti-VEGF antibody, bevacizumab, at PN5 and analyzed the effects 5 days later. Compared to the control animals, anti-VEGF treated animals showed a disruption of the integration of bony tissues to form the alveolar bone process structures, which should contain the periodontal ligaments. Based on these data, we conclude that specific morphogenesis of the alveolar bone process is closely associated with blood vessel formation.
牙槽骨突是承载牙齿的增厚骨嵴,已知其与周围组织存在动态功能相互作用。然而,牙槽骨突发育过程中发生的详细形态变化以及这种形态发生背后的潜在分子机制尚未阐明。在本研究中,我们使用苏木精-伊红(HE)染色和甲苯胺蓝染色(MTC)检查了小鼠发育过程中牙槽骨突的详细形态变化。此外,我们评估了参与血管形成的各种信号分子的精确定位模式,包括CD31、α-平滑肌肌动蛋白(α-SMA)、血管内皮生长因子(VEGF)、骨膜蛋白和转化生长因子-β(TGF-β)。在注射神经末梢染料AM1-43后检查牙槽骨突的神经支配情况。形态学和免疫组织化学数据表明,牙槽骨突发育与血管形成之间存在密切关系。为了更深入地研究血管在牙槽骨突形成中的作用,我们在出生后第5天(PN5)给小鼠微量注射临床上可用的抗VEGF抗体贝伐单抗,并在5天后分析其效果。与对照动物相比,抗VEGF治疗的动物显示出骨组织整合形成牙槽骨突结构(其中应包含牙周韧带)受到破坏。基于这些数据,我们得出结论,牙槽骨突的特定形态发生与血管形成密切相关。