Leonardi Rosalia, Talic Nabeel F, Loreto Carla
Department of Surgery and Medicine, II Dental Unit, University of Catania, Via S. Sofia n.78, Policlinico Universitario, 95125 Catania, Italy.
Acta Histochem. 2007;109(3):215-20. doi: 10.1016/j.acthis.2007.01.002. Epub 2007 Mar 9.
Matrix metalloproteinases (MMPs) are enzymes that play a central role in periodontal ligament (PDL) space remodelling during orthodontic tooth movement. It has previously been shown that messenger RNA levels of MMP-13 increase significantly following the application of orthodontic forces. The aim of the present study was to examine immunolocalisation of MMP-13 and to evaluate if this collagenase is time-dependently and differentially detected within the PDL following the application of orthodontic forces to create areas of compression and tension. This was achieved by placing elastic bands between the maxillary first and second molars of 16 male Sprague-Dawley rats (each weighing 120-200g) for 12 and 24h. The molar-bearing segments were dissected and processed for histological and immunohistochemical examination. Binding of a monoclonal antibody was used to evaluate MMP-13 localization using an indirect streptavidin/biotin immunperoxidase technique. MMP-13 was found to be inducible at the protein level by the application of forces. The PDL and osteoblast-lineage cells showed a time-dependent increase in immunolabelling of MMP-13. Immunolabelling of MMP-13 was detected initially on the compression side, and then on both the compression and the tension sides. Since this increase in MMP-13 immunolabelling occurred very early following the application of an orthodontic force in both PDL and alveolar bone, this would indicate that MMP-13 might play an important role during tooth movement.
基质金属蛋白酶(MMPs)是在正畸牙齿移动过程中牙周膜(PDL)空间重塑中起核心作用的酶。先前已表明,施加正畸力后MMP - 13的信使核糖核酸水平显著增加。本研究的目的是检测MMP - 13的免疫定位,并评估在施加正畸力以产生压缩区和张力区后,这种胶原酶在PDL内是否随时间变化且有差异地被检测到。这是通过在16只雄性Sprague - Dawley大鼠(每只体重120 - 200g)的上颌第一和第二磨牙之间放置弹性带12小时和24小时来实现的。将含磨牙节段解剖并进行组织学和免疫组织化学检查。使用间接链霉亲和素/生物素免疫过氧化物酶技术,通过单克隆抗体的结合来评估MMP - 13的定位。发现通过施加力可在蛋白质水平诱导MMP - 13。PDL和成骨细胞系细胞显示出MMP - 13免疫标记的时间依赖性增加。MMP - 13的免疫标记最初在压缩侧被检测到,然后在压缩侧和张力侧均被检测到。由于在正畸力施加后,PDL和牙槽骨中MMP - 13免疫标记的这种增加很早就出现了,这表明MMP - 13可能在牙齿移动过程中起重要作用。