Department of Biomedical Sciences, Baylor College of Dentistry, Texas A&M Health Science Center, Dallas, TX, USA.
J Periodontal Res. 2013 Apr;48(2):221-7. doi: 10.1111/j.1600-0765.2012.01523.x. Epub 2012 Aug 31.
Dentin sialophosphoprotein (DSPP) and its cleaved products, dentin phosphoprotein (DPP) and dentin sialoprotein (DSP), play important roles in biomineralization. Recently, we observed that DSPP is highly expressed in the alveolar bone and cementum, indicating that this molecule may play an important role in the formation and maintenance of a healthy periodontium, and its deletion may cause increased susceptibility to periodontal diseases. The objective of this investigation was to study the effects of Dspp ablation on periodontal tissues by analyzing Dspp null mice.
Newborn to 6-mo-old Dspp null mice were examined, and the 3- and 6-mo-old Dspp null mice were characterized in detail using X-ray radiography, histology and scanning electron microscopy (backscattered as well as resin-infiltrating). Wild-type mice of the same age groups served as the normal controls.
The Dspp null mice showed significant loss of alveolar bone and cementum, particularly in the furcation and interproximal regions of the molars. The alveolar bone appeared porous while the quantity of cementum was reduced in the apical region. The canalicular systems and osteocytes in the alveolar bone were abnormal, with reduced numbers of canaliculi and altered osteocyte morphology. The loss of alveolar bone and cementum along with the detachment of the periodontal ligaments (PDL) led to the apical migration of the epithelial attachment and formation of periodontal pockets.
Inactivation of DSPP leads to the loss of alveolar bone and cementum and increased susceptibility to bacterial infections in PDL of Dspp null mice. The fact that the loss of DSPP results in periodontal diseases indicates that this molecule plays a vital role in maintaining the health of the periodontium.
牙本质涎磷蛋白(DSPP)及其裂解产物牙本质磷蛋白(DPP)和牙本质涎蛋白(DSP)在生物矿化过程中发挥着重要作用。最近,我们观察到 DSPP 在牙槽骨和牙骨质中高度表达,表明该分子可能在健康牙周组织的形成和维持中发挥重要作用,其缺失可能导致牙周病易感性增加。本研究旨在通过分析 Dspp 缺失小鼠来研究 Dspp 缺失对牙周组织的影响。
对新生至 6 月龄的 Dspp 缺失小鼠进行检查,并对 3 月龄和 6 月龄的 Dspp 缺失小鼠进行详细的 X 射线射线照相、组织学和扫描电子显微镜(背散射以及树脂渗透)分析。相同年龄组的野生型小鼠作为正常对照。
Dspp 缺失小鼠表现出明显的牙槽骨和牙骨质丧失,尤其是在磨牙的分叉和近中区域。牙槽骨呈多孔状,而根尖区域的牙骨质数量减少。牙槽骨中的管腔系统和骨细胞异常,管腔数量减少,骨细胞形态改变。牙槽骨和牙骨质的丧失以及牙周韧带(PDL)的分离导致上皮附着的根尖迁移和牙周袋的形成。
DSPP 的失活导致 Dspp 缺失小鼠的牙槽骨和牙骨质丧失以及对 PDL 细菌感染的易感性增加。DSPP 的缺失导致牙周病的事实表明,该分子在维持牙周组织健康方面起着至关重要的作用。