Institute of Dental Research, Westmead Millennium Institute and Westmead Centre for Oral Health, Westmead, Sydney, New South Wales, Australia.
Bone. 2012 Jan;50(1):265-75. doi: 10.1016/j.bone.2011.10.031. Epub 2011 Nov 4.
Odontoblast synthesis of dentin proceeds through discrete but overlapping phases characterized by formation of a patterned organic matrix followed by remodelling and active mineralization. Microbial invasion of dentin in caries triggers an adaptive response by odontoblasts, culminating in formation of a structurally altered reactionary dentin, marked by biochemical and architectonic modifications including diminished tubularity. Scanning electron microscopy of the collagen framework in reactionary dentin revealed a radically modified yet highly organized meshwork as indicated by fractal and lacunarity analyses. Immuno-gold labelling demonstrated increased density and regular spatial distribution of dentin sialoprotein (DSP) in reactionary dentin. DSP contributes putative hydroxyapatite nucleation sites on the collagen scaffold. To further dissect the formation of this altered dentin matrix, the associated enzymatic machinery was investigated. Analysis of extracted dentin matrix indicated increased activity of matrix metalloproteinase-2 (MMP-2) in the reactionary zone referenced to physiologic dentin. Likewise, gene expression analysis of micro-dissected odontoblast layer revealed up-regulation of MMP-2. Parallel up-regulation of tissue inhibitor of metalloproteinase-2 (TIMP-2) and membrane type 1- matrix metalloproteinase (MT1-MMP) was observed in response to caries. Next, modulation of odontoblastic dentinogenic enzyme repertoire was addressed. In the odontoblast layer expression of Toll-like receptors was markedly altered in response to bacterial invasion. In carious teeth TLR-2 and the gene encoding the corresponding adaptor protein MyD88 were down-regulated whereas genes encoding TLR-4 and adaptor proteins TRAM and Mal/TIRAP were up-regulated. TLR-4 signalling mediated by binding of bacterial products has been linked to up-regulation of MMP-2. Further, increased expression of genes encoding components of the TGF-β signalling pathway, namely SMAD-2 and SMAD-4, may explain the increased synthesis of collagen by odontoblasts in caries. These findings indicate a radical adaptive response of odontoblasts to microbial invasion of dentin with resultant synthesis of modified mineralized matrix.
成牙本质细胞合成牙本质是通过离散但重叠的阶段进行的,其特征是形成有图案的有机基质,然后进行重塑和主动矿化。龋病中牙本质的微生物入侵会引发成牙本质细胞的适应性反应,最终形成结构改变的反应性牙本质,其特征是生化和架构发生改变,包括管腔减少。反应性牙本质胶原纤维的扫描电子显微镜显示,纤维结构分析表明,胶原纤维框架呈现出一种明显改变但高度有序的网格结构。免疫金标记显示,反应性牙本质中牙本质涎磷蛋白(DSP)的密度增加且空间分布更加规则。DSP 在胶原支架上提供了潜在的羟基磷灰石成核位点。为了进一步剖析这种改变的牙本质基质的形成,研究了相关的酶机制。从提取的牙本质基质分析中表明,与生理性牙本质相比,反应区的基质金属蛋白酶-2(MMP-2)活性增加。同样,对微分离的成牙本质细胞层的基因表达分析显示,MMP-2 上调。对龋病的基因表达分析显示,MMP-2 及其组织抑制剂-2(TIMP-2)和膜型 1-基质金属蛋白酶(MT1-MMP)呈平行上调。接下来,研究了成牙本质细胞牙本质生成酶谱的调节。在成牙本质细胞层,细菌入侵导致 Toll 样受体的表达明显改变。在龋病牙中,TLR-2 和编码相应衔接蛋白 MyD88 的基因下调,而编码 TLR-4 和衔接蛋白 TRAM 和 Mal/TIRAP 的基因上调。TLR-4 信号通过结合细菌产物介导 MMP-2 的上调。此外,TGF-β 信号通路的基因编码产物,即 SMAD-2 和 SMAD-4 的表达增加,可能解释了龋病中成牙本质细胞胶原合成增加的原因。这些发现表明,成牙本质细胞对牙本质中微生物入侵的剧烈适应性反应导致了改性矿化基质的合成。