Prajapati S, Ruan Q, Mukherjee K, Nutt S, Moradian-Oldak J
1 Center for Craniofacial Molecular Biology, Herman Ostrow School of Dentistry, University of Southern California, Los Angeles, CA, USA.
2 Mork Family Department of Chemical Engineering and Materials Science, University of Southern California, Los Angeles, CA, USA.
J Dent Res. 2018 Jan;97(1):84-90. doi: 10.1177/0022034517728504. Epub 2017 Aug 28.
Biomimetic synthesis of artificial enamel is a promising strategy for the prevention and restoration of defective enamel. We have recently reported that a hydrogel system composed of chitosan-amelogenin (CS-AMEL) and calcium phosphate is effective in forming an enamel-like layer that has a seamless interface with natural tooth surfaces. Here, to improve the mechanical system function and to facilitate the biomimetic enamel regrowth, matrix metalloproteinase-20 (MMP-20) was introduced into the CS-AMEL hydrogel. Inspired by our recent finding that MMP-20 prevents protein occlusion inside enamel crystals, we hypothesized that addition of MMP-20 to CS-AMEL hydrogel could reinforce the newly grown layer. Recombinant human MMP-20 was added to the CS-AMEL hydrogel to cleave full-length amelogenin during the growth of enamel-like crystals on an etched enamel surface. The MMP-20 proteolysis of amelogenin was studied, and the morphology, composition, and mechanical properties of the newly grown layer were characterized. We found that amelogenin was gradually degraded by MMP-20 in the presence of chitosan. The newly grown crystals in the sample treated with MMP-20-CS-AMEL hydrogel showed more uniform orientation and greater crystallinity than the samples treated with CS-AMEL hydrogel without MMP-20. Stepwise processing of amelogenin by MMP-20 in the CS-AMEL hydrogel prevented undesirable protein occlusion within the newly formed crystals. As a result, both the modulus and hardness of the repaired enamel were significantly increased (1.8- and 2.4-fold, respectively) by the MMP-20-CS-AMEL hydrogel. Although future work is needed to further incorporate other enamel matrix proteins into the system, this study brings us one step closer to biomimetic enamel regrowth.
人工牙釉质的仿生合成是预防和修复牙釉质缺陷的一种很有前景的策略。我们最近报道,由壳聚糖-釉原蛋白(CS-AMEL)和磷酸钙组成的水凝胶系统可有效形成与天然牙齿表面具有无缝界面的牙釉质样层。在此,为改善机械系统功能并促进仿生牙釉质再生,将基质金属蛋白酶-20(MMP-20)引入CS-AMEL水凝胶中。受我们最近发现MMP-20可防止牙釉质晶体内部蛋白质堵塞的启发,我们推测向CS-AMEL水凝胶中添加MMP-20可增强新生长层。将重组人MMP-20添加到CS-AMEL水凝胶中,以便在蚀刻的牙釉质表面上生长牙釉质样晶体的过程中裂解全长釉原蛋白。研究了釉原蛋白的MMP-20蛋白水解作用,并对新生长层的形态、组成和力学性能进行了表征。我们发现,在壳聚糖存在下,釉原蛋白会被MMP-20逐渐降解。与用不含MMP-20的CS-AMEL水凝胶处理的样品相比,用MMP-20-CS-AMEL水凝胶处理的样品中新生长的晶体显示出更均匀的取向和更高的结晶度。MMP-20在CS-AMEL水凝胶中对釉原蛋白的逐步加工可防止新形成的晶体中出现不希望的蛋白质堵塞。结果,MMP-20-CS-AMEL水凝胶使修复后的牙釉质的模量和硬度均显著增加(分别增加1.8倍和2.4倍)。尽管未来需要进一步将其他牙釉质基质蛋白纳入该系统,但这项研究使我们离仿生牙釉质再生又近了一步。