Department of Restorative Dentistry, College of Dentistry, University of Illinois at Chicago, 801 South Paulina street, Chicago, IL 60612, USA.
Arch Oral Biol. 2013 Mar;58(3):254-60. doi: 10.1016/j.archoralbio.2012.09.007. Epub 2012 Oct 27.
This study assessed the micro-morphological changes in demineralized dentine scaffold following incubation with recombinant dentine matrix protein 1 (rDMP1).
Extracted human molar crowns were sectioned into 6 beams (dimensions: 0.50mm×1.70mm×6.00mm), demineralized and incubated overnight in 3 different media (n=4): rDMP1 in bovine serum albumin (BSA), BSA and distilled water. Samples were placed in a chamber with simulated physiological concentrations of calcium and phosphate ions at constant pH 7.4. Samples were immediately processed for transmission electron microscopy (TEM) and field emission-scanning electron microscopy (FE-SEM) after 1 and 2 weeks.
Analysis of the scaffold showed that decalcification process retained the majority of endogenous proteoglycans and phosphoproteins. rDMP1 treated samples promoted deposition of amorphous calcium phosphate (ACP) precursors and needle shaped hydroxyapatite crystals surrounding collagen fibrils. The BSA group presented ACP bound to collagen with no needle-like apatite crystals. Samples kept in distilled water showed no evidence of ACP and crystal apatite. Results from rDMP1 immobilized on dentine matrix suggests that the acidic protein was able to bind to collagen fibrils and control formation of amorphous calcium phosphate and its subsequent transformation into hydroxyapatite crystals after 2 weeks.
These findings suggest a possible bio-inspired strategy to promote remineralization of dentine for reparative and regenerative purposes.
本研究评估了重组牙本质基质蛋白 1(rDMP1)孵育后脱矿牙本质支架的微观形态变化。
从人磨牙冠上切下 6 个牙本质梁(尺寸:0.50mm×1.70mm×6.00mm),进行脱矿处理,并在 3 种不同的培养基中孵育过夜(n=4):牛血清白蛋白(BSA)中的 rDMP1、BSA 和蒸馏水。将样本放置在一个腔室内,其中含有模拟生理浓度的钙和磷酸盐离子,pH 值为 7.4。在孵育 1 周和 2 周后,立即对样本进行透射电子显微镜(TEM)和场发射扫描电子显微镜(FE-SEM)分析。
对支架的分析表明,脱矿过程保留了大部分内源性糖胺聚糖和磷蛋白。rDMP1 处理的样本促进了无定形磷酸钙(ACP)前体的沉积,并在胶原纤维周围形成了针状羟基磷灰石晶体。BSA 组呈现出与胶原结合的 ACP,没有针状磷灰石晶体。保存在蒸馏水中的样本没有 ACP 和晶状磷灰石的证据。固定在牙本质基质上的 rDMP1 的结果表明,酸性蛋白能够与胶原纤维结合,并控制无定形磷酸钙的形成及其在 2 周后转化为羟基磷灰石晶体。
这些发现表明,对于修复和再生目的,促进牙本质再矿化可能存在一种生物启发策略。