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富含亮氨酸的釉原蛋白肽介导的仿生牙釉质再生

Biomimetic Enamel Regeneration Mediated by Leucine-Rich Amelogenin Peptide.

作者信息

Kwak S Y, Litman A, Margolis H C, Yamakoshi Y, Simmer J P

机构信息

1 Center for Biomineralization, Department of Applied Oral Sciences, The Forsyth Institute, Cambridge, MA, USA.

2 Department of Developmental Biology, Harvard School of Dental Medicine, Boston, MA, USA.

出版信息

J Dent Res. 2017 May;96(5):524-530. doi: 10.1177/0022034516688659. Epub 2017 Jan 23.

Abstract

We report here a novel biomimetic approach to the regeneration of human enamel. The approach combines the use of inorganic pyrophosphate (PP) to control the onset and rate of enamel regeneration and the use of leucine-rich amelogenin peptide (LRAP), a nonphosphorylated 56-amino acid alternative splice product of amelogenin, to regulate the shape and orientation of growing enamel crystals. This study builds on our previous findings that show LRAP can effectively guide the formation of ordered arrays of needle-like hydroxyapatite (HA) crystals in vitro and on the known role mineralization inhibitors, like PP, play in the regulation of mineralized tissue formation. Acid-etched enamel surfaces of extracted human molars, cut perpendicular or parallel to the direction of the enamel rods, were exposed to a PP-stabilized supersaturated calcium phosphate (CaP) solution containing 0 to 0.06 mg/mL LRAP for 20 h. In the absence of LRAP, PP inhibition was reversed by the presence of etched enamel surfaces and led to the formation of large, randomly distributed plate-like HA crystals that were weakly attached, regardless of rod orientation. In the presence of 0.04 mg/mL LRAP, however, densely packed mineral layers, comprising bundles of small needle-like HA crystals, formed on etched surfaces that were cut perpendicular to the enamel rods. These crystals were strongly attached, and their arrangement reflected to a significant degree the underlying enamel prism pattern. In contrast, under the same conditions with LRAP, little to no crystal formation was found on enamel surfaces that were cut parallel to the direction of the enamel rods. These results suggest that LRAP preferentially interacts with ab surfaces of mature enamel crystals, inhibiting their directional growth, thus selectively promoting linear growth along the c-axis of enamel crystals. The present findings demonstrate a potential for the development of a new approach to regenerate enamel structure and properties.

摘要

我们在此报告一种用于人类牙釉质再生的新型仿生方法。该方法结合使用无机焦磷酸盐(PP)来控制牙釉质再生的起始和速率,以及使用富含亮氨酸的釉原蛋白肽(LRAP),它是釉原蛋白的一种非磷酸化的56个氨基酸的可变剪接产物,来调节生长中的牙釉质晶体的形状和取向。本研究基于我们之前的发现,即LRAP在体外能有效引导针状羟基磷灰石(HA)晶体有序阵列的形成,以及基于矿化抑制剂(如PP)在矿化组织形成调节中所起的已知作用。将垂直或平行于牙釉质棒方向切割的拔除人类磨牙的酸蚀牙釉质表面,暴露于含有0至0.06 mg/mL LRAP的PP稳定的过饱和磷酸钙(CaP)溶液中20小时。在没有LRAP的情况下,蚀刻牙釉质表面的存在会逆转PP的抑制作用,并导致形成大的、随机分布的板状HA晶体,这些晶体附着较弱,与牙釉质棒的取向无关。然而,在存在0.04 mg/mL LRAP的情况下,在垂直于牙釉质棒切割的蚀刻表面上形成了密集堆积的矿化层,该矿化层由小针状HA晶体束组成。这些晶体附着牢固,并且它们的排列在很大程度上反映了底层的牙釉质棱柱模式。相比之下,在相同的LRAP条件下,在平行于牙釉质棒方向切割的牙釉质表面上几乎没有发现晶体形成。这些结果表明,LRAP优先与成熟牙釉质晶体的ab表面相互作用,抑制其定向生长,从而选择性地促进沿牙釉质晶体c轴的线性生长。目前的研究结果表明开发一种再生牙釉质结构和性能的新方法具有潜力。

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