Mazumder P, Prajapati S, Bapat R, Moradian-Oldak J
Center for Craniofacial Molecular Biology, Division of Biomedical Sciences, Herman Ostrow School of Dentistry, University of Southern California, Los Angeles, CA, USA.
Center for Craniofacial Molecular Biology, Division of Biomedical Sciences, Herman Ostrow School of Dentistry, University of Southern California, Los Angeles, CA, USA
J Dent Res. 2016 Aug;95(9):1042-8. doi: 10.1177/0022034516645389. Epub 2016 May 4.
Amelogenin and ameloblastin are 2 extracellular matrix proteins that are essential for the proper development of enamel. We recently reported that amelogenin and ameloblastin colocalized during the secretory stage of enamel formation when nucleation of enamel crystallites occurs. Direct interactions between the 2 proteins have been also demonstrated in our in vitro studies. Here, we explore interactions between their fragments during enamel maturation. We applied in vivo immunofluorescence imaging, quantitative co-localization analysis, and a new FRET (fluorescence resonance energy transfer) technique to demonstrate ameloblastin and amelogenin interaction in the maturing mouse enamel. Using immunochemical analysis of protein samples extracted from 8-d-old (P8) first molars from mice as a model for maturation-stage enamel, we identified the ~17-kDa ameloblastin (Ambn-N) and the TRAP (tyrosine-rich amelogenin peptide) fragments. We used Ambn-N18 and Ambn-M300 antibodies raised against the N-terminal and C-terminal segments of ameloblastin, as well as Amel-FL and Amel-C19 antibodies against full-length recombinant mouse amelogenin (rM179) and C-terminal amelogenin, respectively. In transverse sections, co-localization images of N-terminal fragments of amelogenin and ameloblastin around the prism boundary revealed the "fish net" pattern of the enamel matrix. Using in vivo FRET microscopy, we further demonstrated spatial interactions between amelogenin and ameloblastin N-terminal fragments. In the maturing mouse enamel, the association of these residual protein fragments created a discontinuity between enamel rods, which we suggest is important for support and maintenance of enamel rods and eventual contribution to unique enamel mechanical properties. We present data that support cooperative functions of enamel matrix proteins in mediating the structural hierarchy of enamel and that contribute to our efforts to design and develop enamel biomimetic material.
釉原蛋白和成釉蛋白是两种细胞外基质蛋白,对牙釉质的正常发育至关重要。我们最近报道,在牙釉质微晶成核的牙釉质形成分泌阶段,釉原蛋白和成釉蛋白共定位。我们的体外研究也证实了这两种蛋白之间的直接相互作用。在此,我们探讨它们的片段在牙釉质成熟过程中的相互作用。我们应用体内免疫荧光成像、定量共定位分析和一种新的荧光共振能量转移(FRET)技术,来证明成釉蛋白和釉原蛋白在成熟小鼠牙釉质中的相互作用。以从8日龄(P8)小鼠第一磨牙提取的蛋白质样本进行免疫化学分析作为成熟阶段牙釉质的模型,我们鉴定出了~17 kDa的成釉蛋白(Ambn-N)和富含酪氨酸的釉原蛋白肽(TRAP)片段。我们使用了针对成釉蛋白N端和C端片段产生的Ambn-N18和Ambn-M300抗体,以及分别针对全长重组小鼠釉原蛋白(rM179)和釉原蛋白C端的Amel-FL和Amel-C19抗体。在横切面上,釉原蛋白和成釉蛋白N端片段在棱柱边界周围的共定位图像显示出牙釉质基质的“鱼网”模式。使用体内FRET显微镜,我们进一步证明了釉原蛋白和成釉蛋白N端片段之间的空间相互作用。在成熟的小鼠牙釉质中,这些残留蛋白片段的结合在釉柱之间产生了间断,我们认为这对于釉柱的支撑和维持以及最终对牙釉质独特机械性能的形成很重要。我们提供的数据支持牙釉质基质蛋白在介导牙釉质结构层次方面的协同功能,并有助于我们设计和开发牙釉质仿生材料的努力。