Bidlack Felicitas B, Xia Yan, Pugach Megan K
Forsyth Institute, Cambridge, MA, United States.
Department of Developmental Biology, Harvard School of Dental Medicine, Boston, MA, United States.
Front Physiol. 2017 Nov 16;8:932. doi: 10.3389/fphys.2017.00932. eCollection 2017.
Mice lacking amelogenin (KO) have hypoplastic enamel. Overexpression of the most abundant amelogenin splice variant M180 and LRAP transgenes can substantially improve KO enamel, but only ~40% of the incisor thickness is recovered and the prisms are not as tightly woven as in WT enamel. This implies that the compositional complexity of the enamel matrix is required for different aspects of enamel formation, such as organizational structure and thickness. The question arises, therefore, how important the ratio of different matrix components, and in particular amelogenin splice products, is in enamel formation. Can optimal expression levels of amelogenin transgenes representing both the most abundant splice variants and cleavage product at protein levels similar to that of WT improve the enamel phenotype of KO mice? Addressing this question, our objective was here to understand dosage effects of amelogenin transgenes () representing the major splice variants M180 and LRAP and cleavage product CTRNC on enamel properties. Amelogenin KO mice were mated with M180, CTRNC and LRAP mice to generate M180 and CTRNC double transgene and M180, CTRNC, LRAP triple transgene mice with transgene hemizygosity (on one allelle) or homozygosity (on both alleles). Transgene homo- vs. hemizygosity was determined by qPCR and relative transgene expression confirmed by Western blot. Enamel volume and mineral density were analyzed by microCT, thickness and structure by SEM, and mechanical properties by Vickers microhardness testing. There were no differences in incisor enamel thickness between amelogenin KO mice with three or two different transgenes, but mice homozygous for a given transgene had significantly thinner enamel than mice hemizygous for the transgene ( < 0.05). The presence of the LRAP did not improve the phenotype of M180/CTRNC/KO enamel. In the absence of endogenous amelogenin, the addition of amelogenin transgenes representing the most abundant splice variants and cleavage product can rescue abnormal enamel properties and structure, but only up to a maximum of ~80% that of molar and ~40% that of incisor wild-type enamel.
缺乏釉原蛋白的小鼠(KO)具有发育不全的牙釉质。最丰富的釉原蛋白剪接变体M180和LRAP转基因的过表达可以显著改善KO小鼠的牙釉质,但仅能恢复约40%的门牙厚度,且棱柱不像野生型牙釉质那样紧密排列。这意味着牙釉质基质的组成复杂性对于牙釉质形成的不同方面,如组织结构和厚度,是必需的。因此,问题就出现了,不同基质成分的比例,特别是釉原蛋白剪接产物的比例,在牙釉质形成中有多重要?代表最丰富剪接变体和裂解产物的釉原蛋白转基因在蛋白质水平上达到与野生型相似的最佳表达水平,能否改善KO小鼠的牙釉质表型?为了解决这个问题,我们的目标是了解代表主要剪接变体M180和LRAP以及裂解产物CTRNC的釉原蛋白转基因对牙釉质特性的剂量效应。将釉原蛋白KO小鼠与M180、CTRNC和LRAP小鼠交配,以产生具有转基因半合子(一个等位基因)或纯合子(两个等位基因)的M180和CTRNC双转基因以及M180、CTRNC、LRAP三转基因小鼠。通过qPCR确定转基因纯合与半合子状态,并通过蛋白质印迹法确认相对转基因表达。通过显微CT分析牙釉质体积和矿物质密度,通过扫描电子显微镜分析厚度和结构,并通过维氏显微硬度测试分析机械性能。具有三种或两种不同转基因的釉原蛋白KO小鼠之间的门牙牙釉质厚度没有差异,但给定转基因纯合的小鼠的牙釉质明显比转基因半合子的小鼠薄(<0.05)。LRAP的存在并没有改善M180/CTRNC/KO牙釉质的表型。在没有内源性釉原蛋白的情况下,添加代表最丰富剪接变体和裂解产物的釉原蛋白转基因可以挽救异常的牙釉质特性和结构,但最多只能达到磨牙野生型牙釉质的约80%和门牙野生型牙釉质的约40%。