Tmem2缺乏导致小鼠牙釉质发育不全和软牙釉质。

IF 8.3 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
P Nag, T Inubushi, J I Sasaki, T Murotani, S Kusano, Y Nakanishi, Y Shiraishi, H Kurosaka, S Imazato, Y Yamaguchi, T Yamashiro
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引用次数: 0

摘要

牙齿由三种矿化组织组成:牙釉质、牙本质和牙骨质。牙齿畸形是最常见的颅面畸形,是由复杂的遗传和环境因素影响牙釉质结构、大小、形状和牙齿萌出引起的。透明质酸(HA)是一种主要的细胞外基质成分,有助于牙周组织的结构和生理功能。跨膜蛋白2 (TMEM2)是一种新型的细胞表面透明质酸酶,在胚胎发生过程中起着关键作用。在这项研究中,我们证实了Tmem2信使RNA在内釉质上皮和分泌前、分泌和成熟成釉细胞中的表达。Tmem2敲入报告小鼠发现Tmem2蛋白定位于分泌性成釉细胞的顶端和基端。上皮特异性Tmem2条件敲除(Tmem2- cko)小鼠的显微计算机断层扫描分析显示,牙釉质层厚度显著减少,牙釉质严重缺乏。Tmem2-CKO小鼠的牙釉质基质蛋白表达明显下调。Tmem2-CKO小鼠牙釉质扫描电镜显示牙釉质棱柱结构不规则,牙釉质显微硬度和密度明显降低,表明成釉细胞分化和牙釉质基质矿化受损。组织学评价显示Tmem2-CKO小鼠细胞与基底膜的粘附较弱。血管素和整合素β1表达的减少和不规则表明Tmem2缺乏减弱了局灶性粘连的形成。此外,Tmem2-CKO小鼠成釉层HA异常积累和claudin 1免疫反应性弱表明紧密连接门功能受损。在分泌性成釉细胞的顶端和基端也观察到不规则的肌动蛋白丝组装。最后,我们证明了tmem2缺陷的mHAT9d小鼠成釉细胞在体外对含ha的底物表现出缺陷的粘附。总的来说,我们的数据强调了TMEM2在粘附到富含ha的细胞外基质、细胞间粘附、成釉细胞分化和牙釉质基质矿化中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tmem2 Deficiency Leads to Enamel Hypoplasia and Soft Enamel in Mouse.

Teeth consist of 3 mineralized tissues: enamel, dentin, and cementum. Tooth malformation, the most common craniofacial anomaly, arises from complex genetic and environmental factors affecting enamel structure, size, shape, and tooth eruption. Hyaluronic acid (HA), a primary extracellular matrix component, contributes to structural and physiological functions in periodontal tissue. Transmembrane protein 2 (TMEM2), a novel cell surface hyaluronidase, has been shown to play a critical role during embryogenesis. In this study, we demonstrate Tmem2 messenger RNA expression in inner enamel epithelium and presecretory, secretory, and mature ameloblasts. Tmem2 knock-in reporter mice reveal TMEM2 protein localization at the apical and basal ends of secretory ameloblasts. Micro-computed tomography analysis of epithelial-specific Tmem2 conditional knockout (Tmem2-CKO) mice shows a significant reduction in enamel layer thickness and severe enamel deficiency. Enamel matrix protein expression was remarkably downregulated in Tmem2-CKO mice. Scanning electron microscopy of enamel from Tmem2-CKO mice revealed an irregular enamel prism structure, while the microhardness and density of enamel were significantly reduced, indicating impaired ameloblast differentiation and enamel matrix mineralization. Histological evaluation indicated weak adhesion between cells and the basement membrane in Tmem2-CKO mice. The reduced and irregular expressions of vinculin and integrin β1 suggest that Tmem2 deficiency attenuated focal adhesion formation. In addition, abnormal HA accumulation in the ameloblast layer and weak claudin 1 immunoreactivity in Tmem2-CKO mice indicate impaired tight junction gate function. Irregular actin filament assembly was also observed at the apical and basal ends of secretory ameloblasts. Last, we demonstrated that Tmem2-deficient mHAT9d mouse ameloblasts exhibit defective adhesion to HA-containing substrates in vitro. Collectively, our data highlight the importance of TMEM2 in adhesion to HA-rich extracellular matrix, cell-to-cell adhesion, ameloblast differentiation, and enamel matrix mineralization.

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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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