Takagiwa Yuri, Higashihori Norihisa, Kano Sakurako, Moriyama Keiji
Maxillofacial Orthognathics, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, Japan.
Maxillofacial Orthognathics, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8549, Japan.
Arch Oral Biol. 2024 Sep;165:106026. doi: 10.1016/j.archoralbio.2024.106026. Epub 2024 Jun 10.
This study aimed to reveal the effects of SET domain bifurcated 1 (SETDB1) on epithelial cells during tooth development.
We generated conditional knockout mice (Setdb1 mice), in which Setdb1 was deleted only in epithelial cells. At embryonic day 14.5 (E14.5), immunofluorescence staining was performed to confirm the absence of SETDB1 within the epithelium of tooth embryos from Setdb1 mice. Mouse embryos were harvested after reaching embryonic day 13.5 (E13.5), and sections were prepared for histological analysis. To observe tooth morphology in detail, electron microscopy and micro-CT analysis were performed at postnatal months 1 (P1M) and 6 (P6M). Tooth embryos were harvested from postnatal day 7 (P7) mice, and the epithelial components of the tooth embryos were isolated and examined using quantitative RT-PCR for the expression of genes involved in tooth development.
Setdb1 mice exhibited enamel hypoplasia, brittle and fragile dentition, and significant abrasion. Coronal sections displayed abnormal ameloblast development, including immature polarization, and a thin enamel layer that detached from the dentinoenamel junction at P7. Electron microscopic analysis revealed characteristic findings such as an uneven surface and the absence of an enamel prism. The expression of Msx2, Amelogenin (Amelx), Ameloblastin (Ambn), and Enamelin (Enam) was significantly downregulated in the epithelial components of tooth germs in Setdb1 mice.
These results indicate that SETDB1 in epithelial cells is important for tooth development and clarify the relationship between the epigenetic regulation of SETDB1 and amelogenesis imperfecta for the first time.
本研究旨在揭示SET结构域分叉1(SETDB1)在牙齿发育过程中对上皮细胞的影响。
我们构建了条件性敲除小鼠(Setdb1小鼠),其中Setdb1仅在上皮细胞中被敲除。在胚胎第14.5天(E14.5),进行免疫荧光染色以确认Setdb1小鼠牙胚上皮内SETDB1的缺失。在胚胎第13.5天(E13.5)后收获小鼠胚胎,并制备切片进行组织学分析。为了详细观察牙齿形态,在出生后1个月(P1M)和6个月(P6M)进行电子显微镜和显微CT分析。从出生后第7天(P7)的小鼠中收获牙胚,并分离牙胚的上皮成分,使用定量RT-PCR检测参与牙齿发育的基因表达。
Setdb1小鼠表现出釉质发育不全、牙列脆弱易碎以及明显磨损。冠状切片显示成釉细胞发育异常,包括极化不成熟,并且在P7时釉质层薄且与牙釉质交界分离。电子显微镜分析揭示了诸如表面不均匀和釉柱缺失等特征性发现。Setdb1小鼠牙胚上皮成分中Msx2、釉原蛋白(Amelx)、成釉蛋白(Ambn)和釉蛋白(Enam)的表达显著下调。
这些结果表明上皮细胞中的SETDB1对牙齿发育很重要,并首次阐明了SETDB1的表观遗传调控与牙釉质发育不全之间的关系。