Itaya Satoshi, Oka Kyoko, Ogata Kayoko, Tamura Shougo, Kira-Tatsuoka Michiko, Fujiwara Naoki, Otsu Keishi, Tsuruga Eichi, Ozaki Masao, Harada Hidemitsu
Section of Pediatric Dentistry, Department of Oral Growth and Development, Fukuoka Dental College.
Biomed Res. 2017;38(1):61-69. doi: 10.2220/biomedres.38.61.
In tooth root development, periodontal ligament (PDL) and cementum are formed by the coordination with the fragmentation of Hertwig's epithelial root sheath (HERS) and the differentiation of dental follicle mesenchymal cells. However, the function of the dental epithelial cells after HERS fragmentation in the PDL is not fully understood. Here, we found that TGF-β regulated HERS fragmentation via epithelial-mesenchymal transition (EMT), and the fragmented epithelial cells differentiated into PDL fibroblastic cells with expressing of PDL extracellular matrix (ECM). In the histochemical analysis, TGF-β was expressed in odontoblast layer adjacent of HERS during root development. Periostin expression was detected around fragmented epithelial cells on the root surface, but not in HERS. In the experiment using an established mouse HERS cell line (HERS01a), TGF-β1 treatment decreased E-cadherin and relatively increased N-cadherin expression. TGF-β1 treatment in HERS01a induced further expression of important ECM proteins for acellular cementum and PDL development such as fibronectin and periostin. Taken together, activation of TGF-βsignaling induces HERS fragmentation through EMT and the fragmented HERS cells contribute to formation of PDL and acellular cementum through periostin and fibronectin expression.
在牙根发育过程中,牙周韧带(PDL)和牙骨质是通过与赫特维希上皮根鞘(HERS)的碎片化以及牙囊间充质细胞的分化协同形成的。然而,HERS碎片化后牙上皮细胞在PDL中的功能尚未完全明确。在此,我们发现转化生长因子-β(TGF-β)通过上皮-间充质转化(EMT)调节HERS碎片化,并且碎片化的上皮细胞通过表达PDL细胞外基质(ECM)分化为PDL成纤维细胞。在组织化学分析中,TGF-β在牙根发育过程中于HERS相邻的成牙本质细胞层表达。在牙根表面碎片化上皮细胞周围检测到骨膜蛋白表达,但在HERS中未检测到。在使用已建立的小鼠HERS细胞系(HERS01a)的实验中,TGF-β1处理降低了E-钙黏蛋白表达并相对增加了N-钙黏蛋白表达。TGF-β1处理HERS01a诱导了无细胞牙骨质和PDL发育的重要ECM蛋白如纤连蛋白和骨膜蛋白的进一步表达。综上所述,TGF-β信号的激活通过EMT诱导HERS碎片化,并且碎片化的HERS细胞通过骨膜蛋白和纤连蛋白的表达促进PDL和无细胞牙骨质的形成。