Department of Oral and Maxillofacial‑Head and Neck Oncology, and Faculty of Oral and Maxillofacial Surgery, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, P.R. China.
Department of Stomatology, Shanghai Tenth People's Hospital, Tongji University, Shanghai 200072, P.R. China.
Mol Med Rep. 2018 Mar;17(3):3537-3544. doi: 10.3892/mmr.2017.8290. Epub 2017 Dec 18.
Protein delta homolog 1 (DLK1) regulates the odontoblastic differentiation of human dental pulp stem cells. It was hypothesized that DLK1 may exert regulatory effects on epithelial‑mesenchymal interactions in tooth development. The present study investigated the expression of DLK1 during the development of mouse enamel and its role in the proliferation and differentiation of ameloblast‑lineage cells (ALCs). DLK1 expression was upregulated in ameloblasts in the first mandibular molar during the entire process of enamel development. The mRNA and protein levels of DLK1 were significantly upregulated following ameloblastic induction in ALCs. In addition, overexpression of DLK1 promoted the proliferation of ALCs, inhibited ameloblastic differentiation, upregulated the expression of amelogenin and enamelin, and downregulated the expression of odontogenic ameloblast‑associated protein and kallikrein 4. The results of the present study suggested that DLK1 may be a potent regulator of ameloblast proliferation and differentiation, and may regulate enamel formation during tooth development.
蛋白 δ 同源物 1(DLK1)调控人牙髓干细胞的成牙本质分化。据推测,DLK1 可能对牙齿发育过程中的上皮-间充质相互作用发挥调节作用。本研究探讨了 DLK1 在小鼠牙釉质发育过程中的表达及其在成釉细胞系(ALCs)增殖和分化中的作用。在第一下颌磨牙釉质发育的整个过程中,DLK1 在成釉细胞中呈上调表达。在 ALCs 中诱导成釉细胞后,DLK1 的 mRNA 和蛋白水平显著上调。此外,过表达 DLK1 促进 ALCs 的增殖,抑制成釉细胞分化,上调釉原蛋白和釉蛋白的表达,下调牙源性成釉细胞相关蛋白和激肽释放酶 4 的表达。本研究结果表明,DLK1 可能是成釉细胞增殖和分化的有效调节剂,并可能在牙齿发育过程中调节牙釉质的形成。