School and Hospital of Stomatology, Shandong University& Shandong Provincial Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration, 44-1Wenhua Road West, 250012, Jinan Shandong, China; Liaocheng People's Hospital, Liaocheng, 252000, Shandong, China.
Jinan Stomatological Hospital, Jinan, 250001, Shandong, China.
Biochem Biophys Res Commun. 2019 Oct 15;518(2):246-252. doi: 10.1016/j.bbrc.2019.08.042. Epub 2019 Aug 12.
Nel-like molecule 1 (Nell-1) is an essential positive regulator of tooth development and odontoblast differentiation. However, its precise mechanism remains undetermined. This study aims to explore the possible receptor or binding protein of Nell-1. Results showed that Nell-1 and Apoptosis related protein 3(APR3) expression levels were high in odontoblasts and inversely correlated. Endogenous Nell-1 co-immunoprecipitated with APR3, and this co-IP was reciprocal. Double immunofluorescence staining revealed that Nell-1 and APR3 colocalized on the nuclear envelope of human dental pulp cells. Nell-1 inhibited the proliferation of these cells co-infected with APR3 through Cyclin D1 downregulation. The interaction of Nell-1 with APR3 stimulated alkaline phosphatase (ALP) activity and promoted the expression and mineralization of DSPP, ALP, OPN, and BSP. The shRNA of APR3 decreased cell differentiation and mineralization. Nell-1 could reciprocally interact with APR3 and stimulate the differentiation and mineralization of human dental pulp cells. Future studies should explore the potential functional connection and the molar mechanism of such interaction.
类内尔蛋白 1(Nell-1)是牙齿发育和成牙本质细胞分化的必需正向调控因子。然而,其确切的机制尚不清楚。本研究旨在探索 Nell-1 的可能受体或结合蛋白。结果表明,Nell-1 和凋亡相关蛋白 3(APR3)在成牙本质细胞中的表达水平较高,呈负相关。内源性 Nell-1 与 APR3 共免疫沉淀,且这种共沉淀是相互的。双免疫荧光染色显示,Nell-1 和 APR3 在人牙髓细胞的核膜上共定位。Nell-1 通过下调 Cyclin D1 抑制共感染 APR3 的这些细胞的增殖。Nell-1 与 APR3 的相互作用刺激碱性磷酸酶(ALP)活性,并促进 DSPP、ALP、OPN 和 BSP 的表达和矿化。APR3 的 shRNA 减少细胞分化和矿化。Nell-1 可以与 APR3 相互作用并刺激人牙髓细胞的分化和矿化。未来的研究应探讨这种相互作用的潜在功能联系和分子机制。