Jiangsu Key Laboratory of Oral Diseases, Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China.
Int J Mol Med. 2019 Jan;43(1):382-392. doi: 10.3892/ijmm.2018.3984. Epub 2018 Nov 7.
Odonto/osteogenic differentiation of stem cells from the apical papilla (SCAPs) is a key process in tooth root formation and development. However, the molecular mechanisms underlying this process remain largely unknown. In the present study, it was identified that guanine and nucleotide binding protein 3 (GNAI3) was at least in part responsible for the odonto/osteogenic differentiation of SCAPs. GNAI3 was markedly induced in mouse tooth root development in vivo and in human SCAPs mineralization in vitro. Notably, knockdown of GNAI3 by lentiviral vectors expressing short‑hairpin RNAs against GNAI3 significantly inhibited the proliferation, cell cycle progression and migration of SCAPs, as well as odonto/osteogenic differentiation of SCAPs in vitro, suggesting that GNAI3 may play an essential role in tooth root development. The promotive role of GNAI3 in odonto/osteogenic differentiation was further confirmed by downregulation of odonto/osteogenic makers in GNAI3‑deficient SCAPs. In addition, knockdown of GNAI3 effectively suppressed activity of c‑Jun N‑terminal kinase (JNK) and extracellular‑signal regulated kinase (ERK) signaling pathways that was induced during SCAPs differentiation, suggesting that GNAI3 promotes SCAPs mineralization at least partially via JNK/ERK signaling. Taken together, the present results implicate GNAI3 as a critical regulator of odonto/osteogenic differentiation of SCAPs in tooth root development, and suggest a possible role of GNAI3 in regeneration processes in dentin or other tissues.
干细胞根尖乳头(SCAPs)的牙骨质/成骨分化是牙根形成和发育的关键过程。然而,这一过程的分子机制在很大程度上尚不清楚。本研究鉴定出鸟嘌呤核苷酸结合蛋白 3(GNAI3)至少部分负责 SCAPs 的牙骨质/成骨分化。GNAI3 在体内小鼠牙根发育和体外人 SCAPs 矿化中明显被诱导。值得注意的是,通过表达针对 GNAI3 的短发夹 RNA 的慢病毒载体敲低 GNAI3 显著抑制了 SCAPs 的增殖、细胞周期进程和迁移,以及体外 SCAPs 的牙骨质/成骨分化,表明 GNAI3 可能在牙根发育中发挥重要作用。GNAI3 下调后,SCAPs 中的牙骨质/成骨标志物表达减少,进一步证实了 GNAI3 在牙骨质/成骨分化中的促进作用。此外,敲低 GNAI3 有效抑制了 SCAPs 分化过程中诱导的 c-Jun N-末端激酶(JNK)和细胞外信号调节激酶(ERK)信号通路的活性,表明 GNAI3 通过 JNK/ERK 信号通路至少部分促进了 SCAPs 的矿化。综上所述,本研究结果表明 GNAI3 是牙根发育中 SCAPs 牙骨质/成骨分化的关键调节因子,并提示 GNAI3 在牙本质或其他组织的再生过程中可能发挥作用。