Guanine and nucleotide binding protein 3 promotes odonto/osteogenic differentiation of apical papilla stem cells via JNK and ERK signaling pathways

Int J Mol Med. 2019 Jan;43(1):382-392. doi: 10.3892/ijmm.2018.3984. Epub 2018 Nov 7.

Abstract

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.

MeSH terms

  • Animals
  • Anthracenes / pharmacology
  • Biomarkers / metabolism
  • Calcification, Physiologic / drug effects
  • Cell Differentiation* / drug effects
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Dental Papilla / cytology*
  • GTP-Binding Protein alpha Subunits, Gi-Go / metabolism*
  • Gene Knockdown Techniques
  • JNK Mitogen-Activated Protein Kinases / metabolism*
  • MAP Kinase Signaling System* / drug effects
  • Male
  • Mice, Inbred C57BL
  • Odontogenesis* / drug effects
  • Osteogenesis* / drug effects
  • Stem Cells / cytology
  • Stem Cells / drug effects
  • Stem Cells / enzymology*
  • Tooth Root / embryology
  • Tooth Root / metabolism
  • Up-Regulation / drug effects
  • Up-Regulation / genetics

Substances

  • Anthracenes
  • Biomarkers
  • pyrazolanthrone
  • JNK Mitogen-Activated Protein Kinases
  • GTP-Binding Protein alpha Subunits, Gi-Go
  • Gnai3 protein, mouse