Maackiain dampens osteoclastogenesis via attenuating RANKL-stimulated NF-κB signalling pathway and NFATc1 activity

J Cell Mol Med. 2020 Nov;24(21):12308-12317. doi: 10.1111/jcmm.15647. Epub 2020 Sep 16.

Abstract

Osteolytic diseases are typified by over-enhanced formation and resorbing function of osteoclasts and have a major impact on human health. Inhibition of osteoclastic differentiation and function is a key strategy for clinical therapy of osteolytic conditions. Maackiain is a natural compound extracted from Sophora flavescens, which has been applied to anti-allergic and anti-tumour treatments. The present results showed that Maackiain could restrain receptor activator of nuclear factor-κB ligand (RANKL)-stimulated osteoclast formation and hydroxyapatite resorption dose-dependently, and interrupt the structures of F-actin belts in the mature osteoclasts. It also repressed the expressions of osteoclast-specific genes and proteins. Furthermore, Maackiain could inhibit RANKL-stimulated NF-κB and calcium signalling pathways, and dampen Nuclear factor of activated T cell cytoplasmic 1 activity, protein expression and translocation into the nucleus. These results revealed that Maackiain may have a potential therapeutic effect on osteoclast-related disorders.

Keywords: maackiain; nuclear factor of activated T cells 1; nuclear factor-κB; osteoclast; receptor activator of nuclear factor-κB ligand.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus
  • Animals
  • Bone Marrow Cells / cytology
  • Bone Resorption / pathology
  • Calcium / metabolism
  • Cell Differentiation / drug effects
  • Cell Survival
  • Female
  • Gene Expression Regulation
  • Macrophages / metabolism
  • Mice
  • NF-kappa B / metabolism*
  • NFATC Transcription Factors / metabolism*
  • Osteoblasts / cytology
  • Osteoclasts / cytology
  • Osteoclasts / drug effects*
  • Osteogenesis / drug effects*
  • Pterocarpans / pharmacology*
  • RANK Ligand / metabolism*
  • Signal Transduction / drug effects

Substances

  • NF-kappa B
  • NFATC Transcription Factors
  • Nfatc1 protein, mouse
  • Pterocarpans
  • RANK Ligand
  • Tnfsf11 protein, mouse
  • Calcium
  • inermin