Tatarinan O, a lignin-like compound from the roots of Acorus tatarinowii Schott inhibits osteoclast differentiation through suppressing the expression of c-Fos and NFATc1

Int Immunopharmacol. 2016 May:34:212-219. doi: 10.1016/j.intimp.2016.03.001. Epub 2016 Mar 9.

Abstract

Osteoclasts (OC) are large multinucleated cells derived from monocyte/macrophage precursors. Suppressing osteoclastogenesis is considered as an effective therapeutic approach to erosive bone disease. The root of Acorus tatarinowii Schott, a well-known traditional Chinese medicine was used to treat rheumatosis and other inflammatory disease. However, the effects of tatarinan O (TO), one of the lignin-like compounds isolated from the roots of Acorus tatarinowii Schott during bone development are still unclear. In the present study, we explored the effect of TO on RANKL-induced osteoclastogenesis in vitro. TO was found to suppress osteoclast differentiation from RANKL-stimulated mouse bone marrow macrophages (BMMs) without significant cytotoxicity. TO also dose-dependently suppressed bone resorption activity of mature osteoclasts. Additionally, TO apparently inhibited the expression of osteoclastic marker genes, such as MMP-9, Cts K and TRAP. Furthermore, our results showed that TO decreased RANKL-induced expression of c-Fos and NFATc1 without influencing NF-κB activation and MAPK phosphorylation. Hence, for the first time we revealed that TO dose-dependently inhibited osteoclastogenesis from RANKL-stimulated mouse BMMs via decreasing the expression of NFATc1 and c-Fos.

Keywords: Bone resorption; NFATc1; Osteoclast; RANKL; Tatarinan O; c-Fos.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acorus / immunology
  • Animals
  • Bone Resorption / drug therapy*
  • Cell Differentiation / drug effects
  • Cells, Cultured
  • Down-Regulation / drug effects
  • Humans
  • Lignans / pharmacology*
  • Macrophages / drug effects
  • Macrophages / physiology
  • Male
  • Medicine, Chinese Traditional
  • Mice
  • Mice, Inbred C57BL
  • NFATC Transcription Factors / genetics
  • NFATC Transcription Factors / metabolism*
  • Osteoclasts / drug effects*
  • Osteoclasts / physiology
  • Plant Roots
  • Proto-Oncogene Proteins c-fos / genetics
  • Proto-Oncogene Proteins c-fos / metabolism*
  • RANK Ligand / physiology

Substances

  • Lignans
  • NFATC Transcription Factors
  • Proto-Oncogene Proteins c-fos
  • RANK Ligand