Heterogeneity and Actin Cytoskeleton in Osteoclast and Macrophage Multinucleation

Int J Mol Sci. 2020 Sep 10;21(18):6629. doi: 10.3390/ijms21186629.

Abstract

Osteoclast signatures are determined by two transcriptional programs, the lineage-determining transcription pathway and the receptor activator of nuclear factor kappa-B ligand (RANKL)-dependent differentiation pathways. During differentiation, mononuclear precursors become multinucleated by cell fusion. Recently, live-cell imaging has revealed a high level of heterogeneity in osteoclast multinucleation. This heterogeneity includes the difference in the differentiation states and the mobility of the fusion precursors, as well as the mode of fusion among the fusion precursors with different numbers of nuclei. In particular, fusion partners often form morphologically distinct actin-based linkages that allow two cells to exchange lipids and proteins before membrane fusion. However, the origin of this heterogeneity remains elusive. On the other hand, osteoclast multinucleation is sensitive to the environmental cues. Such cues promote the reorganization of the actin cytoskeleton, especially the formation and transformation of the podosome, an actin-rich punctate adhesion. This review covers the heterogeneity of osteoclast multinucleation at the pre-fusion stage with reference to the environment-dependent signaling pathway responsible for reorganizing the actin cytoskeleton. Furthermore, we compare osteoclast multinucleation with macrophage fusion, which results in multinucleated giant macrophages.

Keywords: actin; environment-dependent signaling; foreign body giant cells; fusion; macrophage; mechanotransduction; multinucleation; osteoclasts; podosome.

Publication types

  • Review

MeSH terms

  • Actin Cytoskeleton / physiology*
  • Animals
  • Cell Nucleus
  • Humans
  • Osteoclasts / physiology*
  • Phagocytes / physiology*