Cited by 50Bone Metabolism and DiseasesCellular Mechanics and InteractionsPhagocytosis and Immune Regulation

Heterogeneity and Actin Cytoskeleton in Osteoclast and Macrophage Multinucleation

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Takito, Jiro, Nakamura, Masanori·2020·International Journal of Molecular Sciences

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.

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  • Heterogeneity is an integral feature of osteoclast fusion and may be related to the capacity of fusion precursors to adapt to specific bone microenvironments.

    “As reviewed elsewhere,160 heterogeneity is an integral feature of osteoclast fusion and may be related to the capacity of fusion precursors to adapt to specific bone microenvironments.”

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References 174 · Cited by 50

Authors
Takito, J., & Nakamura, M.
Affiliations
SHOWA Medical University (JP)
Corresponding author
Takito, Jiro
Venue
International Journal of Molecular Sciences
Publisher
MDPI AG
Published
2020-09-10
Volume
21
Issue
18
Pages
6629
ISSN
1422-0067 (ISSN-L)
OpenAlex
W3084071956
Cited by
50
References
174
Citations by year
2026: 11 · 2025: 11 · 2024: 6 · 2023: 4 · 2022: 9 · 2021: 8 · 2020: 1
FWCI
0.53
Type
journal article
Language
en
Open access
Locations
  • International Journal of Molecular Sciences (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
  • Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
Keywords
macrophage fusion, actin cytoskeleton, cell fusion, cellular heterogeneity, podosomes, RANKL signaling, osteoclastogenesis, cell adhesion
MeSH terms
Animals, Cell Nucleus, Humans, Actin Cytoskeleton, Osteoclasts, Phagocytes

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