Heterogeneity and Actin Cytoskeleton in Osteoclast and Macrophage Multinucleation
Open accessAbstract
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.”
From Bone remodeling: an operational process ensuring survival and bone mechanical competence (2022) · cites this paper as [160]
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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)
- PMC
- PMC7554939
- 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
- gold
- doi.org
- Licence
- 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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