The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.
The Role of NFAT in Osteoclast Formation
Abstract
Osteoclasts are cells of monocyte-macrophage origin that degrade bone matrix. Receptor activator of NF-kappaB ligand (RANKL) induces osteoclast formation in the presence of macrophage-colony-stimulating factor (M-CSF) and costimulatory signals. RANKL induces activation of the TNF receptor-associated factor 6 (TRAF6) and c-Fos pathways, which lead to the osteoclast-specific event, that is, autoamplification of nuclear factor of activated T cells (NFAT)c1, the master transcription factor for osteoclast differentiation. Autoamplification of NFATc1 is dependent on the calcium signaling of immunoglobulin-like receptors associated with immunoreceptor tyrosine-based activation motif (ITAM)-harboring adaptors. In addition to the calcineurin-NFATc1 axis, calcium signaling activates the calmodulin-dependent kinase pathway, which also plays a critical role in osteoclast formation. Such advances in the understanding of the molecular mechanism of osteoclast differentiation are expected to lead to novel therapeutic approaches to bone diseases.
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“This activates cyclic adenosine monophosphate (cAMP) response element-binding protein (CREB) and the calcineurin pathway [21,24,25,27], a key costimulatory pathway of NFATc1 [21,23] and an important signaling component of a number of immune cell receptors [28] (Figure 4 and Figure 5).”
From Osteoclasts and Microgravity (2020) · cites this paper as [25]
In the citing paper
“NFATc1 binds to its own promoter, switching on an epigenetically controlled autoregulatory cycle that permits efficient induction of the osteoclast-specific genes, tartrate-resistant acid phosphatase (TRAP), cathepsin K, as well as the fusion-specific genes, dendritic cell-specific transmembrane protein (DC-STAMP) and ATPase H+ transporting V0 subunit D2 (ATP6v0d2) [20,25,26] (Figure 3).”
From Osteoclasts and Microgravity (2020) · cites this paper as [25]
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Metadata
- Authors
- TAKAYANAGI, H.
- Affiliations
- Tokyo Medical and Dental University (JP)
- Corresponding author
- TAKAYANAGI, HIROSHI
- ORCID
- TAKAYANAGI, HIROSHI
- Venue
- Annals of the New York Academy of Sciences
- Publisher
- Wiley
- Published
- 2007-11
- Volume
- 1116
- Issue
- 1
- Pages
- 227-237
- ISSN
- 0077-8923 (ISSN-L)
- 1749-6632
- OpenAlex
- W1975505424
- Cited by
- 442
- References
- 36
- Citations by year
- 2026: 6 · 2025: 16 · 2024: 16 · 2023: 21 · 2022: 23 · 2021: 21 · 2020: 33 · 2019: 35 · 2018: 34 · 2017: 28 · 2016: 31 · 2015: 38 · 2014: 19 · 2013: 22 · 2012: 29
- FWCI
- 1.13
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annals of the New York Academy of Sciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Kanae Foundation for the Promotion of Medical Science
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Signaling Pathways in Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Receptors and Signaling
- Keywords
- osteoclastogenesis, NFATc1, RANKL, TRAF6, c-fos, calcineurin, calcium signaling, calcium/calmodulin-dependent protein kinase, ITAM, macrophage colony-stimulating factor, bone resorption, bone disease
- MeSH terms
- Animals, Humans, Osteoclasts, Transcription, Genetic, Signal Transduction, NFATC Transcription Factors, RANK Ligand
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