Bone Resorption by Osteoclasts
Abstract
Osteoporosis, a disease endemic in Western society, typically reflects an imbalance in skeletal turnover so that bone resorption exceeds bone formation. Bone resorption is the unique function of the osteoclast, and anti-osteoporosis therapy to date has targeted this cell. The osteoclast is a specialized macrophage polykaryon whose differentiation is principally regulated by macrophage colony-stimulating factor, RANK ligand, and osteoprotegerin. Reflecting integrin-mediated signals, the osteoclast develops a specialized cytoskeleton that permits it to establish an isolated microenvironment between itself and bone, wherein matrix degradation occurs by a process involving proton transport. Osteopetrotic mutants have provided a wealth of information about the genes that regulate the differentiation of osteoclasts and their capacity to resorb bone.
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Osteoclast formation from macrophages is principally regulated by M-CSF, RANKL, and OPG.
“Formation of osteoclasts from macrophages is principally regulated by macrophage colony-stimulating factor, RANK ligand (RANKL), and osteoprotegerin (OPG) [259].”
From MicroRNAs as Regulators of Phagocytosis (2022) · cites this paper as [259]
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Jo, Y., Sarkar, N., & Bose, S. (2023) · Journal of Materials Chemistry B · doi:10.1039/d2tb02210a · Cited by 22 · see citing works
Olufsen, M., & Arukwe, A. (2011) · Aquatic Toxicology · doi:10.1016/j.aquatox.2011.09.005 · Cited by 20 · see citing works
Peroxidase enzymes inhibit osteoclast differentiation and bone resorption
Panagopoulos, V., Liapis, V., Zinonos, I., Hay, S., Leach, D. A., Ingman, W., DeNichilo, M. O., Atkins, G. J., Findlay, D. M., Zannettino, A. C. W., et al. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.11.007 · Cited by 18 · see citing works
Effect of remifentanil on pre-osteoclast cell differentiation in vitro
Jeon, H.-O., Choi, I.-S., Yoon, J.-Y., Kim, E.-J., Yoon, J.-U., Cho, A.-R., Kim, H.-J., & Kim, C.-H. (2018) · Journal of Dental Anesthesia and Pain Medicine · doi:10.17245/jdapm.2018.18.1.9 · Cited by 4 · see citing works
- Authors
- Teitelbaum, S. L.
- Affiliations
- Barnes-Jewish Hospital (US)
- Corresponding author
- Teitelbaum, Steven L.
- Venue
- Science
- Published
- 2000-09
- Volume
- 289
- Issue
- 5484
- Pages
- 1504-1508
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W1967502057
- Cited by
- 3,962
- References
- 5
- Citations by year
- 2026: 82 · 2025: 123 · 2024: 142 · 2023: 151 · 2022: 159 · 2021: 188 · 2020: 202 · 2019: 199 · 2018: 200 · 2017: 163 · 2016: 155 · 2015: 184 · 2014: 176 · 2013: 161 · 2012: 196
- FWCI
- 7.69
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Health Sciences › Medicine › Rheumatology › Bone and Dental Protein Studies
- Keywords
- bone resorption, osteoclasts, osteoporosis, osteoclastogenesis, macrophage colony-stimulating factor, RANK ligand, osteoprotegerin, integrins, cytoskeleton, matrix degradation, proton transport, bone turnover
- MeSH terms
- Animals, Bone Resorption, Carrier Proteins, Cell Differentiation, Cell Membrane, Glycoproteins, Humans, Macrophages, Membrane Glycoproteins, Osteoclasts, Osteopetrosis, Integrins, Macrophage Colony-Stimulating Factor, Stromal Cells, Receptors, Tumor Necrosis Factor, Receptors, Cytoplasmic and Nuclear, Osteoprotegerin, RANK Ligand, Receptor Activator of Nuclear Factor-kappa B
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