Cell line IDG-SW3 replicates osteoblast-to-late-osteocyte differentiation in vitro and accelerates bone formation in vivo
Open accessAbstract
Osteocytes are the most abundant cells in bone yet are the most challenging to study because they are embedded in a mineralized matrix. We generated a clonal cell line called IDG-SW3 (for Immortomouse/Dmp1-GFP-SW3) from long-bone chips from mice carrying a Dmp1 promoter driving GFP crossed with the Immortomouse, which expresses a thermolabile SV40 large T antigen regulated by interferon γ (IFN-γ). Cells from these mice can be expanded at 33 °C in the presence of IFN-γ and then allowed to resume their original phenotype at 37 °C in the absence of IFN-γ. IDG-SW3 cells are Dmp1-GFP− and T antigen+ under immortalizing conditions but Dmp1-GFP+ and T antigen− under osteogenic conditions. Like osteoblasts, they express alkaline phosphatase and produce and mineralize a type 1 collagen matrix containing calcospherulites. Like early osteocytes, they express E11/gp38, Dmp1, MEPE, and Phex. Like late osteocytes, they develop a dendritic morphology and express SOST/sclerostin and fibroblast growth factor 23 (FGF-23), regulated by parathyroid hormone (PTH) and 1,25-dihydroxyvitamin D3. When cultured on 3D matrices, they express Dmp1-GFP and sclerostin. When the 3D cultures are implanted in calvarial defects in vivo, they accelerate bone healing. This cell line should prove useful for studying osteoblast-to-osteocyte transition, mechanisms for biomineralization, osteocyte function, and regulation of SOST/sclerostin and FGF-23. © 2011 American Society for Bone and Mineral Research
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In the IDG-SW3 dataset, days 3, 14 and 35 represent osteoblast, early osteocyte and mature osteocyte stages, respectively.
“Data from days 3, 14 and 35 represent osteoblast, early osteocyte and mature osteocyte stages, respectively86.”
From Osteocyte transcriptome mapping identifies a molecular landscape controlling skeletal homeostasis and susceptibility to skeletal disease (2021) · cites this paper as [86]
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Guidelines for assessment of bone microstructure in rodents using micro–computed tomography
Bouxsein, M., Boyd, S. K., Christiansen, B., Guldberg, R. E., Jepsen, K. J., & Müller, R. (2010) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.141 · Cited by 4,461 · see citing works
Bonewald, L. F. (2011) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.320 · Cited by 2,287 · see citing works
Self-citationFeng, J. Q., Ward, L. M., Liu, S., Lu, Y., Xie, Y., Yuan, B., Yu, X., Rauch, F., Davis, S. I., Zhang, S., et al. (2006) · Nature Genetics · doi:10.1038/ng1905 · Cited by 1,199 · cited 1× · see citing works
“In hypophosphatemia, Dmp1 and Phex, also produced by the osteocyte, downregulate FGF-23 expression, thereby increasing phosphate reabsorption in the kidney and enabling the body to maintain normal phosphate levels and bone mineral content.((13,33)) Patients with chronic kidney disease, vitamin D deficiency, or hypopho…”
BackgroundSelf-citationFogh, J., & Trempe, G. (1975) · Springer eBooks · doi:10.1007/978-1-4757-1647-4_5 · Cited by 1,008 · see citing works
Sclerostin is a delayed secreted product of osteocytes that inhibits bone formation
Poole, K. E. S., Van Bezooijen, R. L., Loveridge, N., Hamersma, H., Papapoulos, S. E., Löwik, C. W., & Reeve, J. (2005) · The FASEB Journal · doi:10.1096/fj.05-4221fje · Cited by 965 · see citing works
Li, X., Ominsky, M. S., Niu, Q., Sun, N., Daugherty, B., D’Agostin, D. M., Kurahara, C., Gao, Y., Cao, J., Gong, J., et al. (2008) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.080216 · Cited by 938 · see citing works
van Bezooijen, R. L., Roelen, B. A. J., Visser, A., van der Wee-Pals, L. J. A., de Wilt, E., Karperien, M., Hamersma, H. A., Papapoulos, S. E., ten Dijke, P., & Löwik, C. W. G. M. (2004) · The Journal of Experimental Medicine · doi:10.1084/jem.20031454 · Cited by 893 · see citing works
Li, X., Ominsky, M. S., Warmington, K. S., Morony, S., Gong, J., Cao, J., Gao, Y., Shalhoub, V., Tipton, B., Haldankar, R., et al. (2008) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.081206 · Cited by 784 · see citing works
Fogh, J. (1975) · Springer eBooks · doi:10.1007/978-1-4757-1647-4 · Cited by 759 · see citing works
Direct derivation of conditionally immortal cell lines from an H-2Kb-tsA58 transgenic mouse.
Jat, P., Noble, M., Ataliotis, P., Tanaka, Y., Yannoutsos, N., Larsen, L., & Kioussis, D. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.12.5096 · Cited by 744 · see citing works
Bellido, T., Ali, A., Gubrij, I. B., Plotkin, L. I., Fu, Q., O’Brien, C. A., Manolagas, S. C., & Jilka, R. L. (2005) · Endocrinology · doi:10.1210/en.2005-0239 · Cited by 640 · see citing works
SOST is a target gene for PTH in bone
Keller, H., & Kneissel, M. (2005) · Bone · doi:10.1016/j.bone.2005.03.018 · Cited by 618 · see citing works
Characterization of a human osteosarcoma cell line (Saos-2) with osteoblastic properties.
Rodan, S. B., Imai, Y., Thiede, M. A., Wesolowski, G. A., Thompson, D., Bar‐Shavit, Z., Shull, S., Mann, K. G., & Rodan, G. A. (1987) · PubMed · Cited by 588 · see citing works
Establishment of an Osteocyte-like Cell Line, MLO-Y4
Kato, Y., Windle, J. J., Koop, B. A., Mundy, G. R., & Bonewald, L. F. (1997) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.1997.12.12.2014 · Cited by 549 · see citing works
Self-citationControl of Bone Mass and Remodeling by PTH Receptor Signaling in Osteocytes
O’Brien, C. A., Plotkin, L. I., Galli, C., Goellner, J. J., Gortázar, A. R., Allen, M. R., Robling, A. G., Bouxsein, M., Schipani, E., Turner, C. H., et al. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002942 · Cited by 389 · see citing works
Whitehead, R., VanEeden, P. E., Noble, M., Ataliotis, P., & Jat, P. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.2.587 · Cited by 364 · see citing works
Bilezikian, J. P., Raisz, L. G. 1., & Martin, T. J. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-373884-4.x0001-8 · Cited by 335 · see citing works
Sclerostin: Current Knowledge and Future Perspectives
Moester, M. J. C., Papapoulos, S. E., Löwik, C. W. G. M., & van Bezooijen, R. L. (2010) · Calcified Tissue International · doi:10.1007/s00223-010-9372-1 · Cited by 332 · see citing works
Partridge, N. C., Alcorn, D., Michelangeli, V. P., Ryan, G. B., & Martin, T. J. (1983) · PubMed · Cited by 310 · see citing works
Zhang, K., Barragan‐Adjemian, C., Ye, L., Kotha, S. P., Dallas, M., Lu, Y., Zhao, S., Harris, M. A., Harris, S. E., Feng, J. Q., et al. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.02120-05 · Cited by 299 · see citing works
Self-citationFluid Shear-Induced ATP Secretion Mediates Prostaglandin Release in MC3T3-E1 Osteoblasts
Genetos, D. C., Geist, D. J., Liu, D., Donahue, H. J., & Duncan, R. L. (2005) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.041009 · Cited by 279 · see citing works
Patterns of FGF-23, DMP1, and MEPE expression in patients with chronic kidney disease
Pereira, R. C., Jüppner, H., Azucena-Serrano, C. E., Yadin, O., Salusky, I. B., & Wesseling‐Perry, K. (2009) · Bone · doi:10.1016/j.bone.2009.08.008 · Cited by 271 · see citing works
Kalajzić, I., Braut, A., Guo, D., Jiang, X., Kronenberg, M. S., Mina, M., Harris, M. A., Harris, S. E., & Rowe, D. W. (2004) · Bone · doi:10.1016/j.bone.2004.03.006 · Cited by 220 · see citing works
Establishment of an Osteoid Preosteocyte-like Cell MLO-A5 That Spontaneously Mineralizes in Culture
Kato, Y., Boskey, A. L., Spevak, L., Dallas, M., Hori, M., & Bonewald, L. F. (2001) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.2001.16.9.1622 · Cited by 207 · see citing works
Self-citationMechanical Loading Stimulates Dentin Matrix Protein 1 (DMP1) Expression in Osteocytes In Vivo
Gluhak‐Heinrich, J., Ye, L., Bonewald, L. F., Feng, J. Q., MacDougall, M. J., Harris, S. E., & Pavlin, D. (2003) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.2003.18.5.807 · Cited by 200 · see citing works
Self-citationKitase, Y., Barragan, L., Qing, H., Kondoh, S., Jiang, J. X., Johnson, M. L., & Bonewald, L. F. (2010) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.168 · Cited by 199 · see citing works
Self-citationVincent, C., Findlay, D. M., Welldon, K. J., Wijenayaka, A. R., Zheng, T. S., Haynes, D. R., Fazzalari, N. L., Evdokiou, A., & Atkins, G. J. (2009) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.090305 · Cited by 183 · see citing works
FGF-23: More than a regulator of renal phosphate handling?
Jüppner, H., Wolf, M. S., & Salusky, I. B. (2010) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.170 · Cited by 159 · see citing works
Aalami, O., Nacamuli, R. P., Lenton, K. A., Cowan, C. M., Fang, T. D., Fong, K. D., Shi, Y.-Y., Song, H. M., Sahar, D. E., & Longaker, M. T. (2004) · Plastic & Reconstructive Surgery · doi:10.1097/01.prs.0000131016.12754.30 · Cited by 150 · see citing works
Boyan, B. D., Schwartz, Z., Bonewald, L. F., & Swain, L. D. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)80148-x · Cited by 149 · see citing works
Self-citationBarragan‐Adjemian, C., Nicolella, D. P., Dusevich, V., Dallas, M. R., Eick, J. D., & Bonewald, L. F. (2006) · Calcified Tissue International · doi:10.1007/s00223-006-0107-2 · Cited by 142 · see citing works
Self-citationMechanical stimulation in vivo reduces osteocyte expression of sclerostin.
Robling, A. G., Bellido, T., & Turner, C. H. (2006) · PubMed · Cited by 141 · see citing works
Sittichokechaiwut, A., Scutt, A. M., Ryan, A. J., Bonewald, L. F., & Reilly, G. C. (2009) · Bone · doi:10.1016/j.bone.2008.12.027 · Cited by 97 · see citing works
Self-citationBellido, T. (2006) · PubMed · Cited by 69 · see citing works
The phosphate regulating hormone fibroblast growth factor‐23
Marsell, R., & Jonsson, K. B. (2010) · Acta Physiologica · doi:10.1111/j.1748-1716.2010.02163.x · Cited by 28 · see citing works
Conditionally immortalized mouse hepatocytes for use in liver gene therapy
Allen, K. J., Reyes, R., Demmler, K., Mercer, J. F. B., Williamson, R., & Whitehead, R. H. (2000) · Journal of Gastroenterology and Hepatology · doi:10.1046/j.1440-1746.2000.2328.x · Cited by 26 · see citing works
Klein‐Nulend, J., & Bonewald, L. F. (2008) · Elsevier eBooks · doi:10.1016/b978-0-12-373884-4.00028-8 · Cited by 26 · see citing works
Self-citationLocalization of Transgenes and Genotyping of H-2K b -tsA58 Transgenic Mice
Kern, G., & Flucher, B. E. (2005) · BioTechniques · doi:10.2144/05381bm03 · Cited by 15 · see citing works
Flagged first, then by citations
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Research works printed but not linked: 1
- Qing, 2010, PTHR1 in osteocytes plays a major role in perilacunar remodeling through the activation of “osteoclastic” genes in osteocytes, J Bone Min Res.
Cited by
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The Osteocyte: An Endocrine Cell … and More
Dallas, S. L., Prideaux, M., & Bonewald, L. F. (2013) · Endocrine Reviews · doi:10.1210/er.2012-1026 · Cited by 1,042 · see citing works
Self-citationRobling, A. G., & Bonewald, L. F. (2020) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021119-034332 · Cited by 539 · see citing works
Self-citationIn Vitro Bone Cell Models: Impact of Fluid Shear Stress on Bone Formation
Wittkowske, C., Reilly, G. C., Lacroix, D. J., & Perrault, C. M. (2016) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2016.00087 · Cited by 289 · see citing works
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Spatz, J., Wein, M. N., Gooi, J. H., Qu, Y., Garr, J., Liu, X. S., Barry, K. J., Uda, Y., Lai, F., Dedic, C., et al. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.628313 · Cited by 294 · see citing works
Qin, Y., Peng, Y., Zhao, W., Pan, J., Ksiȩżak-Reding, H., Cardozo, C. P., Wu, Y., Pajevic, P. D., Bonewald, L. F., Bauman, W. A., et al. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.770941 · Cited by 282 · see citing works
Self-citationCathepsin K Inhibitors for Osteoporosis: Biology, Potential Clinical Utility, and Lessons Learned
Drake, M. T., Clarke, B. L., Oursler, M. J., & Khosla, S. (2017) · Endocrine Reviews · doi:10.1210/er.2015-1114 · Cited by 268 · see citing works
The osteocyte as a signaling cell
Delgado‐Calle, J., & Bellido, T. (2021) · Physiological Reviews · doi:10.1152/physrev.00043.2020 · Cited by 269 · see citing works
Regulation of Bone Remodeling by Parathyroid HormonePreprint
Wein, M. N., & Kronenberg, H. M. (2018) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a031237 · Cited by 243 · see citing works
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Stern, A. R., Stern, M. M., Dyke, M. E. V., Jähn, K., Prideaux, M., & Bonewald, L. F. (2012) · BioTechniques · doi:10.2144/0000113876 · Cited by 207 · see citing works
Self-citationUda, Y., Azab, E., Sun, N., Shi, C., & Pajevic, P. D. (2017) · Current Osteoporosis Reports · doi:10.1007/s11914-017-0373-0 · Cited by 201 · see citing works
Effects of PTH on osteocyte function
Bellido, T., Saini, V., & Pajevic, P. D. (2013) · Bone · doi:10.1016/j.bone.2012.09.016 · Cited by 196 · see citing works
Role of phosphate sensing in bone and mineral metabolism
Chande, S., & Bergwitz, C. (2018) · Nature Reviews Endocrinology · doi:10.1038/s41574-018-0076-3 · Cited by 189 · see citing works
Osteocyte necrosis triggers osteoclast-mediated bone loss through macrophage-inducible C-type lectin
Andreev, D., Liu, M., Weidner, D., Kachler, K., Faas, M., Grüneboom, A., Schlötzer-Schrehardt, U., Muñoz, L. E., Steffen, U., Grötsch, B., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci134214 · Cited by 188 · see citing works
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Atkins, G. J., & Findlay, D. M. (2012) · Osteoporosis International · doi:10.1007/s00198-012-1915-z · Cited by 185 · see citing works
Sims, N. A., & Martin, T. J. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00041 · Cited by 184 · see citing works
Regulation of bone-renal mineral and energy metabolism: the PHEX, FGF23, DMP1, MEPE ASARM pathway
Rowe, P. S. N. (2012) · Critical Reviews™ in Eukaryotic Gene Expression · doi:10.1615/critreveukargeneexpr.v22.i1.50 · Cited by 173 · see citing works
Uluçkan, Ö., Jiménez, M., Karbach, S. H., Jeschke, A., Graña‐Castro, O., Keller, J., Busse, B., Croxford, A. L., Finzel, S., Koenders, M. I., et al. (2016) · Science Translational Medicine · doi:10.1126/scitranslmed.aad8996 · Cited by 170 · see citing works
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Self-citationIn vitro and in vivo approaches to study osteocyte biology
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HDAC5 Controls MEF2C-Driven Sclerostin Expression in Osteocytes
Wein, M. N., Spatz, J., Nishimori, S., Doench, J., Root, D., Babij, P., Nagano, K., Baron, R., Brooks, D., Bouxsein, M., et al. (2015) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2381 · Cited by 158 · see citing works
Comparative Biocompatibility and Osteogenic Potential of Two Bioceramic Sealers
Giacomino, C. M., Wealleans, J. A., Kuhn, N., & Diogenes, A. R. (2018) · Journal of Endodontics · doi:10.1016/j.joen.2018.08.007 · Cited by 158 · see citing works
Autoregulation of Osteocyte Sema3A Orchestrates Estrogen Action and Counteracts Bone Aging
Hayashi, M., Nakashima, T., Yoshimura, N., Okamoto, K., Tanaka, S., & Takayanagi, H. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2018.12.021 · Cited by 156 · see citing works
Sclerostin's role in bone's adaptive response to mechanical loading
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Phosphate Toxicity in CKD: The Killer among Us
Ritter, C. S., & Slatopolsky, E. (2016) · Clinical Journal of the American Society of Nephrology · doi:10.2215/cjn.11901115 · Cited by 149 · see citing works
Pereira, M., Jeyabalan, J., Jørgensen, C. S., Hopkinson, M., Al-Jazzar, A., Roux, J. P., Chavassieux, P., Orriss, I. R., Cleasby, M. E., & Chenu, C. (2015) · Bone · doi:10.1016/j.bone.2015.08.006 · Cited by 137 · see citing works
Youlten, S. E., Kemp, J. P., Logan, J. G., Ghirardello, E. J., Sergio, C. M., Dack, M. R. G., Guilfoyle, S. E., Leitch, V. D., Butterfield, N. C., Komla-Ebri, D., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22517-1 · Cited by 133 · see citing works
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Bonewald, L. F., & Wacker, M. (2012) · Pediatric Nephrology · doi:10.1007/s00467-012-2309-3 · Cited by 128 · see citing works
Self-citationSt. John, H. C., Bishop, K. A., Meyer, M. B., Benkusky, N. A., Leng, N., Kendziorski, C., Bonewald, L. F., & Pike, J. W. (2014) · Molecular Endocrinology · doi:10.1210/me.2014-1091 · Cited by 127 · see citing works
Self-citationOsteocytic oxygen sensing controls bone mass through epigenetic regulation of sclerostin
Stegen, S., Stockmans, I., Moermans, K., Thienpont, B., Maxwell, P. H., Carmeliet, P., & Carmeliet, G. (2018) · Nature Communications · doi:10.1038/s41467-018-04679-7 · Cited by 126 · see citing works
Prideaux, M., Wijenayaka, A. R., Kumarasinghe, D. D., Ormsby, R. T., Evdokiou, A., Findlay, D. M., & Atkins, G. J. (2014) · Calcified Tissue International · doi:10.1007/s00223-014-9879-y · Cited by 125 · see citing works
Galea, G. L., Meakin, L. B., Sugiyama, T., Zebda, N., Sunters, A., Taipaleenmäki, H., Stein, G. S., van Wijnen, A. J., Lanyon, L. E., & Price, J. S. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.405456 · Cited by 124 · see citing works
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Elefteriou, F., & Yang, X. (2011) · Bone · doi:10.1016/j.bone.2011.08.021 · Cited by 120 · see citing works
Jähn, K., Kelkar, S., Zhao, H., Xie, Y., Tiede-Lewis, L. M., Dusevich, V., Dallas, S. L., & Bonewald, L. F. (2017) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3167 · Cited by 116 · see citing works
“IDG-SW3 are immortalized cells that have been previously established as a suitable in vitro model for osteoblast-toosteocyte differentiation.((9)) Cells were cultured on type I collagen–coated plates and dishes (rat tail type I collagen; BD Biosciences, San Jose, CA, USA) at passages 7 to 25 and seeded at 40,000 cells…”
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Najafova, Z., Tirado-Magallanes, R., Subramaniam, M., Hossan, T., Schmídt, G., Nagarajan, S., Baumgart, S. J., Mishra, V. K., Bedi, U., Hesse, E., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw826 · Cited by 114 · see citing works
Osteon: Structure, Turnover, and Regeneration
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Holdsworth, G., Roberts, S. J., & Ke, H. Z. (2018) · Journal of Molecular Endocrinology · doi:10.1530/jme-18-0176 · Cited by 104 · see citing works
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Sasaki, F., Hayashi, M., Mouri, Y., Nakamura, S., ADACHI, T., & Nakashima, T. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.10.174 · Cited by 101 · see citing works
Paek, K., Kim, S., Tak, S., Kim, M. K., Park, J., Chung, S. H., Park, T. H., & Kim, J. A. (2022) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10313 · Cited by 100 · see citing works
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Kegelman, C. D., Coulombe, J. C., Jordan, K. M., Horan, D. J., Qin, L., Robling, A. G., Ferguson, V. L., Bellido, T., & Boerckel, J. D. (2019) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3876 · Cited by 95 · see citing works
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Nasello, G., Alamán‐Díez, P., Schiavi, J., Pérez, M. Á., McNamara, L. M., & García‐Aznar, J. M. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.00336 · Cited by 80 · see citing works
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Riquelme, M. A., Gu, S., Hua, R., & Jiang, J. X. (2021) · Bone Research · doi:10.1038/s41413-020-00126-w · Cited by 77 · see citing works
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Yee, C. S., Schurman, C. A., White, C. R., & Alliston, T. N. (2019) · Current Osteoporosis Reports · doi:10.1007/s11914-019-00514-0 · Cited by 69 · see citing works
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Creecy, A., Damrath, J. G., & Wallace, J. M. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.578477 · Cited by 68 · see citing works
Brady, R. T., O’Brien, F. J., & Hoey, D. A. (2015) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2015.02.080 · Cited by 67 · see citing works
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Rowe, P. S. (2012) · Cell Biochemistry and Function · doi:10.1002/cbf.2841 · Cited by 67 · see citing works
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Vazquez, M., Evans, B. A. J., Riccardi, D., Evans, S. L., Ralphs, J. R., Dillingham, C. M., & Mason, D. J. (2014) · Frontiers in Endocrinology · doi:10.3389/fendo.2014.00208 · Cited by 67 · see citing works
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Inoue, M., Ono, T., KAMEO, Y., Sasaki, F., Ono, T., ADACHI, T., & Nakashima, T. (2019) · Scientific Reports · doi:10.1038/s41598-019-40463-3 · Cited by 66 · see citing works
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Wein, M. N. (2017) · JBMR Plus · doi:10.1002/jbm4.10021 · Cited by 64 · see citing works
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Zhao, N., Nociti, F. H., Duan, P., Prideaux, M., Zhao, H. L., Foster, B. L., Somerman, M. J., & Bonewald, L. F. (2015) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2690 · Cited by 62 · see citing works
Self-citationIto, N., Findlay, D. M., Anderson, P., Bonewald, L. F., & Atkins, G. J. (2012) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2012.09.029 · Cited by 57 · see citing works
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Yang, Y., Wang, M., Yang, S., Lin, Y., Zhou, Q., Li, H., & Tang, T. (2020) · Biofabrication · doi:10.1088/1758-5090/aba1d0 · Cited by 56 · see citing works
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Xu, R., Zhang, C., Shin, D. Y., Kim, J., Lalani, S., Li, N., Yang, Y.-S., Liu, Y., Eiseman, M., Davis, R. J., et al. (2017) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3184 · Cited by 54 · see citing works
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Zhang, C., Bakker, A. D., Klein‐Nulend, J., & Bravenboer, N. (2019) · Current Osteoporosis Reports · doi:10.1007/s11914-019-00521-1 · Cited by 54 · see citing works
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Shah, K. M., Stern, M., Stern, A. R., Pathak, J. L., Bravenboer, N., & Bakker, A. D. (2016) · BoneKEy Reports · doi:10.1038/bonekey.2016.65 · Cited by 51 · see citing works
Prasadam, I., Farnaghi, S., Feng, J. Q., Gu, W., Perry, S., Crawford, R., & Xiao, Y. (2013) · Arthritis Research & Therapy · doi:10.1186/ar4333 · Cited by 50 · see citing works
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Prideaux, M., Schutz, C., Wijenayaka, A. R., Findlay, D. M., Campbell, D. G., Solomon, L. B., & Atkins, G. J. (2016) · Bone · doi:10.1016/j.bone.2016.04.017 · Cited by 48 · see citing works
Wang, K., Le, L., Chun, B. M., Tiede-Lewis, L. M., Shiflett, L. A., Prideaux, M., Campos, R., Veno, P. A., Xie, Y., Dusevich, V., et al. (2019) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3720 · Cited by 44 · see citing works
Self-citationShao, J., Zhou, Y., & Xiao, Y. (2018) · Bone · doi:10.1016/j.bone.2018.01.010 · Cited by 41 · see citing works
Sánchez‐de‐Diego, C., Artigas, N., Pimenta-Lopes, C., Valer, J. A., Torrejón, B., Gama-Pérez, P., Villena, J. A., García-Rovés, P. M., Rosa, J. L., & Ventura, F. (2019) · iScience · doi:10.1016/j.isci.2019.04.015 · Cited by 41 · see citing works
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Thompson, W. R., Uzer, G., Brobst, K. E., Xie, Z., Sen, B., Yen, S. S., Styner, M., & Rubin, J. E. (2015) · Scientific Reports · doi:10.1038/srep11049 · Cited by 41 · see citing works
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Motyl, K. J., DeMambro, V., Barlow, D. J., Olshan, D. S., Nagano, K., Baron, R., Rosen, C. J., & Houseknecht, K. L. (2015) · Endocrinology · doi:10.1210/en.2015-1099 · Cited by 39 · see citing works
Matsuzaka, T., Matsugaki, A., & Nakano, T. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121203 · Cited by 40 · see citing works
John, H. C. S., Meyer, M. B., Benkusky, N. A., Carlson, A. H., Prideaux, M., Bonewald, L. F., & Pike, J. W. (2014) · Bone · doi:10.1016/j.bone.2014.11.010 · Cited by 39 · see citing works
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Shi, C., Uda, Y., Dedic, C., Azab, E., Sun, N., Hussein, A. I., Petty, C. A., Fulzele, K. S., Mitterberger, M. C., Zwerschke, W., et al. (2017) · The FASEB Journal · doi:10.1096/fj.201700485rr · Cited by 37 · see citing works
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Bernhardt, A., Weiser, E., Wolf, S., Vater, C., & Gelinsky, M. (2019) · Tissue Engineering Part A · doi:10.1089/ten.tea.2018.0338 · Cited by 39 · see citing works
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Zhou, Y., Lin, J., Shao, J., Zuo, Q., Wang, S., Wolff, A., Nguyen, D., Rintoul, L., Du, Z., Gu, Y., et al. (2019) · Bone · doi:10.1016/j.bone.2019.06.027 · Cited by 39 · see citing works
Prideaux, M., Kitase, Y., Kimble, M., O’Connell, T. M., & Bonewald, L. F. (2020) · Bone · doi:10.1016/j.bone.2020.115374 · Cited by 39 · see citing works
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Sottnik, J. L., Campbell, B., Mehra, R., Behbahani‐Nejad, O., Hall, C. L., & Keller, E. T. (2014) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24793 · Cited by 37 · see citing works
FGF23 Is Endogenously Phosphorylated in Bone Cells
Lindberg, I., Pang, H. W., Stains, J. P., Clark, D. J., Yang, A. J., Bonewald, L. F., & Li, K. Z. (2014) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2354 · Cited by 37 · see citing works
Self-citationPrideaux, M., Dallas, S. L., Zhao, N., Johnsrud, E. D., Veno, P. A., Guo, D., Mishina, Y. M., Harris, S. E., & Bonewald, L. F. (2015) · PLoS ONE · doi:10.1371/journal.pone.0125731 · Cited by 37 · see citing works
Self-citationLiu, Z., Solesio, M. E., Schaffler, M. B., Frikha-Benayed, D., Rosen, C. J., Werner, H., Kopchick, J. J., Pavlov, E. V., Abramov, A. Y., & Yakar, S. (2018) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3573 · Cited by 37 · see citing works
Wang, S., Xiao, L., Prasadam, I., Crawford, R., Zhou, Y., & Xiao, Y. (2022) · Molecular Medicine · doi:10.1186/s10020-022-00530-4 · Cited by 39 · see citing works
Upstream Regulators of Fibroblast Growth Factor 23
Ratsma, D. M. A., Zillikens, M. C., & van der Eerden, B. C. J. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2021.588096 · Cited by 36 · see citing works
Prouvé, É., Drouin, B., Chevallier, P., Rémy, M., Durrieu, M., & Laroche, G. (2021) · Macromolecular Bioscience · doi:10.1002/mabi.202100069 · Cited by 36 · see citing works
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Pin, F., Prideaux, M., Huot, J. R., Essex, A. L., Plotkin, L. I., Bonetto, A., & Bonewald, L. F. (2021) · Cancer Letters · doi:10.1016/j.canlet.2021.06.030 · Cited by 36 · see citing works
Self-citationGovey, P. M., Jacobs, J., Tilton, S. C., Loiselle, A. E., Zhang, Y., Freeman, W. M., Waters, K. M., Karin, N. J., & Donahue, H. J. (2014) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2014.03.022 · Cited by 36 · see citing works
Osteocyte RANKL Drives Bone Resorption in Mouse Ligature-Induced Periodontitis
Kittaka, M., Yoshimoto, T., Levitan, M. E., Urata, R., Choi, R. B., Teno, Y., Xie, Y., Kitase, Y., Prideaux, M., Dallas, S. L., et al. (2023) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4897 · Cited by 35 · see citing works
Overcoming physical constraints in bone engineering: ‘the importance of being vascularized’
Genova, T., Munaron, L., Carossa, S., & Mussano, F. D. (2015) · Journal of Biomaterials Applications · doi:10.1177/0885328215616749 · Cited by 35 · see citing works
Impact of flow shear stress on morphology of osteoblast-like IDG-SW3 cells
Xu, H., Duan, J., Ren, L. M., Yang, P., Yang, R., Li, W., Zhao, D., Shang, P., & Jiang, J. X. (2017) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-017-0870-3 · Cited by 34 · see citing works
Saito, S., Hamai, R., Shiwaku, Y., Hasegawa, T., Sakai, S., Tsuchiya, K., Sai, Y., Iwama, R., Amizuka, N., Takahashi, T., et al. (2021) · Acta Biomaterialia · doi:10.1016/j.actbio.2021.05.017 · Cited by 33 · see citing works
Naqvi, S. M., Pérez, J. A. P., Kumar, V., Verbruggen, A. S. K., & McNamara, L. M. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.00601 · Cited by 32 · see citing works
Plotkin, L. I., & Wallace, J. M. (2021) · Bone · doi:10.1016/j.bone.2021.115994 · Cited by 32 · see citing works
Notch expressed by osteocytes plays a critical role in mineralisation
Shao, J., Zhou, Y., Lin, J., Nguyen, T. D., Huang, R., Gu, Y., Friis, T., Crawford, R., & Xiao, Y. (2018) · Journal of Molecular Medicine · doi:10.1007/s00109-018-1625-x · Cited by 31 · see citing works
Staines, K. A., Prideaux, M., Allen, S., Buttle, D. J., Pitsillides, A. A., & Farquharson, C. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25282 · Cited by 30 · see citing works
Different Effects of Fluoride Exposure on the Three Major Bone Cell Types
Jiang, N., Guo, F., Sun, B., Zhang, X., & Xu, H. J. (2019) · Biological Trace Element Research · doi:10.1007/s12011-019-01684-9 · Cited by 29 · see citing works
- Authors
- Woo, S. M., Rosser, J., Dusevich, V., Kalajzic, I., & Bonewald, L. F.
- Affiliations
- University of Missouri–Kansas City (US)
- Department of Reconstructive Sciences, University of Connecticut Health Center, School of Dental Medicine, Farmington, CT, USA
- Corresponding author
- Bonewald, Lynda F
- ORCID
- Bonewald, Lynda F
- Venue
- Journal of Bone and Mineral Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2011-07-06
- Volume
- 26
- Issue
- 11
- Pages
- 2634-2646
- ISSN
- 0884-0431 (ISSN-L)
- 1523-4681
- PMC
- PMC3192242
- OpenAlex
- W1985564086
- Semantic Scholar
- 5073feae7cce21d7166d2f0cfd327c76e4bcb852
- Cited by
- 243
- References
- 39
- Citations by year
- 2026: 9 · 2025: 14 · 2024: 16 · 2023: 17 · 2022: 18 · 2021: 24 · 2020: 22 · 2019: 26 · 2018: 18 · 2017: 14 · 2016: 15 · 2015: 19 · 2014: 14 · 2013: 7 · 2012: 9
- FWCI
- 4.02
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- Journal of Bone and Mineral Research (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- American Association of Endodontists Foundation
- National Institutes of Health
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (R03AR053275, P01AR046798)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Keywords
- osteocytes, SV40 large T antigen, interferon-gamma, sclerostin, fibroblast growth factor 23, parathyroid hormone, 1,25-dihydroxyvitamin D3, bone regeneration, calvarial defect, biomineralization, type I collagen, osteocyte function
- MeSH terms
- Fibroblast Growth Factor-23, Animals, Antigens, Polyomavirus Transforming, Bone and Bones, Calcification, Physiologic, Calcium, Cell Differentiation, Cell Line, Cell Movement, Extracellular Space, Gene Expression Regulation, Microspheres, Osteocytes, Osteogenesis, Time Factors, Transcription Factors, Wound Healing, Biomarkers, Gene Expression Profiling, Fibrillar Collagens, Cell Proliferation, Green Fluorescent Proteins, Mice, Rats
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