The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.
Identity of Osteoclastogenesis Inhibitory Factor (OCIF) and Osteoprotegerin (OPG): A Mechanism by which OPG/OCIF Inhibits Osteoclastogenesis in Vitro1
Abstract
The morphogenesis and remodeling of bone depends on the integrated activity of osteoblasts that form bone and osteoclasts that resorb bone. We previously reported the isolation of a new cytokine termed osteoclastogenesis inhibitory factor, OCIF, which specifically inhibits osteoclast development. Here we report the cloning of a complementary DNA of human OCIF. OCIF is identical to osteoprotegerin (OPG), a soluble member of the tumor-necrosis factor receptor family that inhibits osteoclastogenesis. Recombinant human OPG/OCIF specifically acts on bone tissues and increases bone mineral density and bone volume associated with a decrease of active osteoclast number in normal rats. Osteoblasts or bone marrow-derived stromal cells support osteoclastogenesis through cell-to-cell interactions. A single class of high affinity binding sites for OPG/OCIF appears on a mouse stromal cell line, ST2, in response to 1,25-dihydroxyvitamin D3. An anti-OPG/OCIF antibody that blocks the binding abolishes the biological activity of OPG/OCIF. When the sites are blocked with OPG/OCIF, ST2 cells fail to support osteoclastogenesis. These results suggest that the sites are involved in cell-to-cell signaling between stromal cells and osteoclast progenitors and that OPG/OCIF inhibits osteoclastogenesis by interrupting the signaling through the sites.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“OPG is an atypical member of the TNF receptor family in that it is a secreted protein with no transmembrane domain and no direct signaling properties (4,6).”
From Receptor Activator of Nuclear Factor κB Ligand and Osteoprotegerin Regulation of Bone Remodeling in Health and Disease (2008) · cites this paper as [6]
Citations
Cites
Osteoprotegerin: a novel secreted protein involved in the regulation of bone density.
Simonet, W. S., Lacey, D. L., Dunstan, C. R., Kelley, M., Chang, M.-S., Lüthy, R., Nguyen, H. Q., Wooden, S., Bennett, L., Boone, T., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80209-3 · Cited by 5,130
The polypeptide encoded by the cDNA for human cell surface antigen Fas can mediate apoptosis
Itoh, N., Yonehara, S., Ishii, A., Yonehara, M., Mizushima, S.-I., Sameshima, M., Hase, A., Seto, Y., & Nagata, S. (1991) · Cell · doi:10.1016/0092-8674(91)90614-5 · Cited by 2,736
The TNF receptor superfamily of cellular and viral proteins: Activation, costimulation, and death
Smith, C. A., Farrah, T., & Goodwin, R. G. (1994) · Cell · doi:10.1016/0092-8674(94)90372-7 · Cited by 1,909
Yoshida, H., Hayashi, S.-I., Kunisada, T., Ogawa, M., Nishikawa, S., Okamura, H., Sudo, T., Shultz, L. D., & Nishikawa, S.-I. (1990) · Nature · doi:10.1038/345442a0 · Cited by 1,789
Increased Osteoclast Development After Estrogen Loss: Mediation by Interleukin-6
Jilka, R. L., Hangoc, G., Girasole, G., Passeri, G., Williams, D. C., Abrams, J. S., Boyce, B. F., Broxmeyer, H. E., & Manolagas, S. C. (1992) · Science · doi:10.1126/science.1621100 · Cited by 1,440
Takebe, Y., Seiki, M., Fujisawa, J., Hoy, P., Yokota, K., Arai, K., Yoshida, M., & Arai, N. (1988) · Molecular and Cellular Biology · doi:10.1128/mcb.8.1.466-472.1988 · Cited by 1,330
A novel domain within the 55 kd TNF receptor signals cell death
Tartaglia, L. A., Ayres, T. M., Wong, G. H., & Goeddel, D. V. (1993) · Cell · doi:10.1016/0092-8674(93)90464-2 · Cited by 1,290
Protection from Fas-Mediated Apoptosis by a Soluble Form of the Fas Molecule
Cheng, J., Zhou, T., Liu, C., Shapiro, J. P., Brauer, M. J., Kiefer, M. C., Barr, P. J., & Mountz, J. D. (1994) · Science · doi:10.1126/science.7510905 · Cited by 1,108
Modulation of Osteoclast Differentiation
Suda, T., Takahashi, N., & Martin, T. J. (1992) · Endocrine Reviews · doi:10.1210/edrv-13-1-66 · Cited by 1,004
OSTEOBLASTIC CELLS ARE INVOLVED IN OSTEOCLAST FORMATION
Takahashi, N., Akatsu, T., Udagawa, N., Sasaki, T., Yamaguchi, A., Moseley, J. M., Martin, T. J., & Suda, T. (1988) · Endocrinology · doi:10.1210/endo-123-5-2600 · Cited by 934
Flagged first, then by citations
Cited by
Sorted by citations
Items 301–400 of 999
Current insights into the role of transforming growth factor-β in bone resorption
Fox, S. W., & Lovibond, A. C. (2005) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2005.09.008 · Cited by 90
An introduction to death receptors in apoptosis
Kumar, R., Herbert, P. E., & Warrens, A. Ν. (2005) · International Journal of Surgery · doi:10.1016/j.ijsu.2005.05.002 · Cited by 92
RANKL and RANK as novel therapeutic targets for arthritis
Nakashima, T., & Penninger, J. M. (2003) · Current Opinion in Rheumatology · doi:10.1097/00002281-200305000-00016 · Cited by 89
Disruption of the C5a receptor gene fails to protect against experimental allergic encephalomyelitis
Reiman, R. M., Gerard, C. J., Campbell, I. L., & Barnum, S. R. (2002) · European Journal of Immunology · doi:10.1002/1521-4141(200204)32:4 · Cited by 53
Mechanisms of Bone Fragility: From Osteogenesis Imperfecta to Secondary Osteoporosis
El‐Gazzar, A., & Högler, W. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22020625 · Cited by 89
Osteoclasts and the immune system
Nakashima, T., & Takayanagi, H. (2009) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-009-0089-z · Cited by 88
The role of the sympathetic nervous system in controlling bone metabolism
Togari, A., Arai, M., & Kondo, A. (2005) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.9.5.931 · Cited by 88
Effects of Creatine and Resistance Training on Bone Health in Postmenopausal Women
CHILIBECK, P. D., CANDOW, D. G., LANDERYOU, T., KAVIANI, M., & PAUS-JENSSEN, L. (2015) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000000571 · Cited by 87
Akatsu, T., Murakami, T., Ono, K., Nishikawa, M., Tsuda, E., Mochizuki, S.-I., Fujise, N., Higashio, K., Motoyoshi, K., Yamamoto, M., et al. (1998) · Bone · doi:10.1016/s8756-3282(98)00141-0 · Cited by 87
Self-citationInterleukin-32 Promotes Osteoclast Differentiation but Not Osteoclast Activation
Mabilleau, G., & Sabokbar, A. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004173 · Cited by 88
Interleukin-18 Up-Regulates Osteoprotegerin Expression in Stromal/Osteoblastic Cells
Makiishi-Shimobayashi, C., Tsujimura, T., Iwasaki, T., Yamada, N., Sugihara, A., Okamura, H., Hayashi, S., & Terada, N. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2001.4380 · Cited by 86
Molecular control of bone remodeling and osteoporosis
Kong, Y., & Penninger, J. M. (2000) · Experimental Gerontology · doi:10.1016/s0531-5565(00)00178-9 · Cited by 86
Molecular and Biological Mechanisms of Bone Metastasis
Cecchini, M. G., Wetterwald, A., van der Pluijm, G., & Thalmann, G. N. (2005) · EAU Update Series · doi:10.1016/j.euus.2005.09.006 · Cited by 89
CLONING AND CHARACTERIZATION OF OSTEOCLAST PRECURSORS FROM THE RAW264.7 CELL LINE
Cuetara, B., Crotti, T. N., O’Donoghue, A. J., & McHugh, K. P. (2006) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1290/0510075.1 · Cited by 88
Maı̈moun, L., Couret, I., Mariano‐Goulart, D., Dupuy, A., Micallef, J., Péruchon, E., Ohanna, F., Cristol, J., Rossi, M., & Leroux, J. L. (2005) · Calcified Tissue International · doi:10.1007/s00223-004-0048-6 · Cited by 83
Naylor, K. E., Rogers, A., Fraser, R. B., Hall, V., Eastell, R., & Blumsohn, A. (2003) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2003-030486 · Cited by 84
Nagata, N., Kitaura, H., Yoshida, N., & Nakayama, K. (2003) · Bone · doi:10.1016/s8756-3282(03)00213-8 · Cited by 87
Characterization of monomeric and homodimeric forms of osteoclastogenesis inhibitory factor.
Tomoyasu, A., Goto, M., Fujise, N., Mochizuki, S.-I., Yasuda, H., Morinaga, T., Tsuda, E., & Higashio, K. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.8443 · Cited by 83
Self-citationMegakaryocyte-mediated inhibition of osteoclast development
Kacena, M. A., Nelson, T., Clough, M. E., Lee, S., Lorenzo, J. A., Gundberg, C. M., & Horowitz, M. C. (2006) · Bone · doi:10.1016/j.bone.2006.05.004 · Cited by 83
Paracrine regulation of osteoclast formation and activity: milestones in discovery.
Martin, T. (2004) · PubMed · Cited by 81
Osteoprotegerin and Osteoclast Differentiation Factor in Tooth Eruption
Wise, G. E., Lumpkin, S. J., Huang, H., & Zhang, Q. (2000) · Journal of Dental Research · doi:10.1177/00220345000790120301 · Cited by 82
Pros and Cons of Denosumab Treatment for Osteoporosis and Implication for RANKL Aptamer Therapy
Zhang, N., Zhang, Z., Yu, Y., Zhuo, Z., Zhang, G., & Zhang, B. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.00325 · Cited by 82
Suzuki, K., Kurose, T., Takizawa, M., Maruyama, M., Ushikawa, K., Kikuyama, M., Sugimoto, C., Seino, Y., Nagamatsu, S., & Ishida, H. (2004) · Diabetes Research and Clinical Practice · doi:10.1016/j.diabres.2004.08.006 · Cited by 81
Togari, A., & Arai, M. (2008) · Journal of Pharmacological Sciences · doi:10.1254/jphs.fm0070227 · Cited by 81
Resolvin D2 Restrains Th1 Immunity and Prevents Alveolar Bone Loss in Murine Periodontitis
Mizraji, G., Heyman, O., Dyke, T. E. V., & Wilensky, A. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00785 · Cited by 81
Yamagishi, T., Otsuka, E., & Hagiwara, H. (2001) · Endocrinology · doi:10.1210/en.142.8.3632 · Cited by 82
The role of TNF-receptor family members and other TRAF-dependent receptors in bone resorption.
Gravallese, E. M., Galson, D. L., Goldring, S. R., & Auron, P. E. (2001) · Arthritis Research · doi:10.1186/ar134 · Cited by 81
Recent Advances in Osteoclast Biological Behavior
Sun, Y., Li, J., Xie, X., Gu, F., Sui, Z., Zhang, K., & Yu, T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.788680 · Cited by 83
Inflammation in periodontal tissues in response to mechanical forces.
Yamaguchi, M., & Kasai, K. (2005) · PubMed · Cited by 80
Cowardin, C. A., Ahern, P. P., Kung, V. L., Hibberd, M. C., Cheng, J., Guruge, J. L., Sundaresan, V. M., Head, R. D., Barile, D., Mills, D. A., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1821770116 · Cited by 79
Osteoprotegerin in Cardiometabolic Disorders
de Ciriza, C. P., Lawrie, A., & Varo, N. (2015) · International Journal of Endocrinology · doi:10.1155/2015/564934 · Cited by 78
New roles of osteoblasts involved in osteoclast differentiation
Yamashita, T. (2012) · World Journal of Orthopedics · doi:10.5312/wjo.v3.i11.175 · Cited by 82
Campagnuolo, G., Bolon, B., & Feige, U. (2002) · Arthritis & Rheumatism · doi:10.1002/art.10369 · Cited by 78
Osteoporosis in Chronic Obstructive Pulmonary Disease
Sarkar, M. S., Bhardwaj, R., Madabhavi, I., & Khatana, J. (2015) · Clinical Medicine Insights Circulatory Respiratory and Pulmonary Medicine · doi:10.4137/ccrpm.s22803 · Cited by 84
Ta, H. M., Nguyen, G. T. T., Jin, H. M., Choi, J., Park, H., Kim, N., Hwang, H., & Kim, K. K. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1011686107 · Cited by 78
Furuya, Y., Inagaki, A., Khan, M., Mori, K., Penninger, J. M., Nakamura, M., Udagawa, N., Aoki, K., Ohya, K., Uchida, K., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.426080 · Cited by 77
Self-citationShimizu, S., Asou, Y., Itoh, S., Chung, U., Kawaguchi, H., Shinomiya, K., & Muneta, T. (2007) · Arthritis & Rheumatism · doi:10.1002/art.22941 · Cited by 74
Role of the Osteoclast at the Bone-Implant Interface
Minkin, C., & Marinho, V. C. (1999) · Advances in Dental Research · doi:10.1177/08959374990130011401 · Cited by 76
Relationship between serum RANKL and RANKL in bone
Findlay, D. M., & Atkins, G. J. (2011) · Osteoporosis International · doi:10.1007/s00198-011-1740-9 · Cited by 76
Stern, A., Laughlin, G. A., Bergstrom, J., & Barrett-Connor, E. L. (2007) · European Journal of Endocrinology · doi:10.1530/eje-06-0753 · Cited by 76
1α,25 Dihydroxyvitamin D3 Rapidly Regulates the Mouse Osteoprotegerin Gene Through Dual Pathways
Kondo, T., Kitazawa, R., Maeda, S., & Kitazawa, S. (2004) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.040604 · Cited by 76
Coordinated cytokine expression by stromal and hematopoietic cells during human osteoclast formation
Atkins, G. J., Haynes, D. R., Geary, S. M., Loric, M., Crotti, T. N., & Findlay, D. M. (2000) · Bone · doi:10.1016/s8756-3282(00)00280-5 · Cited by 76
Glucocorticoid-induced osteoporosis: a review on pathophysiology and treatment options.
de Nijs, R. N. J. (2008) · PubMed · Cited by 74
Hyaluronan Increases RANKL Expression in Bone Marrow Stromal Cells Through CD44
Cao, J., Singleton, P. A., Majumdar, S., Boudignon, B. M., Burghardt, A. J., Kurimoto, P., Wronski, T. J., Bourguignon, L., & Halloran, B. P. (2005) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.041014 · Cited by 79
Miyashita, T., Kawakami, A., Nakashima, T., Yamasaki, S., Tamai, M., Tanaka, F., Kamachi, M., Ida, H., Migita, K., Origuchi, T., et al. (2004) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2004.02534.x · Cited by 74
Canonical Wnt Signaling in Osteoblasts Is Required for Osteoclast Differentiation
Glass, D. A., & Karsenty, G. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1346.015 · Cited by 75
Immature and mature megakaryocytes enhance osteoblast proliferation and inhibit osteoclast formation
Ciovacco, W. A., Cheng, Y., Horowitz, M. C., & Kacena, M. A. (2010) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22456 · Cited by 75
Osteoprotegerin and its cognate ligand: a new paradigm of osteoclastogenesis
Hofbauer, L. C., & Heufelder, A. E. (1998) · European Journal of Endocrinology · doi:10.1530/eje.0.1390152 · Cited by 75
Efficient osteoclast differentiation requires local complement activation
Tu, Z., Bu, H., Dennis, J. E., & Lin, F. (2010) · Blood · doi:10.1182/blood-2010-01-263590 · Cited by 74
Crystal Structure of the Extracellular Domain of Mouse RANK Ligand at 2.2-Å Resolution
Ito, S., Wakabayashi, K., Ubukata, O., Hayashi, S., Okada, F., & Hata, T. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m106525200 · Cited by 74
A Novel Osteoblast-derived C-type Lectin That Inhibits Osteoclast Formation
Zhou, H., Kartsogiannis, V., Hu, Y. S., Elliott, J., Quinn, J. M. W., McKinstry, W. J., Gillespie, M. T., & Ng, K. W. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m011554200 · Cited by 76
Decreased Bone Density, Elevated Serum Osteoprotegerin, and β-Cross-Laps in Wilson Disease
Hegedüs, D., Ferencz, V., Lakatos, P. L., Mészáros, S., Lakatos, P. L., Horváth, C., & Szalay, F. (2002) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.2002.17.11.1961 · Cited by 75
Yang, S., Takahashi, N., Yamashita, T., Sato, N., Takahashi, M., Mogi, M., Uematsu, T., Kobayashi, Y., Nakamichi, Y., Takeda, K., et al. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.3.1956 · Cited by 73
Duarte, P. M., Gurgel, B. C. D. V., Sallum, A. W., Filho, G. D. R. N., Sallum, E. A., & Nociti, F. H. (2005) · Journal of Periodontology · doi:10.1902/jop.2005.76.1.107 · Cited by 73
Targeting the RANKL/RANK/OPG Axis for Cancer Therapy
Ming, J., Cronin, S. J. F., & Penninger, J. M. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.01283 · Cited by 75
Osteoclastic differentiation and function regulated by old and new pathways
Blair, H. C., & Zaidi, M. (2006) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-006-9010-4 · Cited by 74
Li, E. K., Tam, L., Griffith, J. F., ZHU, T. Y., Li, T. K., Li, M., Wong, K. C., Chan, M. M., Lam, C. W. K., Chu, F. S. K., et al. (2009) · The Journal of Rheumatology · doi:10.3899/jrheum.081337 · Cited by 71
Ukai, T., Yumoto, H., Gibson, F., & Genco, C. (2007) · Infection and Immunity · doi:10.1128/iai.01241-07 · Cited by 77
Mechanisms involved in bone resorption regulated by vitamin D
Nakamichi, Y., Udagawa, N., Suda, T., & Takahashi, N. (2017) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2017.11.005 · Cited by 71
Molecular genetics of too much bone
Janssens, K. (2002) · Human Molecular Genetics · doi:10.1093/hmg/11.20.2385 · Cited by 72
Fahrleitner, A., Prenner, G., Leb, G., Tscheliessnigg, K. H., Piswanger-Sölkner, C., Obermayer-Pietsch, B., Portugaller, H. R., Berghold, A., & Dobnig, H. (2003) · Bone · doi:10.1016/s8756-3282(02)00926-2 · Cited by 71
The dynamic interplay between osteoclasts and the immune system
Nakashima, T., & Takayanagi, H. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.04.004 · Cited by 72
Clinical development of anti-RANKL therapies for treatment and prevention of bone metastasis
Lipton, A., & Goessl, C. D. (2010) · Bone · doi:10.1016/j.bone.2010.10.161 · Cited by 71
Arko, B., Preželj, J., Kocijančič, A., Komel, R., & Marc, J. (2004) · Maturitas · doi:10.1016/j.maturitas.2004.08.006 · Cited by 71
Lubberts, E., Oppers‐Walgreen, B., Pettit, A. R., van den Bersselaar, L., Joosten, L. A. B., Goldring, S. R., Gravallese, E. M., & van den Berg, W. B. (2002) · Arthritis & Rheumatism · doi:10.1002/art.10607 · Cited by 70
From latency to overt bone metastasis in breast cancer: potential for treatment and prevention
Salvador, F., Lope, A. L., & Gomis, R. R. (2019) · The Journal of Pathology · doi:10.1002/path.5292 · Cited by 73
Cell signalling in macrophages, the principal innate immune effector cells of rheumatoid arthritis
Drexler, S. K., Kong, P. L., Wales, J., & Foxwell, B. M. J. (2008) · Arthritis Research & Therapy · doi:10.1186/ar2481 · Cited by 72
Macrophage-Inflammatory Protein-1α Regulates Preosteoclast Differentiationin Vitro
Scheven, B. A. A., Milne, J. S., Hunter, I., & Robins, S. P. (1999) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.9909 · Cited by 70
Tsangari, H., Findlay, D. M., Kuliwaba, J. S., Atkins, G. J., & Fazzalari, N. L. (2004) · Bone · doi:10.1016/j.bone.2004.02.006 · Cited by 69
Stalvey, M. S., Clines, K. L., Havasi, V., McKibbin, C. R., Dunn, L. K., Chung, W. J., & Clines, G. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080098 · Cited by 69
Cloning and Function of Rabbit Peroxisome Proliferator-activated Receptor δ/β in Mature Osteoclasts
Mano, H., Kimura, C., Fujisawa, Y., Kameda, T., Mikiko, W.-M., Kaneko, H., Kaneda, T., Hakeda, Y., & Kumegawa, M. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.11.8126 · Cited by 67
Osteoprotegerin mitigates tail suspension-induced osteopenia.
Bateman, T. A., Dunstan, C. R., Ferguson, V. L., Lacey, D. L., Ayers, R. A., & Simske, S. J. (2000) · Bone · doi:10.1016/s8756-3282(00)00256-8 · Cited by 66
Creatine supplementation for older adults: Focus on sarcopenia, osteoporosis, frailty and Cachexia
Candow, D. G., Chilibeck, P. D., Forbes, S. C., Fairman, C. M., Gualano, B., & Roschel, H. (2022) · Bone · doi:10.1016/j.bone.2022.116467 · Cited by 76
Villa, I., Mrak, E., Rubinacci, A., Ravasi, F., & GUIDOBONO, F. (2006) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00354.2005 · Cited by 70
Signalling in osteoclasts and the role of Fos/AP1 proteins
Wagner, E. F., & Matsuo, K. (2003) · Annals of the Rheumatic Diseases · doi:10.1136/ard.62.suppl_2.ii83 · Cited by 69
Yamamoto, Y., Udagawa, N., Matsuura, S., Nakamichi, Y., Horiuchi, H., Hosoya, A., Nakamura, M., Ozawa, H., Takaoka, K., Penninger, J. M., et al. (2006) · Endocrinology · doi:10.1210/en.2006-0216 · Cited by 67
RANKL Upregulation Associated With Periodontitis and Porphyromonas gingivalis
Wara‐aswapati, N., Surarit, R., Chayasadom, A., Boch, J. A., & Pitiphat, W. (2007) · Journal of Periodontology · doi:10.1902/jop.2007.060398 · Cited by 68
Agutter, P. S., & Wheatley, D. N. (2000) · BioEssays · doi:10.1002/1521-1878(200011)22:11 · Cited by 56
Brändström, H., Stiger, F., Lind, L., Kahan, T., Melhus, H., & Kindmark, A. (2002) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(02)00137-7 · Cited by 68
Finding a Toll on the Route: The Fate of Osteoclast Progenitors After Toll-Like Receptor Activation
Souza, P. P. C., & Lerner, U. H. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01663 · Cited by 67
Azizieh, F. Y., Shehab, D., Al-Jarallah, K. F., Gupta, R., & Raghupathy, R. (2019) · Biomarker Insights · doi:10.1177/1177271919843825 · Cited by 67
Osteoclasts—the innate immune cells of the bone
Wu, Y., Humphrey, M. B., & Nakamura, M. C. (2008) · Autoimmunity · doi:10.1080/08916930701693180 · Cited by 69
Furuya, Y., Mori, K., Ninomiya, T., Tomimori, Y., Tanaka, S., Takahashi, N., Udagawa, N., Uchida, K., & Yasuda, H. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.246280 · Cited by 68
Self-citationKoide, M., Kobayashi, Y., Ninomiya, T., Nakamura, M., Yasuda, H., Arai, Y., Okahashi, N., Yoshinari, N., Takahashi, N., & Udagawa, N. (2013) · Endocrinology · doi:10.1210/en.2012-1928 · Cited by 67
Self-citationBone remodeling: new aspects of a key process that controls skeletal maintenance and repair
Pogoda, P., Priemel, M., Rueger, J. M., & Amling, M. (2004) · Osteoporosis International · doi:10.1007/s00198-004-1787-y · Cited by 62
Haynes, D. R. (2004) · Inflammation Research · doi:10.1007/s00011-004-1303-z · Cited by 66
Bone remodelling: A signalling system for osteoclast regulation
Filvaroff, E. H., & Derynck, R. (1998) · Current Biology · doi:10.1016/s0960-9822(98)70434-8 · Cited by 66
Mantovani, A., Locati, M., Polentarutti, N., Vecchi, A., & Garlanda, C. (2003) · Journal of Leukocyte Biology · doi:10.1189/jlb.1003473 · Cited by 66
Itonaga, I., Sabokbar, A., Murray, D. W., & Athanasou, N. A. (2000) · Annals of the Rheumatic Diseases · doi:10.1136/ard.59.1.26 · Cited by 66
Pax5-Deficient Mice Exhibit Early Onset Osteopenia with Increased Osteoclast Progenitors
Horowitz, M. C., Xi, Y., Pflugh, D. L., Hesslein, D. G. T., Schatz, D. G., Lorenzo, J., & Bothwell, A. L. M. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.11.6583 · Cited by 65
Neog, M. K., Pragasam, S. J., Krishnan, M., & Rasool, M. (2017) · BioFactors · doi:10.1002/biof.1377 · Cited by 66
Nakamura, I., Tanaka, H., Rodan, G. A., & Duong, L. T. (1998) · Endocrinology · doi:10.1210/en.139.12.5182 · Cited by 65
Nakagawa, N., Yasuda, H., Yano, K., Mochizuki, S.-I., Kobayashi, N., Fujimoto, H., Shima, N., Morinaga, T., Chikazu, D., Kawaguchi, H., et al. (1999) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1999.1601 · Cited by 64
Self-citationEstrogen receptors in breast and bone: from virtue of remodeling to vileness of metastasis
Bado, I., Gugala, Z., Fuqua, S. A. W., & Zhang, X. (2017) · Oncogene · doi:10.1038/onc.2017.94 · Cited by 65
ADRENAL AND GONADAL STEROIDS INHIBIT IL-6 SECRETION BY HUMAN MARROW CELLS
Gordon, C. M., LeBoff, M. S., & Glowacki, J. (2001) · Cytokine · doi:10.1006/cyto.2001.0962 · Cited by 64
Bone effects of vitamin D – Discrepancies between in vivo and in vitro studies
Suda, T., Takahashi, F., & Takahashi, N. (2011) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2011.11.011 · Cited by 66
Ohno, H., Uemura, Y., Murooka, H., Takanashi, H., Tokieda, T., Ohzeki, Y., Kubo, K., & Serizawa, I. (2007) · European Journal of Immunology · doi:10.1002/eji.200737199 · Cited by 64
Influence of bisphosphonates on the osteoblast RANKL and OPG gene expression in vitro
Koch, F. P., Merkel, C., Ziebart, T., Smeets, R., Walter, C., & Al‐Nawas, B. (2010) · Clinical Oral Investigations · doi:10.1007/s00784-010-0477-8 · Cited by 67
Metadata
- Authors
- Yasuda, H., Shima, N., Nakagawa, N., Mochizuki, S.-I., Yano, K., Fujise, N., Sato, Y., Goto, M., Yamaguchi, K., Kuriyama, M., Kanno, T., Murakami, A., Tsuda, E., Morinaga, T., & Higashio, K.
- Affiliations
- Megmilk Snow Brand (Japan) (JP)
- Corresponding author
- Higashio, Kanji
- Venue
- Endocrinology
- Publisher
- The Endocrine Society
- Published
- 1998-03
- Volume
- 139
- Issue
- 3
- Pages
- 1329-1337
- ISSN
- 0013-7227 (ISSN-L)
- 1945-7170
- OpenAlex
- W2167886526
- Cited by
- 1,201
- References
- 33
- Citations by year
- 2026: 7 · 2025: 13 · 2024: 21 · 2023: 15 · 2022: 21 · 2021: 21 · 2020: 29 · 2019: 36 · 2018: 22 · 2017: 38 · 2016: 22 · 2015: 28 · 2014: 36 · 2013: 54 · 2012: 35
- FWCI
- 24.00
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Endocrinology (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
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Bone and Dental Protein Studies
- Keywords
- osteoprotegerin, osteoclastogenesis inhibition, TNF receptor superfamily, bone remodeling, bone mineral density, stromal cells, osteoblasts, cell-to-cell signaling, 1,25-dihydroxyvitamin D3, bone resorption, gene cloning
- MeSH terms
- Amino Acid Sequence, Animals, Cells, Cultured, Cloning, Molecular, Glycoproteins, Humans, Male, Molecular Sequence Data, Osteoclasts, Recombinant Proteins, Bone Density, Bone Remodeling, Rats, Sprague-Dawley, Receptors, Tumor Necrosis Factor, Receptors, Cytoplasmic and Nuclear, Mice, Rats, Osteoprotegerin
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review