The DOI matches its Crossref record; 148 of the 148 references it cites were found in a registry or an index.
The Osteocyte: New Insights
Open accessAbstract
Osteocytes are an ancient cell, appearing in fossilized skeletal remains of early fish and dinosaurs. Despite its relative high abundance, even in the context of nonskeletal cells, the osteocyte is perhaps among the least studied cells in all of vertebrate biology. Osteocytes are cells embedded in bone, able to modify their surrounding extracellular matrix via specialized molecular remodeling mechanisms that are independent of the bone forming osteoblasts and bone-resorbing osteoclasts. Osteocytes communicate with osteoclasts and osteoblasts via distinct signaling molecules that include the RankL/OPG axis and the Sost/Dkk1/Wnt axis, among others. Osteocytes also extend their influence beyond the local bone environment by functioning as an endocrine cell that controls phosphate reabsorption in the kidney, insulin secretion in the pancreas, and skeletal muscle function. These cells are also finely tuned sensors of mechanical stimulation to coordinate with effector cells to adjust bone mass, size, and shape to conform to mechanical demands.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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
“The muscle–bone crosstalk may represent a key point in the development of osteosarcopenia (a musculoskeletal disorder) therapies [135].”
From Exerkines and Sarcopenia: Unveiling the Mechanism Behind Exercise-Induced Mitochondrial Homeostasis (2025) · cites this paper as [135]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph node organogenesis.
Kong, Y.-Y., Yoshida, H., Sarosi, I., Tan, H.-L., Timms, E., Capparelli, C., Morony, S., Oliveira-dos-Santos, A. J., Van, G., Itie, A., et al. (1999) · Nature · doi:10.1038/16852 · Cited by 3,351
Manolagas, S. C. (2000) · Endocrine Reviews · doi:10.1210/edrv.21.2.0395 · Cited by 2,639
Evidence for osteocyte regulation of bone homeostasis through RANKL expression
Nakashima, T., Hayashi, M., Fukunaga, T., Kurata, K., Oh-hora, M., Feng, J. Q., Bonewald, L. F., Kodama, T., Wutz, A., Wagner, E. F., et al. (2011) · Nature Medicine · doi:10.1038/nm.2452 · Cited by 1,778
Shimada, T., Kakitani, M., Yamazaki, Y., Hasegawa, H., Takeuchi, Y., Fujita, T., Fukumoto, S., Tomizuka, K., & Yamashita, T. (2004) · Journal of Clinical Investigation · doi:10.1172/jci19081 · Cited by 1,503
Shimada, T., Kakitani, M., Yamazaki, Y., et al. (2004) · Journal of Clinical Investigation · doi:10.1172/jci200419081 · Cited by 1,368
Mechanical Stimulation of Bone in Vivo Reduces Osteocyte Expression of Sost/Sclerostin
Robling, A. G., Niziolek, P. J., Baldridge, L. A., Condon, K. W., Allen, M. R., Alam, I., Mantila, S. M., Gluhak-Heinrich, J., Bellido, T. M., Harris, S. E., et al. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m705092200 · Cited by 1,350
Self-citationManolagas, S. C. (2000) · Endocrine Reviews · doi:10.1210/er.21.2.115 · Cited by 1,318
Matrix-embedded cells control osteoclast formation
Xiong, J., Onal, M., Jilka, R. L., Weinstein, R. S., Manolagas, S. C., & O'Brien, C. A. (2011) · Nature Medicine · doi:10.1038/nm.2448 · Cited by 1,304
Feng, 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
Sensitivity of osteocytes to biomechanical stress in vitro
Klein‐Nulend, J., van der Plas, A., Semeins, C. M., Ajubi, N. E., Erangos, J. A., Nijweide, P. J., & Burger, E. H. (1995) · The FASEB Journal · doi:10.1096/fasebj.9.5.7896017 · Cited by 776
Research works printed but not linked: 9
- Pawlicki R., 1975, Z. Mikrosk. Anat. Forsch., 89, 393
- von Recklinghausen F., 1910, Untersuchungen über Rachitis und Osteomalacia
- Tanaka-Kamioka K, 1998, J. Bone Miner. Res., 10, 1555
- Zallone AZ, 1983, Basic Appl. Histochem., 27, 191
- Tsourdi E, 2018, J. Musculoskelet. Neuronal Interact., 18, 292
- Wolff J., 1892, Das Gesetz der Transformen der Knochen
- Frost HM., 1960, Henry Ford Hosp. Med. Bull., 8, 208
- Klein-Nulend J, 2014, Osteoporos. Int., 25, 1427
- Smalt R, 1997, Am. J. Physiol., 273, E751
Cited by
Sorted by citations
Advances in pathogenesis and therapeutic strategies for osteoporosis
Song, S., Guo, Y., Yang, Y., & Fu, D. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2022.108168 · Cited by 476
Osteocyte-Related Cytokines Regulate Osteoclast Formation and Bone Resorption
Kitaura, H., Marahleh, A., Ohori, F., Noguchi, T., Shen, W.-R., Qi, J., Nara, Y., Pramusita, A., Kinjo, R., & Mizoguchi, I. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21145169 · Cited by 405
Iantomasi, T., Romagnoli, C., Palmini, G., Donati, S., Falsetti, I., Miglietta, F., Aurilia, C., Marini, F., Giusti, F., & Brandi, M. L. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043772 · Cited by 395
Recent Advances in 3D Printing of Smart Scaffolds for Bone Tissue Engineering and Regeneration
Yuan, X., Zhu, W., Yang, Z., He, N., Chen, F., Han, X., & Zhou, K. (2024) · Advanced Materials · doi:10.1002/adma.202403641 · Cited by 364
The role of autophagy in bone metabolism and clinical significance
Wang, J., Zhang, Y., Cao, J., Wang, Y., Anwar, N., Zhang, Z., Zhang, D., Ma, Y., Xiao, Y., Xiao, L., et al. (2023) · Autophagy · doi:10.1080/15548627.2023.2186112 · Cited by 337
Subchondral Bone Remodeling: A Therapeutic Target for Osteoarthritis
Zhu, X., Chan, Y.-T., Yung, P. S., Tuan, R. S., & Jiang, Y. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.607764 · Cited by 218
Osteocytes in bone aging: Advances, challenges, and future perspectives
Cui, J., Shibata, Y., Zhu, T., Zhou, J. M., & Zhang, J. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101608 · Cited by 185
Cardoneanu, A., Macovei, L., Burlui, A., Mihai, I., Bratoiu, I., Rezus, I., Richter, P., Tamba, B., & Rezuș, E. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010171 · Cited by 168
Vlashi, R., Zhang, X., Wu, M., & Chen, G. (2023) · Genes & Diseases · doi:10.1016/j.gendis.2022.07.011 · Cited by 165
Targeting strategies for bone diseases: signaling pathways and clinical studies
Xu, H., Wang, W., Liu, X., Huang, W. H., Chen, Z., Xu, Y., Yang, H., Bai, J., & Geng, D. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01467-8 · Cited by 177
Autophagy in Bone Remodeling: A Regulator of Oxidative Stress
Zhu, C., Shen, S., Zhang, S., Huang, M., Zhang, L., & Chen, X. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.898634 · Cited by 169
Insights and implications of sexual dimorphism in osteoporosis
Zhang, Y., Xie, N., Sun, X., Nice, E. C., Liou, Y., Huang, C., Zhu, H., & Shen, Z. (2024) · Bone Research · doi:10.1038/s41413-023-00306-4 · Cited by 164
The basics of phosphate metabolism
Wagner, C. A. (2023) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfad188 · Cited by 165
New developments in the biology of fibroblast growth factors
Ornitz, D. M., & Itoh, N. (2022) · WIREs Mechanisms of Disease · doi:10.1002/wsbm.1549 · Cited by 147
Maeda, K., Yoshida, K., Nishizawa, T., Otani, K., Yamashita, Y., Okabe, H., Hadano, Y., Kayama, T., Kurosaka, D., & Saito, M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052871 · Cited by 153
Metabolic regulation of skeletal cell fate and function
Stegen, S., & Carmeliet, G. (2024) · Nature Reviews Endocrinology · doi:10.1038/s41574-024-00969-x · Cited by 166
Bone Marrow Mesenchymal Stromal Cells: Identification, Classification, and Differentiation
Gao, Q., Wang, L., Wang, S., Huang, B., Jing, Y., & Su, J. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.787118 · Cited by 140
Hu, L., Liu, R., & Zhang, L. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.109095 · Cited by 137
Sun, Y., Wan, B., Wang, R., Zhang, B., Luo, P., Diaodiao, W., Nie, J., Chen, D., & Wu, X. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.808303 · Cited by 122
Kahil, K., Weiner, S., Addadi, L., & Gal, A. (2021) · Journal of the American Chemical Society · doi:10.1021/jacs.1c09174 · Cited by 118
Osteoimmunology in Periodontitis and Orthodontic Tooth Movement
Alghamdi, B., Jeon, H. H., Ni, J., Qiu, D., Liu, A., Hong, J. J., Ali, M., Wang, A., Troka, M. E., & Graves, D. T. (2023) · Current Osteoporosis Reports · doi:10.1007/s11914-023-00774-x · Cited by 132
The roles of osteocytes in alveolar bone destruction in periodontitis
Huang, X., Xie, M., Xie, Y., Feng, M., Lu, X., Li, X., & Chen, L. (2020) · Journal of Translational Medicine · doi:10.1186/s12967-020-02664-7 · Cited by 122
Impact of the host response and osteoblast lineage cells on periodontal disease
Zhou, M., & Graves, D. T. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.998244 · Cited by 122
Neuronal Induction of Bone‐Fat Imbalance through Osteocyte Neuropeptide Y
Zhang, Y., Chen, C., Liu, Y., Rao, S., Tan, Y., Qian, Y., Xia, K., Huang, J., Liu, X., Hong, C., et al. (2021) · Advanced Science · doi:10.1002/advs.202100808 · Cited by 110
Regulation of bone homeostasis: signaling pathways and therapeutic targets
Wu, Z., Li, W., Jiang, K., Lin, Z., Qian, C., Wu, M., Xia, Y., Li, N., Zhang, H., Xiao, H.-X., et al. (2024) · MedComm · doi:10.1002/mco2.657 · Cited by 129
Noncancerous disease-targeting AIEgens
Duo, Y., Luo, G., Zhang, W., Wang, R., Xiao, G. G., Li, Z., Li, X., Chen, M., Yoon, J., & Tang, B. Z. (2023) · Chemical Society Reviews · doi:10.1039/d2cs00610c · Cited by 106
Ferroptosis in Osteocytes as a Target for Protection Against Postmenopausal Osteoporosis
Jiang, Z., Qi, G., He, X., Yu, Y., Cao, Y., Zhang, C., Zou, W., & Yuan, H. (2024) · Advanced Science · doi:10.1002/advs.202307388 · Cited by 108
Control of osteocyte dendrite formation by Sp7 and its target gene osteocrin
Wang, J. S., Kamath, T., Mazur, C. M., Mirzamohammadi, F., Rotter, D., Hojo, H., Castro, C. D., Tokavanich, N., Patel, R., Govea, N., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-26571-7 · Cited by 105
Kitaura, H., Marahleh, A., Ohori, F., Noguchi, T., Nara, Y., Pramusita, A., Kinjo, R., Ma, J., Kanou, K., & Mizoguchi, I. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031481 · Cited by 106
The origins and formation of bone-resorbing osteoclasts
Elson, A., Anuj, A., Barnea-Zohar, M., & Reuven, N. (2022) · Bone · doi:10.1016/j.bone.2022.116538 · Cited by 95
Jiang, Y., Wang, Z., Liu, X., Wan, M., Liu, Y., Jiao, B., Liao, X., Luo, Z., Wang, Y., Hong, C., et al. (2022) · Advanced Science · doi:10.1002/advs.202105316 · Cited by 90
Local senolysis in aged mice only partially replicates the benefits of systemic senolysis
Farr, J. N., Saul, D., Doolittle, M. L., Kaur, J., Rowsey, J. L., Vos, S. J., Froemming, M. N., Lagnado, A. B., Zhu, Y., Weivoda, M., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci162519 · Cited by 81
Carbon-Based Nanomaterials for Bone and Cartilage Regeneration: A Review
Liu, H., Chen, J., Qiao, S., & Zhang, W. (2021) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.1c00759 · Cited by 78
Bone-to-Brain: A Round Trip in the Adaptation to Mechanical Stimuli
Gerosa, L., & Lombardi, G. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2021.623893 · Cited by 78
Bone marrow niches in the regulation of bone metastasis
Chen, F., Han, Y., & Kang, Y. (2021) · British Journal of Cancer · doi:10.1038/s41416-021-01329-6 · Cited by 77
Osteocytes directly regulate osteolysis via MYD88 signaling in bacterial bone infection
Yoshimoto, T., Kittaka, M., Doan, A. A. P., Urata, R., Prideaux, M., Rojas, R. E., Harding, C. V., Boom, W. H., Bonewald, L. F., Greenfield, E. M., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34352-z · Cited by 77
Energy metabolism: A newly emerging target of BMP signaling in bone homeostasis
Yang, J., Ueharu, H., & Mishina, Y. M. (2020) · Bone · doi:10.1016/j.bone.2020.115467 · Cited by 76
Osteometabolism: Metabolic Alterations in Bone Pathologies
Srivastava, R. K., Sapra, L., & Mishra, P. K. (2022) · Cells · doi:10.3390/cells11233943 · Cited by 79
Materials‐Mediated In Situ Physical Cues for Bone Regeneration
Liu, S., Zhang, L., Li, Z., Gao, F., Zhang, Q., Bianco, A., Liu, H., Ge, S., & Ma, B. (2023) · Advanced Functional Materials · doi:10.1002/adfm.202306534 · Cited by 73
Metabolic reprogramming in skeletal cell differentiation
Bertels, J., He, G., & Long, F. (2024) · Bone Research · doi:10.1038/s41413-024-00374-0 · Cited by 78
Long, J. T., Leinroth, A. P., Liao, Y., Ren, Y., Mirando, A. J., Nguyen, T., Guo, W., Sharma, D., Rouse, D., Wu, C., et al. (2022) · eLife · doi:10.7554/elife.76932 · Cited by 71
Control of Bone Matrix Properties by Osteocytes
Creecy, A., Damrath, J. G., & Wallace, J. M. (2021) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.578477 · Cited by 68
Crosstalk Between the Neuroendocrine System and Bone Homeostasis
Zhao, Y., Peng, X., Wang, Q., Zhang, Z., Wang, L., Xu, Y., Yang, H., Bai, J., & Geng, D. (2023) · Endocrine Reviews · doi:10.1210/endrev/bnad025 · Cited by 75
Bone Hierarchical Structure: Heterogeneity and Uniformity
Rodríguez-Palomo, A., Østergaard, M., & Birkedal, H. (2023) · Advanced Functional Materials · doi:10.1002/adfm.202307026 · Cited by 72
Osteocytes and Bone Metastasis
Riquelme, M. A., Cardenas, E. R., & Jiang, J. X. (2020) · Frontiers in Endocrinology · doi:10.3389/fendo.2020.567844 · Cited by 65
A cholinergic neuroskeletal interface promotes bone formation during postnatal growth and exercise
Gadomski, S., Fielding, C., García-García, A., Korn, C., Kapeni, C., Ashraf, S., Villadiego, J., Toro, R. D., Domingues, O., Skepper, J. N., et al. (2022) · Cell Stem Cell · doi:10.1016/j.stem.2022.02.008 · Cited by 65
Farr, J. N., Kaur, J., Doolittle, M. L., & Khosla, S. (2020) · Current Osteoporosis Reports · doi:10.1007/s11914-020-00619-x · Cited by 60
Bone metabolism – an underappreciated player
Choi, I. A., Umemoto, A., Mizuno, M., & Park‐Min, K. (2024) · npj Metabolic Health and Disease · doi:10.1038/s44324-024-00010-9 · Cited by 75
Role and Regulation of Transcription Factors in Osteoclastogenesis
Jiang, T., Xia, T., Qiao, F., Wang, N., Jiang, Y., & Xin, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242216175 · Cited by 60
Kindlin-2 regulates skeletal homeostasis by modulating PTH1R in mice
Fu, X., Zhou, B., Yan, Q., Tao, C., Qin, L., Wu, X., Lin, S., Chen, S., Lai, Y., Zou, X., et al. (2020) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-00328-y · Cited by 62
Sadek, K. M., Moshy, S. E., Radwan, I. A., Rady, D., Abbass, M. M. S., El‐Rashidy, A. A., Dörfer, C. E., & El‐Sayed, K. M. F. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054599 · Cited by 64
Hanga-Fărcaș, A., Miere, F. G., Filip, G. A., Clichici, S. V., Fritea, L., Vicaș, L. G., Marian, E., Pallag, A., Jurca, T., Filip, S. M., et al. (2023) · Plants · doi:10.3390/plants12102055 · Cited by 57
Nakai, Y., Praneetpong, N., Ono, W., & Ono, N. (2023) · Journal of Bone Metabolism · doi:10.11005/jbm.2023.30.4.297 · Cited by 66
Yang, J., Dong, D., Luo, X., Zhou, J., Shang, P., & Zhang, H. (2020) · Calcified Tissue International · doi:10.1007/s00223-020-00735-x · Cited by 55
Amino acid metabolism in skeletal cells
Devignes, C.-S., Carmeliet, G., & Stegen, S. (2022) · Bone Reports · doi:10.1016/j.bonr.2022.101620 · Cited by 55
Ma, J., Wang, A., Zhang, H., Liu, B., Geng, Y., Xu, Y., Zuo, G., & Peng, J. (2022) · Bone · doi:10.1016/j.bone.2022.116511 · Cited by 52
Mathavan, N., Singh, A., Marques, F. C., Günther, D., Kuhn, G. A., Wehrle, E., & Müller, R. (2025) · Science Advances · doi:10.1126/sciadv.adp8496 · Cited by 59
Che, H., Gao, Y., Xu, Y., Xu, H., Eils, R., & Tian, M. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02329-1 · Cited by 57
New Advances in Osteocyte Mechanotransduction
Li, X., Kordsmeier, J., & Xiong, J. (2021) · Current Osteoporosis Reports · doi:10.1007/s11914-020-00650-y · Cited by 61
Endocrine Regulation on Bone by Thyroid
Zhu, S., Pang, Y., Xu, J., Chen, X., Zhang, C., Wu, B. Y., & Gao, J. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.873820 · Cited by 58
The role of mechanosensor Piezo1 in bone homeostasis and mechanobiology
Wang, J., Sun, Y., & Li, J. (2022) · Developmental Biology · doi:10.1016/j.ydbio.2022.11.002 · Cited by 52
Sparks, D. S., Savi, F. M., Dlaska, C. E., Saifzadeh, S., Brierly, G. I., Ren, E., Cipitria, A., Reichert, J. C., Wille, M., Schuetz, M., et al. (2023) · Science Advances · doi:10.1126/sciadv.add6071 · Cited by 51
Osteocyte mitochondria inhibit tumor development via STING-dependent antitumor immunity
Zhou, H., Zhang, W., Li, H., Xu, F., Yinwang, E., Xue, Y., Chen, T., Wang, S., Wang, Z., Sun, H., et al. (2024) · Science Advances · doi:10.1126/sciadv.adi4298 · Cited by 52
Zhang, L., Guan, Q., Wang, Z., Feng, J., Zou, J., & Gao, B. (2023) · Aging and Disease · doi:10.14336/ad.2023.1115 · Cited by 58
Is There a Governing Role of Osteocytes in Bone Tissue Regeneration?
Cao, W., Helder, M. N., Bravenboer, N., Wu, G., Jin, J., Bruggenkate, C. M. T., Klein‐Nulend, J., & Schulten, E. A. J. M. (2020) · Current Osteoporosis Reports · doi:10.1007/s11914-020-00610-6 · Cited by 49
Wang, X., Ma, Y., Chen, J., Liu, Y., Liu, G., Wang, P., Wang, B., Taketo, M. M., Bellido, T., & Tu, X. (2022) · Bioactive Materials · doi:10.1016/j.bioactmat.2022.07.017 · Cited by 46
Dallas, S. L., & Moore, D. S. (2020) · Bone · doi:10.1016/j.bone.2020.115463 · Cited by 43
Connexin Gap Junctions and Hemichannels Link Oxidative Stress to Skeletal Physiology and Pathology
Hua, R., Zhang, J., Riquelme, M. A., & Jiang, J. X. (2021) · Current Osteoporosis Reports · doi:10.1007/s11914-020-00645-9 · Cited by 43
New Emerging Biomarkers for Bone Disease: Sclerostin and Dickkopf-1 (DKK1)
Dinçel, A. S., & Jørgensen, N. R. (2022) · Calcified Tissue International · doi:10.1007/s00223-022-01020-9 · Cited by 46
Strategies of Macrophages to Maintain Bone Homeostasis and Promote Bone Repair: A Narrative Review
Hu, Y., Huang, J., Chen, C., Wang, Y., Hao, Z., Chen, T., Wang, J., & Li, J. (2022) · Journal of Functional Biomaterials · doi:10.3390/jfb14010018 · Cited by 44
Circadian Regulation of Bone Remodeling
Kikyo, N. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25094717 · Cited by 43
Hashimoto, R., Minoshima, M., Kikuta, J., Yari, S., Bull, S. D., Ishii, M., & Kikuchi, K. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202006388 · Cited by 41
Iron Oxide Nanoparticles Combined with Static Magnetic Fields in Bone Remodeling
Yang, J., Wu, J., Guo, Z., Zhang, G., & Zhang, H. (2022) · Cells · doi:10.3390/cells11203298 · Cited by 43
Inflammation and mechanical force‐induced bone remodeling
Jeon, H. H., Huang, X., Rojas, L., Sripinun, P., Lee, J., Hong, J. J., & Graves, D. T. (2024) · Periodontology 2000 · doi:10.1111/prd.12619 · Cited by 45
Kim, J., & ADACHI, T. (2021) · Scientific Reports · doi:10.1038/s41598-021-92607-z · Cited by 40
Matsuzaka, T., Matsugaki, A., & Nakano, T. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121203 · Cited by 40
Effect of flavonoids from Rhizoma Drynariae on osteoporosis rats and osteocytes
Jin, H., Jiang, N., Xu, W., Zhang, Z., Yang, Y., Zhang, J., & Xu, H. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113379 · Cited by 40
Jiao, Z., Chai, H., Wang, S., Sun, C., Huang, Q., & Xu, W. (2023) · Journal of Molecular Medicine · doi:10.1007/s00109-023-02319-2 · Cited by 39
Garcia-Moreno, M., Jordan, P. M., Günther, K., Dau, T., Fritzsch, C., Vermes, M., Schoppa, A., Ignatius, A. A., Wildemann, B., Werz, O., et al. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.937466 · Cited by 40
Metabolic Health and Disease: A Role of Osteokines?
Shimonty, A., Bonewald, L. F., & Huot, J. R. (2023) · Calcified Tissue International · doi:10.1007/s00223-023-01093-0 · Cited by 41
The pathogenesis of bone metastasis in solid tumors: a review
Vičić, I., & Belev, B. (2021) · Croatian Medical Journal · doi:10.3325/cmj.2021.62.270 · Cited by 38
Costantini, A., Mäkitie, R. E., Hartmann, M. A., Fratzl‐Zelman, N., Zillikens, M. C., Kornak, U., Søe, K., & Mäkitie, O. (2020) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4668 · Cited by 42
Radiation induces primary osteocyte senescence phenotype and affects osteoclastogenesis in vitro
Wang, Y., Xu, L., Wang, J., Bai, J., Zhai, J., & Zhu, G. (2021) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2021.4909 · Cited by 41
Osteoporosis: interferon-gamma-mediated bone remodeling in osteoimmunology
Li, S., Liu, G., & Hu, S. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1396122 · Cited by 42
Tirado‐Cabrera, I., Martín‐Guerrero, E., Heredero‐Jiménez, S., Ardura, J. A., & Gortázar, A. R. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30849 · Cited by 36
An update on the role of ferroptosis in the pathogenesis of osteoporosis
Wu, X., Fang, X., Lu, F., Chen, Q., Liu, J., & Zheng, L. (2024) · EFORT Open Reviews · doi:10.1530/eor-23-0148 · Cited by 37
Non-bone metastatic cancers promote osteocyte-induced bone destruction
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
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 37
Lin, W., Hu, S., Li, K., Shi, Y., Pan, C., Xu, Z., Li, D., Wang, H. H., Li, B., & Chen, H. (2023) · Small · doi:10.1002/smll.202307595 · Cited by 37
Redox signaling and antioxidant defense in osteoclasts
Tao, H., Li, X., Wang, Q., Yu, L., Peng, Y., Chen, W., Yang, X., Zhou, J., & Geng, D. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2023.12.043 · Cited by 40
Young osteocyte-derived extracellular vesicles facilitate osteogenesis by transferring tropomyosin-1
Wang, Z., Lin, X., Cao, J., Liu, Y.-W., Luo, Z.-W., Rao, S.-S., Wang, Y., Wang, Y.-Y., Chen, C., Zhu, G., et al. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02367-x · Cited by 42
Liu, X., Shen, L., Wan, M., Xie, H., & Wang, Z. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02428-1 · Cited by 33
Sclerostin: From Molecule to Clinical Biomarker
Omran, A. S., Atanasova, D., Landgren, F., & Magnusson, P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23094751 · Cited by 44
Zhang, Y., Ma, S., Nie, J., Liu, Z., Chen, F., Li, A., & Pei, D. (2023) · Small · doi:10.1002/smll.202207951 · Cited by 35
Subchondral osteoclasts and osteoarthritis: new insights and potential therapeutic avenues
Chen, W., Wang, Q., Tao, H., Lu, L., Zhou, J., Wang, Q., Huang, W., & Yang, X. H. (2024) · Acta Biochimica et Biophysica Sinica · doi:10.3724/abbs.2024017 · Cited by 35
Tang, Y., Su, S., Yu, R., Liao, C., Dong, Z., Jia, C., Yau, V., Wu, L., Guo, W., & Zheng, J. (2024) · Cell Death Discovery · doi:10.1038/s41420-024-01969-6 · Cited by 35
The Potential Roles of T Cells in Periapical Lesions
Wang, L., Yang, F., Qiu, Y., Ye, L., Song, D., & Huang, D. (2021) · Journal of Endodontics · doi:10.1016/j.joen.2021.09.016 · Cited by 35
Bone Homeostasis and Gut Microbial-Dependent Signaling Pathways
Zhong, X., Zhang, F., Yin, X., Cao, H., Wang, X., Liu, D., Chen, J., & Chen, X. (2021) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.2104.04016 · Cited by 35
Tang, T., Landis, W. J., Blouin, S., Bertinetti, L., Hartmann, M. A., Berzlanovich, A. M., Weinkamer, R., Wagermaier, W., & Fratzl, P. (2020) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4753 · Cited by 34
Pathological progression of osteoarthritis: a perspective on subchondral bone
Li, X., Chen, W., Liu, D., Chen, P., Wang, S., Li, F., Chen, Q., Lv, S., Li, F., Chen, C., et al. (2024) · Frontiers of Medicine · doi:10.1007/s11684-024-1061-y · Cited by 36
Metadata
- Authors
- Robling, A. G., & Bonewald, L. F.
- Affiliations
- Indiana University School of Medicine (US)
- Corresponding author
- Bonewald, Lynda F.
- Venue
- Annual Review of Physiology
- Publisher
- Annual Reviews
- Published
- 2020-02-10
- Volume
- 82
- Issue
- 1
- Pages
- 485-506
- ISSN
- 0066-4278 (ISSN-L)
- 1545-1585
- PMC
- PMC8274561
- OpenAlex
- W3006279369
- Cited by
- 539
- References
- 146
- Citations by year
- 2026: 67 · 2025: 94 · 2024: 96 · 2023: 114 · 2022: 82 · 2021: 60 · 2020: 26
- FWCI
- 6.75
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Annual Review of Physiology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- IUScholarWorks (Indiana University) (submittedVersion)
- Purdue University Indianapolis (Indiana University) (submittedVersion)
- Funders
- U.S. Department of Veterans Affairs (IK6 BX003783, I01 BX001478)
- National Institutes of Health (PO1AG039355)
- National Institute on Aging (P01AG039355)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (P01AR046798, R61AR073551, R01AR053237)
- 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
- osteocytes, RANKL/OPG axis, phosphate reabsorption, insulin secretion, skeletal muscle function, mechanotransduction, bone mass regulation, bone formation and resorption
- MeSH terms
- Fibroblast Growth Factor-23, Animals, Bone and Bones, Humans, Osteocytes, Bone Remodeling
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