The DOI matches its Crossref record; 49 of the 49 references it cites were found in a registry or an index.
Insulin Signaling in Osteoblasts Integrates Bone Remodeling and Energy Metabolism
Open accessAbstract
The broad expression of the insulin receptor suggests that the spectrum of insulin function has not been fully described. A cell type expressing this receptor is the osteoblast, a bone-specific cell favoring glucose metabolism through a hormone, osteocalcin, that becomes active once uncarboxylated. We show here that insulin signaling in osteoblasts is necessary for whole-body glucose homeostasis because it increases osteocalcin activity. To achieve this function insulin signaling in osteoblasts takes advantage of the regulation of osteoclastic bone resorption exerted by osteoblasts. Indeed, since bone resorption occurs at a pH acidic enough to decarboxylate proteins, osteoclasts determine the carboxylation status and function of osteocalcin. Accordingly, increasing or decreasing insulin signaling in osteoblasts promotes or hampers glucose metabolism in a bone resorption-dependent manner in mice and humans. Hence, in a feed-forward loop, insulin signals in osteoblasts activate a hormone, osteocalcin, that promotes glucose metabolism.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“OCN promoted the survival and function of pancreatic β-cells and increased insulin secretion [209], while insulin itself induced the release of OCN [210].”
From The Role of Exercise in the Interplay between Myokines, Hepatokines, Osteokines, Adipokines, and Modulation of Inflammation for Energy Substrate Redistribution and Fat Mass Loss: A Review (2020) · cites this paper as [210]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Moreover, IL-6 increases production of OCN by osteoblasts [71] (2c), which itself stimulates transient pancreatic secretion of the anorexic hormone insulin and triggers a positive feed-forward mechanism that results in increased OCN and thus more insulin [28,209,210] (2d).”
From The Role of Exercise in the Interplay between Myokines, Hepatokines, Osteokines, Adipokines, and Modulation of Inflammation for Energy Substrate Redistribution and Fat Mass Loss: A Review (2020) · cites this paper as [210]
Experimental — accuracy not yet measured
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
Cell Signaling by Receptor Tyrosine Kinases
Lemmon, M. A., & Schlessinger, J. (2010) · Cell · doi:10.1016/j.cell.2010.06.011 · Cited by 7,929
PARFITT, A. M., Drezner, M. K., Glorieux, F. H., Kanis, J. А., Malluche, H. H., Meunier, P. J., Ott, S. M., & Recker, R. R. (1987) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.5650020617 · Cited by 5,344
Osf2/Cbfa1: A Transcriptional Activator of Osteoblast Differentiation
Ducy, P., Zhang, R., Geoffroy, V., Ridall, A. L., & Karsenty, G. (1997) · Cell · doi:10.1016/s0092-8674(00)80257-3 · Cited by 4,246
Self-citationCell Signaling by Receptor Tyrosine Kinases
Schlessinger, J. (2000) · Cell · doi:10.1016/s0092-8674(00)00114-8 · Cited by 3,774
Bone Histomorphometry : Standardization of Nomenclature, Symbols, and Units
PARFITT, A. M., Drezner, M. K., Glorieux, F. H., Kanis, J. А., Malluche, H. H., Meunier, P. J., Ott, S. M., & Recker, R. R. (1987) · Journal of Bone and Mineral Research · Cited by 3,258
Endocrine regulation of energy metabolism by the skeleton
Lee, N. K., Sowa, H., Hinoi, E., Ferron, M., Ahn, J. D., Confavreux, C., Dacquin, R., Mee, P. J., McKee, M. D., Jung, D. Y., et al. (2007) · Cell · doi:10.1016/j.cell.2007.05.047 · Cited by 2,554
Self-citationIncreased bone formation in osteocalcin-deficient mice
Ducy, P. F., Morris, C., Boyce, B. F., Pinero, G. J., Story, B. M., Dunstan, C. R., Smith, E. A., Bonadio, J. F., Goldstein, S. A., Gundberg, C. M., et al. (1996) · Nature · doi:10.1038/382448a0 · Cited by 1,724
Genetic regulation of osteoclast development and function
Teitelbaum, S. L., & Ross, F. P. (2003) · Nature Reviews Genetics · doi:10.1038/nrg1122 · Cited by 1,720
Insulin-regulated hepatic gluconeogenesis through FOXO1–PGC-1α interaction
Puigserver, P., Rhee, J., Donovan, J., Walkey, C. J., Yoon, J. C., Oriente, F., Kitamura, Y., Altomonte, J., Dong, H., Accili, D., et al. (2003) · Nature · doi:10.1038/nature01667 · Cited by 1,487
Michael, M. D., Kulkarni, R. N., Postic, C., Previs, S. F., Shulman, G. I., Magnuson, M. A., & Kahn, C. R. (2000) · Molecular Cell · doi:10.1016/s1097-2765(05)00015-8 · Cited by 1,296
Research works printed but not linked: 1
- Ferron, M., Hinoi, E., Karsenty, G., and Ducy, P. (2008). Osteocalcin differentially regulates beta cell and adipocyte gene expression and affects the development of metabolic diseases in wild-type mice. Proc. Natl. Acad. Sci. USA 105, 5266–5270. · DOI · Paper page
Cited by
Sorted by citations
Items 401–500 of 999
Urano, T., Shiraki, M., Kuroda, T., Tanaka, S., Urano, F., Uenishi, K., & Inoue, S. (2017) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-017-0857-0 · Cited by 32
VKORC1L1, An Enzyme Mediating the Effect of Vitamin K in Liver and Extrahepatic Tissues
Lacombe, J., & Ferron, M. (2018) · Nutrients · doi:10.3390/nu10080970 · Cited by 30
Laboratory aspects and clinical utility of bone turnover markers.
Bhattoa, H. P. (2018) · Europe PMC (PubMed Central) · Cited by 32
Ribeiro, A. L., Mendes, F. B., Carias, E., Rato, F., Santos, N., Neves, P. L., & Silva, A. P. (2019) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2019.107476 · Cited by 32
New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis
Sabrautzki, S., Rubio‐Aliaga, I., Hans, W., Fuchs, H., Rathkolb, B., Calzada‐Wack, J., Cohrs, C. M., Klaften, M., Seedorf, H., Eck, S. H., et al. (2012) · Mammalian Genome · doi:10.1007/s00335-012-9397-z · Cited by 33
Qu, S. (2014) · Medical Science Monitor · doi:10.12659/msm.890130 · Cited by 32
Role of Inositol Poly-Phosphatases and Their Targets in T Cell Biology
Srivastava, N., Sudan, R., & Kerr, W. G. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00288 · Cited by 32
Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits
Billings, L. K., Hsu, Y., Ackerman, R. J., Dupuis, J., Voight, B. F., Rasmussen‐Torvik, L. J., Herçberg, S., Lathrop, M. G., Barnes, D. R., Langenberg, C., et al. (2012) · Diabetes · doi:10.2337/db11-1515 · Cited by 34
X-ray Crystal Structure of Bovine 3 Glu-Osteocalcin
Malashkevich, V. N., Almo, S. C., & Dowd, T. L. (2013) · Biochemistry · doi:10.1021/bi4010254 · Cited by 32
Temperatures rising: brown fat and bone.
Motyl, K. J., & Rosen, C. J. (2011) · PubMed · Cited by 31
Association between osteocalcin and metabolic syndrome in postmenopausal women
Lee, S. W., Jo, H. H., Kim, M. R., Kim, J. H., & You, Y. O. (2015) · Archives of Gynecology and Obstetrics · doi:10.1007/s00404-015-3656-7 · Cited by 31
Confavreux, C. B., Szulc, P., Casey, R., Varennes, A., Goudable, J., & Chapurlat, R. D. (2014) · European Journal of Endocrinology · doi:10.1530/eje-13-0567 · Cited by 32
Gu, L.-J., Lai, X., Wang, Y., Zhang, J.-M., & Liu, J. (2019) · Medicine · doi:10.1097/md.0000000000016096 · Cited by 31
Merlotti, D., Cosso, R., Eller-Vainicher, C., Vescini, F., Chiodini, I., Gennari, L., & Falchetti, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22010435 · Cited by 34
Bisphosphonates in inflammatory rheumatic diseases
Peris, P., Monegal, A., & Guañabens, N. (2021) · Bone · doi:10.1016/j.bone.2021.115887 · Cited by 31
Critical review of bone health, fracture risk and management of bone fragility in diabetes mellitus
Palui, R., Pramanik, S., Mondal, S., & Ray, S. (2021) · World Journal of Diabetes · doi:10.4239/wjd.v12.i6.706 · Cited by 32
Avilkina, V., Chauveau, C., & Mhenni, O. G. (2021) · Bone · doi:10.1016/j.bone.2021.116232 · Cited by 33
Takashi, Y., & Kawanami, D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042376 · Cited by 30
Yasutake, Y., Mizokami, A., Kawakubo‐Yasukochi, T., Chishaki, S., Takahashi, I., Takeuchi, H., & Hirata, M. (2016) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00334.2015 · Cited by 32
Maekawa, S., Katagiri, S., Takeuchi, Y., Komazaki, R., Ohtsu, A., Udagawa, S., & Izumi, Y. (2016) · Journal of Periodontal Research · doi:10.1111/jre.12387 · Cited by 31
Inter-organ communication and regulation of beta cell function
Hussain, M. A., Akalestou, E., & Song, W. (2016) · Diabetologia · doi:10.1007/s00125-015-3862-7 · Cited by 31
Nisio, A. D., Rocca, M. S., Fadini, G. P., Toni, L. D., Marcuzzo, G., Marescotti, M. C., Sanna, M., Plebani, M., Vettor, R., Avogaro, A., et al. (2016) · Clinical Endocrinology · doi:10.1111/cen.13248 · Cited by 30
Osteocalcin and the physiology of danger
Berger, J. M., & Karsenty, G. (2021) · FEBS Letters · doi:10.1002/1873-3468.14259 · Cited by 32
Protein tyrosine phosphatases in skeletal development and diseases
Yang, H., Wang, L., Shigley, C., & Yang, W. (2022) · Bone Research · doi:10.1038/s41413-021-00181-x · Cited by 32
Effect of Fluoride on Insulin Level of Rats and Insulin Receptor Expression in the MC3T3-E1 Cells
Hu, C., Ren, L., Li, X., Wu, N., Li, G., Liu, Q., & Xu, H. J. (2012) · Biological Trace Element Research · doi:10.1007/s12011-012-9482-x · Cited by 30
Karasik, D., Cheung, C. L., Zhou, Y., Cupples, L. A., Kiel, D. P., & Demissie, S. (2011) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.563 · Cited by 29
Yang, J. W., Hong, N., Shim, J., Rhee, Y., & Kim, H. C. (2018) · Journal of Bone Metabolism · doi:10.11005/jbm.2018.25.2.123 · Cited by 30
Osteocalcin, ovarian senescence, and brain health
Schatz, M., Saravanan, S., d’Adesky, N., Bramlett, H. M., Pérez‐Pinzón, M. A., & Raval, A. P. (2020) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2020.100861 · Cited by 31
Endocrine Regulation of Bone and Energy Metabolism in Hibernating Mammals
Doherty, A. H., Florant, G. L., & Donahue, S. W. (2014) · Integrative and Comparative Biology · doi:10.1093/icb/icu001 · Cited by 29
New Insights into Adhesion Signaling in Bone Formation
Brunner, M., Jurdic, P., Tuckerman, J., Block, M. R., & Bouvard, D. (2013) · International review of cytology · doi:10.1016/b978-0-12-407695-2.00001-9 · Cited by 30
Camerino, C., Conte, E., Caloiero, R., Fonzino, A., Carratù, M. R., Lograno, M. D., & Tricarico, D. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2017.01101 · Cited by 29
The endocrine role of bone: Novel functions of bone-derived cytokines
Wang, H., Zheng, X.-Q., Zhang, Y., Huang, J., Zhou, W., Li, X., Tian, H., Wang, B., Xing, D., Fu, W., et al. (2020) · Biochemical Pharmacology · doi:10.1016/j.bcp.2020.114308 · Cited by 31
Osteocalcin and vascular function: is there a cross-talk?
Tacey, A., Hayes, A., Zulli, A., & Levinger, I. (2021) · Molecular Metabolism · doi:10.1016/j.molmet.2021.101205 · Cited by 29
Leanza, G., Fontana, F., Lee, S.-Y., Remedi, M. S., Schott, C., Ferron, M., Hamilton-Hall, M. N., Alippe, Y., Strollo, R., Napoli, N., et al. (2020) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4303 · Cited by 27
Longitudinal associations of insulin resistance with change in bone mineral density in midlife women
Shieh, A., Greendale, G. A., Cauley, J. A., Srikanthan, P., & Karlamangla, A. S. (2022) · JCI Insight · doi:10.1172/jci.insight.162085 · Cited by 29
Ouyang, J., Wan, W., Zhang, S., Ge, L., Yuan, Q., Zhong, W., Xing, M. M. Q., Li, Q., & Fang, X. (2015) · International Journal of Nanomedicine · doi:10.2147/ijn.s77118 · Cited by 29
Isolation and characterization of human osteoblasts from needle biopsies without in vitro culture
Fujita, K., Roforth, M. M., Atkinson, E. J., Peterson, J. M., Drake, M. T., McCready, L. K., Farr, J. N., Monroe, D. G., & Khosla, S. (2013) · Osteoporosis International · doi:10.1007/s00198-013-2529-9 · Cited by 29
Bone Response to Weight Loss Following Bariatric Surgery
Mele, C., Caputo, M., Ferrero, A., Daffara, T., Cavigiolo, B., Spadaccini, D., Nardone, A., Prodam, F., Aimaretti, G., & Marzullo, P. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.921353 · Cited by 37
The role of bone in energy metabolism: A focus on osteocalcin
Smith, C., Lin, X., Parker, L., Yeap, B. B., Hayes, A., & Levinger, I. (2024) · Bone · doi:10.1016/j.bone.2024.117238 · Cited by 32
Xuan, Y., Sun, L., Liu, D., Zhao, L., Tao, B., Wang, W., Zhao, H., Liu, J., & Ning, G. (2014) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2014-2583 · Cited by 31
Hinton, P. S., Shankar, K., Eaton, L. M., & Rector, R. S. (2015) · Metabolism · doi:10.1016/j.metabol.2015.04.004 · Cited by 28
Zhang, J., Tan, L., Xu, C., He, H., Tian, Q., Zhou, Y. G., Qiu, C., Chen, X., & Deng, H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0138524 · Cited by 29
Zhang, L., Li, P., Tang, Z., Dou, Q., & Feng, B. (2019) · Annals of Translational Medicine · doi:10.21037/atm.2019.06.74 · Cited by 27
Liver-Specific Deletion of Mouse CTCF Leads to Hepatic Steatosis via Augmented PPARγ Signaling
Choi, Y., Song, M.-J., Jung, W.-J., Jeong, H., Park, S., Yang, B., Lee, E.-C., Joo, J.-S., Choi, D., Koo, S.-H., et al. (2021) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2021.07.016 · Cited by 23
What are the effects of leptin on bone and where are they exerted?
Idelevich, A., Sato, K., & Baron, R. (2012) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.1812 · Cited by 27
Insulin, osteoblasts, and energy metabolism: why bone counts calories
Riddle, R. C., & Clemens, T. L. (2014) · Journal of Clinical Investigation · doi:10.1172/jci75554 · Cited by 28
Interorgan Crosstalk Contributing toβ-Cell Dysfunction
Tanabe, K., Amo-Shiinoki, K., Hatanaka, M., & Tanizawa, Y. (2017) · Journal of Diabetes Research · doi:10.1155/2017/3605178 · Cited by 30
Liu, T., Liu, D., Xuan, Y., Zhao, L., Sun, L., Zhao, D., Wang, X., He, Y., Guo, X., Du, R., et al. (2017) · Bone Research · doi:10.1038/boneres.2017.20 · Cited by 29
Rosa, B. V., Blair, H. T., Vickers, M. H., Dittmer, K. E., Morel, P. C. H., Knight, C. G., & Firth, E. C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082378 · Cited by 27
Bone metabolism and fracture risk in type 2 diabetes mellitus
Yamaguchi, T., & Sugimoto, T. (2012) · BoneKEy Reports · doi:10.1038/bonekey.2012.27 · Cited by 26
Vitamin K role in mineral and bone disorder of chronic kidney disease
de Oliveira, R. B., Stinghen, A. E. M., & Massy, Z. A. (2019) · Clinica Chimica Acta · doi:10.1016/j.cca.2019.11.040 · Cited by 27
RANKL induces beige adipocyte differentiation in preadipocytes
Matsuo, F. S., de Araújo, P. H. C., Mota, R. F., Carvalho, A. J. R., de Queiroz, M. S., de Almeida, B. B., Ferreira, K. C. D. O. S., Metzner, R. J. M., Ferrari, G. D., Alberici, L. C., et al. (2020) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00397.2019 · Cited by 27
Low Bone Turnover Markers in Young and Middle-Aged Male Patients with Type 2 Diabetes Mellitus
Liu, X. X., Jiang, L., Liu, Q., Zhang, J., Niu, W., Liu, J., & Zhang, Q. (2020) · Journal of Diabetes Research · doi:10.1155/2020/6191468 · Cited by 27
Weivoda, M. M., & Hohl, R. J. (2011) · Bone · doi:10.1016/j.bone.2011.09.056 · Cited by 27
A unified model for bone–renal mineral and energy metabolism
Rowe, P. S. (2015) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2015.03.006 · Cited by 27
Bone-brain crosstalk and potential associated diseases
Rousseaud, A., Moriceau, S., Ramos-Brossier, M., & Oury, F. (2016) · Hormone Molecular Biology and Clinical Investigation · doi:10.1515/hmbci-2016-0030 · Cited by 28
Mst1/2 Kinases Modulate Glucose Uptake for Osteoblast Differentiation and Bone Formation
Li, W., Deng, Y., Feng, B., & Mak, K. K. (2018) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.3413 · Cited by 28
Hu, Y., Tan, L., Chen, X., Greenbaum, J., & Deng, H. (2018) · Bone · doi:10.1016/j.bone.2018.08.020 · Cited by 28
Mosher, Melton, P. E., Stapleton, Schanfield, & Crawford, C. (2016) · Human Biology · doi:10.13110/humanbiology.88.2.0121 · Cited by 26
Genetic activation of glycolysis in osteoblasts preserves bone mass in type I diabetes
Ji, X., Seeley, R. A., Li, K., Song, F., Liao, X., Song, C., Angelozzi, M., Valeri, A., Marmo, T., Lee, W., et al. (2023) · Cell chemical biology · doi:10.1016/j.chembiol.2023.07.003 · Cited by 28
PHOSPHO1 is a skeletal regulator of insulin resistance and obesity
Suchacki, K. J., Morton, N. M., Vary, C., Huesa, C., Yadav, M. C., Thomas, B. J., Rajoanah, S., Bünger, L., Ball, D., Barrios-Llerena, M. E., et al. (2020) · BMC Biology · doi:10.1186/s12915-020-00880-7 · Cited by 26
Glycemic Control and Bone in Diabetes
Weber, D. R., Long, F., Zemel, B. S., & Kindler, J. M. (2022) · Current Osteoporosis Reports · doi:10.1007/s11914-022-00747-6 · Cited by 29
A Review on the Crosstalk between Insulin and Wnt/β-Catenin Signalling for Bone Health
Wong, S. K., Mohamad, N.-V., Jayusman, P. A., & Ibrahim, N. ‘. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241512441 · Cited by 26
Saucedo, R., Rico, G., Vega, G., Basurto, L., Córdova, L. F. R., Galvan, R., Hernandez, M., Puello, E., & Zárate, A. (2014) · Journal of Endocrinological Investigation · doi:10.1007/s40618-014-0220-4 · Cited by 25
Makinistoglu, M. P., & Karsenty, G. (2014) · Molecular Metabolism · doi:10.1016/j.molmet.2014.10.004 · Cited by 26
Recent advances in vitamin K-dependent Gla-containing proteins and vitamin K nutrition
Shiraki, M., Tsugawa, N., & Okano, T. (2015) · Osteoporosis and Sarcopenia · doi:10.1016/j.afos.2015.07.009 · Cited by 27
Osteocalcin: a new link between bone and energy metabolism. Some evolutionary clues
Fernández‐Real, J. M., & Ricart, W. (2011) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0b013e328346df4e · Cited by 26
Osteocalcin, a bone‐derived hormone with important andrological implications
Toni, L. D., Nisio, A. D., Rocca, M. S., Ponce, M. D. R., Ferlin, A., & Foresta, C. (2017) · Andrology · doi:10.1111/andr.12359 · Cited by 26
Giudici, K. V., Fisberg, R. M., Marchioni, D. M. L., Peters, B. S. E., & Martini, L. A. (2017) · Journal of the American College of Nutrition · doi:10.1080/07315724.2016.1274923 · Cited by 26
Smoking and other determinants of bone turnover
Jorde, R., Stunes, A. K., Kubiak, J., Grimnes, G., Thorsby, P. M., & Syversen, U. (2019) · PLOS ONE · doi:10.1371/journal.pone.0225539 · Cited by 25
Verroken, C., Zmierczak, H., Goemaere, S., Kaufman, J., & Lapauw, B. (2016) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2016-3609 · Cited by 25
GLP-1 signaling is required for improvement of glucose tolerance by osteocalcin
Mizokami, A., Mukai, S., Gao, J., Kawakubo‐Yasukochi, T., Otani, T., Takeuchi, H., Jimi, E., & Hirata, M. (2019) · Journal of Endocrinology · doi:10.1530/joe-19-0288 · Cited by 27
ATRAID regulates the action of nitrogen-containing bisphosphonates on bone
Surface, L. E., Burrow, D. T., Li, J., Park, J., Kumar, S., Lyu, C., Song, N., Yu, Z., Rajagopal, A., Bae, Y., et al. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.aav9166 · Cited by 27
The Roles of FOXO1 in Periodontal Homeostasis and Disease
Ren, L., Yang, J., Wang, J., Zhou, X., & Liu, C. (2021) · Journal of Immunology Research · doi:10.1155/2021/5557095 · Cited by 25
Zhang, L., Li, X., Yu, Y., Zhang, L., Dong, L., Gan, J., Mao, T., Liu, T., Peng, J., & He, L. (2021) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2021.111081 · Cited by 24
The “Connexin” Between Bone Cells and Skeletal Functions
Zappitelli, T., & Aubin, J. E. (2014) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24836 · Cited by 25
Quarles, L. D. (2013) · Seminars in Nephrology · doi:10.1016/j.semnephrol.2012.12.014 · Cited by 25
Oh, J., & Lee, N. K. (2017) · Molecules and Cells · doi:10.14348/molcells.2017.0025 · Cited by 24
Reis, A. M. S., Ribeiro, L. G. R., Ocarino, N. M., Goes, A. M., & Serákides, R. (2015) · BMC Musculoskeletal Disorders · doi:10.1186/s12891-015-0467-8 · Cited by 24
The Effect of Type 2 Diabetes on Bone Biomechanics
Karim, L., Rezaee, T., & Vaidya, R. (2019) · Current Osteoporosis Reports · doi:10.1007/s11914-019-00526-w · Cited by 24
Cheung, C., Sing, C., Lau, W. C. Y., Li, G. H., Lip, G. Y. H., Tan, K. C. B., Cheung, B. M. Y., Chan, E. W., & Wong, I. C. K. (2021) · Cardiovascular Diabetology · doi:10.1186/s12933-021-01263-0 · Cited by 23
Crosstalk between bone and other organs
Yuan, W., & Song, C. (2022) · Medical Review · doi:10.1515/mr-2022-0018 · Cited by 27
Analysis of the Role of Insulin Signaling in Bone Turnover Induced by Fluoride
Liu, Q., Liu, H., Yu, X., Wang, Y., Yang, C., & Xu, H. J. (2015) · Biological Trace Element Research · doi:10.1007/s12011-015-0555-5 · Cited by 24
Bone Development and Remodeling
Maes, C., & Kronenberg, H. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-323-18907-1.00060-3 · Cited by 26
The role of bone in whole-body energy metabolism
Lecka‐Czernik, B., Rosen, C. J., & Napoli, N. (2025) · Nature Reviews Endocrinology · doi:10.1038/s41574-025-01162-4 · Cited by 27
The Importance of the Gastrointestinal Tract in the Control of Bone Mass Accrual
Karsenty, G., & Gershon, M. D. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.06.011 · Cited by 23
Lavet, C., Martin, A., Linossier, M., Vanden‐Bossche, A., Laroche, N., Thomas, M., Gerbaix, M., Ammann, P., Fraissenon, A., Lafage‐Proust, M., et al. (2015) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2596 · Cited by 24
Fowlkes, J. L., Bunn, R. C., Kalaitzoglou, E., Ray, P., Popescu, I. R., & Thrailkill, K. M. (2020) · Scientific Reports · doi:10.1038/s41598-020-65717-3 · Cited by 23
Nakagawa, T., Tsuka, S., Aonuma, F., Nodai, T., Munemasa, T., Tamura, A., Mukaibo, T., Kondo, Y., Masaki, C., & Hosokawa, R. (2020) · Journal of Prosthodontic Research · doi:10.2186/jpr.jpor_2019_629 · Cited by 25
Metabolic Phenotypes and Step by Step Evolution of Type 2 Diabetes: A New Paradigm
Cooper, I. D., Brookler, K. H., Kyriakidou, Y., Elliott, B., & Crofts, C. A. P. (2021) · Biomedicines · doi:10.3390/biomedicines9070800 · Cited by 24
Villafán-Bernal, J. R., Llamas-Covarrubias, M. A., Muñóz-Valle, J. F., Rivera-León, E. A., González-Hita, M. E., Bastidas‐Ramírez, B. E., Gurrola‐Díaz, C. M., Armendáriz‐Borunda, J., & Sánchez‐Enríquez, S. (2014) · Journal of Investigative Medicine · doi:10.2310/jim.0000000000000015 · Cited by 23
Up-regulation of cyclinD1 and Bcl2A1 by insulin is involved in osteoclast proliferation
Lee, J., & Lee, N. K. (2014) · Life Sciences · doi:10.1016/j.lfs.2014.07.006 · Cited by 23
Shim, J., Greenblatt, M. B., Singh, A., Brady, N. J., Hu, D. Z., Drapp, R., Ogawa, W., Kasuga, M., Noda, T., Yang, S., et al. (2011) · Journal of Clinical Investigation · doi:10.1172/jci59466 · Cited by 23
Deficiency of the bone mineralization inhibitor NPP1 protects against obesity and diabetes
Huesa, C., Zhu, D., Glover, J. D., Ferron, M., Karsenty, G., Milne, E., Millán, J. L., Ahmed, S. F., Farquharson, C., Morton, N. M., et al. (2014) · Disease Models & Mechanisms · doi:10.1242/dmm.017905 · Cited by 23
Enhanced and suppressed mineralization by acetoacetate and β-hydroxybutyrate in osteoblast cultures
Saito, A., Yoshimura, K., Miyamoto, Y., Kaneko, K., Chikazu, D., Yamamoto, M., & Kamijo, R. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.03.109 · Cited by 24
Zhang, X., Cheng, Q., Wáng, Y. X. J., Leung, P. S., & Mak, K. K. (2016) · Cell Death and Differentiation · doi:10.1038/cdd.2016.113 · Cited by 23
Insulin and bone health in young adults: The mediator role of lean mass
Torres-Costoso, A. I., Pozuelo‐Carrascosa, D. P., Álvarez‐Bueno, C., Ferri‐Morales, A., Ibarra, J. M., Notario‐Pacheco, B., & Martínez‐Vizcaíno, V. (2017) · PLoS ONE · doi:10.1371/journal.pone.0173874 · Cited by 23
Stechschulte, L. A., & Lecka‐Czernik, B. (2017) · Current Molecular Biology Reports · doi:10.1007/s40610-017-0056-8 · Cited by 23
Park, Y. E., Musson, D. S., Naot, D., & Cornish, J. (2017) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2017.04.001 · Cited by 25
Tangseefa, P., Martin, S. K., Fitter, S., Baldock, P. A. J., Proud, C. G., & Zannettino, A. C. W. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.26163 · Cited by 24
Metadata
- Authors
- Ferron, M., Wei, J., Yoshizawa, T., Del Fattore, A., DePinho, R. A., Teti, A., Ducy, P., & Karsenty, G.
- Affiliations
- Columbia University (US)
- Harvard University (US)
- University of L'Aquila (IT)
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2010-07
- Volume
- 142
- Issue
- 2
- Pages
- 296-308
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC2910411
- OpenAlex
- W1971400919
- Cited by
- 1,123
- References
- 49
- Citations by year
- 2026: 30 · 2025: 47 · 2024: 50 · 2023: 41 · 2022: 43 · 2021: 62 · 2020: 84 · 2019: 65 · 2018: 73 · 2017: 89 · 2016: 75 · 2015: 100 · 2014: 76 · 2013: 84 · 2012: 87
- FWCI
- 37.16
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Archivio Istituzionale della Ricerca - Università degli Studi dell Aquila (submittedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK078042)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (R01AR045548)
- 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 › Endocrinology, Diabetes and Metabolism › Alkaline Phosphatase Research Studies
- Keywords
- insulin signaling, osteoblasts, osteocalcin, bone remodeling, bone resorption, glucose homeostasis, energy metabolism, uncarboxylated osteocalcin, decarboxylation, osteoclasts, feed-forward loop
- MeSH terms
- Animals, Cells, Cultured, Energy Metabolism, Extracellular Matrix, Glucose, Humans, Insulin, Mice, Inbred C57BL, Osteoblasts, Signal Transduction, Osteocalcin, Bone Remodeling, Mice
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