The DOI matches its Crossref record; 53 of the 53 references it cites were found in a registry or an index.
Calcitonin-gene-related peptide stimulates stromal cell osteogenic differentiation and inhibits RANKL induced NF-κB activation, osteoclastogenesis and bone resorption
Open accessAbstract
Previously we observed that capsaicin treatment in rats inhibited sensory neuropeptide signaling, with a concurrent reduction in trabecular bone formation and bone volume, and an increase in osteoclast numbers and bone resorption. Calcitonin gene-related peptide (CGRP) is a neuropeptide richly distributed in sensory neurons innervating the skeleton and we postulated that CGRP signaling regulates bone integrity. In this study we examined CGRP effects on stromal and bone cell differentiation and activity in vitro. CGRP receptors were detected by immunocytochemical staining and real time PCR assays in mouse bone marrow stromal cells (BMSCs) and bone marrow macrophages (BMMs). CGRP effects on BMSC proliferation and osteoblastic differentiation were studied using BrdU incorporation, PCR products, alkaline phosphatase (ALP) activity, and mineralization assays. CGRP effects on BMM osteoclastic differentiation and activity were determined by quantifying tartrate-resistant acid phosphatase positive (TRAP+) multinucleated cells, pit erosion area, mRNA levels of TRAP and cathepsin K, and nuclear factor-κB (NF-κB) nuclear localization. BMSCs, osteoblasts, BMMs, and osteoclasts all expressed CGRP receptors. CGRP (10-10-10-8M) stimulated BMSC proliferation, up-regulated the expression of osteoblastic genes, and increased ALP activity and mineralization in the BMSCs. In BMM cultures CGRP (10-8M) inhibited receptor activator of NF-κB ligand (RANKL) activation of NF-κB. CGRP also down-regulated osteoclastic genes like TRAP and cathepsin K, decreased the numbers of TRAP+ cells, and inhibited bone resorption activity in RANKL stimulated BMMs. These results suggest that CGRP signaling maintains bone mass both by directly stimulating stromal cell osteoblastic differentiation and by inhibiting RANKL induced NF-κB activation, osteoclastogenesis, and bone resorption.
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 cited source says what the claim attributes to it.
In the citing paper
“suggesting that CGRP acts with higher potency to inhibit osteoclast activity than osteoclast differentiation (213).”
From The Activity of Peptides of the Calcitonin Family in Bone (2019) · cites this paper as [213]
The cited source says what the claim attributes to it.
In the citing paper
“In cells cultured from mouse bone marrow and induced to differentiate into osteoclasts by M-CSF and RANKL, the area of resorption pits was reduced by CGRP in a concentration of 0.1 nM or higher, whereas higher concentrations of 10 nM CGRP were required for the inhibition of TRAP-positive cell formation”
From The Activity of Peptides of the Calcitonin Family in Bone (2019) · cites this paper as [213]
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
RAMPs regulate the transport and ligand specificity of the calcitonin-receptor-like receptor
McLatchie, L. M., Fraser, N. J., Main, M. J., Wise, A., Brown, J., Thompson, N., Solari, R., Lee, M. G., & Foord, S. M. (1998) · Nature · doi:10.1038/30666 · Cited by 2,134
Functions of RANKL/RANK/OPG in bone modeling and remodeling
Boyce, B. F., & Xing, L. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.03.018 · Cited by 1,844
Minireview: The OPG/RANKL/RANK System
Khosla, S. (2001) · Endocrinology · doi:10.1210/endo.142.12.8536 · Cited by 1,515
Origins of skeletal pain: sensory and sympathetic innervation of the mouse femur
Mach, D. B., Rogers, S. D., Sabino, M. C., Luger, N. M., Schwei, M. J., Pomonis, J. D., Keyser, C. P., Clohisy, D. R., Adams, D. J., O’Leary, P., et al. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00165-3 · Cited by 676
Rapidly Forming Apatitic Mineral in an Osteoblastic Cell Line (UMR 106—01 BSP)
Stanford, C. M., Jacobson, P. A., Eanes, E. D., Lembke, L. A., & Midura, R. J. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.16.9420 · Cited by 439
Austin, L. A., & Heath, H. (1981) · New England Journal of Medicine · doi:10.1056/nejm198101293040505 · Cited by 417
Substance P- and CGRP-immunoreactive nerves in bone
Bjurholm, A., Andris Kreicbergs, A., Brodin, E., & Schultzberg, M. (1988) · Peptides · doi:10.1016/0196-9781(88)90023-x · Cited by 384
Huhtakangas, J. A., Olivera, C. J., Bishop, J. E., Zanello, L. P., & Norman, A. W. (2004) · Molecular Endocrinology · doi:10.1210/me.2004-0116 · Cited by 337
Gamse, R., Leeman, S. E., Holzer, P. D., & Lembeck, F. (1981) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/bf00500070 · Cited by 316
Shui, C., Spelsberg, T. C., Riggs, B. L., & Khosla, S. (2003) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.2003.18.2.213 · Cited by 231
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–198 of 198
Varied presentations and outcomes of Charcot neuroarthropathy in patients with diabetes mellitus
Rastogi, A., Prakash, M., & Bhansali, A. K. (2018) · International Journal of Diabetes in Developing Countries · doi:10.1007/s13410-018-0700-8 · Cited by 17
Leitão, L., Alves, C. J., Sousa, D. M., Neto, E., Conceição, F., & Lamghari, M. (2019) · The FASEB Journal · doi:10.1096/fj.201900454r · Cited by 16
αCGRP Affects BMSCs’ Migration and Osteogenesis via the Hippo-YAP Pathway
Wang, B., Lin, J., Zhang, Q., Zhang, X., Yu, H., Gong, P., & Xiang, L. (2019) · Cell Transplantation · doi:10.1177/0963689719871000 · Cited by 16
Calcitonin gene-related peptide regulates periodontal tissue regeneration
Miki, K., Takeshita, N., Yamashita, M., Kitamura, M., & Murakami, S. (2024) · Scientific Reports · doi:10.1038/s41598-024-52029-z · Cited by 15
Cracking the Code: The Role of Peripheral Nervous System Signaling in Fracture Repair
Morris, A. J., Parker, R. S., Nazzal, M. K., Natoli, R. M., Fehrenbacher, J. C., Kacena, M. A., & White, F. A. (2024) · Current Osteoporosis Reports · doi:10.1007/s11914-023-00846-y · Cited by 15
Li, X., Hu, L., Wang, X., Liu, H., Zhang, C., Wang, J., Wang, X., & Wang, S. (2024) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2023.12.001 · Cited by 15
Zhao, Z., Fu, X., Zhang, G., Li, Y., Wu, M., & Tan, Y. (2012) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24375 · Cited by 17
Neurologic Regulation and Orthodontic Tooth Movement
Kyrkanides, S., Huang, H., & Faber, R. D. (2015) · Frontiers of oral physiology/Frontiers of oral biology · doi:10.1159/000351900 · Cited by 16
Wang, L., Hou, S., Sabsovich, I., Guo, T., Wei, T., & Kingery, W. S. (2020) · Bone · doi:10.1016/j.bone.2020.115806 · Cited by 15
Self-citationMa, L., Xiang, L., Yao, Y., Yuan, Q., Li, L., & Gong, P. (2013) · Medical Hypotheses · doi:10.1016/j.mehy.2013.04.025 · Cited by 15
Huang, C., Yang, X., Liu, D., Sun, Y.-G., & Dai, X.-M. (2015) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-015-0630-8 · Cited by 15
Terra, S. R., Cardoso, J. C. R., Félix, R. C., Martins, L. A. M., Souza, D. O., Guma, F. T. C. R., Canário, A. V. M., & Schein, V. (2015) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2015.01.010 · Cited by 14
Bio‑Oss� modified by calcitonin gene‑related peptide promotes osteogenesis in vitro
Li, Y., Yang, L., Zheng, Z., Li, Z., Deng, T., Ren, W., Wu, C., & Guo, L. (2017) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2017.5048 · Cited by 13
RANKL and RANK in Cancer Therapy
Onji, M., & Penninger, J. M. (2022) · Physiology · doi:10.1152/physiol.00020.2022 · Cited by 14
Chen, H., Lü, H., Huang, J., Wang, Z., Chen, Y., & Zhang, T. (2021) · Orthopaedic Journal of Sports Medicine · doi:10.1177/23259671211003982 · Cited by 12
Lasschuit, J. W. J., Greenfield, J. R., & Tonks, K. T. T. (2021) · Acta Diabetologica · doi:10.1007/s00592-021-01803-w · Cited by 12
Hydrogel‐Based Systems in Neuro‐Vascularized Bone Regeneration: A Promising Therapeutic Strategy
Li, X., Cui, Y., He, X., & Mao, L. (2024) · Macromolecular Bioscience · doi:10.1002/mabi.202300484 · Cited by 12
Does methamphetamine affect bone metabolism?
Tomita, M., Katsuyama, H., Watanabe, Y., Okuyama, T., Fushimi, S., Ishikawa, T., Nata, M., & Miyamoto, O. (2014) · Toxicology · doi:10.1016/j.tox.2014.01.014 · Cited by 11
Effect of Periodontal Pathogens on Total Bone Volume Fraction: A Phenotypic Study
Zhang, Z., Xie, M., Liu, Y., Li, Y.-X., Wu, K., & Ding, Y. (2020) · Current Medical Science · doi:10.1007/s11596-020-2243-8 · Cited by 11
Effects of CGRP receptor antagonism on glucose and bone metabolism in mice with diet-induced obesity
Köhli, P., Appelt, J., Otto, E., Jahn, D., Baranowsky, A., Bahn, A., Erdmann, C., Müchler, J. M., Mülleder, M., Tsitsilonis, S., et al. (2020) · Bone · doi:10.1016/j.bone.2020.115646 · Cited by 11
Wang, T., Guo, Y., Yuan, Y., Xin, N., Zhang, Q., Guo, Q., & Gong, P. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.02.027 · Cited by 11
Periosteum Organoid: Biomimetic Design Inspired From the Bone Healing Process
Hao, S., Wang, F., Huang, J., Xia, Z., Triffitt, J. T., Xu, C., Bai, L., & Su, J. (2025) · Exploration · doi:10.1002/exp.20240298 · Cited by 11
Strategies for in situ tissue engineering of vascularized bone regeneration (Review)
He, Y., Liang, L., Luo, C., Zhang, Z., & Huang, J. (2023) · Biomedical Reports · doi:10.3892/br.2023.1625 · Cited by 10
Increase of CGRP-Containing Nerve Fibers in the Rat Periodontal Ligament After Luxation
Nagayama, T., Seiryu, M., Deguchi, T., Kano, M., Suzuki, T., Takano‐Yamamoto, T., & Ichikawa, H. (2011) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-011-9767-1 · Cited by 10
Chen, J., Ma, G., Liu, W., Liu, Y., & Ding, Y. (2016) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-016-0780-9 · Cited by 10
Lai, M., Yan, X., Shen, K., Tang, Q., Fang, X., Zhang, C., Zhu, Z., & Hou, Y. (2020) · Colloids and Surfaces A Physicochemical and Engineering Aspects · doi:10.1016/j.colsurfa.2020.124899 · Cited by 10
Xie, D., Xu, Y., Yang, Y., Hua, Z., Li, J., Fu, G., & Wu, Q. (2020) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14540 · Cited by 10
Zeng, X., He, S., Yang, C., Yang, Y., Zheng, G., Wang, H., Liang, L., Xu, C., Cao, P., Wu, X., et al. (2025) · Pharmacological Research · doi:10.1016/j.phrs.2025.107850 · Cited by 9
Nakasa, T., Ikuta, Y., Sumii, J., Nekomoto, A., Kawabata, S., & Adachi, N. (2023) · The Journal of Foot & Ankle Surgery · doi:10.1053/j.jfas.2023.10.004 · Cited by 9
Inhibition of osteogenesis surrounding the titanium implant by CGRP deficiency
Liu, Y., Zheng, G., Liu, L., Wang, Z., Wang, Y., Chen, Q., & Luo, E. (2017) · Connective Tissue Research · doi:10.1080/03008207.2017.1317759 · Cited by 9
Jablonski, H., Polan, C., Wedemeyer, C., Hilken, G., Schlepper, R., Bachmann, H. S., Grabellus, F., Dudda, M., Jäger, M., & Kauther, M. D. (2017) · Bone · doi:10.1016/j.bone.2017.09.006 · Cited by 9
Jochheim, L. S., Odysseos, G., Hidalgo‐Sastre, A., Zhong, S., Staufer, L. M., Kroiss, M., Kabacaoğlu, D., Lange, S., Engleitner, T., Hartmann, D., et al. (2019) · Pancreatology · doi:10.1016/j.pan.2019.05.455 · Cited by 9
Fei, W., Zhang, H., Yuxin, D., Li, S., Zhang, G., & Yinghui, T. (2016) · PubMed Central · doi:10.7518/hxkq.2016.03.014 · Cited by 8
Lago, E. P., Baird, A., Blott, S. C., McPhail, R. E., Ross, A. C., Durward-Akhurst, S. A., & Guest, D. J. (2023) · Animals · doi:10.3390/ani14010116 · Cited by 8
Lei, S., Guo, L., Yue, H., Zhao, D., Zhang, C., Du, W., Huang, L., Wang, J., Dang, Y., Liu, J., et al. (2013) · Orthopaedic Surgery · doi:10.1111/os.12071 · Cited by 8
Chen, Z., Luo, Z., Greenblatt, M. B., Wu, Z., & Xu, R. (2026) · Bone Research · doi:10.1038/s41413-026-00534-4 · Cited by 9
Salvio, G., Petrelli, M., Paolini, S., Baldini, V., Sbaffi, C., Basili, S., Giordano, A., Balercia, G., & Cinti, S. (2023) · Journal of Endocrinological Investigation · doi:10.1007/s40618-022-01999-w · Cited by 7
Long, H., Zheng, L., Gomes, F. C., Zhang, J., Mou, X., & Yuan, H. M. (2013) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2013.04.015 · Cited by 7
A mysterious triangle of blood, bones, and nerves
Asada, N., & Katayama, Y. (2023) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-023-01402-5 · Cited by 8
Wang, S., Xu, S., Shi, Z., Wu, J.-C., Lei, S., & Wang, Y. (2019) · Europe PMC (PubMed Central) · doi:10.7507/1002-1892.201811137 · Cited by 7
Deciphering the skeletal interoceptive circuitry to control bone homeostasis
Wu, Y., Guo, J., Chen, Z., Zhang, F., Chow, B., Chen, Z., Yeung, K., & Qiao, W. (2025) · BMEMat · doi:10.1002/bmm2.12138 · Cited by 6
Hamiti, Y., Liu, K., Wang, S., Yang, X. N., Kadier, X., & Yusufu, A. (2025) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2025.1641476 · Cited by 6
Sensory-neuron-derived CGRPα controls white adipocyte differentiation and tissue plasticity
Dumont, K. D., Seradj, S. H., Wang, Y., Liu, S., Červenka, I., Wu, C., Jannig, P. R., Porsmyr‐Palmertz, M., Baiges‐Gayà, G., Huang, X., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116613 · Cited by 6
Therapeutic approach to "diabetic foot" complications.
Calderini, C., Cioni, F., Haddoub, S., Maccanelli, F., Magotti, M. G., & Tardio, S. (2014) · Acta bio-medica dell'Ateneo parmense/Acta biomedica · Cited by 6
Involvement of sensory neurons in bone defect repair in rats
Henmi, A., Nakamura, M., Echigo, S., & Sasano, Y. (2011) · Journal of Electron Microscopy · doi:10.1093/jmicro/dfr075 · Cited by 6
Liu, Q., Yu, M., Liao, M., Ran, Z., Tang, X., Hu, J., Su, B., Fu, G., & Wu, Q. (2023) · Journal of Molecular Histology · doi:10.1007/s10735-023-10167-0 · Cited by 5
Zhang, Y., Chen, H., Long, X., & Xu, T. (2021) · Regenerative Biomaterials · doi:10.1093/rb/rbab041 · Cited by 6
Impact of TRP Channels in Oral Pathology and Therapeutic Targeting Options: A Narrative Review
Evangeliou, E., Plemmenos, G., Chalazias, A., & Piperi, C. (2023) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026623666230331110443 · Cited by 5
Dual Factor-Loaded Artificial Periosteum Accelerates Bone Regeneration
Yao, M., Liang, S., Zeng, Y., Peng, F., Zhao, X., Du, C., Ma, X., Huang, H., Wang, D., & Zhang, Y. (2024) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.3c01587 · Cited by 4
Guozhu, Y., Yihua, W., Zhu, Y. H., li, D., Tianqi, Z., Jia, L., & Shizhou, Z. (2025) · Regenerative Therapy · doi:10.1016/j.reth.2025.02.016 · Cited by 4
Hamiti, Y., Liu, K., Yang, X. N., Wang, S., Kadier, X., & Yusufu, A. (2025) · Materials Today Bio · doi:10.1016/j.mtbio.2025.102181 · Cited by 5
Zhang, X., Huang, X., Zhang, Y., Xu, Z., Chen, Y., Sun, J. L., Chen, X., Zhang, Y., Wu, W., & Chen, Z. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110949 · Cited by 4
Shiwaku, Y., Okawa, H., Suzuki, I., Sakai, S., Egusa, H., & Suzuki, O. (2024) · Acta Biomaterialia · doi:10.1016/j.actbio.2024.08.054 · Cited by 4
Wei, X., Li, M., You, J., Luo, J., Zhai, J., Zhang, J., Feng, J., Wang, H., & Zhou, Y. (2025) · International Journal of Nanomedicine · doi:10.2147/ijn.s505677 · Cited by 5
The pathogenesis of Charcot osteoarthropathy: the role of the peripheral nervous system
Radikovich, G. G., & Kaminarskaya, Y. A. (2015) · Endocrine Surgery · doi:10.14341/serg201445-14 · Cited by 4
Calcitonin: Survey of new anatomy data to pathology and therapeutic aspects
Faour, O., & Gilloteaux, J. (2017) · Translational Research in Anatomy · doi:10.1016/j.tria.2017.01.001 · Cited by 4
New Generation of Meso and Antiprogestins (SPRMs) into the Osteoporosis Approach
Woźniczka, M., & Błaszczak-Świątkiewicz, K. (2021) · Molecules · doi:10.3390/molecules26216491 · Cited by 4
Pathogenesis of Charcot Neuroarthropathy and Acute Management
Petrova, N. L., & EDMONDS, M. E. (2020) · doi:10.1002/9781119445821.ch19 · Cited by 4
Kocot, N., Pękala, E., Koczurkiewicz, P., Chłoń‐Rzepa, G., Łapa, A., & Wójcik‐Pszczoła, K. (2025) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2025.108301 · Cited by 3
Li, K., Zhang, X., Li, J., & Zheng, X. (2025) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2025.114619 · Cited by 3
Huang, C., Liu, X., Lin, L., Zhang, S., Xu, N., Wang, X., & Lin, J. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1669459 · Cited by 3
The Role of IL-6RA in UHMWPE Promotes Proliferation in Fibro-Like Synovial Cells
Pang, X., Jiang, Y., Zhen, X., Nie, H., Qin, H., Huang, L., & Zhang, L. (2018) · BioMed Research International · doi:10.1155/2018/3928915 · Cited by 3
Petrova, N. L. (2017) · Frontiers in diabetes · doi:10.1159/000480045 · Cited by 3
Naot, D., Musson, D. S., & Cornish, J. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-814841-9.00033-6 · Cited by 4
Wang, L., Ni, Z., Huang, Y., Mao, J., Wu, J., (17594), W. W., Jiang, X., Zhou, L., Tang, J., Xi, K., et al. (2026) · Journal of Materials Chemistry B · doi:10.1039/d5tb02399h · Cited by 2
Self-citationNeuro-osteo crosstalk: The sympathetic nervous system as a key driver of SCI-induced osteoporosis
Bryan, J. A., Jackson, W., Lemmens, N., & Hook, M. A. (2026) · Experimental Neurology · doi:10.1016/j.expneurol.2026.115824 · Cited by 2
The Effects of Calcitonin Gene‐Related Peptide on Cartilage in Osteoarthritis
Ju, Y., Shen, L., Huang, Q., & Huang, Z. (2025) · International Journal of Rheumatic Diseases · doi:10.1111/1756-185x.70357 · Cited by 2
Levasseur, R. (2019) · EMC - Aparato Locomotor · doi:10.1016/s1286-935x(19)42130-8 · Cited by 2
Acid-base Balance and Oxidative Metabolism in Calcified Tissues
Riihonen, R. (2010) · UTUPub (University of Turku) · Cited by 2
Levasseur, R. (2019) · EMC - Podología · doi:10.1016/s1762-827x(19)42712-0 · Cited by 1
Nagayama, T., Fukunaga, T., Yajima, T., Shigemi, S., Sakamoto, M., Seiryu, M., Ichikawa, H., Mizoguchi, I., & Sato, T. (2024) · Clinical and Investigative Orthodontics · doi:10.1080/27705781.2024.2336324 · Cited by 1
Tang, Y., Lin, J., Zhao, T., Sun, L., & Liu, T. (2025) · Biomaterials Science · doi:10.1039/d4bm01635a · Cited by 1
Ishizuka, K. (2022) · Journal of Hard Tissue Biology · doi:10.2485/jhtb.31.87 · Cited by 1
Ma, L., Xiang, L., & Gong, P. (2013) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24562
Pathophysiology of Diabetes and Charcot Neuroarthropathy
Soin, S. P., Hunter, J. G., & Kates, S. L. (2016) · Springer eBooks · doi:10.1007/978-3-319-27623-6_2
Ma, L., Xiang, L., Ma, X., Zhang, S., & Gong, P. (2020) · Journal of Hard Tissue Biology · doi:10.2485/jhtb.29.205
Yang, C.-Z. H.-N., LiuYi-gong, D.-C., & Dai, S.-M. (2015)
Salvio, G., Petrelli, M., Paolini, S., Baldini, V., Sbaffi, C., Basili, S., Giordano, A., Balercia, G., & Cinti, S. (2022) · Research Square · doi:10.21203/rs.3.rs-1335950/v1
Diabetes and Charcot neuroarthropathy: pathophysiology
Pierre-Jerome, C., & Nuaimi, D. M. S. A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-99352-4.00024-3
Mmu_circ_009056 promotes osteogenic differentiation and mineralization of BMSCs via miR-139-3pPreprint
Luo, T., Huang, Z., Ding, C., Su, Z., Zheng, Z., & Guo, L. (2022) · Research Square · doi:10.21203/rs.3.rs-1886368/v1
Lago, E. P., Baird, A., Blott, S. C., McPhail, R. E., Ross, A. K. C., Durward-Akhurst, S. A., & Guest, D. J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.16.545331
Masuyama, T., Sato, I., Ueda, Y., Kawata, S., Yakura, T., & Itoh, M. (2023) · Journal of Oral and Maxillofacial Surgery · doi:10.1016/j.joms.2023.09.012
Role and Research Progress of CGRP in Bone Homeostasis
唐, 晓. (2024) · Advances in Clinical Medicine · doi:10.12677/acm.2024.1492442
Bardiugov, P. S., Artemova, E. V., Parshikov, M. V., & Yarygin, N. V. (2024) · N N Priorov Journal of Traumatology and Orthopedics · doi:10.17816/vto623895
Calcitonin gene-related peptide (CGRP)
Ling, B., Aubdool, A. A., Kodji, X., Brain, S. D., Stanimirovic, D. B., Hamel, É., & Moreno, M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-13825-6.00159-x
Zhang, H., An, Y., Luo, Y., Lei, L., Wen, Z., Chen, X., Li, L., Ong, M. T., Zheng, L., Tong, W., et al. (2026) · Bioactive Materials · doi:10.1016/j.bioactmat.2026.05.003
Sensorineural regulation of skull healing implicates FGF1 signaling in non-healing bonePreprint
Horenberg, A. L., Villapudua, C. U., Xu, M., Zeng, E. Z., Dias, S., Sinha, T., Archer, M., Scheller, E. L., Pathak, A. P., James, A. W., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.24.690319
Therapeutic interleukin-2 rewires skeletal-immune circuits to reverse postmenopausal bone lossPreprint
Zhou, P., Feng, J., Zhang, Y., Liu, Y., Ma, D., Xue, A., Wei, W., Sun, L., Yu, D., & Zheng, T. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.07.696511
Cho, Y., Choi, C. A., Kwon, M., Kwon, J., Ok, H., Ryu, D., Yang, K., Kim, J., & Park, E. H. (2026) · Journal of Cellular Physiology · doi:10.1002/jcp.70140
Qiang, D., Liu, Y., 戴纯刚, Zhang, H., Chen, Z., Zhu, X., Gao, Z., Zhang, Q., Xie, L., & Chen, L. (2026) · Journal of Visualized Experiments · doi:10.3791/69707
The role of sensory nervous system in the regulation of bone formation, remodeling, and repair
Silva, D. (2017) · theses.fr (ABES) · doi:10.70675/4216a1c9z5df6z4e80z9fcaz0ffed4a18391
Rôle des cellules stromales périostéales dans la régénération de la niche hématopoïétique
Marchand, T. (2021) · theses.fr (ABES) · doi:10.70675/c12711fcz3a80z4ed4za5e8zec7f35f79a41
Mardelle, U. (2024) · theses.fr (ABES) · doi:10.70675/1e786d9ez8d0ez41b3z8ac1z367faf59ae53
The Role of Traumatic Brain Injury on Fracture Healing in Polytrauma
Baldini, T. D., Rahmati, M., Shahlaie, K., Price, R., Schneider, P., Khan, S., Lee, M. A., & Saiz, A. M. (2026) · Journal of Neurotrauma · doi:10.1177/08977151261438945
Liu, X., Li, K., Zhang, B., Xu, Z., Xu, W., Wang, X., Ge, S. H., Shao, J., & Li, J. (2026) · Advanced Healthcare Materials · doi:10.1002/adhm.71305
Tsujino, S., Ochi, H., Okada, R., Kamimura, D., Utagawa, K., Shin, T., Yamada, H., Unno, A., Sunamura, S., Akazawa, C., et al. (2026) · Bone Research · doi:10.1038/s41413-026-00563-z
Baral, S., Kulshrestha, S., Viswanathan, V. K., Jain, V. K., Iyengar, K. P., & Regmi, A. (2026) · Calcified Tissue International · doi:10.1007/s00223-026-01619-2
Metadata
- Authors
- Wang, L., Shi, X., Zhao, R., Halloran, B. P., Clark, D. J., Jacobs, C. R., & Kingery, W. S.
- Affiliations
- VA Palo Alto Health Care System (US)
- San Francisco VA Medical Center (US)
- Corresponding author
- Wang, Liping
- Venue
- Bone
- Publisher
- Elsevier BV
- Published
- 2010-05
- Volume
- 46
- Issue
- 5
- Pages
- 1369-1379
- ISSN
- 1873-2763 (ISSN-L)
- 8756-3282
- PMC
- PMC2854244
- OpenAlex
- W2039009902
- Semantic Scholar
- 97501e887b43c9d591e6450a3690e83b185845cc
- Cited by
- 198
- References
- 53
- Citations by year
- 2026: 11 · 2025: 17 · 2024: 16 · 2023: 19 · 2022: 16 · 2021: 8 · 2020: 17 · 2019: 18 · 2018: 18 · 2017: 10 · 2016: 7 · 2015: 14 · 2014: 6 · 2013: 10 · 2012: 3
- FWCI
- 1.47
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Bone (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Department of Veterans Affairs, Veterans Health Administration, Rehabilitation Research and Development Service (A4265R)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK067197)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Keywords
- calcitonin gene-related peptide, mesenchymal stem cells, osteogenic differentiation, osteoclastogenesis, bone resorption, RANKL, NF-κB activation, bone marrow-derived macrophages, CGRP receptor, sensory neuropeptides, bone mass regulation, capsaicin, cathepsin K, traps
- MeSH terms
- Alkaline Phosphatase, Animals, Bone Resorption, Cell Differentiation, Cells, Cultured, Male, Mice, Inbred C57BL, Microscopy, Fluorescence, Osteoclasts, Osteogenesis, Blotting, Western, Calcitonin Gene-Related Peptide, Polymerase Chain Reaction, NF-kappa B, Stromal Cells, Microscopy, Confocal, Cell Proliferation, Mice, RANK Ligand
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