The DOI matches its Crossref record; 56 of the 56 references it cites were found in a registry or an index.
Bidirectional ephrinB2-EphB4 signaling controls bone homeostasis
Open accessAbstract
Bone homeostasis requires a delicate balance between the activities of bone-resorbing osteoclasts and bone-forming osteoblasts. Various molecules coordinate osteoclast function with that of osteoblasts; however, molecules that mediate osteoclast-osteoblast interactions by simultaneous signal transduction in both cell types have not yet been identified. Here we show that osteoclasts express the NFATc1 target gene Efnb2 (encoding ephrinB2), while osteoblasts express the receptor EphB4, along with other ephrin-Eph family members. Using gain- and loss-of-function experiments, we demonstrate that reverse signaling through ephrinB2 into osteoclast precursors suppresses osteoclast differentiation by inhibiting the osteoclastogenic c-Fos-NFATc1 cascade. In addition, forward signaling through EphB4 into osteoblasts enhances osteogenic differentiation, and overexpression of EphB4 in osteoblasts increases bone mass in transgenic mice. These data demonstrate that ephrin-Eph bidirectional signaling links two major molecular mechanisms for cell differentiation--one in osteoclasts and the other in osteoblasts--thereby maintaining bone homeostasis.
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
“The ephrinB2/ephrinB4 binding transduces bidirectional signals, which promote osteoblast differentiation, whereas the reverse signaling (ephrinB4/ephrinB2) inhibits osteoclastogenesis [178] (Figure 5).”
From Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells (2015) · cites this paper as [178]
In the citing paper
“These findings suggest that ephrinB2/ephrinB4 pathway may be involved in the ending of bone resorption and induces osteoblast differentiation in the transition phase [178].”
From Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells (2015) · cites this paper as [178]
In the citing paper
“One of these factors is ephrinB2, a membrane-bound molecule expressed in mature osteoclasts, which bind to ephrinB4, found in the plasma membrane of osteoblasts.”
From Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells (2015) · cites this paper as [178]
In the citing paper
“The communication route between osteoclasts and osteoblasts involves a bidirectional signaling pathway mediated by EphrinB2‐EphB4 that links the suppression of osteoclastogenesis to osteogenesis within each BMU.251”
From Bone remodeling: an operational process ensuring survival and bone mechanical competence (2022) · cites this paper as [251]
Citations
Cites
Etienne-Manneville, S., & Hall, A. (2002) · Nature · doi:10.1038/nature01148 · Cited by 4,965
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
Komori, T., Yagi, H., Nomura, S., Yamaguchi, A., Sasaki, K., Deguchi, K., Shimizu, Y., Bronson, R. T., Gao, Y.-H., Inada, M., et al. (1997) · Cell · doi:10.1016/s0092-8674(00)80258-5 · Cited by 4,244
Cell Shape, Cytoskeletal Tension, and RhoA Regulate Stem Cell Lineage Commitment
McBeath, R., Pirone, D. M., Nelson, C. M., Bhadriraju, K., & Chen, C. S. (2004) · Developmental Cell · doi:10.1016/s1534-5807(04)00075-9 · Cited by 4,182
Nakashima, K., Zhou, X., Kunkel, G., Zhang, Z., Deng, J. M., Behringer, R. R., & de Crombrugghe, B. (2002) · Cell · doi:10.1016/s0092-8674(01)00622-5 · Cited by 3,608
Takayanagi, H., Kim, S., Koga, T., Nishina, H., Isshiki, M., Yoshida, H., Saiura, A., Isobe, M., Yokochi, T., Inoue, J.-I., et al. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00369-6 · Cited by 2,701
Conditional gene targeting in macrophages and granulocytes using LysMcre mice
Clausen, B. E., Burkhardt, C., Reith, W., Renkawitz, R., & Förster, I. (1999) · Transgenic Research · doi:10.1023/a:1008942828960 · Cited by 2,098
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
Wang, H. U., Chen, Z., & Anderson, D. J. (1998) · Cell · doi:10.1016/s0092-8674(00)81436-1 · Cited by 1,684
Reaching a Genetic and Molecular Understanding of Skeletal Development
Karsenty, G., & Wagner, E. F. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00157-0 · Cited by 1,611
c-Fos: a Key Regulator of Osteoclast-Macrophage Lineage Determination and Bone Remodeling
Grigoriadis, A. E., Wang, Z., Cecchini, M. G., Hofstetter, W., Felix, R., Fleisch, H. A., & Wagner, E. F. (1994) · Science · doi:10.1126/science.7939685 · Cited by 1,264
Mechanisms and functions of eph and ephrin signalling
Kullander, K., & Klein, R. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm856 · Cited by 1,158
Batlle, E., Henderson, J. T., Beghtel, H., van den Born, M., Sancho, E., Huls, G. A., Meeldijk, J., Robertson, J. V., van de Wetering, M., Pawson, T. J., et al. (2002) · Cell · doi:10.1016/s0092-8674(02)01015-2 · Cited by 1,154
Adams, R. H., Wilkinson, G. A., Weiss, C., Diella, F., Gale, N. W., Deutsch, U., Risau, W., & Klein, R. (1999) · Genes & Development · doi:10.1101/gad.13.3.295 · Cited by 1,030
Eph receptor signalling casts a wide net on cell behaviour
Pasquale, E. B. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1662 · Cited by 1,013
Parfitt, A. M. (1994) · Journal of Cellular Biochemistry · doi:10.1002/jcb.240550303 · Cited by 1,001
Requirement for NF-κB in osteoclast and B-cell development
Franzoso, G., Carlson, L., Xing, L., Poljak, L., Shores, E. W., Brown, K. D., Leonardi, A., Tran, T., Boyce, B. F., & Siebenlist, U. (1997) · Genes & Development · doi:10.1101/gad.11.24.3482 · Cited by 996
Bone and haematopoietic defects in mice lacking c-fos
Wang, Z., Ovitt, C. E., Grigoriadis, A. E., Möhle-Steinlein, U., Rüther, U., & Wagner, E. F. (1992) · Nature · doi:10.1038/360741a0 · Cited by 932
Autoamplification of NFATc1 expression determines its essential role in bone homeostasis
Asagiri, M., Sato, K., Usami, T., Ochi, S., Nishina, H., Yoshida, H., Morita, I., Wagner, E. F., Mak, T. W., Serfling, E., et al. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20051150 · Cited by 849
Gale, N. W., & Yancopoulos, G. D. (1999) · Genes & Development · doi:10.1101/gad.13.9.1055 · Cited by 794
Jaiswal, R. K., Jaiswal, N., Bruder, S. P., Mbalaviele, G., Marshak, D. R., & Pittenger, M. F. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.13.9645 · Cited by 771
RANKL maintains bone homeostasis through c-Fos-dependent induction of interferon-β
Takayanagi, H., Kim, S., Matsuo, K., Suzuki, H. I., Suzuki, T., Sato, K., Yokochi, T., Oda, H., Nakamura, K., Ida, N., et al. (2002) · Nature · doi:10.1038/416744a · Cited by 719
Self-citationGerety, S. S., Wang, H. U., Chen, Z., & Anderson, D. J. (1999) · Molecular Cell · doi:10.1016/s1097-2765(00)80342-1 · Cited by 713
Nuclear Factor of Activated T-cells (NFAT) Rescues Osteoclastogenesis in Precursors Lacking c-Fos
Matsuo, K., Galson, D. L., Chen, Z., Peng, L., Laplace, C., Wang, K. Z. Q., Bachler, M. A., Amano, H., Aburatani, H., Ishikawa, H., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313973200 · Cited by 570
Self-citationMAPK Pathways Activate and Phosphorylate the Osteoblast-specific Transcription Factor, Cbfa1
Xiao, G., Jiang, D., Thomas, P. E., Benson, M. D., Guan, K., Karsenty, G., & Franceschi, R. T. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.6.4453 · Cited by 552
Liu, W., Toyosawa, S., Furuichi, T., Kanatani, N., Yoshida, C. A., Liu, Y., Himeno, M., Narai, S., Yamaguchi, A., & Komori, T. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.200105052 · Cited by 454
Pfeilschifter, J., & Mundy, G. R. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.7.2024 · Cited by 434
Ishida, N., Hayashi, K., Hoshijima, M., Ogawa, T., Koga, S., Miyatake, Y., Kumegawa, M., Kimura, T., & Takeya, T. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m205063200 · Cited by 377
`Eph'ective signaling: forward, reverse and crosstalk
Murai, K. K., & Pasquale, E. B. (2003) · Journal of Cell Science · doi:10.1242/jcs.00625 · Cited by 363
Suggested Sequential Mode of Control of Changes in Cell Behaviour in Adult Bone Remodelling
Hattner, R. S., Epker, B. N., & Frost, H. M. (1965) · Nature · doi:10.1038/206489a0 · Cited by 348
Ephrin-B1 forward and reverse signaling are required during mouse developmentPreprint
Davy, A., Aubin, J., & Soriano, P. M. (2004) · Genes & Development · doi:10.1101/gad.1171704 · Cited by 296
Skeletal Renewal and Metabolic Bone Disease
Harris, W. H., & Heaney, R. P. (1969) · New England Journal of Medicine · doi:10.1056/nejm196901232800405 · Cited by 279
Retroviral delivery of small interfering RNA into primary cells
Barton, G. M., & Medzhitov, R. M. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.242594499 · Cited by 279
Multiple roles of ephrins in morphogenesis, neuronal networking, and brain functionPreprint
Palmer, A., & Klein, R. (2003) · Genes & Development · doi:10.1101/gad.1093703 · Cited by 272
Cardiovascular ephrinB2 function is essential for embryonic angiogenesis
Gerety, S. S., & Anderson, D. J. (2002) · Development · doi:10.1242/dev.129.6.1397 · Cited by 263
Control of Skeletal Patterning by EphrinB1-EphB Interactions
Compagni, A., Logan, M., Klein, R., & Adams, R. H. (2003) · Developmental Cell · doi:10.1016/s1534-5807(03)00198-9 · Cited by 231
Ephrin signaling in vivo: Look both ways
Davy, A., & Soriano, P. M. (2004) · Developmental Dynamics · doi:10.1002/dvdy.20200 · Cited by 207
Eph receptor–ephrin bidirectional signals that target Ras and Rho proteins
Hooten, N. N., & Pasquale, E. B. (2003) · Cellular Signalling · doi:10.1016/j.cellsig.2003.10.006 · Cited by 199
The insulin-like growth factor system and the coupling of formation to resorption
Hayden, J. M., Mohan, S., & Baylink, D. J. (1995) · Bone · doi:10.1016/8756-3282(95)00186-h · Cited by 199
Steinle, J. J., Meininger, C. J., Forough, R., Wu, G., Wu, M. H., & Granger, H. J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m207221200 · Cited by 182
Wang, F. S., Wang, C. J., Sheen‐Chen, S., Kuo, Y. R., Chen, R., & Yang, K. D. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m104587200 · Cited by 176
Füller, T., Korff, T., Kilian, A., Dandekar, G., & Augustin, H. G. (2003) · Journal of Cell Science · doi:10.1242/jcs.00426 · Cited by 172
Himanen, J., & Nikolov, D. B. (2002) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(02)00096-1 · Cited by 169
Gebbink, M. F. B. G., Kranenburg, O., Poland, M., van Horck, F. P. G., Houssa, B., & Moolenaar, W. H. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.137.7.1603 · Cited by 149
1α,25-dihydroxyvitamin D3 inhibits anti-CD40 plus IL-4-mediated IgE production in vitro
Heine, G., Anton, K., Henz, B. M., & Worm, M. (2002) · European Journal of Immunology · doi:10.1002/1521-4141(200212)32:12 · Cited by 124
Cowan, C. A., Yokoyama, N., Saxena, A., Chumley, M. J., Silvany, R. E., Baker, L. A., Srivastava, D. P., & Henkemeyer, M. J. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.03.026 · Cited by 120
c-Fos suppresses systemic inflammatory response to endotoxin
Ray, N., Kuwahara, M., Takada, Y., Maruyama, K., Kawaguchi, T., Tsubone, H., Ishikawa, H., & Matsuo, K. (2006) · International Immunology · doi:10.1093/intimm/dxl004 · Cited by 110
Self-citationEphrin B2 Induces T Cell Costimulation
Yu, G., Luo, H., Wu, Y., & Wu, J. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.1.106 · Cited by 92
A Phage Display Technique Identifies a Novel Regulator of Cell Differentiation
Sheu, T., Schwarz, E. M., Martinez, D. A., O’Keefe, R. J., Rosier, R. N., Zuscik, M. J., & Puzas, J. E. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m208292200 · Cited by 89
Harmey, D., Stenbeck, G., Nobes, C. D., Lax, A. J., & Grigoriadis, A. E. (2004) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.040105 · Cited by 85
Skeletal Renewal and Metabolic Bone Disease
Harris, W. H., & Heaney, R. P. (1969) · New England Journal of Medicine · doi:10.1056/nejm196901302800507 · Cited by 75
Resorption of auditory ossicles and hearing loss in mice lacking osteoprotegerin
Kanzaki, S., Ito, M., Takada, Y., Ogawa, K., & Matsuo, K. (2006) · Bone · doi:10.1016/j.bone.2006.01.155 · Cited by 69
Self-citationWang, Z., Cohen, K. S., Shao, Y., Mole, P., Dombkowski, D., & Scadden, D. T. (2003) · Blood · doi:10.1182/blood-2003-04-1063 · Cited by 66
Does bone resorption inhibition affect the anabolic response to parathyroid hormone?
Martin, T. J. (2004) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2004.01.002 · Cited by 38
Chemometrical Classification of Ephrin Ligands and Eph Kinases Using GRID/CPCA Approach
Myshkin, E., & Wang, B. (2003) · Journal of Chemical Information and Computer Sciences · doi:10.1021/ci0256586 · Cited by 24
Reduced Expression of Thrombospondins and Craniofacial Dysmorphism in Mice Overexpressing Fra1
Nishiwaki, T., Yamaguchi, T., Chen, Z., Amano, H., Hankenson, K. D., BORNSTEIN, P. K., Toyama, Y., & Matsuo, K. (2006) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.051216 · Cited by 20
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells
Florencio-Silva, R., Sasso, G. R. D. S., Sasso-Cerri, E., Simões, M. J., & Cerri, P. S. (2015) · BioMed Research International · doi:10.1155/2015/421746 · Cited by 2,044
Osteoimmunology: shared mechanisms and crosstalk between the immune and bone systems
Takayanagi, H. (2007) · Nature Reviews Immunology · doi:10.1038/nri2062 · Cited by 1,878
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
Cellular and molecular mechanisms of bone remodeling
Raggatt, L. J., & Partridge, N. C. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.r109.041087 · Cited by 1,402
Eph-Ephrin Bidirectional Signaling in Physiology and Disease
Pasquale, E. B. (2008) · Cell · doi:10.1016/j.cell.2008.03.011 · Cited by 1,281
Metadata
- Authors
- Zhao, C., Irie, N., Takada, Y., Shimoda, K., Miyamoto, T., Nishiwaki, T., Suda, T., & Matsuo, K.
- Affiliations
- Keio University (JP)
- Corresponding author
- Matsuo, Koichi
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2006-08
- Volume
- 4
- Issue
- 2
- Pages
- 111-121
- ISSN
- 1550-4131 (ISSN-L)
- OpenAlex
- W2026387061
- Cited by
- 777
- References
- 56
- Citations by year
- 2026: 25 · 2025: 25 · 2024: 23 · 2023: 34 · 2022: 35 · 2021: 45 · 2020: 49 · 2019: 33 · 2018: 42 · 2017: 42 · 2016: 47 · 2015: 39 · 2014: 46 · 2013: 40 · 2012: 59
- FWCI
- 15.54
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Medicinal Plant Pharmacodynamics Research
- Keywords
- ephrin-B2, EphB4, bidirectional signaling, bone homeostasis, osteoclastogenesis, osteogenic differentiation, osteoblast-osteoclast interaction, NFATc1, c-fos, bone mass, Eph/ephrin signaling
- MeSH terms
- Animals, Base Sequence, Bone and Bones, Cell Differentiation, Cells, Cultured, Homeostasis, Mice, Transgenic, Molecular Sequence Data, Osteoblasts, Osteoclasts, Signal Transduction, Up-Regulation, Proto-Oncogene Proteins c-fos, Receptor, EphB4, Ephrin-B2, NFATC Transcription Factors, 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