Expression and function of semaphorin 7A in bone cells
Open accessAbstract
Background information. Sema‐7A is a glycosylphosphatidylinositol‐anchored semaphorin that was first identified in the immune system. It is a member of a large family of proteins involved in axon guidance signalling. Sema‐7A is expressed in the myeloid and the lymphoid lineage and seems to be involved in cytokine expression and chemotaxy through its receptor Plexin C1. However, it can promote axon outgrowth, acting through a β1 subunit‐containing integrin receptor. Results and conclusions. In the present study, we have investigated its regulation and function in bone cells. Semiquantitative reverse transcriptase—PCR demonstrated that Sema‐7A mRNA is present during all stages of osteoblast differentiation and maturation in mouse calvaria cells and in MC3T3 cell line in vitro. Its expression is also regulated during primary osteoclast differentiation in vitro. We report that Sema‐7A is capable of increasing the migration of MC3T3 cells and that this process is mediated by the mitogen‐activated protein kinase pathway in osteoblasts, probably through the integrin subunit β1. Moreover, the addition of recombinant soluble Sema‐7A to the culture enhances osteoclast fusion. These findings indicate for the first time the possible involvement of Sema‐7A in bone cell differentiation.
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
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?
Semaphorins are involved in cell-cell communication between osteoclasts and osteoblasts during bone remodeling.
“In bone, it has been suggested that semaphorins are also involved in cell-cell communication between osteoclasts and osteoblasts during the bone remodeling cycle [174–176].”
From Biology of Bone Tissue: Structure, Function, and Factors That Influence Bone Cells (2015) · cites this paper as [174]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Osteoclast differentiation and activation
Boyle, W. J., Simonet, W. S., & Lacey, D. L. (2003) · Nature · doi:10.1038/nature01658 · Cited by 6,670 · cited 2× · see citing works
“Osteoclasts are giant multinucleated resorbing cells that result from the fusion of a monocytic precursor in the presence of RANK-L (receptor activator of NF κB ligand) and M-CSF (macrophage colony-stimulating factor) (Burgess et al., 1999; Shevde et al., 2000; Vaananen et al., 2000; Boyle et al., 2003).”
BackgroundControl of osteoblast function and regulation of bone mass
Harada, S.-I., & Rodan, G. A. (2003) · Nature · doi:10.1038/nature01660 · Cited by 1,451 · see citing works
Tamagnone, L., Artigiani, S., Chen, H., He, Z., Ming, G., Song, H., Chédotal, A., Winberg, M. L., Goodman, C. S., Poo, M.-M., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)80063-x · Cited by 1,156 · see citing works
The cell biology of osteoclast function
Väänänen, H. K., Zhao, H., Mulari, M. T. K., & Halleen, J. M. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.3.377 · Cited by 726 · see citing works
The ligand for osteoprotegerin (OPGL) directly activates mature osteoclasts.
Burgess, T. L., Qian, Y.-X., Kaufman, S., Ring, B. D., Van, G., Capparelli, C., Kelley, M., Hsu, H., Boyle, W. J., Dunstan, C. R., et al. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.145.3.527 · Cited by 689 · see citing works
Semaphorin III is needed for normal patterning and growth of nerves, bones and heart
Behar, O., Golden, J. A., Mashimo, H. L., Schöen, F. J., & Fishman, M. C. (1996) · Nature · doi:10.1038/383525a0 · Cited by 583 · see citing works
Semaphorin 7A promotes axon outgrowth through integrins and MAPKs
Pasterkamp, R. J., Peschon, J. J., Spriggs, M. K., & Kolodkin, A. L. (2003) · Nature · doi:10.1038/nature01790 · Cited by 517 · see citing works
Shevde, N. K., Bendixen, A. C., Dienger, K. M., & Pike, J. W. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.130200197 · Cited by 502 · see citing works
Destaing, O., Saltel, F., Géminard, J.-C., Jurdic, P., & Bard, F. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-07-0389 · Cited by 453 · see citing works
Self-citationSemaphorin junction: making tracks toward neural connectivity
Pasterkamp, R. J., & Kolodkin, A. L. (2003) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(03)00003-5 · Cited by 309 · see citing works
Integrin Expression and Function on Human Osteoblast-like Cells
Gronthos, S., Stewart, K., Graves, S. E., Hay, S., & Simmons, P. J. (1997) · Journal of Bone and Mineral Research · doi:10.1359/jbmr.1997.12.8.1189 · Cited by 251 · see citing works
Comeau, M. R., Johnson, R., DuBose, R. F., Petersen, M., Gearing, P., VandenBos, T., Park, L., Farrah, T., Buller, R. M. L., Cohen, J. I., et al. (1998) · Immunity · doi:10.1016/s1074-7613(00)80552-x · Cited by 237 · see citing works
Semaphorins in interactions between T cells and antigen-presenting cells
Kikutani, H., & Kumanogoh, A. (2003) · Nature reviews. Immunology · doi:10.1038/nri1003 · Cited by 192 · see citing works
Love, C. A., Harlos, K., Mavaddat, N., Davis, S. J., Stuart, D. I., Jones, E. Y., & Esnouf, R. M. (2003) · Nature Structural & Molecular Biology · doi:10.1038/nsb977 · Cited by 166 · see citing works
Sema7A is a Potent Monocyte Stimulator
HOLMES, S., DOWNS, A. ‐., Fosberry, A. P., Hayes, P. D., Michalovich, D., MURDOCH, P., Moores, K., Fox, J. M., Deen, K. C., Pettman, G. R., et al. (2002) · Scandinavian Journal of Immunology · doi:10.1046/j.1365-3083.2002.01129.x · Cited by 148 · see citing works
β1 integrins and osteoclast function: Involvement in collagen recognition and bone resorption
Helfrich, M. H., Nesbitt, S. A., Lakkakorpi, P. T., Barnes, M. J., Bodary, S. C., Shankar, G., Mason, W. T., Mendrick, D. L., Väänänen, H. K., & Horton, M. A. (1996) · Bone · doi:10.1016/s8756-3282(96)00223-2 · Cited by 139 · see citing works
Knowing How to Navigate: Mechanisms of Semaphorin Signaling in the Nervous System
He, Z., Wang, K., Koprivica, V., Ming, G., & Song, H. (2002) · Science s STKE · doi:10.1126/stke.2002.119.re1 · Cited by 136 · see citing works
Bonnelye, E., Merdad, L., Kung, V., & Aubin, J. E. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.153.5.971 · Cited by 119 · see citing works
Self-citationOry, S., Munari‐Silem, Y., Fort, P., & Jurdic, P. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.7.1177 · Cited by 111 · see citing works
Self-citationXu, X., Ng, S., Wu, Z., Nguyen, D., Homburger, S. A., Seidel‐Dugan, C., Ebens, A. J., & Luo, Y. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.35.22428 · Cited by 108 · see citing works
Matrix mineralization in MC3T3-E1 cell cultures initiated by β-glycerophosphate pulse
Fratzl‐Zelman, N., Fratzl, P., Hörandner, H., Grabner, B., Varga, F., Ellinger, A., & Klaushofer, K. (1998) · Bone · doi:10.1016/s8756-3282(98)00139-2 · Cited by 79 · see citing works
Togari, A., Mogi, M., Arai, M., Yamamoto, S., & Koshihara, Y. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02700-1 · Cited by 65 · see citing works
New Eukaryotic Semaphorins with Close Homology to Semaphorins of DNA Viruses
Lange, C., Liehr, T., Goen, M., Gebhart, E., Fleckenstein, B., & Ensser, A. (1998) · Genomics · doi:10.1006/geno.1998.5256 · Cited by 51 · see citing works
Bagnard, D., Sainturet, N., Meyronet, D., Perraut, M., Miehe, M., Roussel, G., Aunis, D., Belin, M., & Thomasset, N. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2003.12.007 · Cited by 47 · see citing works
Structure and Function of the Immune Semaphorin CD100/SEMA4D
Elhabazi, A., Marie‐Cardine, A., Ponnat, I. C.-D., Bensussan, A., & Boumsell, L. (2003) · Critical Reviews in Immunology · doi:10.1615/critrevimmunol.v23.i12.40 · Cited by 42 · see citing works
Angelisová, P., Drbal, K., Černý, J., Hilgert, I., & Hořejšf, V. (1999) · Immunobiology · doi:10.1016/s0171-2985(99)80073-4 · Cited by 31 · see citing works
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 · see citing works
Osteoclast–osteoblast communication
Matsuo, K., & Irie, N. (2008) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2008.03.027 · Cited by 780 · see citing works
Pederson, L., Ruan, M., Westendorf, J. J., Khosla, S., & Oursler, M. J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805133106 · Cited by 556 · see citing works
Osteoimmunology: The conceptual framework unifying the immune and skeletal systems
Okamoto, K., Nakashima, T., Shinohara, M., Negishi-Koga, T., Komatsu, N., Terashima, A., Sawa, S., Nitta, T., & Takayanagi, H. (2017) · Physiological Reviews · doi:10.1152/physrev.00036.2016 · Cited by 534 · see citing works
Suppression of bone formation by osteoclastic expression of semaphorin 4D
Negishi-Koga, T., Shinohara, M., Komatsu, N., Bito, H., Kodama, T., Friedel, R. H., & Takayanagi, H. (2011) · Nature Medicine · doi:10.1038/nm.2489 · Cited by 498 · see citing works
Subchondral bone osteoclasts induce sensory innervation and osteoarthritis pain
Zhu, S., Zhu, J., Zhen, G., Hu, Y., An, S., Li, Y., Zheng, Q., Chen, Z., Yang, Y., Wan, M., et al. (2019) · Journal of Clinical Investigation · doi:10.1172/jci121561 · Cited by 456 · see citing works
Yazdani, U., & Terman, J. R. (2006) · Genome biology · doi:10.1186/gb-2006-7-3-211 · Cited by 417 · see citing works
Dynamics of the skeletal muscle secretome during myoblast differentiation
Henningsen, J., Rigbolt, K. T. G., Blagoev, B., Pedersen, B. K., & Kratchmarova, I. (2010) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m110.002113 · Cited by 303 · see citing works
The many faces of semaphorins: from development to pathology
Roth, L., Koncina, E., Šatkauskas, S., Crémel, G., Aunis, D., & Bagnard, D. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-8518-z · Cited by 183 · see citing works
Semaphorin 7A plays a critical role in TGF-β1–induced pulmonary fibrosis
Kang, H., Lee, C. G., Homer, R., & Elias, J. A. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20061273 · Cited by 176 · see citing works
Hota, P. K., & Buck, M. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1019-0 · Cited by 170 · see citing works
Secretome Signature of Invasive Glioblastoma Multiforme
Formolo, C. A., Williams, R., Gordish‐Dressman, H., MacDonald, T. J., Lee, N. H., & Hathout, Y. (2011) · Journal of Proteome Research · doi:10.1021/pr200210w · Cited by 131 · see citing works
Bone cell communication factors and Semaphorins
Negishi-Koga, T., & Takayanagi, H. (2012) · BoneKEy Reports · doi:10.1038/bonekey.2012.183 · Cited by 90 · see citing works
Semaphorins in bone development, homeostasis, and disease
Kang, S., & Kumanogoh, A. (2012) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2012.09.008 · Cited by 87 · see citing works
Zhang, Y., Wei, L., Miron, R. J., Shi, B., & Bian, Z. (2014) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2322 · Cited by 85 · see citing works
Semaphorin 7a Promotes Spreading and Dendricity in Human Melanocytes through β1-Integrins
Scott, G., McClelland, L. A., & Fricke, A. F. (2007) · Journal of Investigative Dermatology · doi:10.1038/sj.jid.5700974 · Cited by 84 · see citing works
Scott, G., McClelland, L. A., Fricke, A. F., & Fender, A. B. (2008) · Journal of Investigative Dermatology · doi:10.1038/jid.2008.329 · Cited by 84 · see citing works
Semaphorins in health and disease
Fard, D., & Tamagnone, L. (2020) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2020.05.006 · Cited by 81 · see citing works
Pasterkamp, R. J., Kolk, S. M., Hellemons, A. J. C. G. M., & Kolodkin, A. L. (2007) · BMC Developmental Biology · doi:10.1186/1471-213x-7-98 · Cited by 81 · see citing works
Zhai, Y., Schilling, K. J., Wang, T., Khatib, M. E., Vinogradov, S. A., Brown, E. B., & Zhang, X. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121041 · Cited by 74 · see citing works
Control of Bone Resorption by Semaphorin 4D Is Dependent on Ovarian Function
Dacquin, R., Domenget, C., Kumanogoh, A., Kikutani, H., Jurdic, P., & Machuca‐Gayet, I. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026627 · Cited by 73 · see citing works
Self-citationSemaphorins in Angiogenesis and Autoimmune Diseases: Therapeutic Targets?
Iragavarapu‐Charyulu, V., Wojcikiewicz, E. P., & Urdaneta, A. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00346 · Cited by 72 · see citing works
Semaphorin Signals in Cell Adhesion and Cell Migration: Functional Role and Molecular Mechanisms
Casazza, A., Fazzari, P., & Tamagnone, L. (2007) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-70956-7_8 · Cited by 71 · see citing works
Semaphorin 7a exerts pleiotropic effects to promote breast tumor progression
Black, S. A., Nelson, A., Gurule, N. J., Futscher, B. W., & Lyons, T. R. (2016) · Oncogene · doi:10.1038/onc.2016.49 · Cited by 65 · see citing works
Garcia‐Areas, R., Libreros, S., Amat, S., Keating, P., Carrió, R., Robinson, P., Blieden, C. R., & Iragavarapu‐Charyulu, V. (2014) · Frontiers in Physiology · doi:10.3389/fphys.2014.00017 · Cited by 62 · see citing works
Sutton, A. L. M., Zhang, X., Dowd, D. R., Kharode, Y. P., Komm, B. S., & MacDonald, P. N. (2008) · Molecular Endocrinology · doi:10.1210/me.2007-0363 · Cited by 61 · see citing works
Xu, R. (2013) · Cell Adhesion & Migration · doi:10.4161/cam.27752 · Cited by 62 · see citing works
Baniwal, S. K., Shah, P. K., Shi, Y., HaDuong, J. H., DeClerck, Y. A., Gabet, Y., & Frenkel, B. (2011) · Osteoporosis International · doi:10.1007/s00198-011-1728-5 · Cited by 56 · see citing works
Semaphorin 7A Contributes to TGF-β–Mediated Liver Fibrogenesis
Minicis, S. D., Rychlicki, C., Agostinelli, L., Saccomanno, S., Trozzi, L., Candelaresi, C., Bataller, R. A., Millán, C., Brenner, D. A., Vivarelli, M., et al. (2013) · American Journal Of Pathology · doi:10.1016/j.ajpath.2013.05.030 · Cited by 55 · see citing works
Verlinden, L., Vanderschueren, D., & Verstuyf, A. (2015) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2015.09.009 · Cited by 55 · see citing works
Koh, J., Oh, B., Lee, J. Y., Lee, J., Kimm, K., Kim, G. S., Park, B. L., Cheong, H. S., Shin, H. D., Hong, J. M., et al. (2005) · Journal of Human Genetics · doi:10.1007/s10038-005-0331-z · Cited by 54 · see citing works
The critical role of the ZNF217 oncogene in promoting breast cancer metastasis to the bone
Bellanger, A., Donini, C. F., Vendrell, J. A., Lavaud, J., Machuca‐Gayet, I., Ruel, M., Vollaire, J., Grisard, E., Győrffy, B., Bièche, I., et al. (2017) · The Journal of Pathology · doi:10.1002/path.4882 · Cited by 51 · see citing works
Self-citationJongbloets, B. C., Ramakers, G. M. J., & Pasterkamp, R. J. (2013) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2013.01.002 · Cited by 49 · see citing works
Huang, S., Li, Z., Liu, Y., Gao, D., Zhang, X., Hao, J., & Yang, F. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.26502 · Cited by 49 · see citing works
Differential marker expression by cultures rich in mesenchymal stem cells
Wetzig, A. R., Alaiya, A. A., Al-Alwan, M. M., Pradez, C. B., Manogaran, P. S., Al‐Mazrou, A., Shinwari, Z., Sleiman, G. M., Ghebeh, H., Alhumaidan, H., et al. (2013) · BMC Cell Biology · doi:10.1186/1471-2121-14-54 · Cited by 46 · see citing works
Hong, L., Li, F., Tang, C., Li, L., Sun, L., Li, X., & Zhu, L. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-02818-x · Cited by 46 · see citing works
Xu, C., & Fan, C. (2007) · Molecular Endocrinology · doi:10.1210/me.2007-0034 · Cited by 45 · see citing works
Ramos, E. K., Tsai, C., Dashzeveg, N. K., Jia, Y., Cao, Y., Manu, M., Taftaf, R., Hoffmann, A. D., El-Shennawy, L., Gritsenko, M. A., et al. (2022) · eLife · doi:10.7554/elife.82669 · Cited by 41 · see citing works
Osteogenesis and Bone Regeneration
Yang, H. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.73955 · Cited by 42 · see citing works
Scott, J. B., Crosnier, C., Bustamante, L. Y., Rayner, J. C., & Wright, G. J. (2013) · Cellular Microbiology · doi:10.1111/cmi.12151 · Cited by 40 · see citing works
Regulation of Osteoblast Differentiation by Slit2 in Osteoblastic Cells
Sun, H., Dai, K., Tang, T., & Zhang, X. (2008) · Cells Tissues Organs · doi:10.1159/000178020 · Cited by 40 · see citing works
Lotz, E. M., Berger, M. B., Boyan, B. D., & Schwartz, Z. (2020) · Bone · doi:10.1016/j.bone.2020.115260 · Cited by 41 · see citing works
Bone scaffolds loaded with siRNA-Semaphorin4d for the treatment of osteoporosis related bone defects
Zhang, Y., Wei, L., Miron, R. J., Shi, B., & Bian, Z. (2016) · Scientific Reports · doi:10.1038/srep26925 · Cited by 39 · see citing works
Kopp, M. A., Brommer, B., Gatzemeier, N., Schwab, J. M., & Prüß, H. (2010) · Glia · doi:10.1002/glia.21045 · Cited by 39 · see citing works
Semaphorin 7A Contributes to West Nile Virus Pathogenesis through TGF-β1/Smad6 Signaling
Sultana, H., Neelakanta, G., Foellmer, H. G., Montgomery, R. R., Anderson, J. F., Koski, R. A., Medzhitov, R. M., & Fikrig, E. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1201140 · Cited by 40 · see citing works
Terpos, E., Ntanasis‐Stathopoulos, I., Christoulas, D., Bagratuni, T., Bakogeorgos, M., Gavriatopoulou, M., Eleutherakis‐Papaiakovou, E., Kanellias, N., Kastritis, E., & Dimopoulos, M. A. (2018) · Blood Cancer Journal · doi:10.1038/s41408-018-0075-6 · Cited by 36 · see citing works
Deng, X., Liang, L., Zhu, D., Zheng, L., Yu, J., Meng, X.-L., Zhao, Y., Sun, X., Pan, T., & Liu, Y. (2018) · International Immunopharmacology · doi:10.1016/j.intimp.2018.04.037 · Cited by 31 · see citing works
Prevention of Alveolar Bone Loss in an Osteoporotic Animal Model via Interference of Semaphorin 4d
Zhang, Y., Wei, L., Miron, R. J., Zhang, Q., & Bian, Z. (2014) · Journal of Dental Research · doi:10.1177/0022034514552676 · Cited by 32 · see citing works
Semaphorins in the development, homeostasis and disease of hormone systems
Giacobini, P., & Prévot, V. (2012) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2012.11.005 · Cited by 31 · see citing works
Liu, X., Tan, N., Zhou, Y., Zhou, X., Chen, H., Wei, H., Chen, J., Xu, X., Zhang, S., Yang, G., et al. (2016) · Stem Cells International · doi:10.1155/2016/2545214 · Cited by 31 · see citing works
Zhang, J., Zhao, C., Sheng, R., Lin, K., Wang, X., & Zhang, S. (2022) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.2c06454 · Cited by 30 · see citing works
NKX2-2 Suppresses Osteosarcoma Metastasis and Proliferation by Downregulating Multiple Target Genes
Chen, H.-M., Liu, W., Zhong, L., Liao, D., Zhang, R., Kang, T., & Wu, Y. (2018) · Journal of Cancer · doi:10.7150/jca.26382 · Cited by 26 · see citing works
PlexinA2 mediates osteoblast differentiation via regulation of Runx2
Oh, J.-E., Kim, H. J., Kim, W.-S., Lee, Z. H., Ryoo, H.-M., Hwang, S. J., Lee, Y., & Kim, H.-H. (2012) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.1471 · Cited by 21 · see citing works
Anoikis resistance in mammary epithelial cells is mediated by semaphorin 7a
Rutherford, T. R., Elder, A. M., & Lyons, T. R. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-04133-5 · Cited by 21 · see citing works
Aniket, A., Reid, R. W., Hall, B., Marriott, I., & El‐Ghannam, A. (2014) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.35326 · Cited by 21 · see citing works
There are many potential medical therapies for atraumatic osteonecrosis
Fessel, J. (2012) · Rheumatology · doi:10.1093/rheumatology/kes241 · Cited by 21 · see citing works
Osteoclast Biology: Regulation of Formation and Function
Choi, Y., Faccio, R., Teitelbaum, S. L., & Takayanagi, H. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800571-2.00004-9 · Cited by 20 · see citing works
Mechanical Tension Alters Semaphorin Expression in the Periodontium
Spencer, A., & Lallier, T. E. (2009) · Journal of Periodontology · doi:10.1902/jop.2009.090212 · Cited by 19 · see citing works
Crosstalk between axon guidance signaling and bone remodeling
Nakanishi, Y., Kang, S., & Kumanogoh, A. (2021) · Bone · doi:10.1016/j.bone.2021.116305 · Cited by 18 · see citing works
Endogenous Semaphorin-7A Impedes Human Lung Fibroblast Differentiation
Esnault, S. J., Torr, E., Bernau, K., Johansson, M. W., KELLY, E. A. B., Sandbo, N. K., & Jarjour, N. N. (2017) · PLoS ONE · doi:10.1371/journal.pone.0170207 · Cited by 18 · see citing works
Satomi, K., Nishimura, K., & Igarashi, K. (2022) · Journal of Periodontal Research · doi:10.1111/jre.13038 · Cited by 17 · see citing works
Verstraelen, S., Nelissen, I., Hooyberghs, J., Witters, H. E., Schoeters, G. E. R., Cauwenberge, P. V., & Heuvel, R. V. D. (2009) · Toxicology in Vitro · doi:10.1016/j.tiv.2009.06.007 · Cited by 16 · see citing works
Serum semaphorin 7A is associated with the risk of acute atherothrombotic stroke
You, T., Zhu, Z., Zheng, X., Zeng, N., Hu, S., Liu, Y., Ren, L., Lu, Q., Tang, C., Ruan, C., et al. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14186 · Cited by 16 · see citing works
Lee, Y., Blount, K. L., Dai, F., Thompson, S., Scher, J. K., Bitterman, S., Droher, M. L., Herzog, E. L., Moeckel, G. W., Karihaloo, A. K., et al. (2018) · Clinical and Experimental Nephrology · doi:10.1007/s10157-018-1542-x · Cited by 13 · see citing works
Netrin-4 Promotes Differentiation and Migration of Osteoblasts
Enoki, Y., Sato, T., Kokabu, S., HAYASHI, N., Iwata, T., Yamato, M., Usui, M., Matsumoto, M., Tomoda, T., Ariyoshi, W., et al. (2018) · In Vivo · doi:10.21873/invivo.11132 · Cited by 14 · see citing works
Brain–Bone Axis in Physiological and Pathological Conditions
Massaccesi, L., Romanelli, M. M. C., & Galliera, E. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26199822 · Cited by 12 · see citing works
Osteolytic cancer cells induce vascular/axon guidance processes in the bone/bone marrow stroma
Hensel, J., Wetterwald, A., Temanni, R., Keller, I., Riether, C., van der Pluijm, G., Cecchini, M. G., & Thalmann, G. N. (2018) · Oncotarget · doi:10.18632/oncotarget.25608 · Cited by 11 · see citing works
SEMA7A: A glycoprotein with therapeutic potential in inflammatory diseases and tumor development
Huang, Q., Wang, Y., Zhang, Z., Yang, Y., Li, H., & Chen, L. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.144907 · Cited by 10 · see citing works
He, M., & Bian, Z. (2016) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2016.10.032 · Cited by 10 · see citing works
Liu, L.-N., Wang, P., Zou, Y.-F., Xu, Z.-W., Cheng, J., Zhang, Y.-Z., Hu, W.-B., & Pan, H.-F. (2019) · Autoimmunity · doi:10.1080/08916934.2019.1642333 · Cited by 8 · see citing works
Semaphorin 7A Accelerates the Inflammatory Osteolysis of Periapical Lesions
Wang, L., Song, Y., Yi, X., Wu, C., Guo, Q., Zhou, X., Song, D., Zhang, L., & Huang, D. (2022) · Journal of Endodontics · doi:10.1016/j.joen.2022.01.020 · Cited by 8 · see citing works
Neuronal Guidance Molecules in Bone Remodeling and Orthodontic Tooth Movement
Şen, S., & Erber, R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231710077 · Cited by 8 · see citing works
Semaphorin 7A: A novel marker of disease activity in Gaucher disease
Franco, M., Reihani, N., Dupuis, L., Collec, E., de Villemeur, T. B., de Person, M., Moussa, F., Berger, M. G., Belmatoug, N., & Kim, C. L. V. (2020) · American Journal of Hematology · doi:10.1002/ajh.25744 · Cited by 8 · see citing works
Alesi, V., Barrano, G., Morara, S., Darelli, D., Petrilli, K., Capalbo, A., Pacella, M., Haass, C., Finocchi, M., Novelli, A., et al. (2011) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.34201 · Cited by 8 · see citing works
Kim, K.-S., Kim, G.-S., Hwang, J., Lee, H., Park, M., Kim, K.-J., Jung, J., Cha, H. S., Shin, H. D., Kang, J.-H., et al. (2007) · BMC Medical Genetics · doi:10.1186/1471-2350-8-70 · Cited by 8 · see citing works
Chen, X., Wang, H., Jia, K., Wang, H., & Ren, T. (2018) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2018.5724 · Cited by 7 · see citing works
RetractedApplication of Proteomics in Apical Periodontitis
Hussein, H., & Kishen, A. (2022) · Frontiers in Dental Medicine · doi:10.3389/fdmed.2022.814603 · Cited by 5 · see citing works
Dalpé, G., Zheng, H., Brown, L., & Culotti, J. G. (2012) · Genetics · doi:10.1534/genetics.112.144253 · Cited by 6 · see citing works
Pan-Cancer Analysis of the Prognostic and Immunological Role of SEMA7A
Yang, L., Zhang, S., Zheng, L., Kong, F., Dang, W., Shen, S., Li, X., Jia, L., Zhang, X., & Lü, N. (2024) · International Journal of General Medicine · doi:10.2147/ijgm.s499872 · Cited by 4 · see citing works
Downregulation of the Autism Spectrum Disorder Gene Shank2 Decreases Bone Mass in Male Mice
Ahmad, M., Stirmlinger, N., Jan, I., Stifel, U., Lee, S., Weingandt, M., Kelp, U., Bockmann, J., Ignatius, A. A., Böckers, T. M., et al. (2022) · JBMR Plus · doi:10.1002/jbm4.10711 · Cited by 4 · see citing works
Gonçalves, C. E. D. S., & Fock, R. A. (2024) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2024.02.002 · Cited by 3 · see citing works
Binet, F., Entz, L., Amiot, M., Tessier, S., Véziers, J., de Beaurepaire, L., André‐Grégoire, G., Dingli, F., Loew, D., Weiss, P., et al. (2025) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00272.2025 · Cited by 3 · see citing works
Análisis de biomarcadores para el seguimiento de pacientes con enfermedad de Gaucher.
Silva-José, T. D. D., Juárez-Vázquez, C. I., & García‐Ortíz, J. E. (2021) · REVISTA BIOMÉDICA · doi:10.32776/revbiomed.v32i3.903 · Cited by 2 · see citing works
Ochman, B., Limanówka, P., Mielcarska, S., Kula, A., Dawidowicz, M., Wagner, W., Hudy, D., Szrot, M., Piecuch, J., Piecuch, J., et al. (2024) · Current Issues in Molecular Biology · doi:10.3390/cimb46090609 · Cited by 1 · see citing works
Traditional Chinese Medicine Therapy for Targeting Osteoblastogenesis
Liu, Y. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.82451 · Cited by 1 · see citing works
Semaphorins in Bone Homeostasis
Hayashi, M., Nakashima, T., & Takayanagi, H. (2015) · Springer eBooks · doi:10.1007/978-4-431-54385-5_8 · Cited by 1 · see citing works
Plexin B2 in mouse and zebrafish development
Perälä, N. M. (2011) · Työväentutkimus Vuosikirja
Zhang, X. (2009) · OhioLink ETD Center (Ohio Library and Information Network)
Gene Expression of Semaphorin 7A During Osteogenic Differentiation in Human Dental Follicle Cells
Kato, R., & Takahashi, K. (2016) · Journal of Hard Tissue Biology · doi:10.2485/jhtb.25.263
- Authors
- Delorme, G., Saltel, F., Bonnelye, E., Jurdic, P., & Machuca‐Gayet, I.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Corresponding author
- Machuca‐Gayet, Irma
- Venue
- Biology of the Cell
- Publisher
- Wiley
- Published
- 2005-07
- Volume
- 97
- Issue
- 7
- Pages
- 589-597
- ISSN
- 0248-4900 (ISSN-L)
- 1768-322X
- OpenAlex
- W2031056152
- Cited by
- 89
- References
- 26
- Citations by year
- 2025: 3 · 2024: 3 · 2022: 7 · 2021: 4 · 2020: 5 · 2019: 4 · 2018: 9 · 2017: 3 · 2016: 5 · 2015: 4 · 2014: 4 · 2013: 5 · 2012: 7
- FWCI
- 1.76
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Biology of the Cell (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ligue Contre le Cancer
- 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
- Health Sciences › Medicine › Rheumatology › Bone and Dental Protein Studies
- Keywords
- SEMA7A, bone cells, osteogenic differentiation, osteoclastogenesis, osteoclast fusion, cell migration, beta1 integrin, MAPK signaling, MC3T3-E1 cells, calvaria cells, GPI-anchored proteins, bone formation
- MeSH terms
- Animals, Cell Differentiation, Cell Movement, Cells, Cultured, Humans, Microscopy, Fluorescence, Osteoblasts, Osteoclasts, RNA, Messenger, Antigens, CD, Semaphorins, Mice, GPI-Linked Proteins
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