Synaptic Cell Adhesion
Open accessAbstract
Chemical synapses are asymmetric intercellular junctions that mediate synaptic transmission. Synaptic junctions are organized by trans-synaptic cell adhesion molecules bridging the synaptic cleft. Synaptic cell adhesion molecules not only connect pre- and postsynaptic compartments, but also mediate trans-synaptic recognition and signaling processes that are essential for the establishment, specification, and plasticity of synapses. A growing number of synaptic cell adhesion molecules that include neurexins and neuroligins, Ig-domain proteins such as SynCAMs, receptor phosphotyrosine kinases and phosphatases, and several leucine-rich repeat proteins have been identified. These synaptic cell adhesion molecules use characteristic extracellular domains to perform complementary roles in organizing synaptic junctions that are only now being revealed. The importance of synaptic cell adhesion molecules for brain function is highlighted by recent findings implicating several such molecules, notably neurexins and neuroligins, in schizophrenia and autism.
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?
There is increasing evidence that neurexins, neuroligins and LRR transmembrane proteins are involved in activity-dependent programs that modulate synapse function.
“There is increasing evidence for the involvement of neurexins, neuroligins and LRR transmembrane proteins in activity-dependent programs that modulate synapse function.”
From Activity-dependent neuronal signalling and autism spectrum disorder (2013) · cites this paper as [16]
Neurexins bind other postsynaptic transmembrane proteins, including LRR transmembrane proteins, in addition to neuroligins, increasing the number of potential trans-synaptic connections.
“In addition to binding neuroligins, neurexins bind other postsynaptic transmembrane proteins, including leucine-rich repeat (LRR) transmembrane proteins, adding to the number of different potential trans-synaptic connections16.”
From Activity-dependent neuronal signalling and autism spectrum disorder (2013) · cites this paper as [16]
Particular neuroligin family members localize specifically to inhibitory or excitatory synapses, suggesting individual neuroligins may specify the formation or function of excitatory and inhibitory synapses.
“Particular neuroligin family members are localized specifically to inhibitory or excitatory synapses, suggesting that individual neuroligins may play a part in specifying the formation or function of excitatory and inhibitory synapses.”
From Activity-dependent neuronal signalling and autism spectrum disorder (2013) · cites this paper as [16]
Neuroligins are postsynaptic membrane proteins that function as neurexin receptors and, together with neurexins, modulate synapse formation and function.
“Neuroligins are postsynaptic membrane proteins that function as neurexin receptors and, working together with neurexins, modulate the formation and function of synapses16,37.”
From Activity-dependent neuronal signalling and autism spectrum disorder (2013) · cites this paper as [16]
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
Berman, H. M. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.1.235 · Cited by 40,196 · see citing works
SWISS‐MODEL and the Swiss‐Pdb Viewer: An environment for comparative protein modeling
Guex, N., & Peitsch, M. (1997) · Electrophoresis · doi:10.1002/elps.1150181505 · Cited by 11,589 · see citing works
Protein structure prediction on the Web: a case study using the Phyre server
Kelley, L. A., & Sternberg, M. J. E. (2009) · Nature Protocols · doi:10.1038/nprot.2009.2 · Cited by 4,154 · see citing works
Gray, E. G., & Whittaker, V. P. (1962) · PubMed · Cited by 2,530 · see citing works
Neurotrophin-regulated signalling pathways
Reichardt, L. F. (2006) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2006.1894 · Cited by 2,195 · see citing works
Neuroligins and neurexins link synaptic function to cognitive disease
Südhof, T. C. (2008) · Nature · doi:10.1038/nature07456 · Cited by 1,849 · see citing works
Self-citationAxo-somatic and axo-dendritic synapses of the cerebral cortex: an electron microscope study.
Eg, G. (1959) · PubMed · Cited by 1,768 · see citing works
ModBase, a database of annotated comparative protein structure models, and associated resources
Pieper, U., Webb, B., Barkan, D. T., Schneidman‐Duhovny, D., Schlessinger, A., Braberg, H., Yang, Z., Meng, E., Pettersen, E. F., Huang, C. C., et al. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq1091 · Cited by 1,069 · see citing works
Neuroligin Expressed in Nonneuronal Cells Triggers Presynaptic Development in Contacting Axons
Scheiffele, P., Fan, J., Choih, J., Fetter, R., & Serafini, T. (2000) · Cell · doi:10.1016/s0092-8674(00)80877-6 · Cited by 1,060 · see citing works
Neurexins Induce Differentiation of GABA and Glutamate Postsynaptic Specializations via Neuroligins
Graf, E. R., Zhang, X., Jin, S., Linhoff, M. W., & Craig, A. M. (2004) · Cell · doi:10.1016/j.cell.2004.11.035 · Cited by 1,001 · see citing works
Quantitative ultrastructural analysis of hippocampal excitatory synapses
Schikorski, T., & Stevens, C. F. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-15-05858.1997 · Cited by 997 · see citing works
A Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice
Tabuchi, K., Blundell, J., Etherton, M. R., Hammer, R. E., Liu, X., Powell, C. M., & Südhof, T. C. (2007) · Science · doi:10.1126/science.1146221 · Cited by 997 · see citing works
Self-citationLTP promotes formation of multiple spine synapses between a single axon terminal and a dendrite
Toni, N., Buchs, P.-A., Nikonenko, I., Bron, C. R., & Muller, D. (1999) · Nature · doi:10.1038/46574 · Cited by 949 · see citing works
Neuroligins Determine Synapse Maturation and Function
Varoqueaux, F., Aramuni, G., Rawson, R. L., Mohrmann, R., Missler, M., Gottmann, K., Zhang, W., Südhof, T. C., & Brose, N. (2006) · Neuron · doi:10.1016/j.neuron.2006.09.003 · Cited by 818 · see citing works
Self-citationSynCAM, a Synaptic Adhesion Molecule That Drives Synapse Assembly
Biederer, T., Sara, Y., Mozhayeva, M. G., Atasoy, D., Liu, X., Kavalali, E. T., & Südhof, T. C. (2002) · Science · doi:10.1126/science.1072356 · Cited by 800 · see citing works
Self-citationBinding of Neuroligins to PSD-95
Irie, M., Hata, Y., Takeuchi, M., Ichtchenko, K., Toyoda, A., Hirao, K., Takai, Y., Rosahl, T. W., & Südhof, T. C. (1997) · Science · doi:10.1126/science.277.5331.1511 · Cited by 749 · see citing works
Self-citationControl of Excitatory and Inhibitory Synapse Formation by Neuroligins
Chih, B., Engelman, H. S., & Scheiffele, P. (2005) · Science · doi:10.1126/science.1107470 · Cited by 716 · see citing works
EphB Receptors Interact with NMDA Receptors and Regulate Excitatory Synapse Formation
Dalva, M. B., Takasu, M. A., Lin, M. Z., Shamah, S. M., Hu, L. S., Gale, N. W., & Greenberg, M. E. (2000) · Cell · doi:10.1016/s0092-8674(00)00197-5 · Cited by 716 · see citing works
α-Neurexins couple Ca2+ channels to synaptic vesicle exocytosis
Missler, M., Zhang, W., Rohlmann, A., Kattenstroth, G., Hammer, R. E., Gottmann, K., & Südhof, T. C. (2003) · Nature · doi:10.1038/nature01755 · Cited by 699 · see citing works
Self-citationNeuroligin 1 is a postsynaptic cell-adhesion molecule of excitatory synapses
Song, J.-Y., Ichtchenko, K., Südhof, T. C., & Brose, N. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.3.1100 · Cited by 696 · see citing works
Postnatal neurodevelopmental disorders: meeting at the synapse?
Zoghbi, H. Y. (2003) · Science · doi:10.1126/science.1089071 · Cited by 691 · see citing works
Neurexins: Synaptic Cell Surface Proteins Related to the α-Latrotoxin Receptor and Laminin
Ushkaryov, Y. A., Petrenko, A. G., Geppert, M., & Südhof, T. C. (1992) · Science · doi:10.1126/science.1621094 · Cited by 688 · see citing works
Neuroligin 1: A splice site-specific ligand for β-neurexins
Ichtchenko, K., Hata, Y., Nguyen, T., Ullrich, B., Missler, M., Moomaw, C. R., & Südhof, T. C. (1995) · Cell · doi:10.1016/0092-8674(95)90396-8 · Cited by 663 · see citing works
Self-citationBourgeron, T. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.06.003 · Cited by 637 · cited 1× · see citing works
“These results endorse the hypothesis that neurodevelopmental disorders can stem from synapse disorganization and imbalanced neuronal excitation and inhibition (Zoghbi 2003; Bourgeron 2009).”
ResultPSA-NCAM is required for activity-induced synaptic plasticity.
Muller, D., Wang, C., Skibo, G. G., Toni, N., Cremer, H., Calaora, V., Rougon, G., & Kiss, J. Z. (1996) · Neuron · doi:10.1016/s0896-6273(00)80174-9 · Cited by 625 · see citing works
Chubykin, A. A., Atasoy, D., Etherton, M. R., Brose, N., Kavalali, E. T., Gibson, J. R., & Südhof, T. C. (2007) · Neuron · doi:10.1016/j.neuron.2007.05.029 · Cited by 594 · see citing works
Jamain, S., Radyushkin, K., Hammerschmidt, K., Granon, S., Boretius, S., Varoqueaux, F., Ramanantsoa, N., Gallego, J., Ronnenberg, A., Winter, D., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711555105 · Cited by 556 · see citing works
Hata, Y., Butz, S., & Sudhof, T. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-08-02488.1996 · Cited by 553 · see citing works
Self-citationNeuroligin 2 is exclusively localized to inhibitory synapses
Varoqueaux, F., Jamain, S., & Brose, N. (2004) · European Journal of Cell Biology · doi:10.1078/0171-9335-00410 · Cited by 552 · see citing works
Control of hippocampal dendritic spine morphology through ephrin-A3/EphA4 signaling
Murai, K. K., Nguyen, L. N., Irie, F., Yamaguchi, Y., & Pasquale, E. B. (2003) · Nature Neuroscience · doi:10.1038/nn994 · Cited by 516 · see citing works
Poulopoulos, A., Aramuni, G., Meyer, G., Soykan, T., Hoon, M., Papadopoulos, T. G., Zhang, M., Paarmann, I., Fuchs, C., Harvey, K., et al. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.023 · Cited by 503 · see citing works
Uchida, N., Honjo, Y., Johnson, K. R., Wheelock, M. J., & Takeichi, M. (1996) · The Journal of cell biology · doi:10.1083/jcb.135.3.767 · Cited by 501 · see citing works
Uemura, T., Lee, S.-J., Yasumura, M., Takeuchi, T., Yoshida, T., Ra, M., Taguchi, R., Sakimura, K., & Mishina, M. (2010) · Cell · doi:10.1016/j.cell.2010.04.035 · Cited by 496 · see citing works
Cadherin Regulates Dendritic Spine Morphogenesis
Togashi, H., Abe, K., Mizoguchi, A., Takaoka, K., Chisaka, O., & Takeichi, M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00748-1 · Cited by 485 · see citing works
Boucard, A. A., Chubykin, A. A., Comoletti, D., Taylor, P., & Südhof, T. C. (2005) · Neuron · doi:10.1016/j.neuron.2005.08.026 · Cited by 470 · see citing works
Ullrich, B., Ushkaryov, Y. A., & Südhof, T. C. (1995) · Neuron · doi:10.1016/0896-6273(95)90306-2 · Cited by 460 · see citing works
Structures, Alternative Splicing, and Neurexin Binding of Multiple Neuroligins
Ichtchenko, K., Nguyen, T., & Südhof, T. C. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.5.2676 · Cited by 459 · see citing works
A stoichiometric complex of neurexins and dystroglycan in brain
Sugita, S., Saito, F., Tang, J., Satz, J., Campbell, K., & Südhof, T. (2001) · Journal of Cell Biology · doi:10.1083/jcb.200105003 · Cited by 453 · see citing works
Etherton, M. R., Blaiss, C. A., Powell, C. M., & Südhof, T. C. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910297106 · Cited by 447 · see citing works
Self-citationFormation of Dendritic Spines with GABAergic Synapses Induced by Whisker Stimulation in Adult Mice
Knott, G. W., Quairiaux, C., Genoud, C., & Welker, E. (2002) · Neuron · doi:10.1016/s0896-6273(02)00663-3 · Cited by 438 · see citing works
Chiu, S.-L., Chen, C.-M., & Cline, H. T. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.014 · Cited by 425 · see citing works
Chih, B., Gollan, L., & Scheiffele, P. (2006) · Neuron · doi:10.1016/j.neuron.2006.06.005 · Cited by 393 · see citing works
Dscam and Sidekick proteins direct lamina-specific synaptic connections in vertebrate retina
Yamagata, M., & Sanes, J. R. (2008) · Nature · doi:10.1038/nature06469 · Cited by 378 · see citing works
LRRTM2 Interacts with Neurexin1 and Regulates Excitatory Synapse Formation
de Wit, J., Sylwestrak, E., O’Sullivan, M. L., Otto, S. J., Tiglio, K., Savas, J. N., Yates, J. R., Comoletti, D., Taylor, P., & Ghosh, A. (2009) · Neuron · doi:10.1016/j.neuron.2009.12.019 · Cited by 376 · see citing works
Structure and Mechanism of Cadherins and Catenins in Cell-Cell Contacts
Pokutta, S., & Weis, W. I. (2007) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010305.104241 · Cited by 375 · see citing works
The liprin protein SYD-2 regulates the differentiation of presynaptic termini in C. elegans
Zhen, M., & Jin, Y. (1999) · Nature · doi:10.1038/43886 · Cited by 374 · see citing works
Ango, F., Cristo, G. D., Higashiyama, H., Bennett, V., Wu, P., & Huang, Z. J. (2004) · Cell · doi:10.1016/j.cell.2004.10.004 · Cited by 371 · see citing works
LRRTM2 Functions as a Neurexin Ligand in Promoting Excitatory Synapse Formation
Ko, J., Fuccillo, M. V., Malenka, R. C., & Südhof, T. C. (2009) · Neuron · doi:10.1016/j.neuron.2009.12.012 · Cited by 369 · see citing works
Linhoff, M. W., Laurén, J., Cassidy, R. M., Dobie, F. A., Takahashi, H., Nygaard, H. B., Airaksinen, M. S., Strittmatter, S. M., & Craig, A. M. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.017 · Cited by 358 · see citing works
N-Cadherin Redistribution during Synaptogenesis in Hippocampal Neurons
Benson, D., & Tanaka, H. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-17-06892.1998 · Cited by 341 · see citing works
Integrins mediate functional pre- and postsynaptic maturation at a hippocampal synapse
Chavis, P., & Westbrook, G. L. (2001) · Nature · doi:10.1038/35077101 · Cited by 332 · see citing works
Neuroligin‐3 is a neuronal adhesion protein at GABAergic and glutamatergic synapses
Budreck, E. C., & Scheiffele, P. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05842.x · Cited by 325 · see citing works
Rex, C. S., Lin, C.-Y., Kramár, E. A., Chen, L. Y., Gall, C. M., & Lynch, G. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4037-06.2007 · Cited by 324 · see citing works
Yamagata, M., Weiner, J. A., & Sanes, J. R. (2002) · Cell · doi:10.1016/s0092-8674(02)00910-8 · Cited by 322 · see citing works
Postsynaptic assembly induced by neurexin-neuroligin interaction and neurotransmitter
Nam, C. I., & Chen, L. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0502038102 · Cited by 322 · see citing works
Role of β-Catenin in Synaptic Vesicle Localization and Presynaptic Assembly
Bamji, S. X., Shimazu, K., Kimes, N. E., Huelsken, J., Birchmeier, W., Lu, B., & Reichardt, L. F. (2003) · Neuron · doi:10.1016/s0896-6273(03)00718-9 · Cited by 310 · see citing works
Structure and Evolution of Neurexin Genes: Insight into the Mechanism of Alternative Splicing
Tabuchi, K., & Südhof, T. C. (2002) · Genomics · doi:10.1006/geno.2002.6780 · Cited by 305 · see citing works
Self-citationRegulation of motor neuron pool sorting by differential expression of type II cadherins
Price, S. R., De Marco Garcia, N. V., Ranscht, B., & Jessell, T. M. (2002) · Cell · doi:10.1016/s0092-8674(02)00695-5 · Cited by 304 · see citing works
Drosophila Liprin-α and the Receptor Phosphatase Dlar Control Synapse Morphogenesis
Kaufmann, N., DeProto, J., Ranjan, R., Wan, H., & Vactor, D. V. (2002) · Neuron · doi:10.1016/s0896-6273(02)00643-8 · Cited by 302 · see citing works
Multiple EphB receptor tyrosine kinases shape dendritic spines in the hippocampus
Henkemeyer, M. J., Itkis, O. S., Ngo, M., Hickmott, P. W., & Ethell, I. M. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200306033 · Cited by 302 · see citing works
Neuregulin-1 Enhances Depolarization-Induced GABA Release
Woo, R., Li, X.-M., Tao, Y., Carpenter‐Hyland, E. P., Huang, Y. Z., Weber, J., Neiswender, H., Dong, X., Wu, J., Gassmann, M., et al. (2007) · Neuron · doi:10.1016/j.neuron.2007.04.009 · Cited by 297 · see citing works
Synaptic Specificity Is Generated by the Synaptic Guidepost Protein SYG-2 and Its Receptor, SYG-1
Shen, K., Fetter, R. D., & Bargmann, C. I. (2004) · Cell · doi:10.1016/s0092-8674(04)00251-x · Cited by 290 · see citing works
Mizoguchi, A., Nakanishi, H., Kimura, K., Matsubara, K., Kuroda, K. O., Katata, T., Honda, T., Kiyohara, Y., Heo, K., Higashi, M., et al. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200103113 · Cited by 289 · see citing works
Siddiqui, T. J., Pancaroglu, R., Kang, Y., Rooyakkers, A., & Craig, A. M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0470-10.2010 · Cited by 284 · see citing works
NGL family PSD-95–interacting adhesion molecules regulate excitatory synapse formation
Kim, S.-H., Burette, A., Chung, H. S., Kwon, S., Woo, J., Lee, H. W., Kim, K., Kim, H., Weinberg, R. J., & Kim, E. (2006) · Nature Neuroscience · doi:10.1038/nn1763 · Cited by 272 · see citing works
Rees, R. P., Bunge, M. B., & Bunge, R. P. (1976) · The Journal of Cell Biology · doi:10.1083/jcb.68.2.240 · Cited by 267 · see citing works
Zuber, B., Nikonenko, I., Klauser, P., Müller, D., & Dubochet, J. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509527102 · Cited by 263 · see citing works
Gamma Protocadherins Are Required for Survival of Spinal Interneurons
Wang, X., Weiner, J. A., Lévi, S., Craig, A. M., Bradley, A., & Sanes, J. R. (2002) · Neuron · doi:10.1016/s0896-6273(02)01090-5 · Cited by 258 · see citing works
LAR receptor protein tyrosine phosphatases in the development and maintenance of excitatory synapses
Dunah, A. W., Hueske, E., Wyszynski, M. W., Hoogenraad, C. C., Jaworski, J., Pak, D. T. S., Simonetta, A., Liu, G., & Sheng, M. (2005) · Nature Neuroscience · doi:10.1038/nn1416 · Cited by 244 · see citing works
TrkB receptor signaling is required for establishment of GABAergic synapses in the cerebellum
Rico, B., Xu, B., & Reichardt, L. F. (2002) · Nature Neuroscience · doi:10.1038/nn808 · Cited by 230 · see citing works
Intracellular and Trans-Synaptic Regulation of Glutamatergic Synaptogenesis by EphB Receptors
Kayser, M. S., McClelland, A. C., Hughes, E. G., & Dalva, M. B. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3072-06.2006 · Cited by 222 · see citing works
Neuroligin-4 is localized to glycinergic postsynapses and regulates inhibition in the retina
Hoon, M., Soykan, T., Falkenburger, B., Hammer, M., Patrizi, A., Schmidt, K., Sassoè-Pognetto, M., Löwel, S., Moser, T., Taschenberger, H., et al. (2011) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1006946108 · Cited by 213 · see citing works
SynCAMs Organize Synapses through Heterophilic Adhesion
Fogel, A. I., Akins, M. R., Krupp, A. J., Stagi, M., Stein, V., & Biederer, T. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2739-07.2007 · Cited by 212 · see citing works
Self-citationGamma protocadherins are required for synaptic development in the spinal cord
Weiner, J. A., Wang, X., Tapia, J. C., & Sanes, J. R. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407931101 · Cited by 208 · see citing works
Araç, D., Boucard, A. A., Özkan, E., Strop, P., Newell, E. W., Südhof, T. C., & Brünger, A. T. (2007) · Neuron · doi:10.1016/j.neuron.2007.12.002 · Cited by 207 · see citing works
Elia, L. P., Yamamoto, M. P., Zang, K., & Reichardt, L. F. (2006) · Neuron · doi:10.1016/j.neuron.2006.05.018 · Cited by 206 · see citing works
Takahashi, H., Arstikaitis, P., Prasad, T., Bartlett, T. E., Wang, Y. T., Murphy, T. H., & Craig, A. M. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.024 · Cited by 193 · see citing works
Synapse development and plasticity: roles of ephrin/Eph receptor signaling
Lai, K., & Ip, N. Y. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.04.009 · Cited by 191 · see citing works
Neurexins Physically and Functionally Interact with GABAA Receptors
Zhang, C., Atasoy, D., Araç, D., Yang, X., Fucillo, M. V., Robison, A. J., Ko, J., Brünger, A. T., & Südhof, T. C. (2010) · Neuron · doi:10.1016/j.neuron.2010.04.008 · Cited by 187 · see citing works
The netrin-G1 ligand NGL-1 promotes the outgrowth of thalamocortical axons
Lin, J. C., Ho, W.-H., Gurney, A. L., & Rosenthal, A. (2003) · Nature Neuroscience · doi:10.1038/nn1148 · Cited by 182 · see citing works
Gibson, J. R., Huber, K., & Südhof, T. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2457-09.2009 · Cited by 181 · see citing works
SynCAM 1 Adhesion Dynamically Regulates Synapse Number and Impacts Plasticity and Learning
Robbins, E. M., Krupp, A. J., de Arce, K. P., Ghosh, A. K., Fogel, A. I., Boucard, A. A., Südhof, T. C., Stein, V., & Biederer, T. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.003 · Cited by 178 · see citing works
Self-citationHines, R. M., Wu, L., Hines, D. J., Steenland, H. W., Mansour, S., Dahlhaus, R., Singaraja, R. R., Cao, X., Sammler, E. M., Hormuzdi, S. G., et al. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0032-08.2008 · Cited by 177 · see citing works
CASK and Protein 4.1 Support F-actin Nucleation on Neurexins
Biederer, T., & Südhof, T. C. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105287200 · Cited by 176 · see citing works
Self-citationLi, J., Ashley, J., Budnik, V., & Bhat, M. A. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.002 · Cited by 171 · see citing works
TrkB Has a Cell-Autonomous Role in the Establishment of Hippocampal Schaffer Collateral Synapses
Luikart, B. W., Nef, S., Virmani, T., Lush, M. E., Liu, Y., Kavalali, E. T., & Parada, L. F. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0041-05.2005 · Cited by 166 · see citing works
Chan, C.-S., Weeber, E. J., Zong, L., Fuchs, E., Sweatt, J. D., & Davis, R. L. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4110-05.2006 · Cited by 165 · see citing works
Ushkaryov, Y. A., Hata, Y., Ichtchenko, K., Moomaw, C. R., Afendis, S. J., Slaughter, C. A., & Südhof, T. C. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)32671-6 · Cited by 160 · see citing works
O'Brien, R., Xu, D., Mi, R., Tang, X., Hopf, C., & Worley, P. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-11-04487.2002 · Cited by 160 · see citing works
Huang, Z., Shimazu, K., Woo, N. H., Zang, K., Müller, U., Lu, B., & Reichardt, L. F. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3526-06.2006 · Cited by 159 · see citing works
Matsuda, K., & Yuzaki, M. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07638.x · Cited by 158 · see citing works
Zhang, W., Rohlmann, A., Sargsyan, V., Aramuni, G., Hammer, R. E., Südhof, T. C., & Missler, M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0497-05.2005 · Cited by 156 · see citing works
Self-citationγ-Protocadherins Are Targeted to Subsets of Synapses and Intracellular Organelles in Neurons
Phillips, G. R., Tanaka, H., Frank, M., Elste, A. M., Fidler, L., Benson, D. L., & Colman, D. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-12-05096.2003 · Cited by 154 · see citing works
Chagnon, M. J., Uetani, N., & Tremblay, M. L. (2004) · Biochemistry and Cell Biology · doi:10.1139/o04-120 · Cited by 152 · see citing works
Laurén, J., Airaksinen, M. S., Saarma, M., & Timmusk, T. (2003) · Genomics · doi:10.1016/s0888-7543(03)00030-2 · Cited by 151 · see citing works
Banovic, D., Khorramshahi, O., Owald, D., Wichmann, C., Riedt, T., Fouquet, W., Tian, R., Sigrist, S. J., & Aberle, H. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.020 · Cited by 151 · see citing works
SALM Synaptic Cell Adhesion-like Molecules Regulate the Differentiation of Excitatory Synapses
Ko, J., Kim, S.-H., Chung, H. S., Kim, K., Han, K., Kim, H., Jun, H., Kaang, B., & Kim, E. (2006) · Neuron · doi:10.1016/j.neuron.2006.04.005 · Cited by 150 · see citing works
Neurexin III alpha: extensive alternative splicing generates membrane-bound and soluble forms.
Ushkaryov, Y. A., & Südhof, T. C. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.14.6410 · Cited by 149 · see citing works
N-cadherin mediates plasticity-induced long-term spine stabilization
Méndez, P., Roo, M. D., Poglia, L., Klauser, P., & Müller, D. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201003007 · Cited by 148 · see citing works
The EphA4 receptor regulates dendritic spine remodeling by affecting β1-integrin signaling pathways
Bourgin, C., Murai, K. K., Richter, M., & Pasquale, E. B. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200610139 · Cited by 147 · see citing works
Dahlhaus, R., Hines, R. M., Eadie, B. D., Kannangara, T. S., Hines, D. J., Brown, C. E., Christie, B. R., & El-Husseini, A. (2009) · Hippocampus · doi:10.1002/hipo.20630 · Cited by 145 · see citing works
Grb4 and GIT1 transduce ephrinB reverse signals modulating spine morphogenesis and synapse formation
Segura, I., Essmann, C. L., Weinges, S., & Acker‐Palmer, A. (2007) · Nature Neuroscience · doi:10.1038/nn1858 · Cited by 145 · see citing works
Complementary expression and neurite outgrowth activity of netrin-G subfamily members
Nakashiba, T., Nishimura, S., Ikeda, T., et al. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00600-1 · Cited by 145 · see citing works
Soler-Llavina, G. J., Fuccillo, M. V., Ko, J., Südhof, T. C., & Malenka, R. C. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1114028108 · Cited by 143 · see citing works
Neuroligin‐1 performs neurexin‐dependent and neurexin‐independent functions in synapse validation
Ko, J., Zhang, C., Araç, D., Boucard, A. A., Brünger, A. T., & Südhof, T. C. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.249 · Cited by 140 · see citing works
Ango, F., Wu, C., van der Want, J. J. L., Wu, P., Schachner, M., & Huang, Z. J. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060103 · Cited by 138 · see citing works
Kakunaga, S., Ikeda, W., Itoh, S., et al. (2005) · Journal of Cell Science · doi:10.1242/jcs.01656 · Cited by 135 · see citing works
A Novel Family of Adhesion-Like Molecules That Interacts with the NMDA Receptor
Wang, C., Chang, K., Petralia, R. S., Wang, Y., Seabold, G. K., & Wenthold, R. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3799-05.2006 · Cited by 130 · see citing works
Hintsch, G. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1181 · Cited by 129 · see citing works
Biederer, T. (2005) · Genomics · doi:10.1016/j.ygeno.2005.08.017 · Cited by 127 · see citing works
Self-citationNCAM promotes assembly and activity-dependent remodeling of the postsynaptic signaling complex
Sytnyk, V., Leshchyns’ka, I., Nikonenko, A. G., & Schachner, M. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200604145 · Cited by 126 · see citing works
Ephrin-B reverse signaling promotes structural and functional synaptic maturation in vivo
Lim, B. K., Matsuda, N., & Poo, M. (2008) · Nature Neuroscience · doi:10.1038/nn2033 · Cited by 117 · see citing works
Bozdagi, O., Wang, X.-B., Nikitczuk, J. S., Anderson, T. R., Bloss, E. B., Radice, G. L., Zhou, Q., Benson, D. L., & Huntley, G. W. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.1223-10.2010 · Cited by 116 · see citing works
Jüngling, K., Eulenburg, V., Moore, R. H., Kemler, R., Leßmann, V., & Gottmann, K. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1013-06.2006 · Cited by 113 · see citing works
Functional dependence of neuroligin on a new non-PDZ intracellular domain
Shipman, S. L., Schnell, E., Hirai, T., Chen, B.-S., Roche, K. W., & Nicoll, R. A. (2011) · Nature Neuroscience · doi:10.1038/nn.2825 · Cited by 111 · see citing works
Togashi, H., Miyoshi, J., Honda, T., Sakisaka, T., Takai, Y., & Takeichi, M. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200601089 · Cited by 110 · see citing works
Morphological Characterization of Molecular Complexes Present in the Synaptic Cleft
́, V. L., Yang, T., Schweikert, G., Förster, F. G., & Baumeister, W. P. (2005) · Structure · doi:10.1016/j.str.2005.02.005 · Cited by 109 · see citing works
The NGL family of leucine-rich repeat-containing synaptic adhesion molecules
Woo, J., Kwon, S., & Kim, E. (2009) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2009.05.008 · Cited by 109 · see citing works
Postsynaptic N -methyl- d -aspartate receptor function requires α-neurexins
Kattenstroth, G., Tantalaki, E., Südhof, T. C., Gottmann, K., & Missler, M. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308626100 · Cited by 108 · see citing works
Self-citationPolo‐Parada, L., Böse, C., Plattner, F., & Landmesser, L. T. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4406-03.2004 · Cited by 105 · see citing works
Ko, J., Soler-Llavina, G. J., Fuccillo, M. V., Malenka, R. C., & Südhof, T. C. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201101072 · Cited by 103 · see citing works
Sun, M., Xing, G., Yuan, L.-D., Gan, G.-M., Knight, D., With, S., He, C.-Z., Han, J., Zeng, X., Fang, M., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3854-10.2011 · Cited by 101 · see citing works
Neurexophilins Form a Conserved Family of Neuropeptide-Like Glycoproteins
Missler, M., & Südhof, T. C. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03630.1998 · Cited by 101 · see citing works
Self-citationMutational analysis of the neurexin/neuroligin complex reveals essential and regulatory components
Reißner, C., Klose, M., Fairless, R., & Missler, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801639105 · Cited by 98 · see citing works
Self-citationCell–cell interactions in synaptogenesis
Akins, M. R., & Biederer, T. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.01.009 · Cited by 97 · see citing works
Self-citationIdentification of functional marker proteins in the mammalian growth cone
Nozumi, M., Togano, T., Takahashi-Niki, K., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904092106 · Cited by 95 · see citing works
Choi, Y.-B., Li, H.-L., Kassabov, S. R., Jin, I., Puthanveettil, S. V., Karl, K. A., Lu, Y., Kim, J.-H., Bailey, C. H., & Kandel, E. R. (2011) · Neuron · doi:10.1016/j.neuron.2011.03.020 · Cited by 94 · see citing works
LG/LNS domains: multiple functions – one business end?
Rudenko, G., Hohenester, E., & Muller, Y. A. (2001) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(01)01832-1 · Cited by 93 · see citing works
Postsynaptic EphrinB3 Promotes Shaft Glutamatergic Synapse Formation
Aoto, J. N., Ting, P. Y., Maghsoodi, B., Xu, N., Henkemeyer, M. J., & Chen, L. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0705-07.2007 · Cited by 93 · see citing works
Modulation of synaptic transmission and plasticity by cell adhesion and repulsion molecules
Dityatev, A. E., Bukalo, O., & Schachner, M. (2008) · Neuron Glia Biology · doi:10.1017/s1740925x09990111 · Cited by 92 · see citing works
Expression and adhesion profiles of SynCAM molecules indicate distinct neuronal functions
Thomas, L. A., Akins, M. R., & Biederer, T. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21773 · Cited by 87 · see citing works
Self-citationSynCAM 1 participates in axo-dendritic contact assembly and shapes neuronal growth cones
Stagi, M., Fogel, A. I., & Biederer, T. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911798107 · Cited by 82 · see citing works
Self-citationThe SALM/Lrfn family of leucine-rich repeat-containing cell adhesion molecules
Nam, J., Mah, W., & Kim, E. (2011) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2011.06.005 · Cited by 77 · see citing works
The Structure of Neurexin 1α Reveals Features Promoting a Role as Synaptic Organizer
Chen, F., Vandavasi, V. G., Murray, B. H., & Rudenko, G. (2011) · Structure · doi:10.1016/j.str.2011.03.012 · Cited by 73 · see citing works
Lyckman, A. W., Horng, S. H., Leamey, C. A., Tropea, D., Watakabe, A., Wart, A. V., McCurry, C., Yamamori, T., & Sur, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0710172105 · Cited by 70 · see citing works
Miller, M. T., Mileni, M., Comoletti, D., Stevens, R. C., Harel, M., & Taylor, P. (2011) · Structure · doi:10.1016/j.str.2011.03.011 · Cited by 69 · see citing works
Fogel, A. I., Li, Y., Giza, J. I., Wang, Q., Lam, T. T., Modis, Y., & Biederer, T. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.120865 · Cited by 66 · see citing works
Self-citationCooper, M. W., & Smith, S. J. (1992) · Journal of Neurobiology · doi:10.1002/neu.480230704 · Cited by 58 · see citing works
CONTACTINS: STRUCTURAL ASPECTS IN RELATION TO DEVELOPMENTAL FUNCTIONS IN BRAIN DISEASE
Zuko, A., Bouyain, S., van der Zwaag, B., & Burbach, J. (2011) · Advances in Protein Chemistry and Structural Biology · doi:10.1016/b978-0-12-386483-3.00001-x · Cited by 56 · see citing works
The SALM Family of Adhesion-like Molecules Forms Heteromeric and Homomeric Complexes
Seabold, G. K., Wang, P. Y., Chang, K., Wang, C.-Y., Wang, Y., Petralia, R. S., & Wenthold, R. J. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m709456200 · Cited by 56 · see citing works
Neuronal Pentraxins Mediate Silent Synapse Conversion in the Developing Visual System
Koch, S. M., & Ullian, E. M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4893-09.2010 · Cited by 55 · see citing works
The neurexin superfamily of Caenorhabditis elegans
Haklai-Topper, L., Soutschek, J., Sabanay, H., Scheel, J., Hobert, O., & Peles, E. (2010) · Gene Expression Patterns · doi:10.1016/j.gep.2010.10.008 · Cited by 49 · see citing works
Netrin‐G2 and netrin‐G2 ligand are both required for normal auditory responsiveness
Zhang, W., Rajan, I., Savelieva, K. V., et al. (2007) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2007.00361.x · Cited by 48 · see citing works
Zhang, Q.-H., Wang, J.-R., Fan, S.-Q., Wang, L.-L., Cao, L., Tang, K., Peng, C., Li, Z., Li, W.-F., Gan, K., et al. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.05.058 · Cited by 40 · see citing works
Presynaptic Targeting of α4β2 Nicotinic Acetylcholine Receptors Is Regulated by Neurexin-1β
Cheng, S., Amici, S. A., Ren, X., McKay, S. B., Treuil, M. W., Lindstrom, J. M., Rao, J., & Anand, R. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.017384 · Cited by 38 · see citing works
Zelano, J., Berg, A., Thams, S., Hailer, N. P., & Cullheim, S. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22186 · Cited by 31 · see citing works
The resilient synapse: insights from genetic interference of synaptic cell adhesion molecules
Piechotta, K., Dudanova, I., & Missler, M. (2006) · Cell and Tissue Research · doi:10.1007/s00441-006-0267-4 · Cited by 29 · see citing works
Self-citationHata, K., Polo‐Parada, L., & Landmesser, L. T. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3847-07.2007 · Cited by 28 · see citing works
7TM-Cadherins: Developmental Roles and Future Challenges
Formstone, C. J. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-7913-1_2 · Cited by 20 · see citing works
Synaptic Specificity Is Generated by the Synaptic Guidepost Protein SYG-2 and Its Receptor, SYG-1
Shen, K., Fetter, R. D., & Bargmann, C. I. (2004) · Cell · doi:10.1016/s0092-8674(04)00407-6 · Cited by 19 · see citing works
Li, J., Budnik, V., Ashley, J., et al. (2020) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/rqsk-bf06 · Cited by 13 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Activity-dependent neuronal signalling and autism spectrum disorder
Ebert, D. H., & Greenberg, M. E. (2013) · Nature · doi:10.1038/nature11860 · Cited by 666 · see citing works
A trans-synaptic nanocolumn aligns neurotransmitter release to receptors
Tang, A.-H., Chen, H., Li, T. P., Metzbower, S. R., MacGillavry, H. D., & Blanpied, T. A. (2016) · Nature · doi:10.1038/nature19058 · Cited by 677 · see citing works
The Postsynaptic Organization of Synapses
Sheng, M., & Kim, E. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005678 · Cited by 603 · see citing works
Profiling cellular diversity in sponges informs animal cell type and nervous system evolution
Musser, J. M., Schippers, K. J., Nickel, M., Mizzon, G., Kohn, A. B., Pape, C., Ronchi, P., Papadopoulos, N., Tarashansky, A. J., Hammel, J. U., et al. (2021) · Science · doi:10.1126/science.abj2949 · Cited by 242 · see citing works
Tao, C.-L., Liu, Y.-T., Sun, R., Zhang, B., Qi, L., Shivakoti, S., Tian, C.-L., Zhang, P., Lau, P.-M., Zhou, Z. H., et al. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.1548-17.2017 · Cited by 207 · see citing works
Cell adhesion and matricellular support by astrocytes of the tripartite synapse
Hillen, A. E. J., Burbach, J. P. H., & Hol, E. M. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.02.002 · Cited by 108 · see citing works
Synaptic Organizers in Alzheimer’s Disease: A Classification Based on Amyloid-β Sensitivity
Lee, A. K., Khaled, H., Chofflet, N., & Takahashi, H. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00281 · Cited by 14 · see citing works
- Authors
- Missler, M., Sudhof, T. C., & Biederer, T.
- Affiliations
- University of Münster (DE)
- Yale University (US)
- Corresponding author
- Biederer, T.
- Venue
- Cold Spring Harbor Perspectives in Biology
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2012-01-25
- Volume
- 4
- Issue
- 4
- Pages
- a005694-a005694
- ISSN
- 1943-0264 (ISSN-L)
- PMC
- PMC3312681
- OpenAlex
- W2150909590
- Cited by
- 255
- References
- 151
- Citations by year
- 2026: 10 · 2025: 19 · 2024: 14 · 2023: 10 · 2022: 8 · 2021: 22 · 2020: 21 · 2019: 18 · 2018: 27 · 2017: 19 · 2016: 19 · 2015: 22 · 2014: 23 · 2013: 15 · 2012: 7
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cold Spring Harbor Perspectives in Biology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Simons Foundation
- Deutsche Forschungsgemeinschaft (SFB 492)
- National Institutes of Health (MH052804)
- National Institute of Mental Health (R01MH089054, R37MH052804)
- National Institute on Drug Abuse (R01DA018928)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Health Sciences › Medicine › Immunology and Allergy › Cell Adhesion Molecules Research
- Keywords
- synaptic cell adhesion molecules, chemical synapses, synaptic transmission, neurexin, neuroligins, receptor tyrosine kinase, receptor tyrosine phosphatase, leucine-rich repeat proteins, synaptic plasticity, schizophrenia, autism spectrum disorder
- MeSH terms
- Cell Adhesion, Humans, Ligands, Synapses, Signal Transduction, Cadherins
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