The DOI matches its Crossref record; 77 of the 79 references it cites were found in a registry or an index.
Postsynaptic Scaffolds of Excitatory and Inhibitory Synapses in Hippocampal Neurons: Maintenance of Core Components Independent of Actin Filaments and Microtubules
Open accessAbstract
The mechanisms responsible for anchoring molecular components of postsynaptic specializations in the mammalian brain are not well understood but are presumed to involve associations with cytoskeletal elements. Here we build on previous studies of neurotransmitter receptors (Allison et al., 1998) to analyze the modes of attachment of scaffolding and signal transducing proteins of both glutamate and GABA postsynaptic sites to either the microtubule or microfilament cytoskeleton. Hippocampal pyramidal neurons in culture were treated with latrunculin A to depolymerize actin, with vincristine to depolymerize microtubules, or with Triton X-100 to extract soluble proteins. The synaptic clustering of PSD-95, a putative NMDA receptor anchoring protein and a core component of the postsynaptic density (PSD), was unaffected by actin depolymerization, microtubule depolymerization, or detergent extraction. The same was largely true for GKAP, a PSD-95-interacting protein. In contrast, the synaptic clustering of Ca(2+)/calmodulin-dependent protein kinase II (CaMKII)alpha, another core component of the PSD, was completely dependent on an intact actin cytoskeleton and was partially disrupted by detergent. Drebrin and alpha-actinin-2, actin-binding proteins concentrated in spines, were also dependent on F-actin for synaptic localization but were unaffected by detergent extraction. Surprisingly, the subcellular distributions of the inhibitory synaptic proteins GABA(A)R and gephyrin, which has a tubulin-binding motif, were unaffected by depolymerization of microtubules or actin or by detergent extraction. These studies reveal an unsuspected heterogeneity in the modes of attachment of postsynaptic proteins to the cytoskeleton and support the idea that PSD-95 and gephyrin may be core scaffolding components independent of the actin or tubulin cytoskeleton.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Lastly, the actin cytoskeleton is known to mediate receptor positioning (Gudheti et al., 2013) and its depolymerization was shown to reduce glutamate receptor accumulations in spines (Allison et al., 2000).”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Allison et al., 2000
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Domain Interaction Between NMDA Receptor Subunits and the Postsynaptic Density Protein PSD-95
Kornau, H., Schenker, L. T., Kennedy, M. B., & Seeburg, P. H. (1995) · Science · doi:10.1126/science.7569905 · Cited by 1,916
(1991) · Medical Entomology and Zoology · Cited by 1,512
Dendritic spine changes associated with hippocampal long-term synaptic plasticity
Engert, F., & Bonhoeffer, T. (1999) · Nature · doi:10.1038/19978 · Cited by 1,412
Rat hippocampal neurons in dispersed cell culture.
Banker, G. A., & Cowan, W. M. (1977) · Brain Research · doi:10.1016/0006-8993(77)90594-7 · Cited by 1,110
Harris, K. M., & Kater, S. B. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.002013 · Cited by 1,020
Naisbitt, S., Kim, E., Tu, J. C., Xiao, B., Sala, C., Valtschanoff, J., Weinberg, R. J., Worley, P. F., & Sheng, M. (1999) · Neuron · doi:10.1016/s0896-6273(00)80809-0 · Cited by 1,009
Postsynaptic clustering of major GABAA receptor subtypes requires the γ2 subunit and gephyrin
Essrich, C., Lorez, M., Benson, J. A., Fritschy, J., & Lüscher, B. (1998) · Nature Neuroscience · doi:10.1038/2798 · Cited by 856
GABAA-receptor-associated protein links GABAA receptors and the cytoskeleton
Wang, H.-B., Bedford, F., Brandon, N., Moss, S., & Olsen, R. (1999) · Nature · doi:10.1038/16264 · Cited by 754
Shen, K., & Meyer, T. (1999) · Science · doi:10.1126/science.284.5411.162 · Cited by 673
Competitive binding of α-actinin and calmodulin to the NMDA receptor
Wyszynski, M., Lin, J., Rao, A., Nigh, E., Beggs, A. H., Craig, A. M., & Sheng, M. (1997) · Nature · doi:10.1038/385439a0 · Cited by 596
Self-citation
Cited by
Sorted by citations
PDZ Domains and the Organization of Supramolecular Complexes
Sheng, M., & Sala, C. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1 · Cited by 1,211
Lacor, P. N., Buniel, M. C., Furlow, P. W., Sanz Clemente, A., Velasco, P. T., Wood, M., Viola, K. L., & Klein, W. L. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3501-06.2007 · Cited by 1,188
Synaptic Targeting by Alzheimer's-Related Amyloid β Oligomers
Lacor, P. N., Buniel, M. C., Chang, L., Fernandez, S. J., Gong, Y., Viola, K. L., Lambert, M. P., Velasco, P. T., Bigio, E. H., Finch, C. E., et al. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.3432-04.2004 · Cited by 954
Subunit-Specific NMDA Receptor Trafficking to Synapses
Barria, A., & Malinow, R. (2002) · Neuron · doi:10.1016/s0896-6273(02)00776-6 · Cited by 515
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
Klein, W. L., Stine, W. B., & Teplow, D. B. (2004) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2004.02.010 · Cited by 494
Lisman (2001) · doi:10.1016/s0896-6273(01)00364-6 · Cited by 480
Constructing inhibitory synapses
Moss, S. J., & Smart, T. G. (2001) · Nature reviews. Neuroscience · doi:10.1038/35067500 · Cited by 467
Phillips, G. R., Huang, J. K., Wang, Y., Tanaka, H., Shapiro, L. S., Zhang, W., Shan, W., Arndt, K., Frank, M., Gordon, R. E., et al. (2001) · Neuron · doi:10.1016/s0896-6273(01)00450-0 · Cited by 438
Gephyrin: a master regulator of neuronal function?
Tyagarajan, S. K., & Fritschy, J. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3670 · Cited by 442
The role of receptor diffusion in the organization of the postsynaptic membrane
Choquet, D., & Triller, A. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1077 · Cited by 427
The actin cytoskeleton: integrating form and function at the synapse
Dillon, C., & Goda, Y. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135757 · Cited by 447
Wenthold, R. J., Prybylowski, K., Standley, S., Sans, N., & Petralia, R. S. (2003) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.43.100901.135803 · Cited by 374
Molecular mechanisms of dendritic spine development and remodeling
Ethell, I. M., & Pasquale, E. B. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.02.003 · Cited by 367
Glutamate receptor dynamics in dendritic microdomains.
Newpher, T. M., & Ehlers, M. D. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.030 · Cited by 356
Role of actin cytoskeleton in dendritic spine morphogenesis
Sekino, Y., Kojima, N., & Shirao, T. (2007) · Neurochemistry International · doi:10.1016/j.neuint.2007.04.029 · Cited by 294
Mechanisms of Synapse Assembly and Disassembly
Goda, Y., & Davis, G. W. (2003) · Neuron · doi:10.1016/s0896-6273(03)00608-1 · Cited by 305
Lüscher, B., & Keller, C. A. (2004) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2004.04.003 · Cited by 280
Rapid recruitment of NMDA receptor transport packets to nascent synapses
Washbourne, P., Bennett, J. E., & McAllister, A. K. (2002) · Nature Neuroscience · doi:10.1038/nn883 · Cited by 284
Activity-Dependent Tuning of Inhibitory Neurotransmission Based on GABAAR Diffusion Dynamics
Bannai, H., Lévi, S., Schweizer, C., Inoue, T., Launey, T., Racine, V., Sibarita, J., Mikoshiba, K., & Triller, A. (2009) · Neuron · doi:10.1016/j.neuron.2009.04.023 · Cited by 270
Frost, N. A., Shroff, H., Kong, H., Betzig, E., & Blanpied, T. A. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.026 · Cited by 275
Huang, Y., Jung, M., Sarkissian, M., & Richter, J. D. (2002) · The EMBO Journal · doi:10.1093/emboj/21.9.2139 · Cited by 270
Stages of Synapse Development Defined by Dependence on F-Actin
Zhang, W., & Benson, D. L. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05169.2001 · Cited by 262
Facilitation of dendritic mRNA transport by CPEBPreprint
Huang, Y., Carson, J. H., Barbarese, E., & Richter, J. D. (2003) · Genes & Development · doi:10.1101/gad.1053003 · Cited by 265
Kneussel, M., & Betz, H. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01627-1 · Cited by 262
Proteomics Analysis of Rat Brain Postsynaptic Density
Li, K. W., Hornshaw, M. P., van der Schors, R. C., Watson, R. B., Tate, S. A., Casetta, B., Jiménez, C. R., Gouwenberg, Y., Gundelfinger, E. D., Smalla, K., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m303116200 · Cited by 249
NMDA Di-Heteromeric Receptor Populations and Associated Proteins in Rat Hippocampus
Al‐Hallaq, R. A., Conrads, T. P., Veenstra, T. D., & Wenthold, R. J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2155-07.2007 · Cited by 264
Takahashi, H., Sekino, Y., Tanaka, S., Mizui, T., Kishi, S., & Shirao, T. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-16-06586.2003 · Cited by 237
Kittler, J. T., Rostaing, P., Schiavo, G., Fritschy, J., Olsen, R. W., Triller, A., & Moss, S. J. (2001) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2001.1005 · Cited by 227
Chen, L., Wang, H., Vicini, S., & Olsen, R. W. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.190133497 · Cited by 208
Papadopoulos, T. G., Körte, M., Eulenburg, V., Kubota, H., Retiounskaia, M., Harvey, R. J., Harvey, K., O’Sullivan, G. A., Laube, B., Hülsmann, S., et al. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601819 · Cited by 204
Induction of Spine Growth and Synapse Formation by Regulation of the Spine Actin Cytoskeleton
Zito, K., Knott, G. W., Shepherd, G. M., Shenolikar, S., & Svoboda, K. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.022 · Cited by 202
Gephyrin Interacts with Dynein Light Chains 1 and 2, Components of Motor Protein Complexes
Fuhrmann, J. C., Kins, S., Rostaing, P., Far, O. E., Kirsch, J., Sheng, M., Triller, A., Betz, H., & Kneussel, M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-13-05393.2002 · Cited by 191
Butkevich, E., Hülsmann, S., Wenzel, D., Shirao, T., Duden, R., & Majoul, I. V. (2004) · Current Biology · doi:10.1016/j.cub.2004.03.063 · Cited by 190
Walikonis, R. S., Oguni, A., Khorosheva, E. M., Jeng, C.-J., Asuncion, F. J., & Kennedy, M. B. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-02-00423.2001 · Cited by 181
Brusés, J. L., Chauvet, N., & Rutishauser, U. S. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-02-00504.2001 · Cited by 212
Gomez, L. L., Alam, S., Smith, K. E., Horne, E., & Dell'Acqua, M. L. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-16-07027.2002 · Cited by 170
Brünig, I., Suter, A., Knuesel, I., Lüscher, B., & Fritschy, J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-12-04805.2002 · Cited by 166
Gephyrin: a central GABAergic synapse organizer
Choii, G., & Ko, J. (2015) · Experimental & Molecular Medicine · doi:10.1038/emm.2015.5 · Cited by 165
Akashi, K., Kakizaki, T., Kamiya, H., Fukaya, M., Yamasaki, M., Abe, M., Natsume, R., Watanabe, M., & Sakimura, K. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5531-08.2009 · Cited by 163
Chamma, I., Heubl, M., Chevy, Q., Renner, M. L., Moutkine, I., Eugène, E., Poncer, J. C., & Lévi, S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5889-12.2013 · Cited by 150
Sharma, K., Fong, D. K., & Craig, A. M. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.01.010 · Cited by 150
Self-citationFong, D. K., Rao, A., Crump, F. T., & Craig, A. M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-06-02153.2002 · Cited by 150
Self-citationLeshchyns’ka, I., Sytnyk, V., Morrow, J. S., & Schachner, M. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200303020 · Cited by 149
Control of the postsynaptic membrane viscosity
Renner, M., Choquet, D., & Triller, A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.4445-08.2009 · Cited by 145
Schell, M. J., Erneux, C., & Irvine, R. F. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m104101200 · Cited by 142
cAMP-Dependent Protein Kinase Mediates Activity-Regulated Synaptic Targeting of NMDA Receptors
Crump, F. T., Dillman, K. S., & Craig, A. M. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05079.2001 · Cited by 140
Self-citationActivity-Induced Rapid Synaptic Maturation Mediated by Presynaptic Cdc42 Signaling
Shen, W., Wu, B., Zhang, Z., Dou, Y., Rao, Z., Chen, Y., & Duan, S. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.017 · Cited by 138
Prange, O., & Murphy, T. H. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-23-09325.2001 · Cited by 128
Oligodendrocytes express synaptic proteins that modulate myelin sheath formation
Hughes, A. N., & Appel, B. (2019) · Nature Communications · doi:10.1038/s41467-019-12059-y · Cited by 128
NCAM 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 124
Robison, A. J., Bass, M. A., Jiao, Y., MacMillan, L. B., Carmody, L. C., Bartlett, R. K., & Colbran, R. J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m502191200 · Cited by 134
Borgesius, N. Z., van Woerden, G. M., Buitendijk, G. H. S., Keijzer, N., Jaarsma, D., Hoogenraad, C. C., & Elgersma, Y. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5105-10.2011 · Cited by 124
Formation of Presynaptic Terminals at Predefined Sites along Axons
Sabo, S. L., Gomes, R. A., & McAllister, A. K. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2052-06.2006 · Cited by 123
Spine microdomains for postsynaptic signaling and plasticity
Newpher, T. M., & Ehlers, M. D. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.02.004 · Cited by 140
Weitzdoerfer, R., Dierssen, M., Fountoulakis, M., & Lübec, G. (2001) · Springer eBooks · doi:10.1007/978-3-7091-6262-0_5 · Cited by 122
O’Connell, K. M. S., Rolig, A. S., Whitesell, J. D., & Tamkun, M. M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1825-06.2006 · Cited by 119
Targets of Caspase-6 Activity in Human Neurons and Alzheimer Disease
Klaiman, G., Petzke, T. L., Hammond, J., & LeBlanc, A. C. (2008) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m800007-mcp200 · Cited by 118
Chen, Y., Wang, Y. Y., Ertürk, A., Kallop, D. Y., Jiang, Z., Weimer, R. M., Kaminker, J. S., & Sheng, M. (2014) · Neuron · doi:10.1016/j.neuron.2014.05.027 · Cited by 111
Dhavan, R., Greer, P. L., Morabito, M. A., Orlando, L. R., & Tsai, L. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-18-07879.2002 · Cited by 116
Welch, J. M., Wang, D., & Feng, G. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20060 · Cited by 113
Spine loss and other dendritic abnormalities in epilepsy
Swann, J. W., Al‐Noori, S., Jiang, M., & Lee, C. L. (2000) · Hippocampus · doi:10.1002/1098-1063(2000)10:5 · Cited by 268
Self-citationSynaptic targeting by Aβ oligomers (ADDLS) as a basis for memory loss in early Alzheimer's disease
Klein, W. L. (2006) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2005.11.003 · Cited by 109
Becher, A., White, J. H. M., & McIlhinney, R. A. J. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00614.x · Cited by 109
Horne, E. A., & Dell’Acqua, M. L. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4340-06.2007 · Cited by 107
Synaptic SAP97 Isoforms Regulate AMPA Receptor Dynamics and Access to Presynaptic Glutamate
Waites, C. L., Specht, C. G., Härtel, K., Leal-Ortiz, S., Genoux, D., Li, D., Drisdel, R. C., Jeyifous, O., Cheyne, J. E., Green, W. N., et al. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.4431-08.2009 · Cited by 109
Activity-Dependent Movements of Postsynaptic Scaffolds at Inhibitory Synapses
Hanus, C., Ehrensperger, M.-V., & Triller, A. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5123-05.2006 · Cited by 105
Cheng, C., Glover, G., Banker, G. A., & Amara, S. G. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-24-10643.2002 · Cited by 89
Synaptic Strength of Individual Spines Correlates with Bound Ca 2+ –Calmodulin-Dependent Kinase II
Asrican, B., Lisman, J. E., & Otmakhov, N. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3587-07.2007 · Cited by 85
Kawaguchi, S., & Hirano, T. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1981-07.2007 · Cited by 87
Aarts, M. M., & Tymianski, M. (2003) · Biochemical Pharmacology · doi:10.1016/s0006-2952(03)00297-1 · Cited by 86
Lalli, G., Gschmeissner, S., & Schiavo, G. (2003) · Journal of Cell Science · doi:10.1242/jcs.00727 · Cited by 84
Shiraishi, Y., Mizutani, A., Mikoshiba, K., & Furuichi, T. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00037-x · Cited by 85
Dendrite-like Process Formation and Cytoskeletal Remodeling Regulated by δ-Catenin Expression
Kim, K., Sirota, A., Chen, Y.-H., Jones, S. B., Dudek, R. W., Lanford, G. W., Thakore, C. U., & Lu, Q. (2002) · Experimental Cell Research · doi:10.1006/excr.2002.5503 · Cited by 82
Telencephalin Slows Spine Maturation
Matsuno, H., Okabe, S., Mishina, M., Yanagida, T., Mori, K., & Yoshihara, Y. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2651-05.2006 · Cited by 86
Transient decrease in F‐actin may be necessary for translocation of proteins into dendritic spines
Ouyang, Y., Wong, M., Capani, F., Rensing, N., Lee, C., Liu, Q., Neusch, C., Martone, M. E., Wu, J. Y., Yamada, K. A., et al. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04521.x · Cited by 82
Albin, S. D., & Davis, G. W. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1538-04.2004 · Cited by 77
Papadopoulos, T. G., Eulenburg, V., Reddy‐Alla, S., Mansuy, I. M., Li, Y., & Betz, H. (2008) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2008.06.006 · Cited by 76
The Role of Collybistin in Gephyrin Clustering at Inhibitory Synapses: Facts and Open Questions
Papadopoulos, T. G., & Soykan, T. (2011) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2011.00011 · Cited by 75
Pak1 regulates dendritic branching and spine formation
Hayashi, K., Ohshima, T., Hashimoto, M., & Mikoshiba, K. (2007) · Developmental Neurobiology · doi:10.1002/dneu.20363 · Cited by 75
α-Actinin Anchors PSD-95 at Postsynaptic Sites
Matt, L., Kim, K., Hergarden, A. C., Patriarchi, T., Malik, Z. A., Park, D. K., Chowdhury, D., Buonarati, O. R., Henderson, P. B., Gökçek-Saraç, Ç., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.01.036 · Cited by 77
Gephyrin: a key regulatory protein of inhibitory synapses and beyond
Groeneweg, F. L., Trattnig, C., Kuhse, J., Nawrotzki, R., & Kirsch, J. (2018) · Histochemistry and Cell Biology · doi:10.1007/s00418-018-1725-2 · Cited by 78
Control of Synapse Structure and Function by Actin and Its Regulators
Gentile, J. E., Carrizales, M. G., & Koleske, A. J. (2022) · Cells · doi:10.3390/cells11040603 · Cited by 72
Xiang, S., Kim, E. Y., Connelly, J. J., Nassar, N. N., Kirsch, J., Winking, J., Schwarz, G., & Schindelin, H. (2006) · Journal of Molecular Biology · doi:10.1016/j.jmb.2006.03.019 · Cited by 73
The Yin–Yang of Dendrite Morphology: Unity of Actin and Microtubules
Georges, P. C., Hadzimichalis, N. M., Sweet, E. S., & Firestein, B. L. (2008) · Molecular Neurobiology · doi:10.1007/s12035-008-8046-8 · Cited by 74
Yao, J., Qi, J., & Chen, G. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1183-06.2006 · Cited by 71
Banks, G. B., Kanjhan, R., Wiese, S., Kneussel, M., Wong, L. M., O’Sullivan, G. A., Sendtner, M., Bellingham, M. C., Betz, H., & Noakes, P. G. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1786-04.2005 · Cited by 67
GIT1 and βPIX Are Essential for GABAA Receptor Synaptic Stability and Inhibitory Neurotransmission
Smith, K. R., Davenport, E. C., Wei, J., Li, X., Pathania, M., Vaccaro, V., Yan, Z., & Kittler, J. T. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.08.061 · Cited by 71
CaMKII, an Enzyme on the Move: Regulation of Temporospatial Localization
Griffith, L. C. (2003) · Molecular Interventions · doi:10.1124/mi.3.7.386 · Cited by 68
Extracellular chaperones prevent Aβ42-induced toxicity in rat brains
Cascella, R., Conti, S., Tatini, F., Evangelisti, E., Scartabelli, T., Casamenti, F., Wilson, M. R., Chiti, F., & Cecchi, C. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2013.04.012 · Cited by 70
Participation of CaMKII in Neuronal Plasticity and Memory Formation
Cammarota, M., Bevilaqua, L. R., Viola, H., Kerr, D. S., Reichmann, B. P., Teixeira, V., Bulla, M. C., Izquierdo, I., & Medina, J. H. (2002) · Cellular and Molecular Neurobiology · doi:10.1023/a:1020763716886 · Cited by 65
Structural Remodeling of the Synapse in Response to Physiological Activity
Huntley, G. W., Benson, D. L., & Colman, D. (2002) · Cell · doi:10.1016/s0092-8674(01)00631-6 · Cited by 64
Aoki, C. J., Kojima, N., Sabaliauskas, N. A., Shah, L. N., Ahmed, T. H., Oakford, J., Ahmed, T., Yamazaki, H., Hanamura, K., & Shirao, T. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22137 · Cited by 66
A network of networks: cytoskeletal control of compartmentalized function within dendritic spines
Frost, N. A., Kerr, J. M., Lu, H. E., & Blanpied, T. A. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.06.009 · Cited by 68
Neural plasticity and memory: molecular mechanism
Amtul, Z., & Rahman, A. (2015) · Reviews in the Neurosciences · doi:10.1515/revneuro-2014-0075 · Cited by 66
The microtubule cytoskeleton at the synapse
Parato, J., & Bartolini, F. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2021.135850 · Cited by 67
Barriers in the brain: resolving dendritic spine morphology and compartmentalization
Adrian, M., Kusters, R., Wierenga, C. J., Storm, C., Hoogenraad, C. C., & Kapitein, L. C. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00142 · Cited by 62
“Lastly, the actin cytoskeleton is known to mediate receptor positioning (Gudheti et al., 2013) and its depolymerization was shown to reduce glutamate receptor accumulations in spines (Allison et al., 2000).”
Wu, H.-Y., Hudry, E., Hashimoto, T., Uemura, K., Fan, Z., Berezovska, O., Grosskreutz, C. L., Bacskai, B. J., & Hyman, B. T. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0227-12.2012 · Cited by 60
Experience‐induced plasticity of thalamocortical axons in both juveniles and adults
Wimmer, V. C., Broser, P. J., Kuner, T., & Bruno, R. M. (2010) · The Journal of Comparative Neurology · doi:10.1002/cne.22483 · Cited by 62
Structure and molecular organization of dendritic spines.
Tashiro, A., & Yuste, R. (2003) · PubMed · doi:10.14670/hh-18.617 · Cited by 60
Metadata
- Authors
- Allison, D. W., Chervin, A. S., Gelfand, V. I., & Craig, A. M.
- Affiliations
- University of Illinois Urbana-Champaign (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2000-06-15
- Volume
- 20
- Issue
- 12
- Pages
- 4545-4554
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6772458
- OpenAlex
- W2148256023
- Cited by
- 245
- References
- 79
- Citations by year
- 2025: 5 · 2024: 3 · 2023: 2 · 2022: 4 · 2021: 10 · 2020: 4 · 2019: 3 · 2018: 4 · 2017: 5 · 2016: 2 · 2015: 5 · 2014: 12 · 2013: 8 · 2012: 7
- FWCI
- 8.28
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Science Foundation
- National Institutes of Health (GM-52111)
- National Institute of General Medical Sciences (R01GM052111, GM52111-01)
- National Institute of Neurological Disorders and Stroke (NS33184, R01NS033184)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- postsynaptic scaffolds, postsynaptic density, actin cytoskeleton, microtubules, PSD-95, GKAP, CaMKIIα, drebrin, ACTN2, GABAA receptor, gephyrin, glutamatergic synapses, inhibitory synapses, hippocampal pyramidal neurons, latrunculin A, vincristine, detergent extraction, dendritic spines
- MeSH terms
- Disks Large Homolog 4 Protein, Actins, Animals, Cells, Cultured, Evoked Potentials, Hippocampus, Marine Toxins, Membrane Proteins, Microtubules, Nerve Tissue Proteins, Neurons, Synapses, Thiazoles, Vincristine, Octoxynol, Bridged Bicyclo Compounds, Heterocyclic, Excitatory Postsynaptic Potentials, Intracellular Signaling Peptides and Proteins, Rats, Thiazolidines
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