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Rapid Actin-Based Plasticity in Dendritic Spines
Open accessAbstract
Dendritic spines have been proposed as primary sites of synaptic plasticity in the brain. Consistent with this hypothesis, spines contain high concentrations of actin, suggesting that they might be motile. To investigate this possibility, we made video recordings from hippocampal neurons expressing actin tagged with green fluorescent protein (GFP-actin). This reagent incorporates into actin-containing structures and allows the visualization of actin dynamics in living neurons. In mature neurons, recordings of GFP fluorescence revealed large actin-dependent changes in dendritic spine shape, similar to those inferred from previous studies using fixed tissues. Visible changes occurred within seconds, suggesting that anatomical plasticity at synapses can be extremely rapid. As well as providing a molecular basis for structural plasticity, the presence of motile actin in dendritic spines implicates the postsynaptic element as a primary site of this phenomenon.
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In the citing paper
“A recent study demonstrated that, in cultured hippocampal neurons, actin distribution in spines changes on a time scale of seconds to minutes in a manner that is perturbed by latrunculin A (Fischer et al., 1998).”
From Regulation of F-Actin Stability in Dendritic Spines by Glutamate Receptors and Calcineurin (1998) · cites this paper as Fischer et al., 1998
In the citing paper
“Morphological alterations of dendritic spines have been shown to have profound effects on the efficacy of synaptic transmission43.”
In the citing paper
“The concentrations of latrunculin A and cytochalasins used here (0.01–1 μM) are similar to those that have been shown previously to alter actin filament organization in cultured cells, prevent lamellipodial ruffling in fibroblasts, inhibit motility and retrograde flow in neuronal growth cones, and arrest dendritic spine motility in hippocampal neurons (3, 4, 7, 10).”
From Dynamic actin filaments are required for stable long-term potentiation (LTP) in area CA1 of the hippocampus (2000) · cites this paper as [10]
Citations
Cites
The Fine Structure of the Nervous System.
Tennyson, V. M. (1970) · Archives of Neurology · doi:10.1001/archneur.1970.00480240094019 · Cited by 1,946
Gonadal steroids regulate dendritic spine density in hippocampal pyramidal cells in adulthood
Gould, E., Woolley, C., Frankfurt, M., & McEwen, B. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-04-01286.1990 · Cited by 1,406
Harris, K. M., & Kater, S. B. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.002013 · Cited by 1,020
Dendritic spines as basic functional units of neuronal integration
Yuste, R., & Denk, W. (1995) · Nature · doi:10.1038/375682a0 · Cited by 950
Evidence for a Role of Dendritic Filopodia in Synaptogenesis and Spine Formation
Ziv, N. E., & Smith, S. J. (1996) · Neuron · doi:10.1016/s0896-6273(00)80283-4 · Cited by 882
Forscher, P., & Smith, S. J. (1988) · The Journal of cell biology · doi:10.1083/jcb.107.4.1505 · Cited by 854
fine structure of the nervous system
Peters, A., Palay, S. L., & Webster, H. D. (1976) · Cited by 796
Moser, M., Trommald, M., & Andersen, P. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.26.12673 · Cited by 617
The Dynamics of Dendritic Structure in Developing Hippocampal Slices
Dailey, M. E., & Smith, S. J. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-09-02983.1996 · Cited by 611
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
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Items 101–200 of 895
Actin-Dependent Regulation of Neurotransmitter Release at Central Synapses
Morales, M., Colicos, M. A., & Goda, Y. (2000) · Neuron · doi:10.1016/s0896-6273(00)00064-7 · Cited by 300
Activity-induced targeting of profilin and stabilization of dendritic spine morphology
Ackermann, M., & Matus, A. I. (2003) · Nature Neuroscience · doi:10.1038/nn1135 · Cited by 289
Self-citationMoore, H., West, A. R., & Grace, A. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(99)00078-5 · Cited by 257
Remodeling of Synaptic Actin Induced by Photoconductive Stimulation
Colicos, M. A., Collins, B., Sailor, M. J., & Goda, Y. (2001) · Cell · doi:10.1016/s0092-8674(01)00579-7 · Cited by 275
Development and Regulation of Dendritic Spine Synapses
Calabrese, B., Wilson, M. S., & Halpain, S. (2006) · Physiology · doi:10.1152/physiol.00042.2005 · Cited by 287
Molecular Control of Cortical Dendrite Development
Whitford, K. L., Dijkhuizen, P. A., Polleux, F., & Ghosh, A. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142932 · Cited by 266
Intracellular trafficking pathways and drug delivery: fluorescence imaging of living and fixed cells
Watson, P. (2004) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2004.05.003 · Cited by 270
Maira, S.-M., Galetić, I., Brazil, D. P., Kaech, S., Ingley, E., Thelen, M., & Hemmings, B. A. (2001) · Science · doi:10.1126/science.1062030 · Cited by 264
Self-citationAlleviating catastrophic forgetting using context-dependent gating and synaptic stabilization
Masse, N. Y., Grant, G. D., & Freedman, D. J. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1803839115 · Cited by 278
Boeckers, T. M., Kreutz, M. R., Winter, C., Zuschratter, W., Smalla, K.-H., Sanmarti-Vila, L., Wex, H., Langnaese, K., Bockmann, J., Garner, C. C., et al. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-15-06506.1999 · Cited by 257
Continual remodeling of postsynaptic density and its regulation by synaptic activity
Okabe, S., Kim, H., Miwa, A., Kuriu, T., & Okado, H. (1999) · Nature Neuroscience · doi:10.1038/12175 · Cited by 257
Portera-Cailliau, C., Pan, D. T., & Yuste, R. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-18-07129.2003 · Cited by 269
Tashiro, A., & Yuste, R. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.04.001 · Cited by 265
Johansson, B. B., & Belichenko, P. V. (2002) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200201000-00011 · Cited by 253
Stability of dendritic spines and synaptic contacts is controlled by αN-catenin
Abe, K., Chisaka, O., Roy, F. M. V., & Takeichi, M. (2004) · Nature Neuroscience · doi:10.1038/nn1212 · Cited by 262
Motile Properties of Vimentin Intermediate Filament Networks in Living Cells
Yoon, M., Moir, R. D., Prahlad, V., & Goldman, R. D. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.143.1.147 · Cited by 252
Majewska, A., Brown, E., Ross, J., & Yuste, R. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-05-01722.2000 · Cited by 248
Remodeling of Synaptic Structure in Sensory Cortical AreasIn Vivo
Majewska, A. K., Newton, J. R., & Sur, M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4454-05.2006 · Cited by 258
Lang, C., Barco, A., Zablow, L., Kandel, E. R., Siegelbaum, S. A., & Zakharenko, S. S. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407581101 · Cited by 245
Remodeling of Synaptic Membranes after Induction of Long-Term Potentiation
Toni, N., Buchs, P.-A., Nikonenko, I., Povilaitite, P., Parisi, L., & Muller, D. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-16-06245.2001 · Cited by 244
McDonald, D., Carrero, G., Andrin, C., de Vries, G., & Hendzel, M. J. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200507101 · Cited by 243
Wong, W. T., Faulkner-Jones, B. E., Sanes, J. R., & Wong, R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-13-05024.2000 · Cited by 242
Form follows function: BDNF and its involvement in sculpting the function and structure of synapses
Zagrebelsky, M., & Korte, M. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.05.029 · Cited by 241
Lin, Y., & Koleske, A. J. (2010) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-153204 · Cited by 255
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
Wegner, A. M., Nebhan, C. A., Hu, L., Majumdar, D., Meier, K. M., Weaver, A. M., & Webb, D. J. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m801555200 · Cited by 241
Contribution of cytoskeleton to the internalization of AMPA receptors
Zhou, Q., Xiao, M., & Nicoll, R. A. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.3.1261 · Cited by 233
Hill, J. J., Hashimoto, T., & Lewis, D. A. (2006) · Molecular Psychiatry · doi:10.1038/sj.mp.4001792 · Cited by 228
Saneyoshi, T., Wayman, G. A., Fortin, D. A., Davare, M. A., Hoshi, N., Nozaki, N., Natsume, T., & Soderling, T. R. (2008) · Neuron · doi:10.1016/j.neuron.2007.11.016 · Cited by 234
Molecular anatomy of the postsynaptic density.
Okabe, S. (2007) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2007.01.006 · Cited by 225
Dendritic Spine Plasticity: Function and Mechanisms
Runge, K., Cardoso, C., & de Chevigny, A. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00036 · Cited by 248
Integrin-driven actin polymerization consolidates long-term potentiation
Kramár, E. A., Lin, B., Rex, C. S., Gall, C. M., & Lynch, G. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601354103 · Cited by 221
GluR1 Links Structural and Functional Plasticity at Excitatory Synapses
Kopec, C. D., Réal, É., Kessels, H. W. H. G., & Malinow, R. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3503-07.2007 · Cited by 226
Gao, X., Deng, P., Xu, Z. C., & Chen, J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0024566 · Cited by 218
A quantitative overview of biophysical forces impinging on neural function
Mueller, J. K., & Tyler, W. J. (2014) · Physical Biology · doi:10.1088/1478-3975/11/5/051001 · Cited by 225
KIF17 Dynamics and Regulation of NR2B Trafficking in Hippocampal Neurons
Guillaud, L., Setou, M., & Hirokawa, N. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00131.2003 · Cited by 218
Regulation of NMDA Receptors by Neuregulin Signaling in Prefrontal Cortex
Gu, Z., Jiang, Q., Fu, A. K. Y., Ip, N. Y., & Yan, Z. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1086-05.2005 · Cited by 220
Synapse formation is regulated by the signaling adaptor GIT1
Zhang, H., Webb, D. J., Asmussen, H., & Horwitz, A. F. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200211002 · Cited by 216
Primary support cultures of hippocampal and substantia nigra neurons
Fath, T., Ke, Y. D., Gunning, P. W., Götz, J., & Ittner, L. M. (2008) · Nature Protocols · doi:10.1038/nprot.2008.199 · Cited by 210
Eom, T., Antar, L. N., Singer, R. H., & Bassell, G. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-32-10433.2003 · Cited by 210
Hasbani, M. J., Schlief, M. L., Fisher, D. A., & Goldberg, M. P. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-07-02393.2001 · Cited by 208
Cortical area and species differences in dendritic spine morphology
Benavides-Piccione, R., Ballesteros-Yáñez, I., DeFelipe, J., & Yuste, R. (2002) · Journal of Neurocytology · doi:10.1023/a:1024134312173 · Cited by 207
Kuriu, T., Inoue, A., Bito, H., Sobue, K., & Okabe, S. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0522-06.2006 · Cited by 219
Enhanced learning after genetic overexpression of a brain growth protein
Routtenberg, A., Cantallops, I., Zaffuto, S., Serrano, P. A., & Namgung, U. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.13.7657 · Cited by 204
Direct Observations of the Mechanical Behaviors of the Cytoskeleton in Living Fibroblasts
Heidemann, S. R., Kaech, S., Buxbaum, R. E., & Matus, A. I. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.145.1.109 · Cited by 204
Self-citationMajewska, A. K., & Sur, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2636949100 · Cited by 207
Localization and translation of mRNA in dentrites and axons
Job, C., & Eberwine, J. (2001) · Nature Reviews Neuroscience · doi:10.1038/35104069 · Cited by 202
Hayashi, K., & Shirao, T. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-10-03918.1999 · Cited by 202
Shaping excitation at glutamatergic synapses
Conti, F., & Weinberg, R. J. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(99)01445-9 · Cited by 203
Regulation of Spine Calcium Dynamics by Rapid Spine Motility
Majewska, A. K., Tashiro, A., & Yuste, R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-22-08262.2000 · Cited by 208
Konradi, C. L., & Heckers, S. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01267-7 · Cited by 201
Ramkumar, A., Jong, B. Y., & Ori-McKenney, K. M. (2017) · Developmental Dynamics · doi:10.1002/dvdy.24599 · Cited by 208
Structural and functional plasticity of dendritic spines – root or result of behavior?
Gipson, C. D., & Olive, M. F. (2016) · Genes Brain & Behavior · doi:10.1111/gbb.12324 · Cited by 214
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
Molecular mechanisms of CaMKII activation in neuronal plasticity
Fink, C. (2002) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(02)00327-6 · Cited by 191
Dendritic pathology in mental retardation: from molecular genetics to neurobiology
Dierssen, M., & Ramakers, G. J. A. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00224.x · Cited by 191
Dendrites are more spiny on mature hippocampal neurons when synapses are inactivated
Kirov, S. A., & Harris, K. M. (1999) · Nature Neuroscience · doi:10.1038/13178 · Cited by 194
Arendt, T. (2003) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2003.09.007 · Cited by 189
Essential Role for the PKC Target MARCKS in Maintaining Dendritic Spine Morphology
Calabrese, B., & Halpain, S. (2005) · Neuron · doi:10.1016/j.neuron.2005.08.027 · Cited by 187
Korkotian, E., & Segal, M. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.21.12068 · Cited by 186
Increase in Neurite Outgrowth Mediated by Overexpression of Actin Depolymerizing Factor
Meberg, P. J., & Bamburg, J. R. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02459.2000 · Cited by 185
Synaptopodin Regulates Plasticity of Dendritic Spines in Hippocampal Neurons
Vlachos, A., Korkotian, E., Schoenfeld, E., Copanaki, E., Deller, T., & Segal, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5528-08.2009 · Cited by 181
Theta Stimulation Polymerizes Actin in Dendritic Spines of Hippocampus
Lin, B., Kramár, E. A., Bi, X., Brücher, F., Gall, C. M., & LYNCH, G. S. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4283-04.2005 · Cited by 187
Electrical compartmentalization in dendritic spines
Yuste, R. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150455 · Cited by 180
A Critical Role for Myosin IIB in Dendritic Spine Morphology and Synaptic Function
Ryu, J., Liu, L., Wong, T. P., Wu, D., Burette, A., Weinberg, R. J., Wang, Y. T., & Sheng, M. (2006) · Neuron · doi:10.1016/j.neuron.2005.12.017 · Cited by 179
Spine dynamics in the brain, mental disorders and artificial neural networks
Kasai, H., Ziv, N. E., Okazaki, H., Yagishita, S., & Toyoizumi, T. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00467-3 · Cited by 184
Regulation of spine morphology and spine density by NMDA receptor signaling in vivo
Ultanir, S. K., Kim, J.-E., Hall, B. J., Deerinck, T., Ellisman, M., & Ghosh, A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704031104 · Cited by 187
Leptin promotes rapid dynamic changes in hippocampal dendritic morphology
O’Malley, D., MacDonald, N., Mizielinska, S., Connolly, C. N., Irving, A. J., & Harvey, J. (2007) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2007.05.001 · Cited by 186
Cougot, N., Bhattacharyya, S. N., Tapia-Arancibia, L., Bordonné, R., Filipowicz, W., Bertrand, E., & Rage, F. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4155-08.2008 · Cited by 185
Listeria monocytogenes Exploits Normal Host Cell Processes to Spread from Cell to Cell✪
Robbins, J. R., Barth, A. I. M., Marquis, H., de Hostos, E. L., Nelson, W. J., & Theriot, J. A. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.146.6.1333 · Cited by 172
Synaptic contact dynamics controlled by cadherin and catenins
Takeichi, M., & Abe, K. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.02.002 · Cited by 176
Actin and the agile spine: How and why do dendritic spines dance?
Halpain, S. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01576-9 · Cited by 169
Coyle, I. P., Koh, Y.-H., Lee, W.-C. M., Slind, J. K., Fergestad, T., Littleton, J. T., & Ganetzky, B. (2004) · Neuron · doi:10.1016/s0896-6273(04)00016-9 · Cited by 168
Shi, Y., Pontrello, C. G., DeFea, K., Reichardt, L. F., & Ethell, I. M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4681-08.2009 · Cited by 171
Woodring, P. J., Litwack, E. D., O’Leary, D. D. M., Lucero, G. R., Wang, J. Y. J., & Hunter, T. R. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200110014 · Cited by 164
Postsynaptic filopodia in muscle cells interact with innervating motoneuron axons
Ritzenthaler, S., Suzuki, E., & CHIBA, A. (2000) · Nature Neuroscience · doi:10.1038/79833 · Cited by 163
Ephrin regulation of synapse formation, function and plasticity
Hruska, M., & Dalva, M. B. (2012) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2012.03.004 · Cited by 174
Bidirectional Regulation of Hippocampal Mossy Fiber Filopodial Motility by Kainate Receptors
Tashiro, A., Dunaevsky, A., Blazeski, R., Mason, C. A., & Yuste, R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00299-x · Cited by 165
Glutamate induces the rapid formation of spine head protrusions in hippocampal slice cultures
Richards, D. A., Mateos, J. M., Hugel, S., de Paola, V., Caroni, P., Gähwiler, B. H., & McKinney, R. A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501881102 · Cited by 161
Calcium regulation of actin dynamics in dendritic spines
Oertner, T. G., & Matus, A. I. (2005) · Cell Calcium · doi:10.1016/j.ceca.2005.01.016 · Cited by 164
Self-citationIntegrated technology for evaluation of brain function and neural plasticity
Rossini, P. M., & Forno, G. D. (2004) · Physical Medicine and Rehabilitation Clinics of North America · doi:10.1016/s1047-9651(03)00124-4 · Cited by 160
A Molecular Clutch between the Actin Flow and N-Cadherin Adhesions Drives Growth Cone Migration
Bard, L., Boscher, C., Lambert, M., Mège, R., Choquet, D., & Thoumine, O. R. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5331-07.2008 · Cited by 156
AMPA receptors as drug targets in neurological disease—advantages, caveats, and future outlook
Chang, P. K. ‐., Verbich, D., & McKinney, R. A. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08165.x · Cited by 155
Filopodia, spines, and the generation of synaptic diversity
Jontes, J. D., & Smith, S. J. (2000) · Neuron · doi:10.1016/s0896-6273(00)00003-9 · Cited by 184
Brain plasticity in health and disease
Johansson, B. B. (2004) · The Keio Journal of Medicine · doi:10.2302/kjm.53.231 · Cited by 158
Neuron-Astrocyte Signaling in the Development and Plasticity of Neural Circuits
Stevens, B. (2008) · Neurosignals · doi:10.1159/000123038 · Cited by 153
Sharma, K., Fong, D. K., & Craig, A. M. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.01.010 · Cited by 150
Helmke, B. P., & Davies, P. F. (2002) · Annals of Biomedical Engineering · doi:10.1114/1.1467926 · Cited by 149
Obermair, G. J., Szabó, Z. M., Bourinet, E., & Flucher, B. E. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2004.03272.x · Cited by 149
C9ORF72 interaction with cofilin modulates actin dynamics in motor neurons
Sivadasan, R., Hornburg, D., Drepper, C., Frank, N., Jablonka, S., Hansel, A., Lojewski, X., Sterneckert, J. L., Hermann, A., Shaw, P. J., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4407 · Cited by 155
Actin cytoskeleton organization in response to integrin-mediated adhesion
Defilippi, P., Olivo, C., Venturino, M., Dolce, L., Silengo, L., & Tarone, G. (1999) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(19991001)47:1 · Cited by 164
Presynaptic Remodeling Contributes to Activity-Dependent Synaptogenesis
Nikonenko, I., Jourdain, P., & Müller, D. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-24-08498.2003 · Cited by 149
Neural mechanisms of attending to items in working memory
Manohar, S., Zokaei, N., Fallon, S. J., Vogels, T. P., & Husain, M. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.03.017 · Cited by 156
Chazeau, A., Mehidi, A., Nair, D. K., Gautier, J. J., Leduc, C., Chamma, I., Kage, F., Kechkar, A., Thoumine, O. R., Rottner, K., et al. (2014) · The EMBO Journal · doi:10.15252/embj.201488837 · Cited by 147
Phosphoinositide-3-Kinase Activation Controls Synaptogenesis and Spinogenesis in Hippocampal Neurons
Cuesto, G., Enríquez-Barreto, L., Caramés, C., Cantarero, M., Gasull, X., Sandi, C., Ferrús, A., Acebes, Á., & Morales, M. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4477-10.2011 · Cited by 142
Glutamate regulates actin-based motility in axonal filopodia
Chang, S., & Camilli, P. V. D. (2001) · Nature Neuroscience · doi:10.1038/90489 · Cited by 141
Regulation of Synaptic Structure by Ubiquitin C-Terminal Hydrolase L1
Cartier, A. E., Djakovic, S. N., Salehi, A., Wilson, S. M., Masliah, E., & Patrick, G. N. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1817-09.2009 · Cited by 141
Insights into Rapid Modulation of Neuroplasticity by Brain Estrogens
Srivastava, D. P., Woolfrey, K. M., & Penzes, P. (2013) · Pharmacological Reviews · doi:10.1124/pr.111.005272 · Cited by 146
Ma, X., Huang, J., Wang, Y., Eipper, B. A., & Mains, R. E. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-33-10593.2003 · Cited by 142
Jin, X., Hu, H., Mathers, P. H., & Agmon, A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-13-05662.2003 · Cited by 137
Metadata
- Authors
- Fischer, M., Kaech, S., Knutti, D., & Matus, A.
- Affiliations
- Friedrich Miescher Institute (CH)
- Corresponding author
- Matus, Andrew
- ORCID
- Kaech, Stefanie
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 1998-05
- Volume
- 20
- Issue
- 5
- Pages
- 847-854
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2111916392
- Cited by
- 905
- References
- 40
- Citations by year
- 2026: 4 · 2025: 7 · 2024: 5 · 2023: 12 · 2022: 16 · 2021: 21 · 2020: 18 · 2019: 17 · 2018: 22 · 2017: 17 · 2016: 33 · 2015: 28 · 2014: 31 · 2013: 30 · 2012: 34
- FWCI
- 20.16
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- 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
- dendritic spines, actin dynamics, synaptic plasticity, structural plasticity, hippocampal neurons, spine motility, postsynaptic elements
- MeSH terms
- Actins, Animals, Cell Line, Dendrites, Fibroblasts, Hippocampus, Indicators and Reagents, Luminescent Proteins, Neuronal Plasticity, Neurons, Synapses, Thiazoles, Cytochalasin D, Microscopy, Video, Bridged Bicyclo Compounds, Heterocyclic, Nucleic Acid Synthesis Inhibitors, Cell Size, Green Fluorescent Proteins, Rats, Thiazolidines
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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.
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