The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.
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.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“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
Cited by
Sorted by citations
Items 301–400 of 895
Postsynaptic actin and neuronal plasticity
Matus, A. I. (1999) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)00018-5 · Cited by 84
Self-citationNOS1AP associates with Scribble and regulates dendritic spine development
Richier, L., Williton, K., Clattenburg, L., Colwill, K., O'Brien, M., Tsang, C., Kolar, A., Zinck, N., Metalnikov, P., Trimble, W. S., et al. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3726-09.2010 · Cited by 81
Okamoto, P. M., Gamby, C., Wells, D. G., Fallon, J. R., & Vallee, R. B. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m104927200 · Cited by 81
Frick, K., Fernandez, S., Bennett, J. C., Prange‐Kiel, J., MacLusky, N., & Léránth, C. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2004.03427.x · Cited by 92
The AMPA Receptor Subunit GluR1 Regulates Dendritic Architecture of Motor Neurons
Inglis, F. M., Crockett, R., Korada, S., Abraham, W. C., Hollmann, M., & Kalb, R. G. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-18-08042.2002 · Cited by 82
ROCK1 and ROCK2 inhibition alters dendritic spine morphology in hippocampal neurons
Swanger, S. A., Mattheyses, A. L., Gentry, E. G., & Herskowitz, J. H. (2015) · Cellular Logistics · doi:10.1080/21592799.2015.1133266 · Cited by 81
The role of drebrin in dendritic spines
Koganezawa, N., Hanamura, K., Sekino, Y., & Shirao, T. (2017) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2017.01.004 · Cited by 80
Development of the outer retina in the mouse
Sharma, R., O’Leary, T. E., Fields, C., & Johnson, D. A. (2003) · Developmental Brain Research · doi:10.1016/s0165-3806(03)00217-7 · Cited by 80
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
Chakravarthy, S., Saiepour, M. H., Bence, M., Perry, S., Hartman, R., Couey, J. J., Mansvelder, H. D., & Levelt, C. N. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506305103 · Cited by 80
DendritesPreprint
Jan, Y. N., & Jan, L. Y. (2001) · Genes & Development · doi:10.1101/gad.916501 · Cited by 82
The new nanophysiology: regulation of ionic flow in neuronal subcompartments
Holcman, D., & Yuste, R. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn4022 · Cited by 78
The discovery of dendritic spines by Cajal in 1888 and its relevance in the present neuroscience
García-López, P., García‐Marín, V., & Freire, M. (2007) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2007.06.002 · Cited by 83
Burianek, L. E., & Soderling, S. H. (2013) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2012.12.005 · Cited by 83
The calcium sensor Copine-6 regulates spine structural plasticity and learning and memory
Reinhard, J. R., Kriz, A., Galic, M., Angliker, N., Rajalu, M., Vogt, K. E., & Rüegg, M. A. (2016) · Nature Communications · doi:10.1038/ncomms11613 · Cited by 77
Control of dendritic spine morphological and functional plasticity by small GTPases.
Woolfrey, K. M., & Srivastava, D. P. (2016) · Neural Plasticity · doi:10.1155/2016/3025948 · Cited by 76
Molecular Mechanisms of Psychostimulant-induced Structural Plasticity
Dietz, D., Dietz, K. C., Nestler, E. J., & Russo, S. J. (2009) · Pharmacopsychiatry · doi:10.1055/s-0029-1202847 · Cited by 78
Spike-Associated Fast Contraction of Dendritic Spines in Cultured Hippocampal Neurons
Korkotian, E., & Segal, M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00314-2 · Cited by 76
Poon, H. F., Farr, S. A., Banks, W. A., Pierce, W. M. J., Klein, J. B., Morley, J. E., & Butterfield, D. A. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2005.02.020 · Cited by 76
Dynamics and pathology of dendritic spines
Halpain, S., Spencer, K., & Graber, S. (2005) · Progress in Brain Research · doi:10.1016/s0079-6123(04)47003-4 · Cited by 88
Muscle arm development in Caenorhabditis elegans
Dixon, S. J., & Roy, P. J. (2005) · Development · doi:10.1242/dev.01883 · Cited by 75
Shirao, T., & Sekino, Y. (2001) · Neuroscience Research · doi:10.1016/s0168-0102(01)00209-7 · Cited by 75
Glial cells in synaptic plasticity
Todd, K. J., Serrano, A., Lacaille, J., & Robitaille, R. (2006) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2005.12.002 · Cited by 74
Sekino, Y., Tanaka, S., Hanamura, K., Yamazaki, H., Sasagawa, Y., Xue, Y., Hayashi, K., & Shirao, T. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.11.003 · Cited by 74
Gao, X., Smith, G. M., & Chen, J. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2008.10.009 · Cited by 77
Therapeutic Potential of Rho-Kinase Inhibitors in Cardiovascular Diseases
Hirooka, Y., & Shimokawa, H. (2005) · American Journal of Cardiovascular Drugs · doi:10.2165/00129784-200505010-00005 · Cited by 74
Cox, P. R., Fowler, V. M., Xu, B., Sweatt, J. D., Paylor, R. E., & Zoghbi, H. Y. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00025-3 · Cited by 74
Byrne, J. H., LaBar, K. S., LeDoux, J. E., Schafe, G. E., & Thompson, R. F. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397179-1.00020-8 · Cited by 74
Brown, C. E., & Murphy, T. H. (2007) · The Neuroscientist · doi:10.1177/1073858407309854 · Cited by 74
Treccani, G., Ardalan, M., Chen, F., Musazzi, L., Popoli, M., Wegener, G., Nyengaard, J. R., & Müller, H. K. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1613-3 · Cited by 73
Proteomics of the Synapse – A Quantitative Approach to Neuronal Plasticity
Dieterich, D. C., & Kreutz, M. R. (2015) · Molecular & Cellular Proteomics · doi:10.1074/mcp.r115.051482 · Cited by 78
Modulation of dendritic spines in epilepsy: Cellular mechanisms and functional implications
Wong, M. (2005) · Epilepsy & Behavior · doi:10.1016/j.yebeh.2005.08.007 · Cited by 74
Electrical Advantages of Dendritic Spines
Gulledge, A. T., Carnevale, N. T., & Stuart, G. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036007 · Cited by 80
Laube, G., Seidenbecher, C. I., Richter, K., Dieterich, D. C., Hoffmann, B., Landwehr, M., Smalla, K., Winter, C., Böckers, T. M., Wolf, G. L., et al. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2001.1078 · Cited by 72
A role for synaptopodin and the spine apparatus in hippocampal synaptic plasticity
Deller, T., Orth, C. B., Turco, D. D., Vlachos, A., Burbach, G. J., Drakew, A., Chabanis, S., Körte, M., Schwegler, H., Haas, C. A., et al. (2006) · Annals of Anatomy - Anatomischer Anzeiger · doi:10.1016/j.aanat.2006.06.013 · Cited by 71
Quantifying neuronal size: Summing up trees and splitting the branch difference
Brown, K. M., Gillette, T. A., & Ascoli, G. A. (2008) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2008.08.005 · Cited by 74
Calcium from internal stores modifies dendritic spine shape
Harris, K. M. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.22.12213 · Cited by 71
Pathologies of axonal transport in neurodegenerative diseases
Liu, X.-A., Rizzo, V., & Puthanveettil, S. V. (2012) · Translational Neuroscience · doi:10.2478/s13380-012-0044-7 · Cited by 73
The discovery of dendritic spines by Cajal
Yuste, R. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2015.00018 · Cited by 80
Activity-Dependent Actin Remodeling at the Base of Dendritic Spines Promotes Microtubule Entry
Schätzle, P., da Silva, M. E., Tas, R. P., Katrukha, E. A., Hu, H. Y., Wierenga, C. J., Kapitein, L. C., & Hoogenraad, C. C. (2018) · Current Biology · doi:10.1016/j.cub.2018.05.004 · Cited by 70
Folding of large multidomain proteins by partial encapsulation in the chaperonin TRiC/CCT
Rüßmann, F., Stemp, M. J., Mönkemeyer, L., Etchells, S. A., Bracher, A., & Hartl, F. U. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1218836109 · Cited by 69
Neuronal post-stroke plasticity in the adult
Rossini, P. M., & Forno, G. D. (2004) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-2004-00263 · Cited by 71
Imaging High-Resolution Structure of GFP-Expressing Neurons in Neocortex In VivoPreprint
Chen, B. E., Lendvai, B., Nimchinsky, E. A., Burbach, B. J., Fox, K., & Svoboda, K. (2000) · Learning & Memory · doi:10.1101/lm.32700 · Cited by 69
Portera‐Cailliau, C. (2011) · The Neuroscientist · doi:10.1177/1073858410395322 · Cited by 72
Rapid plasticity of dendritic spine: hints to possible functions?
Segal, M. (2001) · Progress in Neurobiology · doi:10.1016/s0301-0082(00)00021-6 · Cited by 68
Frotscher, M. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.10.946 · Cited by 69
Konur, S., & Yuste, R. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.07.005 · Cited by 68
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
Drosophila MICAL regulates myofilament organization and synaptic structure
Beuchle, D., Schwarz, H., Langegger, M., Koch, I., & Aberle, H. (2007) · Mechanisms of Development · doi:10.1016/j.mod.2007.01.006 · Cited by 70
Characterization of dendritic spines in the Drosophila central nervous system
Leiss, F., Koper, E., Hein, I., Fouquet, W., Lindner, J., Sigrist, S. J., & Tavosanis, G. (2009) · Developmental Neurobiology · doi:10.1002/dneu.20699 · Cited by 69
Regulated expression of an actin‐associated protein, synaptopodin, during long‐term potentiation
Yamazaki, M., Matsuo, R., Fukazawa, Y., Ozawa, F., & Inokuchi, K. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00552.x · Cited by 67
Dunn, G., Dobbie, I. M., Monypenny, J., Holt, M., & Zicha, D. (2002) · Journal of Microscopy · doi:10.1046/j.0022-2720.2001.001007.x · Cited by 67
Plasticity of Neuron-Glial Interactions Mediated by Astrocytic EphARs
Nestor, M. W., Mok, L., Tulapurkar, M. E., & Thompson, S. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2442-07.2007 · Cited by 66
de Ven, T. V., VanDongen, H. M. A., & VanDongen, A. M. J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2450-05.2005 · Cited by 66
Jiang, J., Suppiramaniam, V. D., & Wooten, M. W. (2006) · Neurosignals · doi:10.1159/000105517 · Cited by 67
Uemura, T., Mori, T., Kurihara, T., Kawase, S., Koike, R., Satoga, M., Cao, X., Li, X., Yanagawa, T., Sakurai, T., et al. (2016) · Scientific Reports · doi:10.1038/srep35861 · Cited by 65
Konur, S., & Yuste, R. (2004) · Journal of Neurobiology · doi:10.1002/neu.10306 · Cited by 66
Cyfip1 Regulates Presynaptic Activity during Development
Hsiao, K., Harony-Nicolas, H., Buxbaum, J. D., Bozdagi-Gunal, O., & Benson, D. L. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.0511-15.2016 · Cited by 64
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
Book Review: On the Function of Dendritic Spines
Yuste, R., & Majewska, A. K. (2001) · The Neuroscientist · doi:10.1177/107385840100700508 · Cited by 67
β-Pix modulates actin-mediated recruitment of synaptic vesicles to synapses
Sun, Y., & Bamji, S. X. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2359-11.2011 · Cited by 63
Lin, Y., Yeckel, M. F., & Koleske, A. J. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4284-12.2013 · Cited by 64
Dynamic distribution of endoplasmic reticulum in hippocampal neuron dendritic spines
Toresson, H., & Grant, S. G. N. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04342.x · Cited by 64
Ito, K., Hirooka, Y., Kishi, T., Kimura, Y., Kaibuchi, K., Shimokawa, H., & Takeshita, A. (2004) · Hypertension · doi:10.1161/01.hyp.0000114602.82140.a4 · Cited by 63
Petrinovic, M. M., Hourez, R., Aloy, E. M., Dewarrat, G., Gall, D., Weinmann, O., Gaudias, J., Bachmann, L. C., Schiffmann, S. N., Vogt, K. E., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1214255110 · Cited by 62
Essential Role for Synaptopodin in Dendritic Spine Plasticity of the Developing Hippocampus
Zhang, X.-L., Poschel, B., Faul, C., Upreti, C., Stanton, P. K., & Mundel, P. H. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2983-12.2013 · Cited by 62
Nakazawa, T., Kuriu, T., Tezuka, T., Umemori, H., Okabe, S., & Yamamoto, T. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05335.x · Cited by 63
Li, J., Erişir, A., & Cline, H. T. (2011) · Neuron · doi:10.1016/j.neuron.2010.12.022 · Cited by 65
Lankhorst, A. J., Duis, S., ter Laak-Poort, M., Joosten, E. A. J., Hamers, F. P. T., & Gispen, W. H. (1999) · Journal of Neurotrauma · doi:10.1089/neu.1999.16.323 · Cited by 61
Abl Family Nonreceptor Tyrosine Kinases Modulate Short-Term Synaptic Plasticity
Moresco, E. M. Y., Scheetz, A. J., Bornmann, W. G., Koleske, A. J., & Fitzsimonds, R. M. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00892.2002 · Cited by 61
Consciousness, the Brain, and Spacetime Geometry
Hameroff, S. R. (2001) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2001.tb05709.x · Cited by 62
Obermair, G. J., Schlick, B., Biase, V. D., Subramanyam, P., Gebhart, M., Baumgartner, S., & Flucher, B. E. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.044271 · Cited by 61
Orchestration of synaptic plasticity through AKAP signaling complexes
Bauman, A. L., Goehring, A. S., & Scott, J. D. (2003) · Neuropharmacology · doi:10.1016/j.neuropharm.2003.09.016 · Cited by 62
Freeze-frame imaging of synaptic activity using SynTagMA
Pérez‐Alvarez, A., Fearey, B. C., O’Toole, R. J., Yang, W., Arganda‐Carreras, I., Lamothe‐Molina, P. J., Moeyaert, B., Mohr, M. A., Panzera, L. C., Schulze, C., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-16315-4 · Cited by 63
Interactions between drebrin and Ras regulate dendritic spine plasticity
Biou, V., Brinkhaus, H., Malenka, R. C., & Matus, A. I. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06269.x · Cited by 61
Self-citationGrossman, S. D., Futter, M., Snyder, G. L., Allen, P. B., Nairn, A. C., Greengard, P., & Hsieh‐Wilson, L. C. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02491.x · Cited by 62
Kalinichenko, S. G., & Okhotin, V. E. (2004) · Neuroscience and Behavioral Physiology · doi:10.1023/b:neab.0000049648.20702.ad · Cited by 60
Goetze, B., Grunewald, B., Baldassa, S., & Kiebler, M. A. (2004) · Journal of Neurobiology · doi:10.1002/neu.20073 · Cited by 60
Petralia, R. S., Wang, Y., Sans, N., Worley, P. F., Hammer, J. A., & Wenthold, R. J. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01553.x · Cited by 60
Synaptic Clustering of PSD-95 Is Regulated by c-Abl through Tyrosine Phosphorylation
de Arce, K. P., Varela‐Nallar, L., Farias, O., Cifuentes, A., Bull, P., Couch, B. A., Koleske, A. J., Inestrosa, N. C., & Alvarez, A. R. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2024-09.2010 · Cited by 59
Egler, V., Korur, S., Failly, M., Boulay, J., Imber, R., Lino, M. M., & Merlo, A. (2008) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-07-4182 · Cited by 59
Lemke, E. A., & Klingauf, J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2971-05.2005 · Cited by 59
Spolidoro, M., Putignano, E., Munafò, C., Maffei, L., & Pizzorusso, T. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhr158 · Cited by 58
Paralemmin-1, a Modulator of Filopodia Induction Is Required for Spine Maturation
Arstikaitis, P., Gauthier-Campbell, C., Herrera, R. C. G., Huang, K., Levinson, J. N., Murphy, T. H., Kilimann, M. W., Sala, C., Colicos, M. A., & El-Husseini, A. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-08-0802 · Cited by 65
Domain Analysis of the Actin-Binding and Actin-Remodeling Activities of Drebrin
Hayashi, K., Ishikawa, R., Kawai‐Hirai, R., Takagi, T., Taketomi, A., & Shirao, T. (1999) · Experimental Cell Research · doi:10.1006/excr.1999.4663 · Cited by 57
Regulation of Synapse Structure and Function by Distinct Myosin II Motors
Rubio, M. D., Johnson, R. C., Miller, C. A., Huganir, R. L., & Rumbaugh, G. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3294-10.2011 · Cited by 59
Shoji‐Kasai, Y., Ageta, H., Hasegawa, Y., Tsuchida, K., Sugino, H., & Inokuchi, K. (2007) · Journal of Cell Science · doi:10.1242/jcs.012450 · Cited by 59
Presynaptic α 2 δ subunits are key organizers of glutamatergic synapses
Schöpf, C. L., Ablinger, C., Geisler, S. M., Stanika, R. I., Campiglio, M., Kaufmann, W. A., Nimmervoll, B., Schlick, B., Brockhaus, J., Missler, M., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1920827118 · Cited by 60
Oray, S., Majewska, A. K., & Sur, M. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj019 · Cited by 61
Lee, S., Salazar, S. V., Cox, T. O., & Strittmatter, S. M. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.2983-18.2018 · Cited by 55
Mohanan, A. G., Gunasekaran, S., Jacob, R. S., & Omkumar, R. V. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.855752 · Cited by 55
Gomes, G. M., Dalmolin, G. D., Bär, J., Karpova, A., Mello, C. F., Kreutz, M. R., & Rubin, M. A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0099184 · Cited by 58
Wong, G. T.-H., Chang, R. C., & Law, A. C.-K. (2012) · Ageing Research Reviews · doi:10.1016/j.arr.2012.08.004 · Cited by 57
Structural plasticity of hippocampal mossy fiber synapses as revealed by high‐pressure freezing
Zhao, S., Studer, D., Chai, X., Graber, W. A., Brose, N., Nestel, S., Young, C. C., Rodriguez, E., Saetzler, K., & Frotscher, M. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23040 · Cited by 60
Hata, Y., & Takai, Y. (1999) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050445 · Cited by 56
Does bouton morphology optimize axon length?
Anderson, J. C., & Martin, K. A. C. (2001) · Nature Neuroscience · doi:10.1038/nn772 · Cited by 55
Control of spine maturation and pruning through proBDNF synthesized and released in dendrites
Orefice, L. L., Shih, C., Xu, H., Waterhouse, E. G., & Xu, B. (2015) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2015.12.010 · Cited by 56
Splice variants of the CaV1.3 L-type calcium channel regulate dendritic spine morphology
Stanika, R. I., Campiglio, M., Pinggera, A., Lee, A., Striessnig, J., Flucher, B. E., & Obermair, G. J. (2016) · Scientific Reports · doi:10.1038/srep34528 · Cited by 55
Imaging of experience-dependent structural plasticity in the mouse neocortex in vivo
Holtmaat, A. J. D. G., Paola, V. D., Wilbrecht, L., & Knott, G. W. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.04.005 · Cited by 57
Ohnishi, H., Kaneko, Y., Okazawa, H., Miyashita, M., Sato, R., Hayashi, A., Tada, K., Nagata, S., Takahashi, M., & Matozaki, T. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.5173-04.2005 · Cited by 55
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
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