The DOI matches its Crossref record; 53 of the 53 references it cites were found in a registry or an index.
Locally dynamic synaptic learning rules in pyramidal neuron dendrites
Open accessAbstract
Long-term potentiation (LTP) of synaptic transmission underlies aspects of learning and memory. LTP is input-specific at the level of individual synapses, but neural network models predict interactions between plasticity at nearby synapses. Here we show in mouse hippocampal pyramidal cells that LTP at individual synapses reduces the threshold for potentiation at neighbouring synapses. After input-specific LTP induction by two-photon glutamate uncaging or by synaptic stimulation, subthreshold stimuli, which by themselves were too weak to trigger LTP, caused robust LTP and spine enlargement at neighbouring spines. Furthermore, LTP induction broadened the presynaptic-postsynaptic spike interval for spike-timing-dependent LTP within a dendritic neighbourhood. The reduction in the threshold for LTP induction lasted approximately 10 min and spread over approximately 10 microm of dendrite. These local interactions between neighbouring synapses support clustered plasticity models of memory storage and could allow for the binding of behaviourally linked information on the same dendritic branch.
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“In addition, Rho-Rock and Ras-ERK signaling pathways lower the threshold for LTP in neighboring spines (Zhu et al., 2002; Harvey and Svoboda, 2007; Harvey et al., 2008; Lee et al., 2009).”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Harvey and Svoboda, 2007
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“These synapses contain AMPARs, but LTP-inducing stimuli cause a rapid addition of AMPARs to the synapse (246–250).”
From Synaptic memory and CaMKII (2023) · cites this paper as [246]
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“Experiments using this approach to induce NMDAR-dependent LTP have shown that LTP can be induced at a single synapse without causing postsynaptic potentiation or depression of neighboring synapses (Matsuzaki et al. 2004;Harvey and Svoboda 2007; but see Engert and Bonhoeffer 1997).”
From NMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD). (2012) · cites this paper as Harvey and Svoboda 2007
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“Insertion of additional receptors therefore is likely to affect the ultrastructure of the synapse, and in fact, spines associated with synapses that underwent LTP enlarge (Matsuzaki et al. 2004;Harvey and Svoboda 2007;Holtmaat and Svoboda 2009;Kasai et al. 2010).”
From NMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD). (2012) · cites this paper as Harvey and Svoboda 2007
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“Furthermore, two-photon glutamate uncaging experiments on single spines indicate that synapses that already express functional AMPARs can be further enhanced by inducing LTP (246–248).”
From Synaptic memory and CaMKII (2023) · cites this paper as [246]
In the citing paper
“Uncaging glutamate near the tip of a single dendritic spine [single spine glutamate uncaging (SSGU)] results in a coordinated increase in spine volume and enhanced synaptic function lasting for more than an hour (20, 21).”
From Synaptic evidence for the efficacy of spaced learning (2012) · cites this paper as [20]
In the citing paper
“Recent studies have shown that induction of plasticity at a single spine transiently lowers the plasticity threshold at adjacent spines (20).”
From Synaptic evidence for the efficacy of spaced learning (2012) · cites this paper as [20]
In the citing paper
“This form of plasticity shares many properties with Schaffer collateral LTP, including dependence on N-methyl-d-aspartate receptors (NMDARs), Rho GTPase signaling, Ca2+/calmodulin-dependent protein kinase II (CaMKII) phosphorylation, F-actin polymerization and synaptic AMPAR insertion (20–24).”
From Synaptic evidence for the efficacy of spaced learning (2012) · cites this paper as [20]
In the citing paper
“The low success rate in adults was unlikely related to technical issues because we used a strong induction protocol (20) that caused structural plasticity in >80% of young spines (Fig. 3C), a value in good agreement with previous studies (20, 21).”
From Synaptic evidence for the efficacy of spaced learning (2012) · cites this paper as [20]
In the citing paper
“Notably, uncaged glutamate is known from past work to produce robust, NMDAR-dependent excitatory responses at nearly all spines (20, 21) under the conditions used in our experiments.”
From Synaptic evidence for the efficacy of spaced learning (2012) · cites this paper as [20]
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Citations
Cites
Two-photon laser scanning fluorescence microscopy
Denk, W., Strickler, J. H., & Webb, W. W. (1990) · Science · doi:10.1126/science.2321027 · Cited by 9,488
Bi, G.-Q., & Poo, M.-M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-24-10464.1998 · Cited by 4,744
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968
A simple method for organotypic cultures of nervous tissue
Stoppini, L., Buchs, P., & Muller, D. (1991) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(91)90128-m · Cited by 3,096
Imaging Neuronal Subsets in Transgenic Mice Expressing Multiple Spectral Variants of GFP
Feng, G., Mellor, R. H., Bernstein, M., Keller-Peck, C., Nguyen, Q. T., Wallace, M., Nerbonne, J. M., Lichtman, J. W., & Sanes, J. R. (2000) · Neuron · doi:10.1016/s0896-6273(00)00084-2 · Cited by 3,042
Homeostatic plasticity in the developing nervous system
Turrigiano, G. G., & Nelson, S. B. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1327 · Cited by 2,485
Structural basis of long-term potentiation in single dendritic spines
Matsuzaki, M., Honkura, N., Ellis-Davies, G. C. R., & Kasai, H. (2004) · Nature · doi:10.1038/nature02617 · Cited by 2,483
Metaplasticity: the plasticity of synaptic plasticity
Abraham, W. C., & Bear, M. F. (1996) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)80018-x · Cited by 1,833
Synaptic tagging and long-term potentiation
Frey, U., & Morris, R. G. M. (1997) · Nature · doi:10.1038/385533a0 · Cited by 1,736 · cited 3×
“Previous studies have suggested that synaptic plasticity can be influenced by prior neural activity 6,7,11,12,41–43 .”
Matsuzaki, M., Ellis-Davies, G. C. R., Nemoto, T., Miyashita, Y., Iino, M., & Kasai, H. (2001) · Nature Neuroscience · doi:10.1038/nn736 · Cited by 1,563 · cited 1×
“1h), consistent with documented relationships between spine volume, postsynaptic density area and the number of AMPA ( a -amino-3-hydroxy-5-methyl-4- isoxazole propionic acid) receptors in the postsynaptic density 14,23,24 .”
ScanImage: Flexible software for operating laser scanning microscopes
Pologruto, T. A., Sabatini, B. L., & Svoboda, K. (2003) · BioMedical Engineering OnLine · doi:10.1186/1475-925x-2-13 · Cited by 1,300
Self-citationA Requirement for the Intercellular Messenger Nitric Oxide in Long-Term Potentiation
Schuman, E. M., & Madison, D. V. (1991) · Science · doi:10.1126/science.1720572 · Cited by 1,135
Transient and persistent dendritic spines in the neocortex in vivo
Holtmaat, A. J. G. D., Trachtenberg, J. T., Wilbrecht, L., Shepherd, G. M., Zhang, X., Knott, G. W., & Svoboda, K. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.003 · Cited by 1,131
Self-citationSpike Timing-Dependent Plasticity of Neural Circuits
Dan, Y., & Poo, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.007 · Cited by 1,029
Principles of two-photon excitation microscopy and its applications to neuroscience
Svoboda, K., & Yasuda, R. (2006) · Neuron · doi:10.1016/j.neuron.2006.05.019 · Cited by 1,027
Self-citationDendritic spines as basic functional units of neuronal integration
Yuste, R., & Denk, W. (1995) · Nature · doi:10.1038/375682a0 · Cited by 950
Generation of Destabilized Green Fluorescent Protein as a Transcription Reporter
Li, X., Zhao, X., Fang, Y., Jiang, X., Duong, T., Fan, C., Huang, C.-C., & Kain, S. R. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.52.34970 · Cited by 846
Cell Type and Pathway Dependence of Synaptic AMPA Receptor Number and Variability in the Hippocampus
Nusser, Z., Lujan, R., Laube, G., Roberts, J. D. B., Molnar, E., & Somogyi, P. (1998) · Neuron · doi:10.1016/s0896-6273(00)80565-6 · Cited by 804
The Life Cycle of Ca2+ Ions in Dendritic Spines
Sabatini, B. L., Oertner, T. G., & Svoboda, K. (2002) · Neuron · doi:10.1016/s0896-6273(02)00573-1 · Cited by 745
Self-citationMartin, K. C., Casadio, A., Zhu, H., Yaping, E., Rose, J. C., Chen, M., Bailey, C. H., & Kandel, E. R. (1997) · Cell · doi:10.1016/s0092-8674(00)80484-5 · Cited by 740
Different modes of expression of AMPA and NMDA receptors in hippocampal synapses
Takumi, Y., Ramírez-León, V., Laake, P., Rinvik, E., & Ottersen, O. P. (1999) · Nature Neuroscience · doi:10.1038/10172 · Cited by 675
Integrative Properties of Radial Oblique Dendrites in Hippocampal CA1 Pyramidal Neurons
Losonczy, A., & Magee, J. C. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.016 · Cited by 641
Calcium stores regulate the polarity and input specificity of synaptic modification
Nishiyama, M., Hong, K., Mikoshiba, K., Poo, M.-M., & Kato, K. (2000) · Nature · doi:10.1038/35046067 · Cited by 635
Furuta, T., Wang, S. S. ‐., Dantzker, J. L. M., Dore, T. M., Bybee, W. J., Callaway, E. M., Denk, W. T., & Tsien, R. Y. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.4.1193 · Cited by 635
Dendritic spikes as a mechanism for cooperative long-term potentiation
Golding, N. L., Staff, N. P., & Spruston, N. (2002) · Nature · doi:10.1038/nature00854 · Cited by 623
Impact of Active Dendrites and Structural Plasticity on the Memory Capacity of Neural Tissue
Poirazi, P., & Mel, B. W. (2001) · Neuron · doi:10.1016/s0896-6273(01)00252-5 · Cited by 601
Casadio, A., Martin, K. C., Giustetto, M., Zhu, H., Chen, M., Bartsch, D., Bailey, C. H., & Kandel, E. R. (1999) · Cell · doi:10.1016/s0092-8674(00)81653-0 · Cited by 503
Specific long-lasting potentiation of synaptic transmission in hippocampal slices
Andersen, P. N., Sundberg, S. H., Sveen, O., & Wigström, H. (1977) · Nature · doi:10.1038/266736a0 · Cited by 489
Glutamate Receptor Exocytosis and Spine Enlargement during Chemically Induced Long-Term Potentiation
Kopec, C. D., Li, B., Wei, W., Boehm, J., & Malinow, R. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3918-05.2006 · Cited by 486
Dendritic spines as individual neuronal compartments for synaptic Ca2+ responses
Müller, W. S., & Connor, J. A. (1991) · Nature · doi:10.1038/354073a0 · Cited by 479
The Influence of Prior Synaptic Activity on the Induction of Long-Term Potentiation
Huang, Y.-Y., Colino, A., Selig, D. K., & Malenka, R. C. (1992) · Science · doi:10.1126/science.1346729 · Cited by 412
A clustered plasticity model of long-term memory engrams.
Govindarajan, A., Kelleher, R. J., & Tonegawa, S. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1937 · Cited by 355
Conservation of total synaptic weight through balanced synaptic depression and potentiation
Royer, S., & Paré, D. (2003) · Nature · doi:10.1038/nature01530 · Cited by 351
Rapid Redistribution of Synaptic PSD-95 in the Neocortex In Vivo
Gray, N. W., Weimer, R. M., Bureau, I., & Svoboda, K. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040370 · Cited by 350
Self-citationState-Dependent Calcium Signaling in Dendritic Spines of Striatal Medium Spiny Neurons
Carter, A. G., & Sabatini, B. L. (2004) · Neuron · doi:10.1016/j.neuron.2004.10.013 · Cited by 347
Malleability of Spike-Timing-Dependent Plasticity at the CA3–CA1 Synapse
Wittenberg, G. M., & Wang, S. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5388-05.2006 · Cited by 334
Facilitation at single synapses probed with optical quantal analysis
Oertner, T. G., Sabatini, B. L., Nimchinsky, E. A., & Svoboda, K. (2002) · Nature Neuroscience · doi:10.1038/nn867 · Cited by 320
Self-citationNMDA Receptor Subunit-Dependent [Ca2+] Signaling in Individual Hippocampal Dendritic Spines
Sobczyk, A., Scheuß, V., & Svoboda, K. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1221-05.2005 · Cited by 294
Self-citationImaging Calcium Concentration Dynamics in Small Neuronal Compartments
Yasuda, R., Nimchinsky, E. A., Scheuß, V., Pologruto, T. A., Oertner, T. G., Sabatini, B. L., & Svoboda, K. (2004) · Science s STKE · doi:10.1126/stke.2192004pl5 · Cited by 278
Self-citationYasuda, R., Harvey, C. D., Zhong, H., Sobczyk, A., Aelst, L. V., & Svoboda, K. (2006) · Nature Neuroscience · doi:10.1038/nn1635 · Cited by 261
Self-citationSynapse specificity of long-term potentiation breaks down at short distances
Engert, F., & Bonhoeffer, T. (1997) · Nature · doi:10.1038/40870 · Cited by 252
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
Weak before strong: dissociating synaptic tagging and plasticity-factor accounts of late-LTP
Frey, U., & Morris, R. (1998) · Neuropharmacology · doi:10.1016/s0028-3908(98)00040-9 · Cited by 242
Release and sequestration of calcium by ryanodine‐sensitive stores in rat hippocampal neurones
Garaschuk, O., Yaari, Y., & Konnerth, A. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.013bl.x · Cited by 228
The Number of Glutamate Receptors Opened by Synaptic Stimulation in Single Hippocampal Spines
Nimchinsky, E. A., Yasuda, R., Oertner, T. G., & Svoboda, K. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5066-03.2004 · Cited by 219
Self-citationTwo-Photon Imaging in Living Brain Slices
Mainen, Z. F., Maletić‐Savatić, M., Shi, S., Hayashi, Y., Malinow, R., & Svoboda, K. (1999) · Methods · doi:10.1006/meth.1999.0776 · Cited by 175
Self-citationHeterosynaptic metaplasticity in the hippocampus in vivo : A BCM-like modifiable threshold for LTP
Abraham, W. C., Mason‐Parker, S. E., Bear, M. F., Webb, S. V., & Tate, W. P. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.181342098 · Cited by 170
Fonseca, R., Nägerl, U. V., Morris, R., & Bonhoeffer, T. (2004) · Neuron · doi:10.1016/j.neuron.2004.10.033 · Cited by 167
Local Sharing as a Predominant Determinant of Synaptic Matrix Molecular Dynamics
Tsuriel, S., Geva, R., Zamorano, P. L., Dresbach, T., Boeckers, T. M., Gundelfinger, E. D., Garner, C. C., & Ziv, N. E. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040271 · Cited by 164
Priming-Induced Shift in Synaptic Plasticity in the Rat Hippocampus
Wang, H., & Wagner, J. J. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.4.2024 · Cited by 126
Role of intercellular interactions in heterosynaptic long-term depression
Scanziani, M., Malenka, R. C., & Nicoll, R. A. (1996) · Nature · doi:10.1038/380446a0 · Cited by 119
Cooperative LTP can map memory sequences on dendritic branches
Mehta, M. R. (2003) · Trends in Neurosciences · doi:10.1016/j.tins.2003.12.004 · Cited by 72
Competing for MemoryHippocampal LTP under Regimes of Reduced Protein Synthesis
FONSECA, R., NAGERL, U., MORRIS, R., & BONHOEFFER, T. (2004) · Neuron · doi:10.1016/s0896-6273(04)00713-5
Flagged first, then by citations
Research works printed but not linked: 1
- Pologruto, T. A. Imaging neural activity and [Ca2+] with genetically encoded calcium indicators and two-photon excitation laser scanning microscopy. PhD thesis, Harvard Univ. (2004)
Cited by
Sorted by citations
Two‐Photon Absorption and the Design of Two‐Photon Dyes
Pawlicki, M., Collins, H. A., Denning, R. G., & Anderson, H. L. (2009) · Angewandte Chemie International Edition · doi:10.1002/anie.200805257 · Cited by 2,022
Experience-dependent structural synaptic plasticity in the mammalian brain
Holtmaat, A., & Svoboda, K. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2699 · Cited by 1,934
Self-citationNMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD).
Luscher, C., & Malenka, R. C. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005710 · Cited by 1,110
Metaplasticity: tuning synapses and networks for plasticity
Abraham, W. C. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2356 · Cited by 1,166
The subcellular organization of neocortical excitatory connections
Petreanu, L., Mao, T., Sternson, S. M., & Svoboda, K. (2009) · Nature · doi:10.1038/nature07709 · Cited by 1,047
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Metadata
- Authors
- Harvey, C. D., & Svoboda, K.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Svoboda, Karel
- Venue
- Nature
- Published
- 2007-12
- Volume
- 450
- Issue
- 7173
- Pages
- 1195-1200
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3425382
- OpenAlex
- W2118069376
- Cited by
- 625
- References
- 53
- Citations by year
- 2026: 20 · 2025: 22 · 2024: 34 · 2023: 34 · 2022: 22 · 2021: 27 · 2020: 24 · 2019: 31 · 2018: 28 · 2017: 32 · 2016: 36 · 2015: 32 · 2014: 48 · 2013: 43 · 2012: 40
- FWCI
- 15.33
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- long-term potentiation, synaptic plasticity, dendritic plasticity, hippocampal pyramidal neurons, dendritic spines, spike-timing-dependent plasticity, synaptic interactions, glutamate uncaging, memory storage, information integration
- MeSH terms
- Animals, Dendrites, Learning, Models, Neurological, Synapses, Long-Term Potentiation, Pyramidal Cells, Glutamic Acid, Excitatory Postsynaptic Potentials, Mice, In Vitro Techniques
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