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Structural plasticity of dendritic spines
Open accessAbstract
Dendritic spines are small mushroom-like protrusions arising from neurons where most excitatory synapses reside. Their peculiar shape suggests that spines can serve as an autonomous postsynaptic compartment that isolates chemical and electrical signaling. How neuronal activity modifies the morphology of the spine and how these modifications affect synaptic transmission and plasticity are intriguing issues. Indeed, the induction of long-term potentiation (LTP) or depression (LTD) is associated with the enlargement or shrinkage of the spine, respectively. This structural plasticity is mainly controlled by actin filaments, the principal cytoskeletal component of the spine. Here we review the pioneering microscopic studies examining the structural plasticity of spines and propose how changes in actin treadmilling might regulate spine morphology.
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“For example, during spine enlargement, rapid actin polymerization provides the mechanical force required for pushing out the spine membrane (Bosch and Hayashi, 2012).”
From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Bosch and Hayashi, 2012
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“Reliable correlates of LTP are the remodelling and enlargement of postsynaptic dendritic spines, which are small protrusions that are associated with most excitatory synapses43.”
From The right time to learn: Mechanisms and optimization of spaced learning (2016) · cites this paper as [43]
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Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424
Tripartite synapses: glia, the unacknowledged partner
Araque, A., Parpura, V., Sanzgiri, R. P., & Haydon, P. G. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01349-6 · Cited by 2,529
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
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 2×
“[28 ,46 ] employed a two-photon-induced glutamate uncaging technique, which allows the controlled release of glutamate in a very small volume compared with other approaches (such as local glutamate application through pipette or conventional UV-mediated uncaging method).”
BackgroundMethodThe importance of dendritic mitochondria in the morphogenesis and plasticity of spines and synapses
Li, Z., Okamoto, K.-I., Hayashi, Y., & Sheng, M. (2004) · Cell · doi:10.1016/j.cell.2004.11.003 · Cited by 1,498
Self-citationDendritic spine changes associated with hippocampal long-term synaptic plasticity
Engert, F., & Bonhoeffer, T. (1999) · Nature · doi:10.1038/19978 · Cited by 1,412
Harris, K., & Stevens, J. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-08-02982.1989 · Cited by 1,073
Harris, K. M., Jensen, F. E., & Tsao, B. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-07-02685.1992 · Cited by 1,036
Shrinkage of dendritic spines associated with long-term depression of hippocampal synapses
Zhou, Q., Homma, K. J., & Poo, M.-M. (2004) · Neuron · doi:10.1016/j.neuron.2004.11.011 · Cited by 1,025
Rapid Dendritic Morphogenesis in CA1 Hippocampal Dendrites Induced by Synaptic Activity
Maletic-Savatic, M., Malinow, R., & Svoboda, K. (1999) · Science · doi:10.1126/science.283.5409.1923 · Cited by 1,009
The Postsynaptic Architecture of Excitatory Synapses: A More Quantitative View
Sheng, M., & Hoogenraad, C. C. (2007) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.76.060805.160029 · Cited by 1,003
LTP promotes formation of multiple spine synapses between a single axon terminal and a dendrite
Toni, N., Buchs, P.-A., Nikonenko, I., Bron, C. R., & Muller, D. (1999) · Nature · doi:10.1038/46574 · Cited by 949
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
Okamoto, K.-I., Nagai, T., Miyawaki, A., & Hayashi, Y. (2004) · Nature Neuroscience · doi:10.1038/nn1311 · Cited by 854
Self-citationActin-based plasticity in dendritic spines
Matus, A. (2000) · Science · doi:10.1126/science.290.5492.754 · Cited by 815
Actin in dendritic spines: connecting dynamics to function
Hotulainen, P., & Hoogenraad, C. C. (2010) · Journal of Cell Biology · doi:10.1083/jcb.201003008 · Cited by 815
Experience-dependent plasticity of dendritic spines in the developing rat barrel cortex in vivo
Lendvai, B., Stern, E. A., Chen, B., & Svoboda, K. (2000) · Nature · doi:10.1038/35009107 · Cited by 802
Superresolution Imaging of Chemical Synapses in the Brain
Dani, A., Huang, B., Bergan, J. F., Dulac, C. G., & Zhuang, X. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.021 · Cited by 748
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
Bidirectional Activity-Dependent Morphological Plasticity in Hippocampal Neurons
Nägerl, U. V., Eberhorn, N., Cambridge, S. B., & Bonhoeffer, T. (2004) · Neuron · doi:10.1016/j.neuron.2004.11.016 · Cited by 602
Spacek, J., & Harris, K. M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-01-00190.1997 · Cited by 599
Local, persistent activation of Rho GTPases during plasticity of single dendritic spines
Murakoshi, H., Wang, H., & Yasuda, R. (2011) · Nature · doi:10.1038/nature09823 · Cited by 564
Petralia, R. S., Esteban, J. A., Wang, Y. –., Partridge, J. G., Zhao, H. –., Wenthold, R. J., & Malinow, R. (1999) · Nature Neuroscience · doi:10.1038/4532 · Cited by 496
The Subspine Organization of Actin Fibers Regulates the Structure and Plasticity of Dendritic Spines
Honkura, N., Matsuzaki, M., Noguchi, J., Ellis-Davies, G. C. R., & Kasai, H. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.013 · Cited by 490
Rapid turnover of actin in dendritic spines and its regulation by activity
Star, E. N., Kwiatkowski, D. J., & Murthy, V. N. (2002) · Nature Neuroscience · doi:10.1038/nn811 · Cited by 481
Ostroff, L. E., Fiala, J. C., Allwardt, B., & Harris, K. M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00785-7 · Cited by 461
Fifkova´, E., & Harreveld, A. V. (1977) · Journal of Neurocytology · doi:10.1007/bf01261506 · Cited by 452
Formation of Dendritic Spines with GABAergic Synapses Induced by Whisker Stimulation in Adult Mice
Knott, G. W., Quairiaux, C., Genoud, C., & Welker, E. (2002) · Neuron · doi:10.1016/s0896-6273(02)00663-3 · Cited by 438
Spine-Neck Geometry Determines NMDA Receptor-Dependent Ca2+ Signaling in Dendrites
Noguchi, J., Matsuzaki, M., Ellis-Davies, G. C. R., & Kasai, H. (2005) · Neuron · doi:10.1016/j.neuron.2005.03.015 · Cited by 419
Korobova, F., & Svitkina, T. (2010) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-07-0596 · Cited by 399
Dynamics and Regulation of Clathrin Coats at Specialized Endocytic Zones of Dendrites and Spines
Blanpied, T. A., Scott, D. B., & Ehlers, M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00979-0 · Cited by 392
A Role of Actin Filament in Synaptic Transmission and Long-Term Potentiation
Kim, C.-H., & Lisman, J. E. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-11-04314.1999 · Cited by 386
Krucker, T., Siggins, G. R., & Halpain, S. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.100139797 · Cited by 374
Glutamate induces de novo growth of functional spines in developing cortex
Kwon, H.-B., & Sabatini, B. L. (2011) · Nature · doi:10.1038/nature09986 · Cited by 368
The postsynaptic density proteins Homer and Shank form a polymeric network structure
Hayashi, M. K., Tang, C., Verpelli, C., Narayanan, R., Stearns, M. H., Xu, R.-M., Li, H., Sala, C., & Hayashi, Y. (2009) · Cell · doi:10.1016/j.cell.2009.01.050 · Cited by 356
Self-citationNeuronal activity regulates diffusion across the neck of dendritic spines
Bloodgood, B. L., & Sabatini, B. L. (2005) · Science · doi:10.1126/science.1114816 · Cited by 344
ADF/cofilin-mediated actin dynamics regulate AMPA receptor trafficking during synaptic plasticity
Gu, J., Lee, C. W., Fan, Y., Komlos, D., Tang, X., Sun, C., Yu, K., Hartzell, H. C., Chen, G., Bamburg, J. R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2634 · Cited by 344
Okamoto, K.-I., Narayanan, R., Lee, S. H., Murata, K., & Hayashi, Y. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701656104 · Cited by 328
Self-citationSTED Nanoscopy of Actin Dynamics in Synapses Deep Inside Living Brain Slices
Urban, N. T., Willig, K. I., Hell, S. W., & Nägerl, U. V. (2011) · Biophysical Journal · doi:10.1016/j.bpj.2011.07.027 · Cited by 309
Plasticity of perisynaptic astroglia during synaptogenesis in the mature rat hippocampus
Witcher, M. R., Kirov, S. A., & Harris, K. M. (2006) · Glia · doi:10.1002/glia.20415 · Cited by 306
Laminar Organization of the NMDA Receptor Complex within the Postsynaptic Density
Valtschanoff, J. G., & Weinberg, R. J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-04-01211.2001 · Cited by 301
Contributions of dendritic spines and perforated synapses to synaptic plasticity
Calverley, R. K. S., & Jones, D. G. (1990) · Brain Research Reviews · doi:10.1016/0165-0173(90)90002-6 · Cited by 277
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
Lu, J., Helton, T. D., Blanpied, T. A., Rácz, B., Newpher, T. M., Weinberg, R. J., & Ehlers, M. D. (2007) · Neuron · doi:10.1016/j.neuron.2007.06.041 · Cited by 273
Patterson, M. A., Szatmari, E. M., & Yasuda, R. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913875107 · Cited by 259
Yuste, R. (2010) · doi:10.7551/mitpress/9780262013505.001.0001 · Cited by 241
Van Harreveld, A., & Fifkova, E. (1975) · Experimental Neurology · doi:10.1016/0014-4886(75)90055-2 · Cited by 239
Dendritic spine geometry: functional implication and regulation
Hayashi, Y., & Majewska, A. K. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.006 · Cited by 237
Self-citationSpine Expansion and Stabilization Associated with Long-Term Potentiation
Yang, Y., Wang, X.-B., Frerking, M., & Zhou, Q. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.3998-07.2008 · Cited by 222
Okamoto, K., Bosch, M., & Hayashi, Y. (2009) · Physiology · doi:10.1152/physiol.00029.2009 · Cited by 213
Self-citationPetersen, J. D., Chen, X., Vinadé, L., Döṣemeci, A., Lisman, J. E., & Reese, T. S. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-35-11270.2003 · Cited by 212
Changes in the postsynaptic density with long‐term potentiation in the dentate gyrus
Desmond, N. L., & Levy, W. B. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902530405 · Cited by 207
Majewska, A. K., & Sur, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2636949100 · Cited by 207
Desmond, N. L., & Levy, W. B. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902530404 · Cited by 207
Fifkova´, E., & Anderson, C. L. (1981) · Experimental Neurology · doi:10.1016/0014-4886(81)90197-7 · Cited by 195
Hosokawa, T., Rusakov, D., Bliss, T., & Fine, A. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-08-05560.1995 · Cited by 187
Ding, J. B., Takasaki, K. T., & Sabatini, B. L. (2009) · Neuron · doi:10.1016/j.neuron.2009.07.011 · Cited by 177
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
Izeddin, I., Specht, C. G., Lelek, M., Darzacq, X., Triller, A., Zimmer, C., & Dahan, M. (2011) · PLoS ONE · doi:10.1371/journal.pone.0015611 · Cited by 154
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
Optical induction of plasticity at single synapses reveals input-specific accumulation of αCaMKII
Zhang, Y.-P., Holbro, N., & Oertner, T. G. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802940105 · Cited by 140
Bliss, T. V. P., & Lømo, T. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010273 · Cited by 135
Regulation of spine and synapse formation by activity-dependent intracellular signaling pathways
Saneyoshi, T., Fortin, D. A., & Soderling, T. R. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.09.013 · Cited by 133
Fifkov/'a, E. (1985) · Brain Research Reviews · doi:10.1016/0165-0173(85)90012-8 · Cited by 130
Dendritic spines do not split during hippocampal LTP or maturation
Fiala, J. C., Allwardt, B. A., & Harris, K. M. (2002) · Nature Neuroscience · doi:10.1038/nn830 · Cited by 124
Popov, V. I., Davies, H. A., Rogachevsky, V. V., Patrushev, I., Errington, M. L., Gabbott, P. L. A., Bliss, T. V. P., & Stewart, M. G. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.06.029 · Cited by 121
Independent Expression of Synaptic and Morphological Plasticity Associated with Long-Term Depression
Wang, X.-B., Yang, Y., & Zhou, Q. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2015-07.2007 · Cited by 100
The Spine Apparatus, Synaptopodin, and Dendritic Spine Plasticity
Segal, M., Vlachos, A., & Korkotian, E. (2010) · The Neuroscientist · doi:10.1177/1073858409355829 · Cited by 91
Oray, S., Majewska, A. K., & Sur, M. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj019 · Cited by 61
Imaging Living Synapses at the Nanoscale by STED Microscopy
Nägerl, U. V., & Bonhoeffer, T. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0990-10.2010 · Cited by 54
He, K., Lee, A., Song, L., Kanold, P. O., & Lee, H. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00913.2010 · Cited by 43
Rapid turnover of spinules at synaptic terminals
Tao-Cheng, J.-H., Döṣemeci, A., Gallant, P. E., Miller, S., Galbraith, J. A., Winters, C. A., Azzam, R. N., & Reese, T. S. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.02.031 · Cited by 43
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Metadata
- Authors
- Bosch, M., & Hayashi, Y.
- Affiliations
- Massachusetts Institute of Technology (US)
- RIKEN Center for Brain Science (JP)
- Corresponding author
- Hayashi, Yasunori
- Venue
- Current Opinion in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2012-06
- Volume
- 22
- Issue
- 3
- Pages
- 383-388
- ISSN
- 0959-4388 (ISSN-L)
- PMC
- PMC4281347
- OpenAlex
- W1983230142
- Cited by
- 415
- References
- 73
- Citations by year
- 2026: 14 · 2025: 19 · 2024: 22 · 2023: 21 · 2022: 14 · 2021: 37 · 2020: 29 · 2019: 30 · 2018: 39 · 2017: 31 · 2016: 27 · 2015: 38 · 2014: 44 · 2013: 33 · 2012: 15
- FWCI
- 2.79
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Current Opinion in Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- RIKEN
- NIH (R01DA17310)
- 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, structural plasticity, dendritic spine morphology, actin cytoskeleton, actin treadmilling, long-term potentiation, long-term depression, synaptic plasticity, postsynaptic compartment, excitatory synapses
- MeSH terms
- Animals, Models, Biological, Neuronal Plasticity, Neurons, Ultrasonography, Dendritic Spines
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