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Developmental regulation of spine motility in the mammalian central nervous system
Open accessAbstract
The function of dendritic spines, postsynaptic sites of excitatory input in the mammalian central nervous system (CNS), is still not well understood. Although changes in spine morphology may mediate synaptic plasticity, the extent of basal spine motility and its regulation and function remains controversial. We investigated spine motility in three principal neurons of the mouse CNS: cerebellar Purkinje cells, and cortical and hippocampal pyramidal neurons. Motility was assayed with time-lapse imaging by using two-photon microscopy of green fluorescent protein-labeled neurons in acute and cultured slices. In all three cell types, dendritic protrusions (filopodia and spines) were highly dynamic, exhibiting a diversity of morphological rearrangements over short (<1-min) time courses. The incidence of spine motility declined during postnatal maturation, but dynamic changes were still apparent in many spines in late-postnatal neurons. Although blockade or induction of neuronal activity did not affect spine motility, disruption of actin polymerization did. We hypothesize that this basal motility of dendritic protrusions is intrinsic to the neuron and underlies the heightened plasticity found in developing CNS.
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“Because spine motility rates decrease during development (Dunaevsky et al., 1999; Majewska and Sur, 2003), this measure is a mark of synapse maturation.”
From Pathogenic SYNGAP1 Mutations Impair Cognitive Development by Disrupting Maturation of Dendritic Spine Synapses (2012) · cites this paper as Dunaevsky et al., 1999
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Cites
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
Axo-somatic and axo-dendritic synapses of the cerebral cortex: an electron microscope study.
Eg, G. (1959) · PubMed · Cited by 1,768
Dendritic spine changes associated with hippocampal long-term synaptic plasticity
Engert, F., & Bonhoeffer, T. (1999) · Nature · doi:10.1038/19978 · Cited by 1,412
Jacobson, M. (1978) · Springer eBooks · doi:10.1007/978-1-4757-4951-9 · Cited by 1,218
Harris, K. M., & Kater, S. B. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.002013 · Cited by 1,020
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
Dendritic spines as basic functional units of neuronal integration
Yuste, R., & Denk, W. (1995) · Nature · doi:10.1038/375682a0 · Cited by 950
Self-citationRapid Actin-Based Plasticity in Dendritic Spines
Fischer, M., Kaech, S., Knutti, D., & Matus, A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80467-5 · Cited by 905
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
Synaptogenesis Via Dendritic Filopodia in Developing Hippocampal Area CA1
Fiala, J. C., Feinberg, M., Popov, V., & Harris, K. M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-21-08900.1998 · Cited by 758
Woolley, C. S., & McEwen, B. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-12-07680.1994 · Cited by 679
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
Allison, D. W., Gelfand, V. I., Spector, I., & Craig, A. M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-07-02423.1998 · Cited by 556
Miniature synaptic events maintain dendritic spines via AMPA receptor activation
McKinney, R. A., Capogna, M., Dürr, R., Gähwiler, B. H., & Thompson, A. S. M. (1999) · Nature Neuroscience · doi:10.1038/4548 · Cited by 523
Eng, H., Lund, K., & Campenot, R. B. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00001.1999 · Cited by 507
Calcium-induced actin depolymerization reduces NMDA channel activity
Rosenmund, C., & Westbrook, G. L. (1993) · Neuron · doi:10.1016/0896-6273(93)90197-y · Cited by 503
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
Diversity Revealed by a Novel Family of Cadherins Expressed in Neurons at a Synaptic Complex
Kohmura, N., Senzaki, K., Hamada, S., Kai, N., Yasuda, R., Watanabe, M., Ishii, H., Yasuda, M., Mishina, M., & Yagi, T. (1998) · Neuron · doi:10.1016/s0896-6273(00)80495-x · Cited by 444
High actin concentrations in brain dendritic spines and postsynaptic densities.
Matus, A., Ackermann, M., Pehling, G., Byers, H. R., & Fujiwara, K. (1982) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.79.23.7590 · Cited by 401
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
Koch, C., & Zador, A. M. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-02-00413.1993 · Cited by 372
Liu, G., Choi, S., & Tsien, R. W. (1999) · Neuron · doi:10.1016/s0896-6273(00)81099-5 · Cited by 356
Destabilization of Cortical Dendrites and Spines by BDNF
Horch, H. W., Krüttgen, A., Portbury, S. D., & Katz, L. C. (1999) · Neuron · doi:10.1016/s0896-6273(00)80785-0 · Cited by 345
Anatomical Correlates of Functional Plasticity in Mouse Visual Cortex
Antonini, A., Fagiolini, M., & Stryker, M. P. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-11-04388.1999 · Cited by 337
A Role for the Cadherin Family of Cell Adhesion Molecules in Hippocampal Long-Term Potentiation
Tang, L., Hung, C. P., & Schuman, E. M. (1998) · Neuron · doi:10.1016/s0896-6273(00)80497-3 · Cited by 335
Morphological analysis of dendritic spine development in primary cultures of hippocampal neurons
Papa, M., Bundman, M. C., Greenberger, V., & Segal, M. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00001.1995 · Cited by 330
Cytoplasmic actin in neuronal processes as a possible mediator of synaptic plasticity.
Fifková, E., & Delay, R. J. (1982) · The Journal of cell biology · doi:10.1083/jcb.95.1.345 · Cited by 309
Yuste, R., Majewska, A. K., Cash, S. S., & Denk, W. T. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-06-01976.1999 · Cited by 288
Self-citationSlices Have More Synapses than Perfusion-Fixed Hippocampus from both Young and Mature Rats
Kirov, S. A., Sorra, K. E., & Harris, K. M. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-08-02876.1999 · Cited by 279
Independent regulation of calcium revealed by imaging dendritic spines
Guthrie, P. B., Segal, M., & Kater, S. B. (1991) · Nature · doi:10.1038/354076a0 · Cited by 262
Cell-cell interactions influence survival and differentiation of purified purkinje cells in vitro
Hatten, C. A. B. E., Blazeski, R., & Mason, C. A. (1994) · Neuron · doi:10.1016/0896-6273(94)90268-2 · Cited by 260
Self-citationCrick, F. (1982) · Trends in Neurosciences · doi:10.1016/0166-2236(82)90020-0 · Cited by 254
Hosokawa, T., Rusakov, D., Bliss, T., & Fine, A. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-08-05560.1995 · Cited by 187
Shimada, A., Mason, C. A., & Morrison, M. E. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-21-08559.1998 · Cited by 165
Self-citationVolatile anesthetics block actin-based motility in dendritic spines
Kaech, S., Brinkhaus, H., & Matus, A. I. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.18.10433 · Cited by 135
Control of spine formation by electrical activity in the adult rat cerebellum
Bravin, M., Morando, L., Vercelli, A., Rossi, F., & Strata, P. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.4.1704 · Cited by 122
Wickens, J. R. (1988) · Progress in Neurobiology · doi:10.1016/0301-0082(88)90013-5 · Cited by 112
A strategy for the analysis of gene expression during neural development.
Arnold, D., Feng, L., Kim, J., & Heintz, N. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.21.9970 · Cited by 63
Persistence of individual dendritic spines in living brain slices.
Hosokawa, T., Bliss, T. V. P., & Fine, A. (1992) · NeuroReport · doi:10.1097/00001756-199206000-00005 · Cited by 33
Flagged first, then by citations
Research works printed but not linked: 2
- R Y Cajal Rev Trimest Histol Norm Pat 1, 1–10 (1888).
- E G Gray J Anat 83, 420–433 (1959).
Cited by
Sorted by citations
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
Morphological Changes in Dendritic Spines Associated with Long-Term Synaptic Plasticity
Yuste, R., & Bonhoeffer, T. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1071 · Cited by 1,269
Self-citationDistinct morphological stages of dentate granule neuron maturation in the adult mouse hippocampus
Zhao, C., Teng, E. M., Summers, R. G., Ming, G.-L., & Gage, F. H. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.3648-05.2006 · Cited by 1,257
Structure and function of dendritic spines
Nimchinsky, E. A., Sabatini, B. L., & Svoboda, K. (2002) · Annual Review of Physiology · doi:10.1146/annurev.physiol.64.081501.160008 · Cited by 1,208
Long-term dendritic spine stability in the adult cortex
Grutzendler, J., Kasthuri, N., & Gan, W.-B. (2002) · Nature · doi:10.1038/nature01276 · Cited by 1,198
Metadata
- Authors
- Dunaevsky, A., Tashiro, A., Majewska, A., Mason, C., & Yuste, R.
- Affiliations
- Columbia University (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1999-11-09
- Volume
- 96
- Issue
- 23
- Pages
- 13438-13443
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC23966
- OpenAlex
- W2156678388
- Cited by
- 412
- References
- 39
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 4 · 2023: 9 · 2022: 10 · 2021: 9 · 2020: 12 · 2019: 8 · 2018: 8 · 2017: 9 · 2016: 9 · 2015: 11 · 2014: 21 · 2013: 12 · 2012: 16
- FWCI
- 7.97
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Columbia Academic Commons (Columbia University)
- Funders
- National Institutes of Health
- National Eye Institute (R01 EY111787)
- National Institute of Neurological Disorders and Stroke (F32NS010370, R01 NS16951, NS10370, R01NS016951)
- National Institute of Environmental Health Sciences (R01ES016951)
- 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 › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- dendritic protrusions, filopodia, postnatal development, synaptic plasticity, Purkinje cells, pyramidal neurons, hippocampal neurons, actin polymerization, neuronal activity, dendritic morphology, central nervous system development
- MeSH terms
- Animals, Brain, Dendrites, Luminescent Proteins, Mice, Inbred C57BL, Green Fluorescent Proteins, Mice
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