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Sleep promotes branch-specific formation of dendritic spines after learning
Open accessAbstract
To sleep, perchance to remember: Many researchers believe sleep helps us consolidate our memories, but no one knows quite how. Yang et al. investigated the precise role of sleep in changing mouse brain structures (see the Perspective by Euston and Steenland). When mice learned motor tasks, small protuberances—or “spines”—formed on some of the dendritic branches of specific brain neurons. These spines represent the physical correlate of a memory. But the neurons grew and retained these spines better when the mice slept after learning the task. Neurons that fired during learning fired again during subsequent slow-wave sleep, allowing the mice to conserve the newly formed spines—and memories. Science , this issue p. 1173 ; see also p. 1087
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“(C) Sleep downscaling also entails a reduction of dendritic synaptic spines, with branches involved in prior learning (red) being spared (assessed by two-photon imaging, 164 left).”
From Sleep—A brain-state serving systems memory consolidation (2023) · cites this paper as [164]
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“At the morphological level, there is evidence that synaptic downscaling during sleep is not ubiquitous but may spare some select synapses that are particularly large or were involved in prior encoding, resulting in increased connectivity at these synapses 163,164,228,231 (Figure 2C).”
From Sleep—A brain-state serving systems memory consolidation (2023) · cites this paper as [164]
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“On a morphological level, SWS following motor task training was found to support branch-specific spine formation in a subset of cells in motor cortex.164”
From Sleep—A brain-state serving systems memory consolidation (2023) · cites this paper as [164]
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“Thus, similar to spine formation during learning, also spine formation during post-training SWS only pertained to select dendritic branches of motor cortex pyramidal cells.164”
From Sleep—A brain-state serving systems memory consolidation (2023) · cites this paper as [164]
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Ultrasensitive fluorescent proteins for imaging neuronal activity
Chen, T.-W., Wardill, T. J., Sun, Y., Pulver, S. R., Renninger, S. L., Baohan, A., Schreiter, E. R., Kerr, R. A., Orger, M. B., Jayaraman, V., et al. (2013) · Nature · doi:10.1038/nature12354 · Cited by 6,474
Diekelmann, S., & Born, J. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2762 · Cited by 3,760
Reactivation of hippocampal ensemble memories during sleep
Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118
Sleep-dependent memory consolidation
Stickgold, R. (2005) · Nature · doi:10.1038/nature04286 · Cited by 1,857
Coordinated memory replay in the visual cortex and hippocampus during sleep
Ji, D., & Wilson, M. A. (2007) · Nature Neuroscience · doi:10.1038/nn1825 · Cited by 1,669
Roffwarg, H. P., Muzio, J. N., & Dement, W. C. (1966) · Science · doi:10.1126/science.152.3722.604 · Cited by 1,559
Sleep and synaptic homeostasis: a hypothesis
Tononi, G., & Cirelli, C. (2003) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2003.09.004 · Cited by 1,217
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
Self-citationStably maintained dendritic spines are associated with lifelong memories
Yang, G., Pan, F., & Gan, W.-B. (2009) · Nature · doi:10.1038/nature08577 · Cited by 1,182
Self-citationThe role of sleep in learning and memory
Maquet, P. (2001) · Science · doi:10.1126/science.1062856 · Cited by 1,177
Replay of neuronal firing sequences in rat hippocampus during sleep following spatial experience
Skaggs, W. E., & McNaughton, B. L. (1996) · Science · doi:10.1126/science.271.5257.1870 · Cited by 1,173
Clues to the functions of mammalian sleep
Siegel, J. M. (2005) · Nature · doi:10.1038/nature04285 · Cited by 1,040
Structural Changes Accompanying Memory Storage
Bailey, C. H., & Kandel, E. R. (1993) · Annual Review of Physiology · doi:10.1146/annurev.ph.55.030193.002145 · Cited by 856
Vyazovskiy, V. V., Cirelli, C., Pfister-Genskow, M., Faraguna, U., & Tononi, G. (2008) · Nature Neuroscience · doi:10.1038/nn2035 · Cited by 837
Pavlides, C., & Winson, J. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-08-02907.1989 · Cited by 684
Bursting of Thalamic Neurons and States of Vigilance
Llinás, R. R., & Steriade, M. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00166.2006 · Cited by 682
Ontogenesis of the states of sleep in rat, cat, and guinea pig during the first postnatal month
Jouvet-Mounier, D., Astic, L., & Lacote, D. (1969) · Developmental Psychobiology · doi:10.1002/dev.420020407 · Cited by 571
Sleep Enhances Plasticity in the Developing Visual Cortex
Frank, M. G., Issa, N. P., & Stryker, M. P. (2001) · Neuron · doi:10.1016/s0896-6273(01)00279-3 · Cited by 523
Song replay during sleep and computational rules for sensorimotor vocal learning
Dave, A. S., & Margoliash, D. (2000) · Science · doi:10.1126/science.290.5492.812 · Cited by 458
Thinned-skull cranial window technique for long-term imaging of the cortex in live mice
Yang, G., Pan, F., Parkhurst, C. N., Grutzendler, J., & Gan, W. (2010) · Nature Protocols · doi:10.1038/nprot.2009.222 · Cited by 445
Self-citationThe slow (<1 Hz) rhythm of non-REM sleep: a dialogue between three cardinal oscillators
Crunelli, V., & Hughes, S. W. (2010) · Nature Neuroscience · doi:10.1038/nn.2445 · Cited by 435
Tennant, K. A., Adkins, D. L., Donlan, N. A., Asay, A. L., Thomas, N. J., Kleim, J. A., & Jones, T. A. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq159 · Cited by 419
Synapse elimination and indelible memory
Lichtman, J. W., & Colman, H. (2000) · Neuron · doi:10.1016/s0896-6273(00)80893-4 · Cited by 380
Bhatt, D. H., Zhang, S., & Gan, W.-B. (2009) · Annual Review of Physiology · doi:10.1146/annurev.physiol.010908.163140 · Cited by 380
Self-citationCircadian glucocorticoid oscillations promote learning-dependent synapse formation and maintenance.
Liston, C., Cichon, J. M., Jeanneteau, F., Jia, Z., Chao, M. V., & Gan, W.-B. (2013) · Nature Neuroscience · doi:10.1038/nn.3387 · Cited by 358
Self-citationSleep and Synaptic Homeostasis: Structural Evidence in Drosophila
Bushey, D., Tononi, G., & Cirelli, C. (2011) · Science · doi:10.1126/science.1202839 · Cited by 357
Sleep and waking modulate spine turnover in the adolescent mouse cortex
Maret, S., Faraguna, U., Nelson, A. B., Cirelli, C., & Tononi, G. (2011) · Nature Neuroscience · doi:10.1038/nn.2934 · Cited by 315
Sleep Oscillations in the Thalamocortical System Induce Long-Term Neuronal Plasticity
Chauvette, S., Seigneur, J., & Timofeev, I. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.034 · Cited by 304
Ribeiro, S., Gervasoni, D., Soares, E. S., Zhou, Y., Lin, S.-C., Pantoja, J., Lavine, M., & Nicolelis, M. A. L. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020024 · Cited by 272
Use-Dependent Plasticity in Clock Neurons Regulates Sleep Need in Drosophila
Donlea, J. M., Ramanan, N., & Shaw, P. J. (2009) · Science · doi:10.1126/science.1166657 · Cited by 251
Mechanisms of sleep-dependent consolidation of cortical plasticity
Aton, S. J., Seibt, J., Dumoulin, M., Jha, S. K., Steinmetz, N., Coleman, T., Naidoo, N., & Frank, M. G. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.007 · Cited by 244
Cellular and molecular connections between sleep and synaptic plasticity
Benington, J. H., & Frank, M. G. (2003) · Progress in Neurobiology · doi:10.1016/s0301-0082(03)00018-2 · Cited by 244
Behavioral State Modulation of Auditory Activity in a Vocal Motor System
Dave, A. S., Yu, A. C., & Margoliash, D. (1998) · Science · doi:10.1126/science.282.5397.2250 · Cited by 230
Synaptic plasticity in sleep: learning, homeostasis and disease
Wang, G., Grone, B., Colas, D., Appelbaum, L., & Mourrain, P. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.07.005 · Cited by 172
Protein Synthesis during Sleep Consolidates Cortical Plasticity In Vivo
Seibt, J., Dumoulin, M. C., Aton, S. J., Coleman, T., Watson, A., Naidoo, N., & Frank, M. G. (2012) · Current Biology · doi:10.1016/j.cub.2012.02.016 · Cited by 162
Yang, G., & Gan, W. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20996 · Cited by 131
Self-citationErasing Synapses in Sleep: Is It Time to Be SHY?
Frank, M. G. (2012) · Neural Plasticity · doi:10.1155/2012/264378 · Cited by 117
Sleep to Upscale, Sleep to Downscale: Balancing Homeostasis and Plasticity
Born, J., & Feld, G. B. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.007 · Cited by 73
Neuronal plasticity and thalamocortical sleep and waking oscillations
Timofeev, I. (2011) · Progress in brain research · doi:10.1016/b978-0-444-53839-0.00009-0 · Cited by 44
NREM delta stimulation following MK-801 is a response of sleep systems
Campbell, I. G., & Feinberg, I. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.6.3714 · Cited by 41
Transcranial Two-Photon Imaging of Synaptic Structures in the Cortex of Awake Head-Restrained Mice
Yang, G., Pan, F., Chang, P. C.-Y., Gooden, F., & Gan, W. (2013) · Methods in molecular biology · doi:10.1007/978-1-62703-411-1_3 · Cited by 37
Self-citationActivity of motor cortex neurons during backward locomotion
Zelenin, P. V., Deliagina, T. G., Orlovsky, G. N., Karayannidou, A., Stout, E. E., Sirota, M. G., & Beloozerova, I. N. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00120.2011 · Cited by 28
Differences in gene expression during sleep and wakefulness
Cirelli, C., & Tononi, G. (1999) · Annals of Medicine · doi:10.3109/07853899908998787 · Cited by 26
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Mechanisms of systems memory consolidation during sleep
Klinzing, J. G., Niethard, N., & Born, J. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0467-3 · Cited by 1,176
Synaptic Neurexin Complexes: A Molecular Code for the Logic of Neural Circuits
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Dudai, Y., Karni, A., & Born, J. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.004 · Cited by 741
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Metadata
- Authors
- Yang, G., Lai, C. S. W., Cichon, J., Ma, L., Li, W., & Gan, W.-B.
- Affiliations
- New York University (US)
- Peking University (CN)
- Corresponding author
- Gan, Wen-Biao
- Venue
- Science
- Published
- 2014-06-06
- Volume
- 344
- Issue
- 6188
- Pages
- 1173-1178
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC4447313
- OpenAlex
- W2088321899
- Semantic Scholar
- 0a583ef013a40265cc574b8f97597b48824ef580
- Cited by
- 616
- References
- 43
- Citations by year
- 2026: 31 · 2025: 39 · 2024: 42 · 2023: 37 · 2022: 54 · 2021: 55 · 2020: 63 · 2019: 61 · 2018: 56 · 2017: 63 · 2016: 50 · 2015: 49 · 2014: 14
- FWCI
- 32.73
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- The HKU Scholars Hub (University of Hong Kong) (submittedVersion)
- Funders
- U.S. Department of Agriculture
- Utah State University
- Louisiana State University
- National Institute of Neurological Disorders and Stroke (R01NS047325, P01NS074972)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- sleep, dendritic spines, motor learning, motor cortex, layer 5 pyramidal neurons, synaptogenesis, memory consolidation, NREM sleep
- MeSH terms
- Animals, Female, Learning, Male, Mice, Mutant Strains, Motor Cortex, Sleep, REM, Dendritic Spines, Mice
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