The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.
Sleep and waking modulate spine turnover in the adolescent mouse cortex
Open accessAbstract
Cortical development involves synaptic formation and elimination. Although synaptogenesis predominates in the early stages and pruning in the later stages, the two processes are thought to happen concurrently. In adults, synaptic strength is modulated by behavioral state, and we asked whether synaptic remodeling may be affected by sleep and waking states. Using two-photon microscopy in adolescent mice, we found that waking results in a net increase in cortical spines, whereas sleep is associated with net spine loss.
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“In juvenile mice in vivo, two-photon microscopy in the sensorimotor cortex revealed a net decrease in spine growth across periods of sleep, although there was also significant spine growth at the same time (772).”
From About Sleep's Role in Memory (2013) · cites this paper as [772]
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“In adult mice, no similar changes were observed.”
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“The mechanisms mediating synaptic plasticity during critical periods in essential aspects differ from those during later life (838) and differences in the regulation of synaptic plasticity may still exist between juveniles and adults (772).”
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Cites
Why do many psychiatric disorders emerge during adolescence?
Paus, T., Keshavan, M., & Giedd, J. N. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2513 · Cited by 3,123
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Tononi, G., & Cirelli, C. (2006) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2005.05.002 · Cited by 2,151
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
Vyazovskiy, V. V., Olcese, U., Hanlon, E. C., Nir, Y., Cirelli, C., & Tononi, G. (2011) · Nature · doi:10.1038/nature10009 · Cited by 865
Self-citationVyazovskiy, V. V., Cirelli, C., Pfister-Genskow, M., Faraguna, U., & Tononi, G. (2008) · Nature Neuroscience · doi:10.1038/nn2035 · Cited by 837
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(1994) · Progress in Brain Research · doi:10.1016/s0079-6123(08)60543-9 · Cited by 565
Neural activity and the dynamics of central nervous system development
Hua, J. Y., & Smith, S. J. (2004) · Nature Neuroscience · doi:10.1038/nn1218 · Cited by 450
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Bushey, D., Tononi, G., & Cirelli, C. (2011) · Science · doi:10.1126/science.1202839 · Cited by 357
Self-citationDash, M. B., Douglas, C. L., Vyazovskiy, V. V., Cirelli, C., & Tononi, G. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5486-08.2009 · Cited by 286
Self-citationInhibitory synaptogenesis in mouse somatosensory cortex
DeFelipe, J. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.7.619 · Cited by 284
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Brook, J. B. H., Salo, T., Luo, A. C., Bagautdinova, J., Rush, S., Alexander‐Bloch, A. F., Baller, E. B., Calkins, M. E., Cieslak, M., Cooper, E. C., et al. (2026) · Aperture Neuro · doi:10.52294/001c.151820 · Cited by 4
Simayi, R., Santoni, L., Galizia, S., Avvisati, R., Biecher, E., de Vivo, L., & Bellesi, M. (2026) · Communications Biology · doi:10.1038/s42003-026-09666-z
Chen, Y., Li, M., Zhao, Z., Xu, X., Huang, Y., Chen, R., Zhao, R., Wang, G., Jiang, F., & Xu, X. (2026) · Nature Communications · doi:10.1038/s41467-026-70135-6 · Cited by 2
The sleeping brain at work : perceptual processing and learning in human sleep Thomas Andrillon
Andrillon, T. (2016) · theses.fr (ABES) · doi:10.70675/db586b86zc952z428fza153z70690caa929f
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Bochereau, A. (2020) · theses.fr (ABES) · doi:10.70675/8f206effz0c76z40d0z91e6z15ccb174c9f1
Ma, J., Braun, A., Oskamp, A., Kricsfalussy-Hrabár, L., Hermes, N., Djakkani, S., Holz, U., Jakobs, S., Klein, S., Stüsgen, S., et al. (2026) · iScience · doi:10.1016/j.isci.2026.116676
Andrys, N. R. R., Johnson, E. A., Rowe, E. B., Millisor, L. A., McDole, B. K., Baratta, M., Radley, J., & Spencer, R. L. (2026) · Brain Structure and Function · doi:10.1007/s00429-026-03176-8
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Cornford, J. H., Pogodin, R., Ghosh, A., Sheng, K., Bicknell, B. A., Codol, O., Li, P., Clark, B. A., Lajoie, G., & Richards, B. A. (2026) · Neuron · doi:10.1016/j.neuron.2026.08.026
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Metadata
- Authors
- Maret, S., Faraguna, U., Nelson, A. B., Cirelli, C., & Tononi, G.
- Affiliations
- University of Wisconsin–Madison (US)
- Corresponding author
- Cirelli, Chiara
- Tononi, Giulio
- Venue
- Nature Neuroscience
- Published
- 2011-10-09
- Volume
- 14
- Issue
- 11
- Pages
- 1418-1420
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- PMC
- PMC3203346
- OpenAlex
- W2045436209
- Cited by
- 315
- References
- 15
- Citations by year
- 2026: 12 · 2025: 13 · 2024: 19 · 2023: 23 · 2022: 23 · 2021: 14 · 2020: 29 · 2019: 26 · 2018: 16 · 2017: 35 · 2016: 21 · 2015: 15 · 2014: 23 · 2013: 28 · 2012: 16
- FWCI
- 9.00
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- CINECA IRIS Institutial research information system (University of Pisa) (submittedVersion)
- Funders
- National Institutes of Health (DP1OD000579)
- National Institute of Mental Health (R01MH091326)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- synaptic plasticity, sleep, wakefulness, synaptic pruning, synaptogenesis, synaptic remodeling, adolescent brain development, cortical development, behavioral state
- MeSH terms
- Animals, Animals, Newborn, Bacterial Proteins, Cerebral Cortex, Electroencephalography, Electromyography, Luminescent Proteins, Mice, Transgenic, Motor Activity, Neurons, Sleep, Ultrasonography, Wakefulness, Microscopy, Confocal, Dendritic Spines, Mice
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