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Critical-Period Plasticity in the Visual Cortex
Open accessAbstract
In many regions of the developing brain, neuronal circuits undergo defined phases of enhanced plasticity, termed critical periods. Work in the rodent visual cortex has led to important insights into the cellular and molecular mechanisms regulating the timing of the critical period. Although there is little doubt that the maturation of specific inhibitory circuits plays a key role in the opening of the critical period in the visual cortex, it is less clear what puts an end to it. In this review, we describe the established mechanisms and point out where more experimental work is needed. We also show that plasticity in the visual cortex is present well before, and long after, the peak of the critical period.
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“It is now well established, largely from studies in rodent primary visual cortex, that the maturation of GABAergic inhibition mediated by a fast-spiking PV interneuron network is a crucial mechanism for triggering the onset and regulating the progression of the critical period for functional wiring in V1 (16,46).”
From MeCP2 regulates the timing of critical period plasticity that shapes functional connectivity in primary visual cortex (2015) · cites this paper as [46]
In the citing paper
“After eye opening, visual experience further refines and elaborates circuits that are critical for normal visual function.”
From Role of emergent neural activity in visual map development (2014) · cites this paper as [7]
In the citing paper
“Though visual experience has a clear role in directing the refinement of synaptic connectivity [7]”
From Role of emergent neural activity in visual map development (2014) · cites this paper as [7]
Citations
Cites
Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex
Hubel, D. H., & Wiesel, T. N. (1962) · The Journal of Physiology · doi:10.1113/jphysiol.1962.sp006837 · Cited by 13,680
The period of susceptibility to the physiological effects of unilateral eye closure in kittens
Hubel, D. H., & Wiesel, T. N. (1970) · The Journal of Physiology · doi:10.1113/jphysiol.1970.sp009022 · Cited by 3,030
Model of autism: increased ratio of excitation/inhibition in key neural systems
Rubenstein, J. L. R., & Merzenich, M. M. (2003) · Genes, Brain and Behavior · doi:10.1034/j.1601-183x.2003.00037.x · Cited by 2,768
SINGLE-CELL RESPONSES IN STRIATE CORTEX OF KITTENS DEPRIVED OF VISION IN ONE EYE
Wiesel, T. N., & Hubel, D. H. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.1003 · Cited by 2,628
Driving fast-spiking cells induces gamma rhythm and controls sensory responses
Cardin, J. A., Carlén, M., Meletis, K., Knoblich, U., Zhang, F., Deisseroth, K., Tsai, L.-H., & Moore, C. I. (2009) · Nature · doi:10.1038/nature08002 · Cited by 2,603
Neocortical excitation/inhibition balance in information processing and social dysfunction
Yizhar, O., Fenno, L. E., Prigge, M., Schneider, F., Davidson, T. J., O’Shea, D. J., Sohal, V. S., Goshen, I., Finkelstein, J., Paz, J. T., et al. (2011) · Nature · doi:10.1038/nature10360 · Cited by 2,454
Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators
Tian, L., Hires, S. A., Mao, T., Huber, D., Chiappe, M. E., Chalasani, S. H., Petreanu, L., Akerboom, J., McKinney, S. A., Schreiter, E. R., et al. (2009) · Nature Methods · doi:10.1038/nmeth.1398 · Cited by 1,967
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
The development and application of optogenetics
Fenno, L., Yizhar, O., & Deisseroth, K. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113817 · Cited by 1,822
Reactivation of Ocular Dominance Plasticity in the Adult Visual Cortex
Pizzorusso, T., Medini, P., Berardi, N., Chierzi, S., Fawcett, J. W., & Maffei, L. (2002) · Science · doi:10.1126/science.1072699 · Cited by 1,679
Research works printed but not linked: 4
- Heinroth O. 1910. Beiträge zur Biologie, namentlich Ethologie und Psychologie der Anatiden. In Verhandlungen des V. Internationalen Ornitologen-Kongresses, Berlin , ed. H Schalow, pp. 589–702. Berlin: Deutsche Ornithologische Gesellschaft
- Joliot AH, 1991, New Biol., 3, 1121
- Nottebohm F, 1978, Serinus canarius, 46, 298
- Van LC, 1996, Gene Expr., 5, 245
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Lau, B. Y. B., Krishnan, K., Huang, Z. J., & Shea, S. D. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1964-19.2019 · Cited by 42
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Steinmetz, J. D., Sapp, R. W., Brott, B. K., Lee, H., Miyamichi, K., Luo, L., Cheng, S., Djurisic, M. R., & Shatz, C. J. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu243 · Cited by 38
Yuan, T., & Bellone, C. (2013) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2013.04.056 · Cited by 38
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Nogo Receptor 1 Confines a Disinhibitory Microcircuit to the Critical Period in Visual Cortex
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Lu, J., Tucciarone, J., Lin, Y., & Huang, Z. J. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1400694111 · Cited by 35
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Chen, C., Ma, X., Wei, J., Shakir, N., Zhang, J. K., Zhang, L., Nehme, A., Cui, Y., Ferguson, D., Bai, F., et al. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-02132-4 · Cited by 32
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Xu, X., Hanganu‐Opatz, I. L., & Bieler, M. (2020) · Frontiers in Neurorobotics · doi:10.3389/fnbot.2020.00007 · Cited by 30
Akol, I., Kalogeraki, E., Pielecka-Fortuna, J., Fricke, M., & Löwel, S. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0902-21.2021 · Cited by 29
Greifzu, F., Kalogeraki, E., & Löwel, S. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.02.014 · Cited by 28
Strettoi, E., Marco, B. D., Orsini, N., & Napoli, D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031138 · Cited by 28
Glial regulation of critical period plasticity
Starkey, J., Horstick, E. J., & Ackerman, S. D. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1247335 · Cited by 31
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Sieben, K., Bieler, M., Röder, B., & Hanganu‐Opatz, I. L. (2015) · PLoS Biology · doi:10.1371/journal.pbio.1002304 · Cited by 28
Li, X., Wu, X., Lu, T., Kuang, C., Si, Y., Zheng, W., Li, Z., & Xue, Y.-X. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25063412 · Cited by 28
Liu, L., Zhang, Y., Men, S., Li, X., Hou, S., & Ju, J. (2023) · Hippocampus · doi:10.1002/hipo.23503 · Cited by 27
Perineuronal net, CSPG receptor and their regulation of neural plasticity.
Miao, Q., Ye, Q., & Zhang, X.-H. (2014) · PubMed · Cited by 27
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Park, S., Haak, K. V., Cho, H. B., Valk, S. L., Bethlehem, R. A. I., Milham, M. P., Bernhardt, B. C., Martino, A. D., & Hong, S. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.699813 · Cited by 26
Pedrosa, L. R. R., Coimbra, G. D. S., Corrêa, M. G., Dias, I. A., & Bahia, C. P. (2022) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2022.763245 · Cited by 26
Zhang, H., Mu, L., Wang, D., Xia, D., Salmon, A. E., Liu, Q., & Wong‐Riley, M. T. T. (2018) · The Journal of Physiology · doi:10.1113/jp275814 · Cited by 26
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Izmi, N., Carhart-Harris, R. L., & Kettner, H. (2024) · Frontiers in Child and Adolescent Psychiatry · doi:10.3389/frcha.2024.1364617 · Cited by 26
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Ferrer, C., & García, N. V. D. M. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.866999 · Cited by 25
Hsu, C. T., Choi, J. T. Y., & Sehgal, A. (2020) · SLEEP · doi:10.1093/sleep/zsaa265 · Cited by 24
Behavioral Signatures of a Developing Neural Code
Avitan, L., Pujic, Z., Mölter, J., McCullough, M., Zhu, S., Sun, B., Myhre, A.-E., & Goodhill, G. J. (2020) · Current Biology · doi:10.1016/j.cub.2020.06.040 · Cited by 24
Parr, A. C., Perica, M. I., Calabro, F. J., Foran, W., Moon, C., Hetherington, H. P., & Luna, B. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02860-7 · Cited by 23
Wong‐Riley, M. T. T. (2021) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2021.1025 · Cited by 23
Frantz, M. G., Kast, R. J., Dorton, H. M., CHAPMAN, K. S. M., & McGee, A. W. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv014 · Cited by 23
Neuregulin directed molecular mechanisms of visual cortical plasticity
Grieco, S. F., Holmes, T. C., & Xu, X. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24414 · Cited by 23
Schlüter, A., Roßberger, S., Dannehl, D., Janssen, J. M., Vorwald, S., Hanne, J., Schultz, C., Mauceri, D., & Engelhardt, M. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00318 · Cited by 22
Pielecka-Fortuna, J., Kalogeraki, E., Fortuna, M. G., & Löwel, S. (2015) · eLife · doi:10.7554/elife.11290 · Cited by 21
Ossandón, J., Stange, L., Gudi-Mindermann, H., Rimmele, J. M., Sourav, S., Bottari, D., Kekunnaya, R., & Röder, B. (2023) · NeuroImage · doi:10.1016/j.neuroimage.2023.120171 · Cited by 21
Maya‐Vetencourt, J. F., & Pizzorusso, T. (2013) · Journal of Experimental Neuroscience · doi:10.4137/jen.s12958 · Cited by 21
Evidence for Competition for Target Innervation in the Medial Prefrontal Cortex
Guirado, R., Umemori, J., Sipilä, P., & Ċastrén, E. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv280 · Cited by 21
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Pielecka-Fortuna, J., Wagener, R. J., Martens, A., Goetze, B., Schmidt, K.-F., Staiger, J. F., & Löwel, S. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0866-x · Cited by 21
Birch, E. E. (2012) · Nature · doi:10.1038/487441a · Cited by 20
Urbančič, N. B., Battelino, S., & Vozel, D. (2023) · Children · doi:10.3390/children11010002 · Cited by 20
Brown, A. P. Y., Cossell, L., & Margrie, T. W. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.03.073 · Cited by 20
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Achiro, J. M., Shen, J., & Bottjer, S. W. (2017) · eLife · doi:10.7554/elife.26973 · Cited by 18
Hsu, C.-L., Chou, C., Huang, S.-C., Lin, C., Lin, M.-Y., Tung, C.-C., Lin, C.-Y., Lai, I. P., Zou, Y., Youngson, N. A., et al. (2018) · Human Molecular Genetics · doi:10.1093/hmg/ddy023 · Cited by 18
Chen, A. N., & Meliza, C. D. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2137-19.2019 · Cited by 18
Beshara, S. P., Beston, B. R., Pinto, J. G. A., & Murphy, K. M. (2015) · eNeuro · doi:10.1523/eneuro.0126-15.2015 · Cited by 18
Li, Y., Wang, L., Zhang, X., Huang, M., Li, S., Wang, X., Chen, L., Jiang, B., & Yang, Y. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.10.015 · Cited by 18
Fu, Y., & Depue, R. A. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.09.026 · Cited by 18
Frequency representation within the human brain: Stability versus plasticity
Lim, H. H., Lenarz, M., Joseph, G., & Lenarz, T. (2013) · Scientific Reports · doi:10.1038/srep01474 · Cited by 17
Marin, I. A., Gutman-Wei, A. Y., Chew, K. S., Raissi, A. J., Djurisic, M. R., & Shatz, C. J. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2203965119 · Cited by 18
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Rączy, K., Hölig, C., Guerreiro, M. J. S., Lingareddy, S., Kekunnaya, R., & Röder, B. (2022) · Brain Communications · doi:10.1093/braincomms/fcac146 · Cited by 17
Brown, T. C., & McGee, A. W. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3002096 · Cited by 17
Litvin, D. G., Dick, T. E., Smith, C. B., & Jacono, F. J. (2018) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2018.03.031 · Cited by 17
Lombaert, N., Hennes, M., Gilissen, S. R. J., Schevenels, G., Aerts, L., Vanlaer, R., Geenen, L., Eeckhaut, A. V., Smolders, I. J., Nys, J., et al. (2018) · Molecular Brain · doi:10.1186/s13041-018-0404-5 · Cited by 17
Anodal occipital tDCS enhances spontaneous alpha activity
Dong, G., Wang, Y., & Chen, X. (2020) · Neuroscience Letters · doi:10.1016/j.neulet.2020.134796 · Cited by 17
Multiple Roles for Nogo Receptor 1 in Visual System Plasticity
Stephany, C.-É., Frantz, M. G., & McGee, A. W. (2015) · The Neuroscientist · doi:10.1177/1073858415614564 · Cited by 17
Visual–tactile processing in primary somatosensory cortex emerges before cross‐modal experience
Bieler, M., Sieben, K., Schildt, S., Röder, B., & Hanganu‐Opatz, I. L. (2017) · Synapse · doi:10.1002/syn.21958 · Cited by 17
Ferrer, C., Hsieh, H. V., & Wollmuth, L. P. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00495.2018 · Cited by 17
Chagas, L. D. S., Trindade, P., Gomes, A. L. T., Mendonça, H. R., Campello‐Costa, P., Faria‐Melibeu, A. D. C., Linden, R., & Serfaty, C. A. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.10.002 · Cited by 17
Critical periods and Autism Spectrum Disorders, a role for sleep
Medina, E., Peterson, S., Ford, K., Singletary, K. G., & Peixoto, L. (2022) · Neurobiology of Sleep and Circadian Rhythms · doi:10.1016/j.nbscr.2022.100088 · Cited by 16
van Lier, M., Smit‐Rigter, L. A., Krimpenfort, R., Saiepour, M. H., Ruimschotel, E., Kamphuis, W., Heimel, J. A., & Levelt, C. N. (2019) · eNeuro · doi:10.1523/eneuro.0277-18.2018 · Cited by 16
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Metadata
- Authors
- Levelt, C. N., & Hübener, M.
- Affiliations
- Netherlands Institute for Neuroscience (NL)
- Max Planck Society (DE)
- Venue
- Annual Review of Neuroscience
- Publisher
- Annual Reviews
- Published
- 2012-07-21
- Volume
- 35
- Issue
- 1
- Pages
- 309-330
- ISSN
- 0147-006X (ISSN-L)
- 1545-4126
- OpenAlex
- W2100171700
- Cited by
- 402
- References
- 151
- Citations by year
- 2026: 23 · 2025: 32 · 2024: 25 · 2023: 18 · 2022: 27 · 2021: 25 · 2020: 31 · 2019: 20 · 2018: 40 · 2017: 34 · 2016: 22 · 2015: 37 · 2014: 35 · 2013: 23 · 2012: 9
- FWCI
- 2.55
- Type
- journal article
- Language
- en
- Open access
- green
- zenodo.org
- Licence
- other-oa
- Locations
- Annual Review of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- KNAW Research Portal (The Royal Netherlands Academy of Arts and Sciences) (publishedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- KNAW research portal (Royal Academy of Art and Sciences (KNAW)) (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Zenodo (CERN European Organization for Nuclear Research) (submittedVersion, other-oa)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- critical period, critical period plasticity, visual cortex, cortical development, inhibitory circuits, neuronal maturation
- MeSH terms
- Aging, Animals, Critical Period, Psychological, Humans, Models, Neurological, Neural Inhibition, Synaptic Transmission, Neuronal Plasticity, Visual Cortex, Signal Transduction, Dominance, Ocular
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