Critical Period Plasticity Matches Binocular Orientation Preference in the Visual Cortex
Open accessAbstract
SUMMARY Changes of ocular dominance in the visual cortex can be induced by visual manipulations during a critical period in early life. However, the role of critical period plasticity in normal development is unknown. Here we show that at the onset of this time window, the preferred orientations of individual cortical cells in the mouse are mismatched through the two eyes and the mismatch decreases and reaches adult levels by the end of the period. Deprivation of visual experience during this period irreversibly blocks the binocular matching of orientation preference, but has no effect in adulthood. The critical period of binocular matching can be delayed by long-term visual deprivation from birth, like that of ocular dominance plasticity. These results demonstrate that activity-dependent changes induced by normal visual experience during the well-studied critical period serve to match eye-specific inputs in the cortex, thus revealing a physiological role for critical period plasticity during normal development.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
A major function of critical period plasticity is to promote experience-dependent matching of orientation tuning through the two eyes.
“A major function of critical period plasticity is to promote the experience-dependent matching of orientation tuning through the two eyes (42).”
From MeCP2 regulates the timing of critical period plasticity that shapes functional connectivity in primary visual cortex (2015) · cites this paper as [42]
Shortly after eye opening, V1 neurons exhibit orientation tuning and respond to both eyes, but orientation preference is binocularly mismatched; this mismatch is progressively corrected through visual experience during the critical period.
“Shortly after eye opening, V1 neurons exhibit orientation tuning and respond to stimulus to both eyes, but the orientation preference is binocularly mismatched.This initial mismatch is then progressively corrected through visual experience during the critical period, such that individual binocular neurons become tuned to similar orientations through the two eyes (42),”
From MeCP2 regulates the timing of critical period plasticity that shapes functional connectivity in primary visual cortex (2015) · cites this paper as [42]
The degree of binocular orientation matching in ~P30 MeCP2-null mice is significantly worse than age-matched WT and remains at a pre-critical-period level.
“The degree of matching in ∼P30 MeCP2 -/y mice was significantly worse than agematched WTs (which had reached the adult level by P30, Fig. 7L) and in fact remained at a level preceding the critical period (∼P20 WT mice) and similar to that observed after long-term visual deprivation from birth (42).”
From MeCP2 regulates the timing of critical period plasticity that shapes functional connectivity in primary visual cortex (2015) · cites this paper as [42]
Those cells are tuned to matching orientations in both eyes.
“that are tuned to the same orientation in the two eyes [97]”
From Role of emergent neural activity in visual map development (2014) · cites this paper as [97]
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 · see citing works
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 · see citing works
The effect of dark rearing on the time course of the critical period in cat visual cortex
Mower, G. D. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90001-y · Cited by 220 · see citing works
Rapid critical period induction by tonic inhibition in visual cortex
Iwai, Y., Fagiolini, M., Obata, K., & Hensch, T. K. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-17-06695.2003 · Cited by 201 · see citing works
Sensitive periods for visual calibration of the auditory space map in the barn owl optic tectum
Brainard, M. S., & Knudsen, E. I. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-10-03929.1998 · Cited by 176 · see citing works
A precritical period for plasticity in visual cortex
Feller, M. B., & Scanziani, M. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.01.012 · Cited by 92 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Critical periods in speech perception: New directions
Werker, J. F., & Hensch, T. K. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-015104 · Cited by 774 · see citing works
Development and plasticity of the primary visual cortex
Espinosa, J. S., & Stryker, M. P. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.009 · Cited by 672 · see citing works
Removing brakes on adult brain plasticity: From molecular to behavioral interventions
Bavelier, D., Levi, D. M., Li, R. W., Dan, Y., & Hensch, T. K. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4812-10.2010 · Cited by 589 · see citing works
Structural plasticity upon learning: regulation and functions
Caroni, P., Donato, F., & Muller, D. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3258 · Cited by 491 · see citing works
Developmental timing and critical windows for the treatment of psychiatric disorders
Marín, O. (2016) · Nature Medicine · doi:10.1038/nm.4225 · Cited by 374 · see citing works
Developmental mechanisms of topographic map formation and alignment
Cang, J., & Feldheim, D. A. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062012-170341 · Cited by 275 · see citing works
Role of emergent neural activity in visual map development
Ackman, J. B., & Crair, M. C. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.11.011 · Cited by 219 · see citing works
Development of direction selectivity in mouse cortical neurons
Rochefort, N. L., Narushima, M., Grienberger, C., Marandi, N., Hill, D. N., & Konnerth, A. (2011) · Neuron · doi:10.1016/j.neuron.2011.06.013 · Cited by 178 · see citing works
Toyoizumi, T., Miyamoto, H., Yazaki-Sugiyama, Y., Atapour, N., Hensch, T. K., & Miller, K. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.022 · Cited by 158 · see citing works
Lensjø, K. K., Christensen, A. C., Tennøe, S., Fyhn, M., & Hafting, T. (2017) · eneuro · doi:10.1523/eneuro.0379-16.2017 · Cited by 133 · see citing works
Sensory experience during locomotion promotes recovery of function in adult visual cortex
Kaneko, M., & Stryker, M. P. (2014) · eLife · doi:10.7554/elife.02798 · Cited by 126 · see citing works
He, L.-J., Liu, N., Cheng, T.-L., Chen, X.-J., Li, Y.-D., Shu, Y.-S., Qiu, Z.-L., & Zhang, X.-H. (2014) · Nature Communications · doi:10.1038/ncomms6036 · Cited by 107 · see citing works
Regional and temporal specificity of intrinsic plasticity mechanisms in rodent primary visual cortex
Nataraj, K., & Turrigiano, G. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4455-11.2011 · Cited by 23 · see citing works
- Authors
- Wang, B.-S., Sarnaik, R., & Cang, J.
- Affiliations
- Northwestern University (US)
- Corresponding author
- Cang, Jianhua
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2010-01
- Volume
- 65
- Issue
- 2
- Pages
- 246-256
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC2822731
- OpenAlex
- W2014906957
- Cited by
- 209
- References
- 6
- Citations by year
- 2026: 10 · 2025: 13 · 2024: 9 · 2023: 15 · 2022: 17 · 2021: 11 · 2020: 18 · 2019: 15 · 2018: 8 · 2017: 21 · 2016: 11 · 2015: 7 · 2014: 15 · 2013: 18 · 2012: 8
- FWCI
- 7.56
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1293 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Brain Research Foundation
- Neurosciences Research Foundation
- Stryker
- National Eye Institute (EY-018621, R01EY018621)
- 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 plasticity, ocular dominance, visual cortex development, visual deprivation, orientation maps, binocular matching, activity-dependent development, mouse visual system
- MeSH terms
- Age Factors, Animals, Animals, Newborn, Mice, Inbred C57BL, Neuronal Plasticity, Orientation, Photic Stimulation, Sensory Deprivation, Visual Cortex, Vision, Binocular, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review