Decline of the Critical Period of Visual Plasticity Is Concurrent with the Reduction of NR2B Subunit of the Synaptic NMDA Receptor in Layer 4
Open accessAbstract
The specific composition of NMDA receptor subunits is thought to underlie the developmental plasticity of the cortex revealed by unbalanced binocular stimulation. However, evidence that NR2 subunits change in correlation with the critical period at locations that are relevant to visual plasticity has been missing. Using preembedding and postembedding immunostaining, as well as electron microscopy, we quantified the volumetric densities of NR1-, NR2A-, and NR2B-containing synapses in layers 4 and 2/3 of the ferret visual cortex at different postnatal ages. Before eye opening, NR2A is encountered infrequently at postsynaptic sites in layer 4, but it increases sharply by postnatal day 34. In the subsequent weeks, postsynaptic NR2A labeling increases gradually in both layers 4 and 2/3 to become the most prevalent subunit in the adult animal. The NR2B subunit is the more prevalent subunit at the onset of the critical period of cortical plasticity. However, it displays different developmental patterns in layers 4 and 2/3. Although no change occurs in synaptic NR2B density in layer 2/3, in layer 4, NR2B maintains its high levels through the peak of the critical period and then becomes significantly reduced by the end of the peak of the critical period. This low level is maintained throughout adulthood. Our results demonstrate a correlation between the loss of NR2B subunits from layer 4 synaptic sites and the decline of the critical period, suggesting that the presence of NR2B subunits at synaptic sites could be a permissive factor regulating the ocular dominance plasticity of the developing cortex.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
Together these findings suggest that the switch from NR2B to NR2A dominated receptors terminates the critical period of experience-dependent plasticity for establishment of ocular dominance columns in the visual cortex.
“Together these findings suggest that the switch from NR2B to NR2A dominated receptors terminates the critical period of experience-dependent plasticity for establishment of ocular dominance columns in the visual cortex.”
From A role for synaptic plasticity in the adolescent development of executive function (2013) · cites this paper as [106]
In “A developmental switch or specificity for individual inputs?” (page unavailable), the paper explicitly proposes that loss of NR2B-containing receptors at specific synapses—not a switch to NR2A-dominated receptor composition—is related to declining plasticity. It reports that the NR2A/NR2B ratio keeps rising beyond the critical period, so it does not support the proposed switch as what terminates that period. (LLM, conf=0.85)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Synaptic Activity and the Construction of Cortical Circuits
Katz, L. C., & Shatz, C. J. (1996) · Science · doi:10.1126/science.274.5290.1133 · Cited by 3,048 · see citing works
Monyer, H., Burnashev, N., Laurie, D. J., Sakmann, B., & Seeburg, P. H. (1994) · Neuron · doi:10.1016/0896-6273(94)90210-0 · Cited by 2,989 · see citing works
Heteromeric NMDA receptors: molecular and functional distinction of subtypes
Monyer, H., Sprengel, R., Schoepfer, R., Herb, A., Higuchi, M., Lomeli, H., Burnashev, N., Sakmann, B., & Seeburg, P. H. (1992) · Science · doi:10.1126/science.256.5060.1217 · Cited by 2,541 · see citing works
CORTICAL PLASTICITY: From Synapses to Maps
Buonomano, D. V., & Merzenich, M. M. (1998) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.21.1.149 · Cited by 2,083 · see citing works
Plasticity of ocular dominance columns in monkey striate cortex
Hubel, D. H., Wiesel, T. N., LeVay, S., Barlow, H. B., & Gaze, R. M. (1977) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1977.0050 · Cited by 1,642 · see citing works
Changing subunit composition of heteromeric NMDA receptors during development of rat cortex
Sheng, M., Cummings, J., Roldan, L. A., Jan, Y. N., & Jan, L. Y. (1994) · Nature · doi:10.1038/368144a0 · Cited by 1,170 · see citing works
The development of ocular dominance columns in normal and visually deprived monkeys
Le Vay, S., Wiesel, T. N., & Hubel, D. H. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901910102 · Cited by 1,123 · see citing works
Blockade of "NMDA" Receptors Disrupts Experience-Dependent Plasticity of Kitten Striate Cortex
Kleinschmidt, A. K., Bear, M. F., & Singer, W. (1987) · Science · doi:10.1126/science.2443978 · Cited by 906 · see citing works
Activity-Dependent Decrease in NMDA Receptor Responses During Development of the Visual Cortex
Carmignoto, G., & Vicini, S. (1992) · Science · doi:10.1126/science.1279803 · Cited by 716 · see citing works
NR2A Subunit Expression Shortens NMDA Receptor Synaptic Currents in Developing Neocortex
Flint, A. C., Maisch, U. S., Weishaupt, J. H., Kriegstein, A. R., & Monyer, H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-07-02469.1997 · Cited by 615 · see citing works
Bear, M., Kleinschmidt, A., Gu, Q., & Singer, W. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-03-00909.1990 · Cited by 488 · see citing works
Developmental switch in the expression of NMDA receptors occurs in vivo and in vitro
Williams, K. L., Russell, S. L., Shen, Y. M., & Molinoff, P. B. (1993) · Neuron · doi:10.1016/0896-6273(93)90317-k · Cited by 456 · see citing works
Chan, J., Aoki, C. J., & Pickel, V. M. (1990) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(90)90015-8 · Cited by 447 · see citing works
NMDA receptors in the visual cortex of young kittens are more effective than those of adult cats
Tsumoto, T., Hagihara, K., Sato, H., & Hata, Y. (1987) · Nature · doi:10.1038/327513a0 · Cited by 440 · see citing works
Gilbert, C. D. (1998) · Physiological Reviews · doi:10.1152/physrev.1998.78.2.467 · Cited by 383 · see citing works
Quinlan, E. M., Olstein, D. H., & Bear, M. F. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.22.12876 · Cited by 382 · see citing works
Polyneuronal innervation of spiny stellate neurons in cat visual cortex
Ahmed, B., Anderson, J. C., Douglas, R. J., Martin, K. A. C., & Nelson, J. C. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903410105 · Cited by 338 · see citing works
Dynamic Regulation of Receptive Fields and Maps in the Adult Sensory Cortex
Weinberger, N. M. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.18.030195.001021 · Cited by 311 · see citing works
The location and function of NMDA receptors in cat and kitten visual cortex
Fox, K., Sato, H., & Daw, N. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-07-02443.1989 · Cited by 307 · see citing works
Peters, A., & Payne, B. R. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.1.69 · Cited by 303 · see citing works
Rapid Development and Plasticity of Layer 2/3 Maps in Rat Barrel Cortex In Vivo
Stern, E. A., Maravall, M., & Svoboda, K. (2001) · Neuron · doi:10.1016/s0896-6273(01)00360-9 · Cited by 276 · see citing works
Mechanisms of visual plasticity: Hebb synapses, NMDA receptors, and beyond
Rauschecker, J. P. (1991) · Physiological Reviews · doi:10.1152/physrev.1991.71.2.587 · Cited by 274 · see citing works
The critical period for ocular dominance plasticity in the Ferret's visual cortex
Issa, N. P., Trachtenberg, J. T., Chapman, B., Zahs, K. R., & Stryker, M. P. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-16-06965.1999 · Cited by 243 · see citing works
Relative numbers of cortical and brainstem inputs to the lateral geniculate nucleus
Erişir, A., Horn, S. C. V., & Sherman, S. M. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.4.1517 · Cited by 234 · see citing works
Estimation of the number of synapses in the cerebral cortex: methodological considerations
DeFelipe, J. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.7.722 · Cited by 193 · see citing works
Techniques to optimize post-embedding single and double staining for amino acid neurotransmitters.
Phend, K. D., Weinberg, R. J., & Rustioni, A. (1992) · Journal of Histochemistry & Cytochemistry · doi:10.1177/40.7.1376741 · Cited by 186 · see citing works
The effect of varying stimulus intensity on NMDA-receptor activity in cat visual cortex
Fox, K., Sato, H., & Daw, N. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.64.5.1413 · Cited by 185 · cited 2× · see citing works
“Indeed, in layer 4, the site of thalamocortical projection, NMDA-mediated responses are the strongest in early development (Tsumoto et al., 1987; Fox et al., 1989; Lu et al., 2001), although they become more prominent in layer 2/3 in adulthood ( Fox et al., 1989, 1990; Shirokawa et al., 1989; Currie et al., 1994).”
BackgroundPhend, K. D., Rustioni, A., & Weinberg, R. J. (1995) · Journal of Histochemistry & Cytochemistry · doi:10.1177/43.3.7532656 · Cited by 182 · see citing works
Lu, H., Gonzalez, E., & Crair, M. C. (2001) · Neuron · doi:10.1016/s0896-6273(01)00501-3 · Cited by 180 · see citing works
Stress-induced activation of nitric oxide-producing neurons in the rat brain
Krukoff, T. L., & Khalili, P. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970127)377:4 · Cited by 167 · see citing works
Development Of Local Circuits In Mammalian Visual Cortex
Katz, L. C., & Callaway, E. M. (1992) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.15.030192.000335 · Cited by 164 · see citing works
Portera‐Cailliau, C., Price, D. L., & Martin, L. J. (1996) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1996.66020692.x · Cited by 151 · see citing works
Roberts, E. B., & Ramoa, A. S. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.5.2587 · Cited by 150 · see citing works
Gu, Q., Bear, M. F., & Singer, W. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90183-1 · Cited by 144 · see citing works
Roberts, E. B., Meredith, M. A., & Ramoa, A. S. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.3.1021 · Cited by 135 · see citing works
Colonnier, M., & Beaulieu, C. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902310205 · Cited by 114 · see citing works
Development of Horizontal Projections in Layer 2/3 of Ferret Visual Cortex
Durack, J. C., & Katz, L. C. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.2.178 · Cited by 113 · see citing works
The development of synapses in cat visual cortex.
Cragg, B. G. (1972) · PubMed · Cited by 93 · see citing works
Chen, L., Cooper, N. G. F., & Mower, G. D. (2000) · Molecular Brain Research · doi:10.1016/s0169-328x(00)00076-0 · Cited by 86 · see citing works
Philpot, B. D., Weisberg, M. P., Ramos, M. S., Sawtell, N. B., Tang, Y., Tsien, J. Z., & Bear, M. F. (2001) · Neuropharmacology · doi:10.1016/s0028-3908(01)00136-8 · Cited by 85 · see citing works
Morphological properties of intracellularly labeled layer I neurons in rat neocortex
Zhou, F.-M., & Hablitz, J. J. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19961209)376:2 · Cited by 79 · see citing works
Shirokawa, T., Nishigori, A., Kimura, F., & Tsumoto, T. (1989) · Experimental Brain Research · doi:10.1007/bf00230237 · Cited by 78 · see citing works
Mechanisms of plasticity in the visual cortex. The Friedenwald Lecture.
Daw, N. W. (1994) · PubMed · Cited by 76 · see citing works
Plasticity of orientation preference maps in the visual cortex of adult cats
Godde, B., Leonhardt, R., Cords, S. M., & Dinse, H. R. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.082407499 · Cited by 73 · see citing works
Development of Y‐axon innervation of cortical area 18 in the cat.
Friedlander, M. J., & Martin, K. A. C. (1989) · The Journal of Physiology · doi:10.1113/jphysiol.1989.sp017756 · Cited by 59 · see citing works
Ghosh, S. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970407)380:2 · Cited by 53 · see citing works
Younossi‐Hartenstein, A., Ehlers, U., & Hartenstein, V. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000124)416:4 · Cited by 33 · see citing works
Postnatal development of NR1, NR2A and NR2B immunoreactivity in the visual cortex of the rat
Cao, Z., Lickey, M. E., Liu, L., Kirk, E., & Gordon, B. (2000) · Brain Research · doi:10.1016/s0006-8993(99)02450-6 · Cited by 25 · see citing works
Development of NR1, NR2A and NR2B mRNA in NR1 immunoreactive cells of rat visual cortex
Cao, Z., Liu, L., Lickey, M. E., & Gordon, B. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02343-x · Cited by 24 · see citing works
Aoki, C. J. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(96)00160-5 · Cited by 24 · see citing works
NMDA receptors in layers II and III of rat cerebral cortex
Currie, S. N., Wang, X. F., & Daw, N. W. (1994) · Brain Research · doi:10.1016/0006-8993(94)90801-x · Cited by 18 · see citing works
Preservation and contrast without osmication or section staining
Locke, M. (1994) · Microscopy Research and Technique · doi:10.1002/jemt.1070290102 · Cited by 15 · see citing works
Cornea-Hébert (1999) · doi:10.1002/(sici)1096-9861(19990628)409:2
Flagged first, then by citations
Cited by
Sorted by citations
Rasch, B., & Born, J. (2013) · Physiological Reviews · doi:10.1152/physrev.00032.2012 · Cited by 2,783 · see citing works
“As a consequence of maturational processes, critical period plasticity is linked to a distinct biochemical milieu, a change in the subunit composition of NMDA receptors in forebrain synapses from a predominance of NR2B subunits at birth to a prevalence of synaptic NR2A subunits towards the end of the critical period,…”
BackgroundRole of NMDA Receptor Subtypes in Governing the Direction of Hippocampal Synaptic Plasticity
Liu, L., Wong, T. P., Pozza, M. F., Lingenhoehl, K., Wang, Y., Sheng, M., Auberson, Y. P., & Wang, Y. T. (2004) · Science · doi:10.1126/science.1096615 · Cited by 1,106 · see citing works
Adolescence as a neurobiological critical period for the development of higher-order cognition
Larsen, B., & Luna, B. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.005 · Cited by 853 · see citing works
Regulation of NMDA receptor subunit expression and its implications for LTD, LTP, and metaplasticity
Yashiro, K., & Philpot, B. D. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.07.046 · Cited by 649 · see citing works
Sale, A., Maya Vetencourt, J. F., Medini, P., Cenni, M. C., Baroncelli, L., De Pasquale, R., & Maffei, L. (2007) · Nature Neuroscience · doi:10.1038/nn1899 · Cited by 492 · see citing works
A role for synaptic plasticity in the adolescent development of executive function
Selemon, L. D. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.7 · Cited by 439 · see citing works
“decline in layer 4 at the end of the critical period for plasticity of ocular dominance columns but remain high in layer 2/3.(106)”
BackgroundWerker, J. F., & Tees, R. C. (2005) · Developmental Psychobiology · doi:10.1002/dev.20060 · Cited by 374 · see citing works
Homeostatic plasticity and NMDA receptor trafficking
Pérez-Otaño, I., & Ehlers, M. D. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.03.004 · Cited by 356 · see citing works
Liu, X.-B., Murray, K. D., & Jones, E. G. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2476-04.2004 · Cited by 316 · see citing works
Hearing Loss Raises Excitability in the Auditory Cortex
Kotak, V. C., Fujisawa, S., Lee, F. A., Karthikeyan, O., Aoki, C. J., & Sanes, D. H. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.5169-04.2005 · Cited by 288 · see citing works
BDNF regulates the expression and traffic of NMDA receptors in cultured hippocampal neurons
Caldeira, M. V., Melo, C. V., Pereira, D. B., Carvalho, R. F., Carvalho, A. L., & Duarte, C. B. (2007) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2007.02.019 · Cited by 266 · see citing works
GABA Neuron Alterations, Cortical Circuit Dysfunction and Cognitive Deficits in Schizophrenia
González‐Burgos, G., Fish, K. N., & Lewis, D. A. (2011) · Neural Plasticity · doi:10.1155/2011/723184 · Cited by 244 · see citing works
Gray, J. D., Milner, T. A., & McEwen, B. S. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.08.034 · Cited by 242 · see citing works
Ontogeny of postsynaptic density proteins at glutamatergic synapses
Petralia, R. S., Sans, N., Wang, Y.-X., & Wenthold, R. J. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.03.013 · Cited by 236 · see citing works
Wang, H., Stradtman, G. G., Wang, X.-J., & Gao, W.-J. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804318105 · Cited by 199 · see citing works
Sanchez, V., Feinstein, S. D., Lunardi, N., Joksovic, P. M., Boscolo, A., Todorovic, S. M., & Jevtović‐Todorović, V. (2011) · Anesthesiology · doi:10.1097/aln.0b013e3182303a63 · Cited by 180 · see citing works
Lunardi, N., Ori, C., Erişir, A., & Jevtović‐Todorović, V. (2009) · Neurotoxicity Research · doi:10.1007/s12640-009-9088-z · Cited by 176 · see citing works
Vision and Cortical Map Development
WHITE, L. E., & Fitzpatrick, D. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.011 · Cited by 168 · see citing works
Dumas, T. C. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.08.002 · Cited by 169 · see citing works
Franks, K. M., & Isaacson, J. S. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.024 · Cited by 138 · see citing works
Dow-Edwards, D. L., MacMaster, F. P., Peterson, B. S., Niesink, R. J. M., Andersen, S. L., & Braams, B. R. (2019) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2019.106834 · Cited by 146 · see citing works
Distribution of Extrasynaptic NMDA Receptors on Neurons
Petralia, R. S. (2012) · The Scientific World JOURNAL · doi:10.1100/2012/267120 · Cited by 121 · see citing works
Cho, K. K. A., Khibnik, L. A., Philpot, B. D., & Bear, M. F. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808104106 · Cited by 114 · see citing works
Zhang, Z., Jiao, Y.-Y., & Sun, Q. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.11.045 · Cited by 113 · see citing works
Coleman, J. E., Nahmani, M., Gavornik, J. P., Haslinger, R., Heynen, A. J., Erişir, A., & Bear, M. F. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1248-10.2010 · Cited by 100 · see citing works
Gonzalez-Burgos, G., Kroener, S., Zaitsev, A. V., Povysheva, N. V., Krimer, L. S., Barrionuevo, G., & Lewis, D. A. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm095 · Cited by 95 · see citing works
Murphy, K. M., Beston, B. R., Boley, P. M., & Jones, D. G. (2005) · Developmental Psychobiology · doi:10.1002/dev.20053 · Cited by 90 · see citing works
NMDA Receptor NR2 Subunit Dependence of the Slow Component of Magnesium Unblock
Clarke, R. J., & Johnson, J. W. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0577-06.2006 · Cited by 89 · see citing works
NR2 subunit‐dependence of NMDA receptor channel block by external Mg2+
Qian, A., Buller, A. L., & Johnson, J. W. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.076737 · Cited by 81 · see citing works
Kielland, A., Bochorishvili, G., Corson, J. A., Zhang, L., Rosin, D. L., Heggelund, P., & Zhu, J. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.001 · Cited by 68 · see citing works
Experience-Dependent Synaptic Plasticity in V1 Occurs without Microglial CX3CR1
Schecter, R. W., Maher, E. E., Welsh, C. A., Stevens, B., Erişir, A., & Bear, M. F. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2679-16.2017 · Cited by 71 · see citing works
Aoki, C. J., Kojima, N., Sabaliauskas, N. A., Shah, L. N., Ahmed, T. H., Oakford, J., Ahmed, T., Yamazaki, H., Hanamura, K., & Shirao, T. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22137 · Cited by 65 · see citing works
Drzewiecki, C. M., & Juraska, J. M. (2020) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2020.173044 · Cited by 67 · see citing works
Xu, J., Yu, L., Cai, R., Zhang, J., & Sun, X. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.07.018 · Cited by 59 · see citing works
Janssen, W. G. M., Vissavajjhala, P., Andrews, G., Moran, T. M., Hof, P. R., & Morrison, J. H. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.08.020 · Cited by 59 · see citing works
Zhang, Z., & Sun, Q. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20844 · Cited by 59 · see citing works
Surface trafficking of NMDA receptors: Gathering from a partner to another
Ladépêche, L., Dupuis, J. P., & Groc, L. (2013) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2013.10.005 · Cited by 57 · see citing works
Erişir, A., & Dreusicke, M. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20507 · Cited by 52 · see citing works
Wang, G., Bochorishvili, G., Chen, Y., Salvati, K. A., Zhang, P., Dubel, S. J., Perez-Reyes, E., Snutch, T. P., Stornetta, R. L., Deisseroth, K., et al. (2015) · Genes & Development · doi:10.1101/gad.260869.115 · Cited by 53 · see citing works
Ionotropic glutamate receptors: Which ones, when, and where in the mammalian neocortex
Hadzic, M., Jäck, A., & Wahle, P. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24103 · Cited by 49 · see citing works
Synaptic and Molecular Mechanisms Regulating Plasticity during Early Learning
Nordeen, K. W., & Nordeen, E. J. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1298.018 · Cited by 46 · see citing works
Drebrin a content correlates with spine head size in the adult mouse cerebral cortex
Kobayashi, C., Aoki, C. J., Kojima, N., Yamazaki, H., & Shirao, T. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21408 · Cited by 43 · see citing works
Lopez‐Rojas, J., & Kreutz, M. R. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.02.021 · Cited by 43 · see citing works
Zhu, J., Zongze, Z., Qiuyue, Y., Peng, F., Qi, Z., Yanlin, W., & Chang, C. (2020) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2020.01.018 · Cited by 42 · see citing works
Trafficking and Targeting of NMDA Receptors
Petralia, R. S., Wenthold, R. J., & Al‐Hallaq, R. A. (2008) · Frontiers in neuroscience · doi:10.1201/9781420044157.ch8 · Cited by 41 · see citing works
Kim, H.-S., Jang, H., Cho, K., Hahn, S. J., Kim, M.-J., Yoon, S. H., Jo, Y., Kim, M.-S., & Rhie, D. (2006) · Brain Research · doi:10.1016/j.brainres.2006.05.046 · Cited by 40 · see citing works
Kanold, P. O., Kim, Y. A., GrandPré, T., & Shatz, C. J. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.171215 · Cited by 39 · see citing works
Beston, B. R., Jones, D. G., & Murphy, K. M. (2010) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2010.00138 · Cited by 36 · see citing works
Wang, L., Fontanini, A., & Maffei, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0622-12.2012 · Cited by 36 · see citing works
Dynamic regulation of NMDAR function in the adult brain by the stress hormone corticosterone
Tse, Y. C., Bagot, R. C., & Wong, T. P. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00009 · Cited by 34 · see citing works
Perica, M. I., & Luna, B. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105378 · Cited by 34 · see citing works
Bi, C., Cui, Y., Mao, Y., Dong, S., Zhang, J., & Sun, X. (2006) · Brain Research · doi:10.1016/j.brainres.2006.06.056 · Cited by 34 · see citing works
Gene expression analysis of the critical period in the visual cortex
Ossipow, V., Pellissier, F., Schaad, O., & Ballivet, M. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.05.003 · Cited by 34 · see citing works
Development of Glutamatergic Proteins in Human Visual Cortex across the Lifespan
Siu, C. R., Beshara, S. P., Jones, D. G., & Murphy, K. M. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2304-16.2017 · Cited by 32 · see citing works
Tse, Y. C., Lai, C., Lai, S., Liu, J., Yung, K. K. L., Shum, D. K., & Chan, Y. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21688 · Cited by 31 · see citing works
Ohno, T., Maeda, H., Murabe, N., Kamiyama, T., Yoshioka, N., Mishina, M., & Sakurai, M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906551107 · Cited by 30 · see citing works
Visual system plasticity in mammals: the story of monocular enucleation-induced vision loss
Nys, J., Scheyltjens, I., & Arckens, L. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00060 · Cited by 29 · see citing works
Receptive Field Self-Organization in a Model of the Fine Structure in V1 Cortical Columns
Lücke, J. (2009) · Neural Computation · doi:10.1162/neco.2009.07-07-584 · Cited by 27 · see citing works
Howe, M. W., Feig, S. L., Osting, S., & Haberly, L. B. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21534 · Cited by 26 · see citing works
McVea, D. A., Murphy, T. H., & Mohajerani, M. H. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00103 · Cited by 22 · see citing works
Aoki, C. J., & Santiago, A. N. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.990354 · Cited by 20 · see citing works
Mao, Y., Zang, S., Zhang, J., & Sun, X. (2006) · Brain Research · doi:10.1016/j.brainres.2005.12.077 · Cited by 21 · see citing works
Maya‐Vetencourt, J. F., & Pizzorusso, T. (2013) · Journal of Experimental Neuroscience · doi:10.4137/jen.s12958 · Cited by 20 · see citing works
Code Under Construction: Neural Coding Over Development
Avitan, L., & Goodhill, G. J. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.05.011 · Cited by 18 · see citing works
Lai, S., Lai, C., Tse, Y. C., Yung, K. K. L., Shum, D. K., & Chan, Y. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06523.x · Cited by 19 · see citing works
Schweitzer, B., Singh, J., Fejtova, A., Groc, L., Heine, M., & Frischknecht, R. (2017) · Scientific Reports · doi:10.1038/s41598-017-07003-3 · Cited by 19 · see citing works
The distinct role of NR2B subunit in the enhancement of visual plasticity in adulthood
Liu, H., Li, Y., Wang, Y., Wang, X., An, X., Wang, S., Chen, L., Liu, G., & Yang, Y. (2015) · Molecular Brain · doi:10.1186/s13041-015-0141-y · Cited by 19 · see citing works
Postnatal development of excitatory postsynaptic currents in nucleus accumbens medium spiny neurons
Zhang, L., & Warren, R. A. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.05.002 · Cited by 19 · see citing works
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 · see citing works
McKeon, S. D., Perica, M. I., Calabro, F. J., Foran, W., Hetherington, H. P., Moon, C., & Luna, B. (2024) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2024.102695 · Cited by 16 · see citing works
Corson, J. A., Nahmani, M., Lubarsky, K., Badr, N., Wright, C., & Erişir, A. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.07.016 · Cited by 17 · see citing works
Aoki, C. J., Lee, J., Nedelescu, H., Ahmed, T. H., Ho, A., & Shen, J. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22151 · Cited by 16 · see citing works
Layer-specific Production of Nitric Oxide during Cortical Circuit Formation in Postnatal Mouse Brain
Imura, T. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh135 · Cited by 16 · see citing works
Father’s care uniquely influences male neurodevelopment
Danoff, J. S., Ramos, E. N., Hinton, T. D., Perkeybile, A. M., Graves, A. J., Quinn, G. C., Lightbody-Cimer, A. R., Gordevičius, J., Milčiūtė, M., Brooke, R. T., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2308798120 · Cited by 15 · see citing works
Developmental remodeling of corticocortical feedback circuits in ferret visual cortex
Khalil, R., & Levitt, J. B. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23591 · Cited by 15 · see citing works
Development of Cross-Orientation Suppression and Size Tuning and the Role of Experience
Popović, M., Stacy, A. K., Kang, M., Nanu, R., Oettgen, C. E., Wise, D. L., Fiser, J., & Hooser, S. D. V. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2886-17.2018 · Cited by 13 · see citing works
Possible role of cooperative action of NMDA receptor and GABA function in developmental plasticity
Kubota, S., & Kitajima, T. (2010) · Journal of Computational Neuroscience · doi:10.1007/s10827-010-0212-0 · Cited by 13 · see citing works
Synaptic and intrinsic mechanisms underlying development of cortical direction selectivity
Roy, A., Osik, J. J., Meschede-Krasa, B., Alford, W. T., Leman, D. P., & Hooser, S. D. V. (2020) · eLife · doi:10.7554/elife.58509 · Cited by 12 · see citing works
May, O. L., Erişir, A., & Hill, D. L. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21708 · Cited by 12 · see citing works
Cui, Y., Zhang, J., Cai, R., & Sun, X. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21936 · Cited by 12 · see citing works
Postnatal development of chorda tympani axons in the rat nucleus of the solitary tract
Wang, S., Corson, J. A., Hill, D. L., & Erişir, A. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23093 · Cited by 11 · see citing works
Maeda, H., Ohno, T., & Sakurai, M. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.10.010 · Cited by 11 · see citing works
Talaei, S. A., Azami, A., & Salami, M. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.01.024 · Cited by 10 · see citing works
Koster, K. P., Flores-Barrera, E., de la Villarmois, E. A., Caballero, A., Tseng, K. Y., & Yoshii, A. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1113-23.2023 · Cited by 10 · see citing works
Wang, W., Zhang, Z., Shang, J., Jiang, Z., Wang, S., Liu, Y. U., & Zhang, L. (2008) · Neuroscience Research · doi:10.1016/j.neures.2008.06.002 · Cited by 10 · see citing works
Lo, F.-S., & Zhao, S.-C. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.01.023 · Cited by 10 · see citing works
Developmental profile of tissue plasminogen activator in postnatal Long Evans rat visual cortex.
Zheng, S., Yin, Z. Q., & Zeng, Y. X. (2008) · PubMed Central · Cited by 9 · see citing works
The mouse olfactory peduncle 4: Development of synapses, perineuronal nets, and capillaries
Collins, L. N., & Brunjes, P. C. (2019) · The Journal of Comparative Neurology · doi:10.1002/cne.24778 · Cited by 8 · see citing works
Lee, C., Joo, K., Kim, M., Rhie, D., & Jang, H. (2015) · Journal of Neuroscience Research · doi:10.1002/jnr.23604 · Cited by 7 · see citing works
Sanchez, V., Bakhti‐Suroosh, A., Chen, A., Brunzell, D. H., Erişir, A., & Lynch, W. J. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14408 · Cited by 7 · see citing works
Petralia, R. S., & Wenthold, R. J. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-055-3_2 · Cited by 6 · see citing works
Reduction of APOE accounts for neurobehavioral deficits in fetal alcohol spectrum disorders
Hwang, H. M., Yamashita, S., Matsumoto, Y., Ito, M., Edwards, A., Sasaki, J., Dutta, D. J., Mohammad, S., Yamashita, C., Wetherill, L. F., et al. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02586-6 · Cited by 5 · see citing works
Foraging and inertia: Understanding the developmental dynamics of overt visual attention
Wass, S. V., Amadó, M. P., Northrop, T., Haresign, I. M., & Phillips, E. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105991 · Cited by 4 · see citing works
Cao, Z., Liu, L., Lickey, M. E., Graves, A., Pham, T. A., & Gordon, B. (2006) · Experimental Brain Research · doi:10.1007/s00221-006-0647-8 · Cited by 5 · see citing works
Molecular Properties and Cell Biology of the NMDA Receptor
Wenthold, R. J., Al‐Hallaq, R. A., Swanwick, C. C., & Petralia, R. S. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_12 · Cited by 5 · see citing works
Experience-Dependent Synaptic Plasticity in the Developing Cerebral Cortex
Aoki, C. J., & Erişir, A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-418675-0.00013-4 · Cited by 4 · see citing works
High Magnesium Promotes the Recovery of Binocular Vision from Amblyopia via TRPM7
Dai, M., Li, J., Hao, X., Li, N., Zheng, M., He, M., & Gu, Y. (2024) · Neuroscience Bulletin · doi:10.1007/s12264-024-01242-x · Cited by 4 · see citing works
Joo, K., Rhie, D., & Jang, H. (2015) · Korean Journal of Physiology and Pharmacology · doi:10.4196/kjpp.2015.19.6.523 · Cited by 4 · see citing works
Isoo, N., Ohno, T., Isowaki, M., Fukuda, S., Murabe, N., Mizukami, H., Ozawa, K., Mishina, M., & Sakurai, M. (2016) · Scientific Reports · doi:10.1038/srep34196 · Cited by 3 · see citing works
Talaei, S. A., Tameh, A. A., & Salami, M. (2016) · Europe PMC (PubMed Central) · doi:10.22038/ijbms.2016.7473 · Cited by 3 · see citing works
- Authors
- Erisir, A., & Harris, J. L.
- Affiliations
- University of Virginia (US)
- ORCID
- Harris, Janna L.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2003-06-15
- Volume
- 23
- Issue
- 12
- Pages
- 5208-5218
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC3119651
- OpenAlex
- W1528276351
- Cited by
- 111
- References
- 53
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 4 · 2023: 3 · 2022: 2 · 2020: 4 · 2019: 4 · 2018: 3 · 2017: 4 · 2016: 6 · 2015: 5 · 2014: 2 · 2013: 5 · 2012: 5
- FWCI
- 2.54
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Eye Institute (R01EY012138, R01-EY12138)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- critical period, visual plasticity, NMDA receptor subunits, NR2B, NR2A, NR1, synaptic density, layer 4, layer 2/3, visual cortex development, ocular dominance plasticity, binocular stimulation, ferrets, postnatal development, postsynaptic sites
- MeSH terms
- Age Factors, Animals, Critical Period, Psychological, Ferrets, Immunohistochemistry, Microscopy, Electron, Neuronal Plasticity, Synapses, Visual Cortex, Receptors, N-Methyl-D-Aspartate, Protein Subunits, Dominance, Ocular
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