Structural and functional recovery from early monocular deprivation in adult rats
Open accessAbstract
Visual deficits caused by abnormal visual experience during development are hard to recover in adult animals. Removal of chondroitin sulfate proteoglycans from the mature extracellular matrix with chondroitinase ABC promotes plasticity in the adult visual cortex. We tested whether chondroitinase ABC treatment of adult rats facilitates anatomical, functional, and behavioral recovery from the effects of a period of monocular deprivation initiated during the critical period for monocular deprivation. We found that chondroitinase ABC treatment coupled with reverse lid-suturing causes a complete recovery of ocular dominance, visual acuity, and dendritic spine density in adult rats. Thus, manipulations of the extracellular matrix can be used to promote functional recovery in the adult cortex.
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?
Maturation of the ECM and PNNs is negatively correlated with the expression of synaptic plasticity.
“The maturation of the ECM in general, and PNNs in particular, has been negatively correlated with the expression of synaptic plasticity.”
From Light reintroduction after dark exposure reactivates plasticity in adults via perisynaptic activation of MMP-9 (2017) · cites this paper as Pizzorusso et al., 2006
The rescue of structural and functional plasticity in Mmp9−/− mouse by hyaluronidase supports the assertion that degradation of the extracellular environment reactivates ocular dominance plasticity in adults.
“Nonetheless, the rescue of structural and functional plasticity in Mmp9−/− mouse by hyaluronidase supports the assertion that degradation of the extracellular environment reactivates ocular dominance plasticity in adults (Pizzorusso et al., 2002; Pizzorusso et al., 2006).”
From Light reintroduction after dark exposure reactivates plasticity in adults via perisynaptic activation of MMP-9 (2017) · cites this paper as Pizzorusso et al., 2006
The decrease in spine density caused by long-term monocular deprivation is recovered by chondroitinase treatment.
“In addition, the decrease in spine density caused by long-term monocular deprivation is recovered by chondroitinase treatment (Pizzorusso et al., 2006).”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Pizzorusso et al., 2006
Removal of chondroitin sulfate proteoglycans by chondroitinase in adult animals restores juvenile levels of plasticity in the rat visual cortex and allows complete recovery of visual acuity in rats that experienced monocular deprivation during the critical period.
“They showed that removal of CSPGs by chondroitinase [a bacterial enzyme which degrades GAGs, including chondroitin sulfate and hyaluronan, disrupting the structure of the perineuronal net; see Galtrey and Fawcett (2007) for review] in adult animals restores juvenile levels of plasticity in the rat visual cortex, and allow a complete recovery of visual acuity in rats which experienced monocular”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Pizzorusso et al., 2006
Cites
Regeneration beyond the glial scar
Silver, J., & Miller, J. H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1326 · Cited by 3,090 · 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
Chondroitinase ABC promotes functional recovery after spinal cord injury
Bradbury, E. J., Moon, L. D. F., Popat, R. J., King, V. R., Bennett, G. S., Patel, P. N., Fawcett, J. W., & McMahon, S. B. (2002) · Nature · doi:10.1038/416636a · Cited by 2,357 · see citing works
Critical period plasticity in local cortical circuits
Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323 · see citing works
The glial scar and central nervous system repair
Fawcett, J. W., & Asher, R. A. (1999) · Brain Research Bulletin · doi:10.1016/s0361-9230(99)00072-6 · Cited by 1,808 · see citing works
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 · see citing works
Self-citationLong-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 · see citing works
Huang, Z. J., Kirkwood, A., Pizzorusso, T., Porciatti, V., Morales, B., Bear, M. F., Maffei, L., & Tonegawa, S. (1999) · Cell · doi:10.1016/s0092-8674(00)81509-3 · Cited by 1,198 · see citing works
Self-citationTransient and persistent dendritic spines in the neocortex in vivo
Holtmaat, A. J. G. D., Trachtenberg, J. T., Wilbrecht, L., Shepherd, G. M., Zhang, X., Knott, G. W., & Svoboda, K. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.003 · Cited by 1,131 · see citing works
Local GABA Circuit Control of Experience-Dependent Plasticity in Developing Visual Cortex
Hensch, T. K., Fagiolini, M., Mataga, N., Stryker, M. P., Baekkeskov, S., & Kash, S. F. (1998) · Science · doi:10.1126/science.282.5393.1504 · Cited by 910 · see citing works
Fagiolini, M., Pizzorusso, T., Berardi, N., Domenici, L., & Maffei, L. (1994) · Vision Research · doi:10.1016/0042-6989(94)90210-0 · Cited by 656 · see citing works
Self-citationExperience-driven plasticity of visual cortex limited by myelin and nogo receptor
McGee, A. W., Yang, Y., Fischer, Q. S., Daw, N. W., & Strittmatter, S. M. (2005) · Science · doi:10.1126/science.1114362 · Cited by 643 · see citing works
Apical dendritic spines of the visual cortex and light deprivation in the mouse
Valverde, P. (1967) · Experimental Brain Research · doi:10.1007/bf00237559 · Cited by 483 · see citing works
NMDA Receptor-Dependent Ocular Dominance Plasticity in Adult Visual Cortex
Sawtell, N. B., Frenkel, M. Y., Philpot, B. D., Nakazawa, K., Tonegawa, S., & Bear, M. F. (2003) · Neuron · doi:10.1016/s0896-6273(03)00323-4 · Cited by 482 · see citing works
Specific GABA <sub>A</sub> Circuits for Visual Cortical Plasticity
Fagiolini, M., Fritschy, J.-M., Löw, K., Möhler, H., Rudolph, U., & Hensch, T. K. (2004) · Science · doi:10.1126/science.1091032 · Cited by 471 · see citing works
Blakemore, C. B., & Sluyters, R. C. V. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010478 · Cited by 452 · see citing works
Wisteria floribunda agglutinin-labelled nets surround parvalbumin-containing neurons
Härtig, W., Brauer, K., & Brückner, G. (1992) · NeuroReport · doi:10.1097/00001756-199210000-00012 · Cited by 440 · see citing works
Experience-dependent pruning of dendritic spines in visual cortex by tissue plasminogen activator
Mataga, N., Mizuguchi, Y., & Hensch, T. K. (2004) · Neuron · doi:10.1016/j.neuron.2004.11.028 · Cited by 371 · see citing works
Multicolor “DiOlistic” Labeling of the Nervous System Using Lipophilic Dye Combinations
Gan, W., Grutzendler, J., Wong, W. T., Wong, R., & Lichtman, J. W. (2000) · Neuron · doi:10.1016/s0896-6273(00)00031-3 · Cited by 331 · see citing works
Dendritic Spine Dynamics Are Regulated by Monocular Deprivation and Extracellular Matrix Degradation
Oray, S., Majewska, A., & Sur, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.12.001 · Cited by 296 · see citing works
Molecular basis of plasticity in the visual cortex
Berardi, N., Pizzorusso, T., Ratto, G. M., & Maffei, L. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00168-1 · Cited by 284 · see citing works
Self-citationHockfield, S., Kalb, R. G., Zaremba, S., & Fryer, H. (1990) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1990.055.01.049 · Cited by 271 · see citing works
Monocular deprivation induces homosynaptic long-term depression in visual cortex
Rittenhouse, C. D., Shouval, H. Z., Paradiso, M. A., & Bear, M. F. (1999) · Nature · doi:10.1038/16922 · Cited by 228 · see citing works
Effects of early unilateral blur on the macaque's visual system. II. Anatomical observations
Hendrickson, A. E., Movshon, J. A., Eggers, H., Gizzi, M., Boothe, R., & Kiorpes, L. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-05-01327.1987 · Cited by 216 · see citing works
Majewska, A. K., & Sur, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2636949100 · Cited by 203 · see citing works
Effects of early unilateral blur on the macaque's visual system. III. Physiological observations
Movshon, J. A., Hm, E., Gizzi, M., Hendrickson, A. E., Kiorpes, L., & Boothe, R. G. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-05-01340.1987 · Cited by 200 · see citing works
Brückner, G., Bringmann, A., Härtig, W., Köppe, G., Delpech, B., & Brauer, K. (1998) · Experimental Brain Research · doi:10.1007/s002210050463 · Cited by 162 · see citing works
A Morphological Correlate of Synaptic Scaling in Visual Cortex
Wallace, W., & Bear, M. F. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1110-04.2004 · Cited by 139 · see citing works
Swindale, N. V., Vital‐Durand, F., & Blakemore, C. B. (1981) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1981.0074 · Cited by 132 · see citing works
Nerve growth factor prevents the amblyopic effects of monocular deprivation.
Domenici, L., Berardi, N., Carmignoto, G., Vantini, G., & Maffei, L. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.19.8811 · Cited by 115 · see citing works
Self-citationWegner, F., Härtig, W., Bringmann, A., Grosche, J., Wohlfarth, K., Zuschratter, W., & Brückner, G. (2003) · Experimental Neurology · doi:10.1016/s0014-4886(03)00313-3 · Cited by 107 · see citing works
The extent of visual recovery from early monocular or binocular visual deprivation in kittens.
Mitchell, D. E. (1988) · The Journal of Physiology · doi:10.1113/jphysiol.1988.sp016939 · Cited by 86 · see citing works
Correlated binocular activity guides recovery from monocular deprivation
Kind, P. C., Mitchell, D. E., Ahmed, B., Blakemore, C. B., Bonhoeffer, T., & Sengpiel, F. (2002) · Nature · doi:10.1038/416430a · Cited by 82 · see citing works
Liao, D. S., Krahe, T. E., Prusky, G. T., Medina, A. E., & Ramoa, A. S. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00266.2004 · Cited by 73 · see citing works
Experience‐dependent plasticity of visual acuity in rats
Prusky, G. T., West, P. W. R., & Douglas, R. M. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00236.x · Cited by 71 · see citing works
Blakemore, C. B., Vital‐Durand, F., & Garey, L. J. (1981) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1981.0072 · Cited by 68 · see citing works
Konur, S., & Yuste, R. (2004) · Journal of Neurobiology · doi:10.1002/neu.10306 · Cited by 65 · see citing works
Mitchell, D. E., & MacKinnon, S. E. (2002) · Clinical and Experimental Optometry · doi:10.1111/j.1444-0938.2002.tb03067.x · Cited by 42 · see citing works
Temporal Aspects of Contrast Visual Evoked Potentials in the Pigmented Rat: Effect of Dark Rearing
Pizzorusso, T., Fagiolini, M., Porciatti, V., & Maffei, L. (1997) · Vision Research · doi:10.1016/s0042-6989(96)00172-1 · Cited by 30 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Plasticity during stroke recovery: from synapse to behaviour
Murphy, T. H., & Corbett, D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2735 · Cited by 1,938 · see citing works
PTPσ Is a Receptor for Chondroitin Sulfate Proteoglycan, an Inhibitor of Neural Regeneration
Shen, Y., Tenney, A. P., Busch, S. A., Horn, K. P., Cuascut, F. X., Liu, K., He, Z., Silver, J., & Flanagan, J. G. (2009) · Science · doi:10.1126/science.1178310 · Cited by 682 · see citing works
Microglial Remodeling of the Extracellular Matrix Promotes Synapse Plasticity
Nguyen, P. T., Dorman, L. C., Pan, S., Vainchtein, I. D., Han, R. T., Nakao-Inoue, H., Taloma, S. E., Barron, J. J., Molofsky, A. B., Kheirbek, M. A., et al. (2020) · Cell · doi:10.1016/j.cell.2020.05.050 · Cited by 615 · 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
The dual role of the extracellular matrix in synaptic plasticity and homeostasis
Dityatev, A., Schachner, M., & Sonderegger, P. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2898 · Cited by 559 · see citing works
Animals lacking link protein have attenuated perineuronal nets and persistent plasticity
Carulli, D., Pizzorusso, T., Kwok, J. C. F., Putignano, E., Poli, A., Forostyak, S., Andrews, M. R., Deepa, S. S., Glant, T. T., & Fawcett, J. W. (2010) · Brain · doi:10.1093/brain/awq145 · Cited by 495 · see citing works
Self-citationCritical period regulation across multiple timescales
Reh, R. K., Dias, B. G., Nelson, C. A., Kaufer, D., Werker, J. F., Kolb, B., Levine, J. D., & Hensch, T. K. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1820836117 · Cited by 492 · 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
Self-citationThe role of extracellular matrix in CNS regeneration
Busch, S. A., & Silver, J. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.09.004 · Cited by 468 · see citing works
Extracellular matrix of the central nervous system: from neglect to challenge
Zimmermann, D. R., & Dours-Zimmermann, M. T. (2008) · Histochemistry and Cell Biology · doi:10.1007/s00418-008-0485-9 · Cited by 465 · see citing works
Critical-Period Plasticity in the Visual Cortex
Levelt, C. N., & Hübener, M. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113813 · Cited by 402 · see citing works
Environment and Brain Plasticity: Towards an Endogenous Pharmacotherapy
Sale, A., Berardi, N., & Maffei, L. (2014) · Physiological Reviews · doi:10.1152/physrev.00036.2012 · Cited by 402 · see citing works
Self-citationExtracellular matrix and perineuronal nets in CNS repair
Kwok, J. C. F., Dick, G., Wang, D., & Fawcett, J. W. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20974 · Cited by 395 · see citing works
Otx2 Binding to Perineuronal Nets Persistently Regulates Plasticity in the Mature Visual Cortex
Beurdeley, M., Spatazza, J., Lee, H. H. C., Sugiyama, S., Bernard, C., Di Nardo, A. A., Hensch, T. K., & Prochiantz, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0394-12.2012 · Cited by 398 · see citing works
The perineuronal net and the control of CNS plasticity
Wang, D., & Fawcett, J. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1375-y · Cited by 373 · see citing works
Enrich the environment to empower the brain
Sale, A., Berardi, N., & Maffei, L. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2008.12.004 · Cited by 341 · see citing works
Self-citationNurturing brain plasticity: Impact of environmental enrichment
Baroncelli, L., Braschi, C., Spolidoro, M., Begenisic, T., Sale, A., & Maffei, L. (2010) · Cell Death & Differentiation · doi:10.1038/cdd.2009.193 · Cited by 330 · see citing works
Self-citationReducing Intracortical Inhibition in the Adult Visual Cortex Promotes Ocular Dominance Plasticity
Harauzov, A., Spolidoro, M., DiCristo, G., De Pasquale, R., Cancedda, L., Pizzorusso, T., Viegi, A., Berardi, N., & Maffei, L. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2233-09.2010 · Cited by 319 · see citing works
Self-citationCritical period revisited: impact on vision
Morishita, H., & Hensch, T. K. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.05.009 · Cited by 311 · see citing works
Autism: A “Critical Period” Disorder?
LeBlanc, J. J., & Fagiolini, M. (2011) · Neural Plasticity · doi:10.1155/2011/921680 · Cited by 301 · see citing works
Mauney, S. A., Athanas, K. M., Pantazopoulos, H., Shaskan, N., Passeri, E., Berretta, S., & Woo, T.-U. W. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.05.007 · Cited by 291 · see citing works
Sensory Deprivation Alters Aggrecan and Perineuronal Net Expression in the Mouse Barrel Cortex
McRae, P. A., Rocco, M. M., Kelly, G., Brumberg, J. C., & Matthews, R. T. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5425-06.2007 · Cited by 272 · see citing works
Very long-term memories may be stored in the pattern of holes in the perineuronal net
Tsien, R. Y. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1310158110 · Cited by 244 · see citing works
Reinhard, S. M., Razak, K., & Ethell, I. M. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00280 · Cited by 219 · see citing works
Perineuronal Nets Enhance the Excitability of Fast-Spiking Neurons
Balmer, T. S. (2016) · eneuro · doi:10.1523/eneuro.0112-16.2016 · Cited by 220 · see citing works
Perineuronal net formation and structure in aggrecan knockout mice
Giamanco, K. A., Morawski, M., & Matthews, R. T. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.08.032 · Cited by 207 · see citing works
Faissner, A., Pyka, M., Geissler, M., Sobik, T., Frischknecht, R., Gundelfinger, E. D., & Seidenbecher, C. (2010) · Brain Research Reviews · doi:10.1016/j.brainresrev.2010.01.001 · Cited by 207 · see citing works
Putignano, E., Lonetti, G., Cancedda, L., Ratto, G., Costa, M., Maffei, L., & Pizzorusso, T. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.007 · Cited by 196 · see citing works
Self-citationMassey, J. M., Amps, J., Viapiano, M. S., Matthews, R. T., Wagoner, M. R., Whitaker, C. M., Alilain, W., Yonkof, A. L., Khalyfa, A., Cooper, N. G. F., et al. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2007.03.029 · Cited by 185 · see citing works
Extracellular matrix abnormalities in schizophrenia
Berretta, S. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.08.010 · Cited by 179 · 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
Hylin, M. J., Orsi, S. A., Moore, A. N., & Dash, P. K. (2013) · Learning & Memory · doi:10.1101/lm.030197.112 · Cited by 143 · see citing works
Carulli, D., Rhodes, K. E., & Fawcett, J. W. (2007) · Journal of Comparative Neurology · doi:10.1002/cne.21231 · Cited by 158 · see citing works
Ye, Q., & Miao, Q.-L. (2013) · Matrix Biology · doi:10.1016/j.matbio.2013.04.001 · Cited by 146 · see citing works
de Vivo, L., Landi, S., Panniello, M., Baroncelli, L., Chierzi, S., Mariotti, L., Spolidoro, M., Pizzorusso, T., Maffei, L., & Ratto, G. M. (2013) · Nature Communications · doi:10.1038/ncomms2491 · Cited by 148 · see citing works
Self-citationVetencourt, J. F. M., Tiraboschi, E., Spolidoro, M., Castrén, E., & Maffei, L. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07488.x · Cited by 138 · see citing works
Self-citationThe perineuronal net component of the extracellular matrix in plasticity and epilepsy
McRae, P. A., & Porter, B. E. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.08.007 · Cited by 143 · 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
Converting juvenile into adult plasticity: a role for the brain's extracellular matrix
Gundelfinger, E. D., Frischknecht, R., Choquet, D., & Heine, M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07253.x · Cited by 136 · see citing works
Pyka, M., Wetzel, C., Aguado, A., Geissler, M., Hatt, H., & Faissner, A. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07690.x · Cited by 131 · see citing works
Removal of perineuronal nets disrupts recall of a remote fear memory
Thompson, E. H., Lensjø, K. K., Wigestrand, M. B., Malthe-Sørenssen, A., Hafting, T., & Fyhn, M. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1713530115 · Cited by 118 · see citing works
Soleman, S., Yip, P. K., Duricki, D. A., & Moon, L. D. F. (2012) · Brain · doi:10.1093/brain/aws027 · Cited by 123 · see citing works
Ciucci, F., Putignano, E., Baroncelli, L., Landi, S., Berardi, N., & Maffei, L. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000475 · Cited by 119 · see citing works
Self-citationNowicka, D., Soulsby, S., Skangiel‐Kramska, J., & Glazewski, S. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06996.x · Cited by 110 · see citing works
Plasticity in the adult brain: lessons from the visual system
Spolidoro, M., Sale, A., Berardi, N., & Maffei, L. (2009) · Experimental Brain Research · doi:10.1007/s00221-008-1509-3 · Cited by 111 · see citing works
Self-citationDelayed anti-Nogo-A therapy improves function after chronic stroke in adult rats
Tsai, S.-Y., Papadopoulos, C. M., Schwab, M. E., & Kartje, G. L. (2011) · Stroke · doi:10.1161/strokeaha.110.590083 · Cited by 106 · see citing works
Otx2-PNN interaction to regulate cortical plasticity
Bernard, C., & Prochiantz, A. (2016) · Neural Plasticity · doi:10.1155/2016/7931693 · Cited by 102 · see citing works
Sandvig, I., Augestad, I. L., Håberg, A. K., & Sandvig, A. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.13959 · Cited by 94 · see citing works
Perineuronal nets and schizophrenia: The importance of neuronal coatings
Bitanihirwe, B. K. Y., & Woo, T.-U. W. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.03.018 · Cited by 95 · see citing works
Nabel, E. M., & Morishita, H. (2013) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2013.00146 · Cited by 85 · see citing works
Murase, S., Lantz, C. L., & Quinlan, E. M. (2017) · eLife · doi:10.7554/elife.27345 · Cited by 87 · see citing works
Environmental regulation of the neural epigenome
Caldji, C., Hellstrom, I. C., Zhang, T.-Y., Diorio, J., & Meaney, M. J. (2011) · FEBS Letters · doi:10.1016/j.febslet.2011.03.032 · Cited by 82 · see citing works
Diverse functions of perineuronal nets
Karetko, M., & Skangiel-Kramska, J. (2009) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2009-1766 · Cited by 76 · see citing works
Plasticity of the visual cortex and treatment of amblyopia
Sengpiel, F. (2014) · Current Biology · doi:10.1016/j.cub.2014.05.063 · Cited by 72 · see citing works
Bekku, Y., Saito, M., Moser, M., Fuchigami, M., Maehara, A., Nakayama, M., Kusachi, S., Ninomiya, Y., & Oohashi, T. (2012) · Journal of Comparative Neurology · doi:10.1002/cne.23009 · Cited by 65 · see citing works
Nakamura, M., Nakano, K., Morita, S., Nakashima, T., Oohira, A., & Miyata, S. (2009) · Brain Research · doi:10.1016/j.brainres.2008.11.022 · Cited by 54 · see citing works
Biomaterial Approaches to Modulate Reactive Astroglial Response
Zuidema, J. M., Gilbert, R. J., & Gottipati, M. K. (2018) · Cells Tissues Organs · doi:10.1159/000494667 · Cited by 46 · see citing works
Karetko-Sysa, M., Skangiel-Kramska, J., & Nowicka, D. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.05.022 · Cited by 45 · see citing works
Arbat-Plana, A., Torres-Espín, A., Navarro, X., & Udina, E. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2014.10.009 · Cited by 40 · see citing works
Optimization of visual training for full recovery from severe amblyopia in adults
Eaton, N. C., Sheehan, H. M., & Quinlan, E. M. (2016) · Learning & Memory · doi:10.1101/lm.040295.115 · Cited by 28 · see citing works
DACS, novel matrix structure composed of chondroitin sulfate proteoglycan in the brain
Hayashi, N., Tatsumi, K., Okuda, H., Yoshikawa, M., Ishizaka, S., Miyata, S., Manabe, T., & Wanaka, A. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.10.040 · Cited by 30 · see citing works
Chemistry and Function of Glycosaminoglycans in the Nervous System
Schwartz, N. B., & Domowicz, M. S. (2014) · Advances in Neurobiology · doi:10.1007/978-1-4939-1154-7_5 · Cited by 25 · see citing works
- Authors
- Pizzorusso, T., Medini, P., Landi, S., Baldini, S., Berardi, N., & Maffei, L.
- Affiliations
- Neuroscience Institute (IT)
- Scuola Normale Superiore (IT)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2006-05-30
- Volume
- 103
- Issue
- 22
- Pages
- 8517-8522
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC1482523
- OpenAlex
- W1986126224
- Cited by
- 367
- References
- 39
- Citations by year
- 2026: 8 · 2025: 16 · 2024: 7 · 2023: 9 · 2022: 16 · 2021: 8 · 2020: 27 · 2019: 12 · 2018: 22 · 2017: 22 · 2016: 12 · 2015: 19 · 2014: 31 · 2013: 28 · 2012: 27
- FWCI
- 9.55
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed (publishedVersion)
- Florence Research (University of Florence) (submittedVersion)
- Scuola Normale Superiore di Pisa (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
- monocular deprivation, chondroitinase ABC, chondroitin sulfate proteoglycans, extracellular matrix, ocular dominance, visual acuity, dendritic spine density, critical period, functional recovery
- MeSH terms
- Aging, Animals, Behavior, Animal, Electrophysiology, Spine, Time Factors, Vision Disorders, Visual Cortex, Vision, Monocular, Chondroitin ABC Lyase, Rats
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