The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.
Enhanced cognitive flexibility in reversal learning induced by removal of the extracellular matrix in auditory cortex
Open accessAbstract
Significance: The brain’s extracellular matrix (ECM) mediates structural stability by enwrapping synaptic contacts fundamental for long-term memory storage. Whether the ECM in the adult brain might thereby govern learning-related plasticity, lifelong memory reformation, and higher cognitive functions is largely unknown. Here, we enzymatically degraded the ECM in the auditory cortex of adult Mongolian gerbils during a reversal learning task. Such local weakening of the structurally rigid ECM specifically accelerated strategy changes required for reversal learning. It neither affected general sensory learning nor erased already established, learned memory traces. Thus, ECM modulation might promote the cognitive flexibility that can build on learned behaviors, and has further implications to develop new tools for guided neuroplasticity with therapeutic potential.
Overview
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
Verification
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In adult mammalian life, auditory learning is limited, but cortex-dependent auditory relearning regains the agility of the juvenile state after ECM digestion [140] (Fig. 2F).”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [140]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“This treatment promotes neuronal plasticity in different neocortical regions, such as the visual (Pizzorusso et al., 2002) and auditory cortices (Happel et al., 2014).”
From Perineuronal Nets Regulate the Inhibitory Perisomatic Input onto Parvalbumin Interneurons and γ Activity in the Prefrontal Cortex (2020) · cites this paper as Happel et al., 2014
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.
Citations
Cites
Critical period plasticity in local cortical circuits
Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323
Balleine, B. W., & O'Doherty, J. P. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.131 · Cited by 1,775
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
Recanzone, G., Schreiner, C., & Merzenich, M. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-01-00087.1993 · Cited by 1,266
A disinhibitory microcircuit for associative fear learning in the auditory cortex
Letzkus, J. J., Wolff, S. B. E., Meyer, E. M. M., Tovote, P., Courtin, J., Herry, C., & Lüthi, A. (2011) · Nature · doi:10.1038/nature10674 · Cited by 840 · cited 1×
“Indeed, auditory associative learning has been correlated with structural changes of topographic connections within primary ACx (19, 29–31), changes in interneuron activity (32, 33), and Ca-dependent synaptic processing (34).”
BackgroundHyaluronidases: Their Genomics, Structures, and Mechanisms of Action
Stern, R., & Jedrzejas, M. J. (2006) · Chemical Reviews · doi:10.1021/cr050247k · Cited by 806
Perineuronal Nets Protect Fear Memories from Erasure
Gogolla, N., Caroni, P., Lüthi, A., & Herry, C. (2009) · Science · doi:10.1126/science.1174146 · Cited by 760
The Restless Engram: Consolidations Never End
Dudai, Y. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150500 · Cited by 644
Decision theory, reinforcement learning, and the brain
Dayan, P., & Daw, N. D. (2008) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.8.4.429 · Cited by 580
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
Dias, R., Robbins, T. W., & Roberts, A. C. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-23-09285.1997 · Cited by 555
Brain extracellular matrix affects AMPA receptor lateral mobility and short-term synaptic plasticity
Frischknecht, R., Heine, M., Perrais, D., Seidenbecher, C. I., Choquet, D., & Gundelfinger, E. D. (2009) · Nature Neuroscience · doi:10.1038/nn.2338 · Cited by 554
Self-citationSurface Mobility of Postsynaptic AMPARs Tunes Synaptic Transmission
Heine, M., Groc, L., Frischknecht, R., Béïque, J.-C., Lounis, B., Rumbaugh, G., Huganir, R. L., Cognet, L., & Choquet, D. (2008) · Science · doi:10.1126/science.1152089 · Cited by 518
Self-citationExperience leaves a lasting structural trace in cortical circuits
Hofer, S. B., Mrsic-Flogel, T. D., Bonhoeffer, T., & Hübener, M. (2009) · Nature · doi:10.1038/nature07487 · Cited by 514
Learning and cognitive flexibility: frontostriatal function and monoaminergic modulation
Kehagia, A. A., Murray, G. K., & Robbins, T. W. (2010) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.01.007 · Cited by 398
Perineuronal nets — a specialized form of extracellular matrix in the adult nervous system
Celio, M. R., & Blümcke, I. (1994) · Brain Research Reviews · doi:10.1016/0165-0173(94)90006-x · Cited by 386
Corticostriatal neurons in auditory cortex drive decisions during auditory discrimination
Znamenskiy, P., & Zador, A. M. (2013) · Nature · doi:10.1038/nature12077 · Cited by 351
Overlapping neural systems mediating extinction, reversal and regulation of fear
Schiller, D., & Delgado, M. R. (2010) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2010.04.002 · Cited by 294
Brakebusch, C., Seidenbecher, C. I., Asztely, F., Rauch, U., Matthies, H., Meyer, H., Krug, M., Böckers, T. M., Zhou, X., Kreutz, M. R., et al. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.21.7417-7427.2002 · Cited by 264
Bukalo, O., Schachner, M., & Dityatev, A. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00082-3 · Cited by 236
Bordi, F., & LeDoux, J. E. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-07-02493.1992 · Cited by 218
Kochlamazashvili, G., Henneberger, C., Bukalo, O., Dvoretskova, E., Senkov, O., Lievens, P. M.-J., Westenbroek, R., Engel, A. K., Catterall, W. A., Rusakov, D. A., et al. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.030 · Cited by 215
Neurocan Is Dispensable for Brain Development
Zhou, X.-H., Brakebusch, C., Matthies, H., Oohashi, T., Hirsch, E., Moser, M., Krug, M., Seidenbecher, C. I., Boeckers, T. M., Rauch, U., et al. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.17.5970-5978.2001 · Cited by 206
Edeline, J., & Weinberger, N. M. (1993) · Behavioral Neuroscience · doi:10.1037//0735-7044.107.1.82 · Cited by 205
Learning-induced plasticity in animal and human auditory cortex
Ohl, F. W., & Scheich, H. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.07.002 · Cited by 197
Self-citationModulation of Perineuronal Nets and Parvalbumin with Developmental Song Learning
Balmer, T. S., Carels, V. M., Frisch, J. L., & Nick, T. A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2974-09.2009 · Cited by 181
Ohl, F. W., Wetzel, W., Wagner, T., Rech, A., & Scheich, H. (1999) · Learning & Memory · doi:10.1101/lm.6.4.347 · Cited by 160
Self-citationde 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
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
Self-citationBudinger, E., Heil, P. F., & Scheich, H. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00142.x · Cited by 135
Brückner, G., Seeger, G., Brauer, K., Härtig, W., Kacza, J., & Bigl, V. (1994) · Brain Research · doi:10.1016/s0006-8993(09)90012-9 · Cited by 132
Inhibitory Plasticity in a Lateral Band Improves Cortical Detection of Natural Vocalizations
Galindo-Leon, E. E., Lin, F. G., & Liu, R. C. (2009) · Neuron · doi:10.1016/j.neuron.2009.05.001 · Cited by 120
Extracellular matrix in plasticity and epileptogenesis
Dityatev, A. E., & Fellin, T. (2008) · Neuron Glia Biology · doi:10.1017/s1740925x09000118 · Cited by 111
van der Schaaf, M. E., van Schouwenburg, M. R., Geurts, D. E. M., Schellekens, A. F. A., Buitelaar, J. K., Verkes, R. J., & Cools, R. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs344 · Cited by 102
Activity-Induced Synaptic Capture and Exocytosis of the Neuronal Serine Protease Neurotrypsin
Frischknecht, R., Fejtová, A., Viesti, M., Stephan, A. H., & Sonderegger, P. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3398-07.2008 · Cited by 90
Self-citationDopaminergic Modulation of Auditory Cortex-Dependent Memory Consolidation through mTOR
Schicknick, H., Schott, B. H., Budinger, E., Smalla, K., Riedel, A., Seidenbecher, C. I., Scheich, H., Gundelfinger, E. D., & Tischmeyer, W. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn026 · Cited by 88
Salgado, H., Bellay, T., Nichols, J., Bose, M., Martinolich, L., Perrotti, L. I., & Atzori, M. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00060.2007 · Cited by 86
Lim, H. H., Lenarz, T., Joseph, G., Battmer, R., Samii, A., Samii, M., Patrick, J. F., & Lenarz, M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3123-07.2007 · Cited by 71
Tan, C. L., Andrews, M. R., Kwok, J. C. F., Heintz, T. G., Gumy, L. F., Fässler, R., & Fawcett, J. W. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5472-11.2012 · Cited by 64
Deep Brain Stimulation of Nucleus Accumbens Region in Alcoholism Affects Reward Processing
Heldmann, M., Berding, G., Voges, J., Bogerts, B., Galazky, I., Müller, U., Baillot, G., Heinze, H., & Münte, T. F. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036572 · Cited by 60
Bowes, C., Massey, J. M., Burish, M. J., Cerkevich, C. M., & Kaas, J. H. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1121604109 · Cited by 54
Kraus, M., Schicknick, H., Wetzel, W., Frank, O., Staak, S., & Tischmeyer, W. (2002) · Learning & Memory · doi:10.1101/lm.47502 · Cited by 42
Self-citationNMDA receptor antagonism impairs reversal learning in developing rats.
Chadman, K. K., Watson, D. J., & Stanton, M. E. (2006) · Behavioral Neuroscience · doi:10.1037/0735-7044.120.5.1071 · Cited by 39
Miyata, S., Akagi, A., Hayashi, N., Watanabe, K., & Oohira, A. (2004) · Brain Research · doi:10.1016/j.brainres.2004.05.034 · Cited by 37
Deliano, M., Scheich, H., & Ohl, F. W. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.1949-09.2009 · Cited by 34
Self-citationWatson, D. J., & Stanton, M. E. (2009) · Learning & Memory · doi:10.1101/lm.1448009 · Cited by 30
Spectral integration plasticity in cat auditory cortex induced by perceptual training
Keeling, M. D., Calhoun, B. M., Krüger, K., Polley, D. B., & Schreiner, C. E. (2007) · Experimental Brain Research · doi:10.1007/s00221-007-1115-9 · Cited by 17
Research works printed but not linked: 1
- 10.1037/0735-7044.107.1.82 · DOI
Cited by
Sorted by citations
Perineuronal nets stabilize the grid cell network
Christensen, A. C., Lensjø, K. K., Lepperød, M. E., Dragly, S.-A., Sutterud, H., Blackstad, J. S., Fyhn, M., & Hafting, T. (2021) · Nature Communications · doi:10.1038/s41467-020-20241-w · Cited by 1,865
The roles of perineuronal nets and the perinodal extracellular matrix in neuronal function
Fawcett, J. W., Oohashi, T., & Pizzorusso, T. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0196-3 · Cited by 589
Casting a Wide Net: Role of Perineuronal Nets in Neural Plasticity
Sorg, B. A., Berretta, S., Blacktop, J. M., Fawcett, J. W., Kitagawa, H., Kwok, J. C. F., & Miquel, M. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2351-16.2016 · Cited by 454
Lensjø, K. K., Lepperød, M. E., Dick, G., Hafting, T., & Fyhn, M. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.2504-16.2016 · Cited by 281
Slaker, M., Churchill, L., Todd, R. P., Blacktop, J. M., Zuloaga, D. G., Raber, J., Darling, R. A., Brown, T. E., & Sorg, B. A. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.3592-14.2015 · Cited by 208
Metadata
- Authors
- Happel, M. F. K., Niekisch, H., Castiblanco Rivera, L. L., Ohl, F. W., Deliano, M., & Frischknecht, R.
- Affiliations
- Otto-von-Guericke-Universität Magdeburg (DE)
- Department of Systems Physiology of Learning and
- Center for Behavioral Brain Sciences (DE)
- Leibniz Institute for Neurobiology (DE)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2014-02-03
- Volume
- 111
- Issue
- 7
- Pages
- 2800-2805
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3932855
- OpenAlex
- W2074133215
- Cited by
- 176
- References
- 47
- Citations by year
- 2026: 9 · 2025: 18 · 2024: 11 · 2023: 11 · 2022: 13 · 2021: 15 · 2020: 22 · 2019: 12 · 2018: 14 · 2017: 18 · 2016: 12 · 2015: 10 · 2014: 10
- FWCI
- 9.30
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- Leibniz-Gemeinschaft
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neuroscience and Music Perception
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- extracellular matrix, auditory cortex, cognitive flexibility, reversal learning, synaptic plasticity, neuroplasticity, Mongolian gerbil
- MeSH terms
- Acoustic Stimulation, Analysis of Variance, Animals, Auditory Cortex, Cognition, Discrimination Learning, Extracellular Matrix, Fluorescence, Gerbillinae, Immunohistochemistry, Male, Neuronal Plasticity, Reversal Learning, Memory, Long-Term
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