Morphology of perineuronal nets in tenascin-R and parvalbumin single and double knockout mice

Perineuronal nets: past and present

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Brain extracellular matrix

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Perineuronal nets — a specialized form of extracellular matrix in the adult nervous system

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Cortical neurons immunoreactive for the potassium channel Kv3.1b subunit are predominantly surrounded by perineuronal nets presumed as a buffering system for cations

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Interactions of the chondroitin sulfate proteoglycan phosphacan, the extracellular domain of a receptor-type protein tyrosine phosphatase, with neurons, glia, and neural cell adhesion molecules.

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The C-type lectin domains of lecticans, a family of aggregating chondroitin sulfate proteoglycans, bind tenascin-R by protein– protein interactions independent of carbohydrate moiety

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Isolation and characterization of developmentally regulated chondroitin sulfate and chondroitin/keratan sulfate proteoglycans of brain identified with monoclonal antibodies

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Mice Deficient for Tenascin-R Display Alterations of the Extracellular Matrix and Decreased Axonal Conduction Velocities in the CNS

Weber, P., Bartsch, U., Rasband, M. N., Czaniera, R., Lang, Y., Bluethmann, H., Margolis, R. U., Levinson, S. R., Shrager, P., Montag, D., et al. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-11-04245.1999 · Cited by 247 · see citing works

TAG-1/Axonin-1 Is a High-affinity Ligand of Neurocan, Phosphacan/Protein-tyrosine Phosphatase-ζ/β, and N-CAM

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Prolonged contraction-relaxation cycle of fast-twitch muscles in parvalbumin knockout mice

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High Affinity Binding and Overlapping Localization of Neurocan and Phosphacan/Protein-tyrosine Phosphatase-ζ/β with Tenascin-R, Amphoterin, and the Heparin-binding Growth-associated Molecule

Milev, P., Chiba, A., Häring, M., Rauvala, H., Schachner, M., Ranscht, B., Margolis, R. K., & Margolis, R. U. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.12.6998 · Cited by 190 · see citing works

The versican C-type lectin domain recognizes the adhesion protein tenascin-R.

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Purification, characterization and developmental expression of a brain-specific chondroitin sulfate proteoglycan, 6B4 proteoglycan/phosphacan

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Neurons Produce a Neuronal Cell Surface-Associated Chondroitin Sulfate Proteoglycan

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Occurrence of a N-terminal proteolytic fragment of neurocan, not a C-terminal half, in a perineuronal net in the adult rat cerebrum

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‘Perineuronal nets’ around cortical interneurons expressing parvalbumin are rich in tenascin

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Postmitotic expression of ankyrinR and beta R-spectrin in discrete neuronal populations of the rat brain

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Phosphacan immunoreactivity is associated with perineuronal nets around parvalbumin-expressing neurones

Haunsø, A., Celio, M. R., Margolis, R. K., & Menoud, P.-A. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01596-6 · Cited by 52 · see citing works

Temporal and spatial appearance of the membrane cytoskeleton and perineuronal nets in the rat neocortex

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Untitled work

Hagihara (1999) · doi:10.1002/(sici)1096-9861(19990726)410:2

Extracellular matrix of the central nervous system: from neglect to challenge

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Chondroitin sulphate proteoglycans: preventing plasticity or protecting the CNS?

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Tenascins and the Importance of Adhesion ModulationPreprint

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Crosstalk between glia, extracellular matrix and neurons

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Reduction in parvalbumin expression not loss of the parvalbumin-expressing GABA interneuron subpopulation in genetic parvalbumin and shank mouse models of autism

Filice, F., Vörckel, K. J., Sungur, A. Ö., Wöhr, M., & Schwaller, B. (2016) · Molecular Brain · doi:10.1186/s13041-016-0192-8 · Cited by 240 · see citing works

Modification of extracellular matrix by enzymatic removal of chondroitin sulfate and by lack of tenascin-R differentially affects several forms of synaptic plasticity in the hippocampus

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Parvalbumin-Deficiency Facilitates Repetitive IPSCs and Gamma Oscillations in the Hippocampus

Vreugdenhil, M., Jefferys, J. G. R., Celio, M. R., & Schwaller, B. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00576.2002 · Cited by 219 · 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

Distribution and synthesis of extracellular matrix proteoglycans, hyaluronan, link proteins and tenascin‐R in the rat spinal cord

Galtrey, C. M., Kwok, J. C. F., Carulli, D., Rhodes, K. E., & Fawcett, J. W. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06108.x · Cited by 203 · see citing works

Contributions of astrocytes to synapse formation and maturation — Potential functions of the perisynaptic extracellular matrix

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Parvalbumin deficiency affects network properties resulting in increased susceptibility to epileptic seizures

Schwaller, B., Tetko, I. V., Tandon, P., Silveira, D. C., Vreugdenhil, M., Henzi, T., Potier, M.-C., Celio, M. R., & Villa, A. E. P. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2003.12.006 · Cited by 169 · see citing works

Promoting plasticity in the spinal cord with chondroitinase improves functional recovery after peripheral nerve repair

Galtrey, C. M., Asher, R. A., Nothias, F., & Fawcett, J. W. (2007) · Brain · doi:10.1093/brain/awl372 · Cited by 166 · see citing works

Behavioral alterations in mice deficient for the extracellular matrix glycoprotein tenascin-R

Freitag, S., Schachner, M., & Morellini, F. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(03)00109-8 · Cited by 93 · see citing works

Proteolytic Remodeling of Perineuronal Nets: Effects on Synaptic Plasticity and Neuronal Population Dynamics

Bozzelli, P. L., Alaiyed, S., Kim, E., Villapol, S., & Conant, K. E. (2018) · Neural Plasticity · doi:10.1155/2018/5735789 · Cited by 90 · see citing works

Prenatal Valproate Exposure Differentially Affects Parvalbumin-Expressing Neurons and Related Circuits in the Cortex and Striatum of Mice

Lauber, E., Filice, F., & Schwaller, B. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00150 · Cited by 87 · see citing works

Dysregulation of Parvalbumin Expression in the Cntnap2−/− Mouse Model of Autism Spectrum Disorder

Lauber, E., Filice, F., & Schwaller, B. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00262 · Cited by 86 · see citing works

Severe cognitive and motor coordination deficits in Tenascin‐R‐deficient mice

Sallaz, M., & Montag, D. (2003) · Genes Brain & Behavior · doi:10.1034/j.1601-183x.2003.00003.x · Cited by 80 · 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

Monoclonal antibody Cat-315 detects a glycoform of receptor protein tyrosine phosphatase beta/phosphacan early in CNS development that localizes to extrasynaptic sites prior to synapse formation

Diño, M. R., Harroch, S., Hockfield, S. J., & Matthews, R. T. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.07.054 · Cited by 76 · see citing works

Parvalbumin neurons and perineuronal nets in the mouse prefrontal cortex

Ueno, H., Suemitsu, S., Okamoto, M., Matsumoto, Y., & Ishihara, T. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.11.035 · Cited by 76 · see citing works

Reduced extracellular space in the brain of tenascin‐R‐ and HNK‐1‐sulphotransferase deficient mice

Syková, E., Voříšek, I., Mazel, T., Antonova, T., & Schachner, M. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04375.x · Cited by 73 · see citing works

Tenascins and inflammation in disorders of the nervous system

Jakovčevski, I., Miljković, D. M., Schachner, M., & Anđjus, P. R. (2012) · Amino Acids · doi:10.1007/s00726-012-1446-0 · Cited by 62 · see citing works

The extracellular matrix glycoprotein tenascin-C and matrix metalloproteinases modify cerebellar structural plasticity by exposure to an enriched environment

Stamenković, V., Stamenković, S., Jaworski, T., Gawlak, M., Jovanović, M., Jakovčevski, I., Wilczynski, G. M., Kaczmarek, L., Schachner, M., Radenović, L., et al. (2016) · Brain Structure and Function · doi:10.1007/s00429-016-1224-y · Cited by 60 · see citing works

Hepatocyte growth factor (HGF) modulates GABAergic inhibition and seizure susceptibility

Bae, M. H., Bissonette, G. B., Mars, W. M., Michalopoulos, G. K., Achim, C. L., Depireux, D. A., & Powell, E. M. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.10.011 · Cited by 50 · see citing works

Perineuronal nets show intrinsic patterns of extracellular matrix differentiation in organotypic slice cultures

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Disturbance of perineuronal nets in the perilesional area after photothrombosis is not associated with neuronal death

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

Sensory experience-dependent formation of perineuronal nets and expression of Cat-315 immunoreactive components in the mouse somatosensory cortex

Ueno, H., Suemitsu, S., Okamoto, M., Matsumoto, Y., & Ishihara, T. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.04.041 · Cited by 45 · see citing works

Extracellular matrix and synapse formation

Yang, L., Wei, M., Xing, B., & Zhang, C. (2022) · Bioscience Reports · doi:10.1042/bsr20212411 · Cited by 40 · see citing works

The potential of memory enhancement through modulation of perineuronal nets

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Chondroitin Sulfate Proteoglycan Tenascin-R Regulates Glutamate Uptake by Adult Brain Astrocytes

Okuda, H., Tatsumi, K., Morita, S., Shibukawa, Y., Korekane, H., Horii-Hayashi, N., Wada, Y., Taniguchi, N., & Wanaka, A. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.504787 · Cited by 33 · see citing works

From molecules to behavior: Implications for perineuronal net remodeling in learning and memory

Sanchez, B., Kraszewski, P., Lee, S., & Cope, E. C. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.16036 · Cited by 37 · see citing works

The protein tyrosine phosphatase RPTPζ/phosphacan is critical for perineuronal net structure

Eill, G. J., Sinha, A., Morawski, M., Viapiano, M. S., & Matthews, R. T. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.010830 · Cited by 32 · see citing works

The protein tyrosine phosphatase RPTPζ/phosphacan is critical for perineuronal net structure

Eill, G. J., Sinha, A., Morawski, M., Viapiano, M. S., & Matthews, R. T. (2020) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)49907-8 · Cited by 32 · see citing works

Structural and Functional Modulation of Perineuronal Nets: In Search of Important Players with Highlight on Tenascins

Jakovljević, A., Tucić, M., Blažíková, M., Korenić, A., Missirlis, Y. F., Stamenković, V., & Anđjus, P. R. (2021) · Cells · doi:10.3390/cells10061345 · Cited by 30 · see citing works

A newly identified mouse hypothalamic area having bidirectional neural connections with the lateral septum: the perifornical area of the anterior hypothalamus rich in chondroitin sulfate proteoglycans

Horii‐Hayashi, N., Sasagawa, T., Hashimoto, T., Kaneko, T., Takeuchi, K., & Nishi, M. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.13024 · Cited by 27 · see citing works

A cross-species genetic analysis identifies candidate genes for mouse anxiety and human bipolar disorder

Ashbrook, D. G., Williams, R. W., Lu, L., & Hager, R. (2015) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2015.00171 · Cited by 24 · see citing works

The Role and Modulation of Spinal Perineuronal Nets in the Healthy and Injured Spinal Cord

Sánchez-Ventura, J., Lane, M. A., & Udina, E. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.893857 · Cited by 25 · see citing works

Early Days of Tenascin-R Research: Two Approaches Discovered and Shed Light on Tenascin-R

Rathjen, F. G., & Hodge, R. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2020.612482 · Cited by 16 · see citing works

The Extracellular Matrix in Neural Development, Plasticity, and Regeneration

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A review of functional heterogeneity among astrocytes and the CS56-specific antibody-mediated detection of a subpopulation of astrocytes in adult brains

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Cntnap2 loss drives striatal neuron hyperexcitability and behavioral inflexibility

Cording, K. R., Tu, E. M., Wang, H., Agopyan-Miu, A. H. C. W., & Bateup, H. S. (2025) · eLife · doi:10.1101/2024.05.09.593387 · Cited by 8 · see citing works

Multiple Species and Functions of Proteoglycans in the Central Nervous System

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Contactin-1 is a critical neuronal cell surface receptor for perineuronal net structure

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Perineuronal nets’ role in metabolism

Zhang, N., Song, B., Bai, P., Du, L. Q., Chen, L., Xu, Y., & Zeng, T. (2024) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00154.2024 · Cited by 4 · see citing works

Cntnap2 loss drives striatal neuron hyperexcitability and behavioral inflexibilityPreprint

Cording, K. R., Tu, E. M., Wang, H., Agopyan-Miu, A. H. C. W., & Bateup, H. S. (2024) · eLife · doi:10.7554/elife.100162.1 · Cited by 4 · see citing works

Cntnap2 loss drives striatal neuron hyperexcitability and behavioral inflexibilityPreprint

Cording, K. R., Tu, E. M., Wang, H., Agopyan-Miu, A. H. C. W., & Bateup, H. S. (2024) · eLife · doi:10.7554/elife.100162 · Cited by 4 · see citing works

Quantitative Morphological Analyses of the Striatum and Cerebellum of Tenascin-R deficient mice

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Astrocytic Regulation of Aberrant Perineuronal Net Formation in Mecp2 ‐Null Neocortex

Sinha, A., Kowalchuk, A. M., Khatibi, N., Matthews, R. T., & MacDonald, J. L. (2026) · Journal of Neurochemistry · doi:10.1111/jnc.70503 · Cited by 2 · see citing works

Microglial NLRP3 inflammasome activation leads to perineuronal net loss in cocultured neurons

Tarakcioglu, E., Tüfekçi, K. U., & Genç, Ş. (2025) · Molecular Biology Reports · doi:10.1007/s11033-025-11145-3 · Cited by 1 · see citing works

Glucocorticoids Modulate Expression of Perineuronal Net Component Genes and Parvalbumin During Development of Mouse Cortical Neurons

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Proteoglycans of the Central Nervous System

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Recycling as a mechanism for extracellular matrix remodeling at the synapse

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Cntnap2 loss drives striatal neuron hyperexcitability and behavioral inflexibilityPreprint

Cording, K. R., Tu, E. M., Wang, H., Agopyan-Miu, A. H. C. W., & Bateup, H. S. (2025) · eLife · doi:10.7554/elife.100162.2 · Cited by 1 · see citing works

Distribution and functions of the extracellular matrix protein matrilin-2 in the nervous system of mice

Malin, D. (2005)

Auswirkungen von Tenascin–C, –R und –C/R–Defizienz auf den skelettalen Phänotyp von Mäusen mit hohem Lebensalter

Herberholz, M. (2005) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.4893

Reviewer #2 (Public Review): Cntnap2 loss drives striatal neuron hyperexcitability and behavioral inflexibility

Cording, K. R., Tu, E. M., Wang, H., et al. (2024) · eLife · doi:10.7554/elife.100162.1.sa1

eLife Assessment: Cntnap2 loss drives striatal neuron hyperexcitability and behavioral inflexibility

Ding, J. (2024) · eLife · doi:10.7554/elife.100162.1.sa3

Reviewer #1 (Public Review): Cntnap2 loss drives striatal neuron hyperexcitability and behavioral inflexibility

Cording, K. R., Tu, E. M., Wang, H., et al. (2024) · eLife · doi:10.7554/elife.100162.1.sa2

Reviewer #3 (Public Review): Cntnap2 loss drives striatal neuron hyperexcitability and behavioral inflexibility

Cording, K. R., Tu, E. M., Wang, H., et al. (2024) · eLife · doi:10.7554/elife.100162.1.sa0

Synaptic changes upon removal of extracellular perineuronal nets in adult mouse visual cortex

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Postnatal development of perineuronal nets in wild-type mice and in a mutant deficient in tenascin-R

Br�ckner, G., Grosche, J., Schmidt, S., H�rtig, W., Margolis, R. U., Delpech, B., Seidenbecher, C. I., Czaniera, R., & Schachner, M. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001225)428:4

Postnatal development of perineuronal nets in wild-type mice and in a mutant deficient in tenascin-R

Br�ckner, G., Grosche, J., Schmidt, S., H�rtig, W., Margolis, R. U., Delpech, B., Seidenbecher, C. I., Czaniera, R., & Schachner, M. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001225)428:4

Phosphacan immunoreactivity is associated with perineuronal nets around parvalbumin-expressing neurones

Haunsø, A., Celio, M. R., Margolis, R. K., & Menoud, P.-A. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01596-6 · Cited by 52 · see citing works

Tenascin-R promotes assembly of the extracellular matrix of perineuronal nets via clustering of aggrecan

Morawski, M., Dityatev, A., Hartlage-Rübsamen, M., Blosa, M., Holzer, M., Flach, K., Pavlica, S., Dityateva, G., Grosche, J., Brückner, G., et al. (2014) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2014.0046 · Cited by 100 · see citing works

Mice Deficient for Tenascin-R Display Alterations of the Extracellular Matrix and Decreased Axonal Conduction Velocities in the CNS

Weber, P., Bartsch, U., Rasband, M. N., Czaniera, R., Lang, Y., Bluethmann, H., Margolis, R. U., Levinson, S. R., Shrager, P., Montag, D., et al. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-11-04245.1999 · Cited by 247 · see citing works

Tenascin-R and perineuronal nets of extracellular matrix

Haunsø, A. (2000)