The DOI matches its Crossref record; 228 of the 228 references it cites were found in a registry or an index.
The roles of perineuronal nets and the perinodal extracellular matrix in neuronal function
Abstract
Perineuronal nets (PNNs) are extracellular matrix (ECM) chondroitin sulfate proteoglycan (CSPG)-containing structures that surround the soma and dendrites of various mammalian neuronal cell types. PNNs appear during development around the time that the critical periods for developmental plasticity end and are important for both their onset and closure. A similar structure - the perinodal ECM - surrounds the axonal nodes of Ranvier and appears as myelination is completed, acting as an ion-diffusion barrier that affects axonal conduction speed. Recent work has revealed the importance of PNNs in controlling plasticity in the CNS. Digestion, blocking or removal of PNNs influences functional recovery after a variety of CNS lesions. PNNs have further been shown to be involved in the regulation of memory and have been implicated in a number of psychiatric disorders.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
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?
In the citing paper
“PNNs are reticular CSPG-containing ECM structures surrounding the soma and proximal dendrites of a subpopulation of CNS neurons and important for controlling neuroplasticity [1, 13].”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [1]
In the citing paper
“The lectican family of CSPGs (also called aggrecan-family CSPGs) are found within PNNs, including aggrecan, brevican, neurocan, and versican [1].”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [1]
In the citing paper
“PNNs are now being considered as a target for the treatment of impaired memory.”
From The extracellular matrix and perineuronal nets in memory (2022) · cites this paper as [1]
In the citing paper
“It has to be taken also into account that PNNs exclusively enwrap the soma and most proximal segments of dendrites (Celio et al., 1998;Fawcett et al., 2019)”
From Perineuronal Nets Regulate the Inhibitory Perisomatic Input onto Parvalbumin Interneurons and γ Activity in the Prefrontal Cortex (2020) · cites this paper as Fawcett et al., 2019
In the citing paper
“PNNs form preferentially around fast-spiking parvalbumin (PV)+ GABAergic interneurons throughout the brain during the closure of the critical period of plasticity, effectively “locking” proximal synapses in place and providing synaptic stability [21] soon after synaptic pruning is completed by developmental microglia [22].”
From Microglia facilitate loss of perineuronal nets in the Alzheimer's disease brain (2020) · cites this paper as [21]
In the citing paper
“Although contrasting effects of PNN ablation on certain (specifically object recognition) memory tasks and measures of plasticity suggest this is not the case for all types of memory [21, 29, 87], such differences may also be at least partly attributable to the PNN ablation method utilized (e.g. enzymatic digestion vs genetic deletion of PNN components) which can produce differential effects on”
From Microglia facilitate loss of perineuronal nets in the Alzheimer's disease brain (2020) · cites this paper as [21]
In the citing paper
“Depending on side chain sulphation pattern, CSPGs can also be preferentially incorporated into conventional PNNs”
From Microglial depletion prevents extracellular matrix changes and striatal volume reduction in a model of Huntington's disease (2020) · cites this paper as Fawcett et al., 2019
In the citing paper
“stabilizing the neuronal circuitry and inhibiting plasticity (Wang and Fawcett, 2012; Fawcett et al. , 2019).”
From Microglial depletion prevents extracellular matrix changes and striatal volume reduction in a model of Huntington's disease (2020) · cites this paper as Fawcett et al. , 2019
Citations
Cites
1 retracted
Matrix Metalloproteinase (MMP) 9 Transcription in Mouse Brain Induced by Fear Learning
Ganguly, K., Rejmak, E., Mikosz, M., Nikolaev, E., Knapska, E., & Kaczmarek, L. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.457903 · Cited by 106
RetractedStructural basis of long-term potentiation in single dendritic spines
Matsuzaki, M., Honkura, N., Ellis-Davies, G. C. R., & Kasai, H. (2004) · Nature · doi:10.1038/nature02617 · Cited by 2,483
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
Self-citationReactivation 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
Self-citationHensch, T. K. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144327 · Cited by 1,300
Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder
Gandal, M. J., Zhang, P., Hadjimichael, E., Walker, R. L., Chen, C., Liu, S., Won, H., van Bakel, H., Varghese, M., Wang, Y., et al. (2018) · Science · doi:10.1126/science.aat8127 · Cited by 1,247
Cortical parvalbumin interneurons and cognitive dysfunction in schizophrenia
Lewis, D. A., Curley, A. A., Glausier, J. R., & Volk, D. W. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2011.10.004 · Cited by 1,071
Fitch, M. T., & Silver, J. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2007.05.014 · Cited by 1,007
Genome-wide association studies of brain imaging phenotypes in UK Biobank
Elliott, L. T., Sharp, K., Alfaro-Almagro, F., Shi, S., Miller, K. L., Douaud, G., Marchini, J., & Smith, S. M. (2018) · Nature · doi:10.1038/s41586-018-0571-7 · Cited by 834
Allen, B., Ingram, E., Takao, M., Smith, M. J., Jakes, R., Virdee, K., Yoshida, H., Holzer, M., Craxton, M., Emson, P. C., et al. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-21-09340.2002 · Cited by 763
Cited by
Sorted by citations
Microglia in neurodegenerative diseases: mechanism and potential therapeutic targets
Gao, C., Jiang, J., Tan, Y., & Chen, S. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01588-0 · Cited by 1,616
Sharkey, K. A., & Mawe, G. M. (2022) · Physiological Reviews · doi:10.1152/physrev.00018.2022 · Cited by 447
Psychedelics reopen the social reward learning critical period
Nardou, R., Sawyer, E., Song, Y. J., Wilkinson, M., Padovan-Hernandez, Y., de Deus, J. L., Wright, N., Lama, C., Faltin, S., Goff, L. A., et al. (2023) · Nature · doi:10.1038/s41586-023-06204-3 · Cited by 358
Regulation of axonal regeneration after mammalian spinal cord injury
Zheng, B., & Tuszynski, M. H. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00562-y · Cited by 328
Dietary palmitic acid promotes a prometastatic memory via Schwann cells
Pascual, G., Domínguez, D., Elosua-Bayés, M., Beckedorff, F., Laudanna, C., Bigas, C., Douillet, D., Greco, C. M., Symeonidi, A., Hernández, I., et al. (2021) · Nature · doi:10.1038/s41586-021-04075-0 · Cited by 322
Microglia facilitate loss of perineuronal nets in the Alzheimer's disease brain
Crapser, J. D., Spangenberg, E. E., Barahona, R. A., Arreola, M. A., Hohsfield, L. A., & Green, K. N. (2020) · EBioMedicine · doi:10.1016/j.ebiom.2020.102919 · Cited by 280
To Kill a Microglia: A Case for CSF1R Inhibitors
Green, K. N., Crapser, J. D., & Hohsfield, L. A. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.07.001 · Cited by 265
Dual roles of astrocytes in plasticity and reconstruction after traumatic brain injury
Zhou, Y., Shao, A., Yao, Y., Tu, S., Deng, Y., & Zhang, J. (2020) · Cell Communication and Signaling · doi:10.1186/s12964-020-00549-2 · Cited by 211
Microglia-mediated degradation of perineuronal nets promotes pain
Tansley, S., Gu, N., Guzmán, A. U., Cai, W., Wong, C., Lister, K. C., Muñoz-Pino, E., Yousefpour, N., Roome, R. B., Heal, J., et al. (2022) · Science · doi:10.1126/science.abl6773 · Cited by 195
Self-citationThe extracellular matrix as modifier of neuroinflammation and remyelination in multiple sclerosis
Ghorbani, S., & Yong, V. W. (2021) · Brain · doi:10.1093/brain/awab059 · Cited by 191
New insights into glial scar formation after spinal cord injury
Tran, A. P., Warren, P. M., & Silver, J. (2021) · Cell and Tissue Research · doi:10.1007/s00441-021-03477-w · Cited by 188
Microglia as hackers of the matrix: sculpting synapses and the extracellular space
Crapser, J. D., Arreola, M. A., Tsourmas, K. I., & Green, K. N. (2021) · Cellular & Molecular Immunology · doi:10.1038/s41423-021-00751-3 · Cited by 178
The extracellular matrix and perineuronal nets in memory
Fawcett, J. W., Fyhn, M., Jendelova, P., Kwok, J. C. F., Ruzicka, J., & Sorg, B. A. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01634-3 · Cited by 169
Self-citationMechanisms of node of Ranvier assembly
Rasband, M. N., & Peles, E. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-00406-8 · Cited by 180
Early Detection and Preventive Intervention in Schizophrenia: From Fantasy to Reality
Lieberman, J. A., Small, S. A., & Girgis, R. R. (2019) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2019.19080865 · Cited by 165
Crapser, J. D., Ochaba, J., Soni, N., Reidling, J. C., Thompson, L. M., & Green, K. N. (2020) · Brain · doi:10.1093/brain/awz363 · Cited by 157
Fast-spiking parvalbumin-positive interneurons in brain physiology and Alzheimer’s disease
Hijazi, S., Smit, A. B., & van Kesteren, R. E. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02168-y · Cited by 157
The role of astrocyte‐mediated plasticity in neural circuit development and function
Perez-Catalan, N. A., Doe, C. Q., & Ackerman, S. D. (2021) · Neural Development · doi:10.1186/s13064-020-00151-9 · Cited by 146
A shift in the mechanisms controlling hippocampal engram formation during brain maturation
Ramsaran, A. I., Wang, Y., Golbabaei, A., Aleshin, S. E., de Snoo, M. L., Yeung, B.-R. A., Rashid, A. J., Awasthi, A., Lau, J., Tran, L. M., et al. (2023) · Science · doi:10.1126/science.ade6530 · Cited by 155
Venturino, A., Schulz, R., De Jesús-Cortés, H., Maes, M. E., Nagy, B., Reilly-Andújar, F., Colombo, G., Cubero, R. J. A., Schoot Uiterkamp, F. E., Bear, M. F., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109313 · Cited by 140
Semaphorins in Adult Nervous System Plasticity and Disease
Carulli, D., de Winter, F., & Verhaagen, J. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.672891 · Cited by 137
Shifting Developmental Trajectories During Critical Periods of Brain Formation
Dehorter, N., & del Pino, I. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00283 · Cited by 143
Wingert, J. C., & Sorg, B. A. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.673210 · Cited by 129
Dual and multi-targeted nanoparticles for site-specific brain drug delivery
Luo, Y., Yang, H., Zhou, Y., & Hu, B. (2019) · Journal of Controlled Release · doi:10.1016/j.jconrel.2019.11.037 · Cited by 132
An Extracellular Perspective on CNS Maturation: Perineuronal Nets and the Control of Plasticity
Carulli, D., & Verhaagen, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052434 · Cited by 136
The Interstitial System of the Brain in Health and Disease
Shetty, A. K., & Zanirati, G. (2020) · Aging and Disease · doi:10.14336/ad.2020.0103 · Cited by 121
Microglial MERTK eliminates phosphatidylserine‐displaying inhibitory post‐synapses
Park, J., Choi, Y., Jung, E., Lee, S., Sohn, J., & Chung, W. (2021) · The EMBO Journal · doi:10.15252/embj.2020107121 · Cited by 118
Communication, Cross Talk, and Signal Integration in the Adult Hippocampal Neurogenic Niche
Vicidomini, C., Guo, N., & Sahay, A. (2020) · Neuron · doi:10.1016/j.neuron.2019.11.029 · Cited by 108
Carceller, H., Guirado, R., Ripolles-Campos, E., Teruel-Marti, V., & Nacher, J. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.0291-20.2020 · Cited by 112
Gottschling, C., Wegrzyn, D., Denecke, B., & Faissner, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-50404-9 · Cited by 111
Cerebellar plasticity and associative memories are controlled by perineuronal nets
Carulli, D., Broersen, R., de Winter, F., Muir, E. M., Mešković, M., de Waal, M., de Vries, S., Boele, H.-J., Canto, C. B., De Zeeuw, C. I., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1916163117 · Cited by 110
Tewari, B. P., Chaunsali, L., Prim, C. E., & Sontheimer, H. W. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1022754 · Cited by 115
Lupori, L., Totaro, V., Cornuti, S., Ciampi, L., Carrara, F., Grilli, E., Viglione, A., Tozzi, F., Putignano, E., Mazziotti, R. M., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112788 · Cited by 113
Self-citationWareham, L. K., Baratta, R. O., Buono, B. J. D., Schlumpf, E., & Calkins, D. J. (2024) · Molecular Neurodegeneration · doi:10.1186/s13024-024-00704-0 · Cited by 111
Formation of memory assemblies through the DNA-sensing TLR9 pathway
Jovasevic, V., Wood, E. M., Cicvaric, A., Zhang, H., Petrovic, Z., Carboncino, A., Parker, K., Bassett, T. E., Moltesen, M., Yamawaki, N., et al. (2024) · Nature · doi:10.1038/s41586-024-07220-7 · Cited by 102
Organ‐On‐A‐Chip Models of the Blood–Brain Barrier: Recent Advances and Future Prospects
Kawakita, S., Mandal, K., Mou, L., Mecwan, M. M., Zhu, Y., Li, S., Sharma, S., Hernández, A. L., Nguyen, H. T., Maity, S., et al. (2022) · Small · doi:10.1002/smll.202201401 · Cited by 103
Programming tissue-sensing T cells that deliver therapies to the brain
Simic, M., Watchmaker, P. B., Gupta, S., Wang, Y., Sagan, S. A., Duecker, J., Shepherd, C., Diebold, D., Pineo-Cavanaugh, P. L., Haegelin, J., et al. (2024) · Science · doi:10.1126/science.adl4237 · Cited by 98
Arreola, M. A., Soni, N., Crapser, J. D., Hohsfield, L. A., Elmore, M. R. P., Matheos, D. P., Wood, M. A., Swarup, V., Mortazavi, A., & Green, K. N. (2021) · Science Advances · doi:10.1126/sciadv.abg1601 · Cited by 92
Müller, L., Benedetto, S. D., & Müller, V. (2025) · Cells · doi:10.3390/cells14010054 · Cited by 102
Nodes of Ranvier during development and repair in the CNS
Lubetzki, C., Sol‐Foulon, N., & Desmazières, A. (2020) · Nature Reviews Neurology · doi:10.1038/s41582-020-0375-x · Cited by 95
Alaiyed, S., McCann, M., Mahajan, G., Rajkowska, G., Stockmeier, C. A., Kellar, K. J., Wu, J. Y., & Conant, K. (2020) · The Journal of Neuroscience · doi:10.1523/jneurosci.2387-19.2020 · Cited by 84
Molecular signature of extracellular matrix pathology in schizophrenia
Pantazopoulos, H., Katsel, P., Haroutunian, V. H., Chelini, G., Klengel, T., & Berretta, S. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.15009 · Cited by 83
Glypicans and Heparan Sulfate in Synaptic Development, Neural Plasticity, and Neurological Disorders
Kamimura, K., & Maeda, N. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.595596 · Cited by 81
Bilchak, J. N., Caron, G., & Côté, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094858 · Cited by 84
Tissue-specific parameters for the design of ECM-mimetic biomaterials
Tonti, O. R., Larson, H., Lipp, S. N., Luetkemeyer, C. M., Makam, M., Vargas, D., Wilcox, S. M., & Calve, S. (2021) · Acta Biomaterialia · doi:10.1016/j.actbio.2021.04.017 · Cited by 84
Ultrasound as a versatile tool for short- and long-term improvement and monitoring of brain function
Blackmore, D. G., Razansky, D., & Götz, J. (2023) · Neuron · doi:10.1016/j.neuron.2023.02.018 · Cited by 75
Astrocytes require perineuronal nets to maintain synaptic homeostasis in mice
Tewari, B. P., Woo, A. M., Prim, C. E., Chaunsali, L., Patel, D. C., Kimbrough, I. F., Engel, K., Browning, J. L., Campbell, S. L., & Sontheimer, H. W. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01714-3 · Cited by 85
Mesenchymal Stem Cells in Treatment of Spinal Cord Injury and Amyotrophic Lateral Sclerosis
Syková, E., Cizkova, D., & Kubinová, Š. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.695900 · Cited by 79
Aggrecan in Cardiovascular Development and Disease
Koch, C. D., Lee, C. M., & Apte, S. (2020) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155420952902 · Cited by 76
Strackeljan, L., Baczynska, E., Cangalaya, C., Baidoe-Ansah, D., Wlodarczyk, J., Kaushik, R., & Dityatev, A. (2021) · Cells · doi:10.3390/cells10081862 · Cited by 71
Parvalbumin interneuron deficits in schizophrenia
Marín, Ó. (2024) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2024.02.010 · Cited by 79
Chondroitin 6-sulphate is required for neuroplasticity and memory in ageing
Yang, S., Gigout, S., Molinaro, A., Naito-Matsui, Y., Hilton, S., Foscarin, S., Nieuwenhuis, B., Tan, C. L., Verhaagen, J., Pizzorusso, T., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01208-9 · Cited by 70
Self-citationExtracellular Matrix Proteins Involved in Alzheimer's Disease
Ma, J., Ma, C., Li, J., Sun, Y., Ye, F., Liu, K., & Zhang, H. (2020) · Chemistry - A European Journal · doi:10.1002/chem.202000782 · Cited by 70
Neuroplasticity of the visual cortex: in sickness and in health
Baroncelli, L., & Lunghi, C. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113515 · Cited by 79
Role of glia and extracellular matrix in controlling neuroplasticity in the central nervous system
Dzyubenko, E., & Hermann, D. M. (2023) · Seminars in Immunopathology · doi:10.1007/s00281-023-00989-1 · Cited by 73
Wang, L., Sorum, A. W., Huang, B.-S., Kern, M. K., Su, G., Pawar, N., Huang, X., Liu, J., Pohl, N. L. B., & Hsieh‐Wilson, L. C. (2023) · Nature Chemistry · doi:10.1038/s41557-023-01248-4 · Cited by 70
Developmental coupling of cerebral blood flow and fMRI fluctuations in youth
Baller, E. B., Valcarcel, A. M., Adebimpe, A., Alexander-Bloch, A., Cui, Z., Gur, R., Gur, R. E., Larsen, B., Linn, K. A., O'Donnell, C., et al. (2021) · bioRxiv · doi:10.1016/j.celrep.2022.110576 · Cited by 65
Pathogenic hypothalamic extracellular matrix promotes metabolic disease
Beddows, C. A., Shi, F., Horton, A. L., Dalal, S., Zhang, P., Ling, C., Yong, V. W., Loh, K., Cho, H., Karagiannis, C., et al. (2024) · Nature · doi:10.1038/s41586-024-07922-y · Cited by 66
Blackmore, D. G., Turpin, F. R., Palliyaguru, T., Evans, H. T., Chicoteau, A., Lee, W., Pelekanos, M., Nguyen, N., Song, J. H., Sullivan, R., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01129-7 · Cited by 64
Melrose, J., Hayes, A. J., & Bix, G. J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115583 · Cited by 69
Tanti, A., Belliveau, C., Nagy, C., Maitra, M., Denux, F., Perlman, K., Chen, F. Y., Mpai, R., Canonne, C., Théberge, S., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01372-y · Cited by 71
Local diffusion in the extracellular space of the brain
Tønnesen, J., Hrabětová, S., & Soria, F. N. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105981 · Cited by 66
Microglia maintain the normal structure and function of the hippocampal astrocyte network
Du, Y., Brennan, F. H., Popovich, P. G., & Zhou, M. (2022) · Glia · doi:10.1002/glia.24179 · Cited by 61
Perineuronal Net Dynamics in the Pathophysiology of Epilepsy
Chaunsali, L., Tewari, B. P., & Sontheimer, H. W. (2021) · Epiliepsy currents/Epilepsy currents · doi:10.1177/15357597211018688 · Cited by 60
Update on Perineuronal Net Staining With Wisteria floribunda Agglutinin (WFA)
Härtig, W., Meinicke, A., Michalski, D., Schob, S., & Jäger, C. (2022) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2022.851988 · Cited by 60
Perineuronal net degradation rescues CA2 plasticity in a mouse model of Rett syndrome
Carstens, K. E., Lustberg, D. J., Shaughnessy, E. K., McCann, K. E., Alexander, G. M., & Dudek, S. M. (2021) · Journal of Clinical Investigation · doi:10.1172/jci137221 · Cited by 57
Lesnikova, A., Casarotto, P. C., Fred, S. M., Voipio, M., Winkel, F., Steinzeig, A., Antila, H., Umemori, J., Biojone, C., & Castrén, E. (2021) · The Journal of Neuroscience · doi:10.1523/jneurosci.2228-20.2020 · Cited by 56
Diurnal changes in perineuronal nets and parvalbumin neurons in the rat medial prefrontal cortex
Harkness, J. H., Gonzalez, A. E., Bushana, P. N., Jorgensen, E. T., Hegarty, D. M., Nardo, A. A. D., Prochiantz, A., Wisor, J. P., Aicher, S. A., Brown, T. E., et al. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02229-4 · Cited by 55
Stevens, S. R., Longley, C. M., Ogawa, Y., Teliska, L. H., Arumanayagam, A. S., Nair, S., Oses-Prieto, J. A., Burlingame, A. L., Cykowski, M. D., Xue, M., et al. (2021) · eLife · doi:10.7554/elife.66491 · Cited by 53
Yu, Z., Chen, N., Hu, D., Chen, W., Yuan, Y., Meng, S., Zhang, W., Lu, L., Han, Y., & Shi, J. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00004 · Cited by 52
BDNF receptor TrkB as the mediator of the antidepressant drug action
Casarotto, P. C., Umemori, J., & Ċastrén, E. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.1032224 · Cited by 53
Step by step: cells with multiple functions in cortical circuit assembly
Cossart, R., & Garel, S. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00585-6 · Cited by 54
Perineuronal Nets: Subtle Structures with Large Implications
Carceller, H., Gramuntell, Y., Klimczak, P., & Nácher, J. (2022) · The Neuroscientist · doi:10.1177/10738584221106346 · Cited by 54
Li, H., Ghorbani, S., Ling, C., Yong, V. W., & Xue, M. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106282 · Cited by 52
Neural Tissue Homeostasis and Repair Is Regulated via CS and DS Proteoglycan Motifs
Hayes, A. J., & Melrose, J. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.696640 · Cited by 52
Tortorella, I., Argentati, C., Emiliani, C., Morena, F., & Martino, S. (2022) · Cells · doi:10.3390/cells11193093 · Cited by 47
Redox regulation, protein S-nitrosylation, and synapse loss in Alzheimer’s and related dementias
Oh, C.-K., Nakamura, T., Zhang, X., & Lipton, S. A. (2024) · Neuron · doi:10.1016/j.neuron.2024.10.013 · Cited by 52
Functional bioengineered models of the central nervous system
Rouleau, N., Murugan, N. J., & Kaplan, D. L. (2023) · Nature Reviews Bioengineering · doi:10.1038/s44222-023-00027-7 · Cited by 49
Dervan, A. G., Franchi, A., Almeida-González, F. R., Dowling, J. K., Kwakyi, O., McCoy, C. E., O’Brien, F. J., & Hibbitts, A. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13122161 · Cited by 46
Westacott, L. J., & Wilkinson, L. S. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.840266 · Cited by 48
Chondroitin 4- O -sulfation regulates hippocampal perineuronal nets and social memory
Huang, H., Joffrin, A. M., Zhao, Y., Miller, G. M., Zhang, G. C., Oka, Y., & Hsieh‐Wilson, L. C. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2301312120 · Cited by 43
A 3D bioprinted cortical organoid platform for modeling human brain development
Cadena, M. A., Sing, A., Taylor, K., Jin, L., Ning, L., Salar Amoli, M., Singh, Y., Lanjewar, S. N., Tomov, M. L., Serpooshan, V., et al. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202401603 · Cited by 39
Chen, H., Chen, C., Mandhani, N., Short-Miller, J. C., Smucker, M. R., Sun, Y., & Kuan, C.-Y. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1171-20.2020 · Cited by 40
Reichelt, A. C., Lemieux, C. A., Princz‐Lebel, O., Singh, A., Bussey, T. J., & Saksida, L. M. (2021) · Scientific Reports · doi:10.1038/s41598-021-85092-x · Cited by 40
Inhibitory control in neuronal networks relies on the extracellular matrix integrity
Dzyubenko, E., Fleischer, M., Manrique‐Castano, D., Borbor, M., Kleinschnitz, C., Faissner, A., & Hermann, D. M. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03861-3 · Cited by 38
The mechanisms of perineuronal net abnormalities in contributing aging and neurological diseases
Dong, Y., Zhao, K., Qin, X., Du, G., & Gao, L. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.102092 · Cited by 39
Yu, Z., Han, Y., Hu, D., Chen, N., Zhang, Z., Chen, W., Xue, Y.-X., Meng, S., Lü, L., Zhang, W., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01495-w · Cited by 39
Yang, R., Zhang, Y., Kang, J., Zhang, C., & Ning, B. (2024) · Aging and Disease · doi:10.14336/ad.2023.0512 · Cited by 38
Neurotrophins and Their Receptors: BDNF’s Role in GABAergic Neurodevelopment and Disease
Caño, C. H.-D., Varela-Andrés, N., Cebrián-León, A., & Deogracias, R. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25158312 · Cited by 39
Emerging approaches to enhance human brain organoid physiology
Pagliaro, A., Artegiani, B., & Hendriks, D. F. G. (2025) · Trends in Cell Biology · doi:10.1016/j.tcb.2024.12.001 · Cited by 37
Neurocan Contributes to Perineuronal Net Development
Schmidt, S., Arendt, T., Morawski, M., & Sonntag, M. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.06.040 · Cited by 36
Sánchez-Ventura, J., Giménez‐Llort, L., Penas, C., & Udina, E. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113533 · Cited by 38
Enzymatic Degradation of Cortical Perineuronal Nets Reverses GABAergic Interneuron Maturation
Willis, A., Pratt, J. A., & MORRIS, B. J. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-02772-z · Cited by 38
Cells of the Central Nervous System: An Overview of Their Structure and Function
Bigbee, J. W. (2022) · Advances in neurobiology · doi:10.1007/978-3-031-12390-0_2 · Cited by 47
Zhang, L., Gao, Y.-Z., Zhao, C., Xia, J., Yang, J., & Ji, M. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109382 · Cited by 37
Primary cilia are required for the persistence of memory and stabilization of perineuronal nets
Jovasevic, V., Zhang, H., Sananbenesi, F., Guedea, A. L., Soman, K. V., Wiktorowicz, J. E., Fischer, A., & Radulovic, J. (2021) · iScience · doi:10.1016/j.isci.2021.102617 · Cited by 32
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 41
Santos‐Silva, T., Colodete, D. A. E., Lisboa, J. R., Freitas, I. D. S., Lopes, C. F. B., Hadera, V., Lima, T. S. A., Souza, A. J., & Gomes, F. V. (2024) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.13994 · Cited by 39
Extracellular Metalloproteinases in the Plasticity of Excitatory and Inhibitory Synapses
Wiera, G., & Mozrzymas, J. W. (2021) · Cells · doi:10.3390/cells10082055 · Cited by 36
Non-Cell-Autonomous Factors Implicated in Parvalbumin Interneuron Maturation and Critical Periods
Gibel-Russo, R., Benacom, D., & Nardo, A. A. D. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.875873 · Cited by 37
Metadata
- Authors
- Fawcett, J. W., Oohashi, T., & Pizzorusso, T.
- Affiliations
- Czech Academy of Sciences (CZ)
- Okayama University (JP)
- Neuroscience Institute (IT)
- Corresponding author
- Fawcett, James W.
- Venue
- Nature Reviews Neuroscience
- Published
- 2019-07-01
- Volume
- 20
- Issue
- 8
- Pages
- 451-465
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- OpenAlex
- W2955918581
- Semantic Scholar
- e14cf9b70c48b98946ffcfb2145a00841a74cb04
- Cited by
- 589
- References
- 228
- Citations by year
- 2026: 85 · 2025: 114 · 2024: 89 · 2023: 83 · 2022: 74 · 2021: 79 · 2020: 54 · 2019: 9
- FWCI
- 6.19
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nature reviews. Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Florence Research (University of Florence) (submittedVersion)
- Scuola Normale Superiore di Pisa (submittedVersion)
- Funders
- Medical Research Council (MR/R004463/1, MR/R004544/1)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- perineuronal nets, chondroitin sulfate proteoglycans, extracellular matrix, critical period, developmental plasticity, CNS plasticity, memory regulation, mental illness, nodes of Ranvier, myelination
- MeSH terms
- Animals, Mental Disorders, Central Nervous System Diseases, Extracellular Matrix, Humans, Memory, Models, Neurological, Neuronal Plasticity, Neurons
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