Activity‐dependent formation and functions of chondroitin sulfate‐rich extracellular matrix of perineuronal nets
Abstract
Extracellular matrix molecules—including chondroitin sulfate proteoglycans, hyaluronan, and tenascin‐R—are enriched in perineuronal nets (PNs) associated with subsets of neurons in the brain and spinal cord. In the present study, we show that similar cell type‐dependent extracellular matrix aggregates are formed in dissociated cell cultures prepared from early postnatal mouse hippocampus. Starting from the 5th day in culture, accumulations of lattice‐like extracellular structures labeled with Wisteria floribunda agglutinin were detected at the cell surface of parvalbumin‐expressing interneurons, which developed after 2–3 weeks into conspicuous PNs localized around synaptic contacts at somata and proximal dendrites, as well as around axon initial segments. Physiological recording and intracellular labeling of PN‐expressing neurons revealed that these are large fast‐spiking interneurons with morphological characteristics of basket cells. To study mechanisms of activity‐dependent formation of PNs, we performed pharmacological analysis and found that blockade of action potentials, transmitter release, Ca 2+ permeable AMPA subtype of glutamate receptors or L‐type Ca 2+ voltage‐gated channels strongly decreased the extracellular accumulation of PN components in cultured neurons. Thus, we suggest that Ca 2+ influx via AMPA receptors and L‐type channels is necessary for activity‐dependent formation of PNs. To study functions of chondroitin sulfate‐rich PNs, we treated cultures with chondroitinase ABC that resulted in a prominent reduction of several major PN components. Removal of PNs did not affect the number and distribution of perisomatic GABAergic contacts but increased the excitability of interneurons in cultures, implicating the extracellular matrix of PNs in regulation of interneuronal activity. © 2007 Wiley Periodicals, Inc. Develop Neurobiol, 2007
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PNNs are found primarily around fast-spiking, parvalbumin (PV)-containing GABAergic interneurons in many brain regions, but not all regions.
“PNNs are found primarily around fast--spiking, parvalbumin (PV)--containing GABAergic interneurons in many brain regions (Hartig et al., 1992;Schuppel et al., 2002;Dityatev et al., 2007), but not all regions (e.g., cerebellum; see below).”
From Casting a Wide Net: Role of Perineuronal Nets in Neural Plasticity (2016) · cites this paper as Dityatev et al., 2007
PNNs are formed during development in an activity-dependent manner.
“PNNs are formed during development (Brückner et al., 2000) in an activity-dependent manner (Dityatev et al., 2007).”
From Perineuronal Nets Regulate the Inhibitory Perisomatic Input onto Parvalbumin Interneurons and γ Activity in the Prefrontal Cortex (2020) · cites this paper as Dityatev et al., 2007
Abnormal glutamatergic transmission, polymorphisms of genes encoding for some PNN components, and altered CSPG expression in glial cells may, independently or in conjunction, cause defective PNN maturation.
“Abnormal glutamatergic transmission, polymorphisms of genes encoding for some of their components and altered CSPG expression in glial cells may, independently or in conjunction, cause defective PNN maturation.3, 5, 6, 7, 59”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [59]
PNN maturation occurs in an experience-dependent manner, requiring neuronal activation through glutamatergic excitation, availability of key PNN components, expression on neurons of ECM surface receptors, and transcription factors inducing neuronal maturation.
“Their maturation occurs in an experience-dependent manner, requiring (i) neuronal activation through glutamatergic excitation,78 (ii) availability of key PNN components, such as specific CSPGs, link proteins and tenascin R, (iii) expression on neurons of ECM surface receptors79, 80 and (iv) transcription factors inducing neuronal maturation.25, 38”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [78]
These functions underlie the role of the adult ECM in neuronal excitability, receptor desensitization, long-term potentiation and long-term depression.
“Overall, these functions underlie the role of the adult ECM to neuronal excitability, receptor desensitization, long-term potentiation and long-term depression.59, 87, 88, 90, 91, 92, 93”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [59]
PNNs surround inhibitory fast spiking parvalbumin-positive GABAergic interneurons and are also associated with excitatory pyramidal neurons in the cerebral cortex.
“PNNs surround inhibitory fast spiking parvalbumin-positive GABAergic interneurons12–14, but are also associated with further subpopulations, for example excitatory pyramidal neurons in the cerebral cortex15,16.”
From Elimination of the four extracellular matrix molecules tenascin-C, tenascin-R, brevican and neurocan alters the ratio of excitatory and inhibitory synapses (2019) · cites this paper as [14]
Hippocampal neurons in culture after ChABC treatment show higher excitability.
“These data are in agreement with the report of Dityatev and colleagues who found a higher excitability of hippocampal neurons in culture after ChABC treatment14.”
From Elimination of the four extracellular matrix molecules tenascin-C, tenascin-R, brevican and neurocan alters the ratio of excitatory and inhibitory synapses (2019) · cites this paper as [14]
CSPGs like aggrecan or brevican are incorporated into perineuronal nets through their interaction with TnR and hyaluronic acid.
“Several reports suggest that CSPGs like aggrecan or brevican are incorporated into perineuronal nets through their interaction with TnR and hyaluronic acid14,53,54.”
From Elimination of the four extracellular matrix molecules tenascin-C, tenascin-R, brevican and neurocan alters the ratio of excitatory and inhibitory synapses (2019) · cites this paper as [14]
Parvalbumin levels and perineuronal net labeling are regulated in an activity-dependent manner.
“Levels of PV (Kinney et al, 2006) and PNN labeling (Dityatev et al, 2007;Giamanco and Matthews, 2012) are regulated in an activity-dependent manner.”
From Reduced Labeling of Parvalbumin Neurons and Perineuronal Nets in the Dorsolateral Prefrontal Cortex of Subjects with Schizophrenia (2016) · cites this paper as Dityatev et al, 2007
Perineuronal nets regulate the survival and excitability of parvalbumin interneurons and the stabilization of sensory circuits.
“PNNs regulate survival (Morawski et al. 2004(Morawski et al. , 2015;;Cabungcal et al. 2013) and excitability of PV interneurons (Dityatev et al. 2007;Carulli et al. 2010;Balmer 2016), and stabilization of sensory circuits (Pizzorusso et al. 2002;McRae et al. 2007).”
From Genetic Reduction of Matrix Metalloproteinase-9 Promotes Formation of Perineuronal Nets Around Parvalbumin-Expressing Interneurons and Normalizes Auditory Cortex Responses in Developing Fmr1 Knock-Out Mice (2018) · cites this paper as Dityatev et al. 2007
PNN enzymatic digestion results in increased excitability of interneurons.
“Consistently, PNN enzymatic digestion results in increased excitability of interneurons (Dityatev et al., 2007).”
From Losing the sugar coating: Potential impact of perineuronal net abnormalities on interneurons in schizophrenia (2015) · cites this paper as Dityatev et al., 2007
PNN gradual maturation around somata and dendrites stabilizes successful synapses, restricting plasticity, regulating synaptogenesis, and maintaining mature forms of learning.
“PNN gradual maturation around somata and dendrites stabilizes successful synapses, restricting plasticity, regulating synaptogenesis and maintaining mature forms of learning (Bukalo et al., 2001; Carulli et al., 2013b; Dityatev et al., 2007; Faissner et al., 2010; Gundelfinger et al., 2010; McRae and Porter, 2012; Pyka et al., 2011).”
From Losing the sugar coating: Potential impact of perineuronal net abnormalities on interneurons in schizophrenia (2015) · cites this paper as Dityatev et al., 2007
In mouse visual cortex slices, blocking glutamate receptors and presynaptic N- and P/Q-type calcium channels left PNN growth unchanged, which suggests that neuronal activity is necessary for PNN development but glutamatergic transmission is not.
“blockage of glutamate receptors and presynaptic N- and P/Q-type calcium channels (both implicated in glutamate release) did not affect PNN growth, indicating that neuronal activity is required but that glutamatergic neurotransmission is not essential for PNN development (Dityatev et al., 2007)”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Dityatev et al., 2007
Blocking sodium channels inhibits PNN formation in mouse visual cortex slices.
“blockage of sodium channels inhibits the formation of PNNs (Dityatev et al., 2007)”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Dityatev et al., 2007
PNN formation is activity-dependent.
“Formation of PNNs has been found to be activity-dependent.”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Dityatev et al., 2007
PNN formation is driven by neuronal activity.
“Accumulating evidence suggests that PNN formation is driven by neuronal activity (Dityatev et al., 2007)”
From Adult neurogenesis, glia, and the extracellular matrix (2019) · cites this paper as Dityatev et al., 2007
Cites
Wessel, D., & Flügge, U. (1984) · Analytical Biochemistry · doi:10.1016/0003-2697(84)90782-6 · Cited by 3,997 · see citing works
Hyaluronan: from extracellular glue to pericellular cue
Toole, B. P. (2004) · Nature Reviews Cancer · doi:10.1038/nrc1391 · Cited by 2,125 · 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
Defined types of cortical interneurone structure space and spike timing in the hippocampus
Somogyi, P., & Klausberger, T. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2004.078915 · Cited by 927 · see citing works
Kv3 channels: voltage-gated K+ channels designed for high-frequency repetitive firing
Rudy, B., & McBain, C. J. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01892-0 · Cited by 781 · see citing works
Lecticans: organizers of the brain extracellular matrix
Yamaguchi, Y. (2000) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000690 · Cited by 642 · see citing works
Interneuron Diversity series: Rhythm and mood in perisomatic inhibition
Freund, T. F. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00227-3 · Cited by 641 · see citing works
Extracellular matrix molecules and synaptic plasticity
Dityatev, A., & Schachner, M. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1115 · Cited by 564 · see citing works
Self-citationNovel hyaluronidase from streptomyces
Takaichi, O. H. Y. A., & Kaneko, Y. (1970) · Biochimica et Biophysica Acta (BBA) - Enzymology · doi:10.1016/0005-2744(70)90139-7 · Cited by 519 · see citing works
Perineuronal nets: past and present
Celio, M. R., Spreafico, R., De Biasi, S., & Vitellaro-Zuccarello, L. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01298-3 · Cited by 497 · 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
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
Self-citationSubmillisecond AMPA receptor-mediated signaling at a principal neuron-interneuron synapse
Geiger, J. R. P., Lübke, J., Roth, A., Frotscher, M., & Jonas, P. (1997) · Neuron · doi:10.1016/s0896-6273(00)80339-6 · Cited by 407 · see citing works
Martina, M., Schultz, J. H., Ehmke, H., Monyer, H., & Jonas, P. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-20-08111.1998 · Cited by 396 · see citing works
Mapping by monoclonal antibody detection of glycosaminoglycans in connective tissues
Couchman, J., Caterson, B., Christner, J. E., & Baker, J. R. (1984) · Nature · doi:10.1038/307650a0 · Cited by 382 · see citing works
Rutherford, L. C., DeWan, A., Lauer, H. M., & Turrigiano, G. G. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-12-04527.1997 · Cited by 381 · see citing works
Localization of Ca2+Channel Subtypes on Rat Spinal Motor Neurons, Interneurons, and Nerve Terminals
Westenbroek, R. E., Hoskins, L., & Catterall, W. A. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-16-06319.1998 · Cited by 377 · see citing works
Brückner, G., Brauer, K., Härtig, W., Wolff, J. R., Rickmann, M. J., Derouiche, A., Delpech, B., Girard, N., Oertel, W. H., & Reichenbach, A. (1993) · Glia · doi:10.1002/glia.440080306 · Cited by 358 · see citing works
Self-citationAggrecan Glycoforms Contribute to the Molecular Heterogeneity of Perineuronal Nets
Matthews, R. T., Kelly, G. M., Zerillo, C. A., Gray, G., Tiemeyer, M., & Hockfield, S. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-17-07536.2002 · Cited by 341 · see citing works
Carulli, D., Rhodes, K. E., Brown, D. J., Bonnert, T. P., Pollack, S. J., Oliver, K., Strata, P., & Fawcett, J. W. (2006) · Journal of Comparative Neurology · doi:10.1002/cne.20822 · Cited by 341 · see citing works
Härtig, W., Derouiche, A., Welt, K., Brauer, K., Grosche, J., Mäder, M., Reichenbach, A., & Brückner, G. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01784-9 · Cited by 339 · see citing works
Self-citationCellular signaling by neural cell adhesion molecules of the immunoglobulin superfamily
Crossin, K. L., & Krushel, L. A. (2000) · Developmental Dynamics · doi:10.1002/(sici)1097-0177(200006)218:2 · Cited by 283 · see citing works
Aspberg, A., Miura, R., Bourdoulous, S., Shimonaka, M., Heinegård, D., Schachner, M., Ruoslahti, E., & Yamaguchi, Y. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.19.10116 · Cited by 275 · 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 · cited 2× · see citing works
“, 2002), it is likely that aggrecan is the proteoglycan that contributes most to the structure of PNs (Hockfield et al., 1990; Lander et al., 1997; Matthews et al., 2002).”
BackgroundJ1-160 and J1-180 are oligodendrocyte-secreted nonpermissive substrates for cell adhesion.
Pesheva, P., Spieß, E., & Schachner, M. (1989) · The Journal of Cell Biology · doi:10.1083/jcb.109.4.1765 · Cited by 270 · see citing works
Self-citationBrakebusch, 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 · see citing works
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
Self-citationBukalo, O., Schachner, M., & Dityatev, A. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00082-3 · Cited by 236 · see citing works
Self-citationParvalbumin-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
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 · see citing works
Two Distinct Chondroitin Sulfate ABC Lyases
Hamai, A., Hashimoto, N., Mochizuki, H., Kato, F., Makiguchi, Y., Horie, K., & Suzuki, S. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.14.9123 · Cited by 203 · see citing works
Lander, C., Kind, P., Maleski, M., & Hockfield, S. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-06-01928.1997 · Cited by 195 · see citing works
Dityatev, A. E., Dityatev, A. E., & Schachner, M. (2000) · Neuron · doi:10.1016/s0896-6273(00)81151-4 · Cited by 173 · see citing works
Self-citationBrückner, 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
Self-citationNeurocan and phosphacan: two major nervous tissue-specific chondroitin sulfate proteoglycans.
Margolis, R. K., Rauch, U., Maurel, P., & Margolis, R. U. (1996) · PubMed · Cited by 160 · see citing works
Magazanik, L. G., Buldakova, S., Samoilova, M., Гмиро, В. Е., Mellor, I. R., & Usherwood, P. N. R. (1997) · The Journal of Physiology · doi:10.1111/j.1469-7793.1997.655ba.x · Cited by 143 · see citing works
Guimaraes, A., Zaremba, S., & Hockfield, S. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-09-03014.1990 · Cited by 128 · see citing works
John, N., Krügel, H., Frischknecht, R., Smalla, K.-H., Schultz, C., Kreutz, M. R., Gundelfinger, E. D., & Seidenbecher, C. I. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.01.011 · Cited by 122 · cited 6× · see citing works
“Another recent study revealed that both excitatory and inhibitory synapses in dissociated hippocampal cultures are embedded in the extracellular matrix of PNs (John et al., 2006).”
BackgroundInfluentialBrückner, G., Grosche, J., Hartlage‐Rübsamen, M., Schmidt, S., & Schachner, M. (2003) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(03)00036-x · Cited by 116 · see citing works
Self-citationAxon initial segment ensheathed by extracellular matrix in perineuronal nets
Brückner, G., Szeöke, S., Pavlica, S., Grosche, J., & Kacza, J. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.11.068 · Cited by 114 · see citing works
Self-citationNeurons Produce a Neuronal Cell Surface-Associated Chondroitin Sulfate Proteoglycan
Lander, C., Zhang, H., & Hockfield, S. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-01-00174.1998 · Cited by 107 · see citing works
Morris, N. P., & Henderson, Z. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00970.x · Cited by 98 · see citing works
Köppe, G., Brückner, G., Härtig, W., Delpech, B., & Bigl, V. (1997) · The Histochemical Journal · doi:10.1023/a:1026408716522 · Cited by 95 · see citing works
Self-citationBerghuis, P., Dobszay, M. B., Sousa, K. M., Schulte, G., Mager, P. P., Härtig, W., Görcs, T. J., Zilberter, Y., Ernfors, P., & Harkany, T. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03561.x · Cited by 93 · see citing works
Perineuronal nets of extracellular matrix around parvalbumin‐containing neurons of the hippocampus
Celio, M. R. (1993) · Hippocampus · doi:10.1002/hipo.1993.4500030709 · Cited by 89 · see citing works
Naegele, J. R., & Katz, L. C. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-02-00540.1990 · Cited by 88 · see citing works
Recognition molecules and neural repair
Loers, G., & Schachner, M. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04409.x · Cited by 88 · see citing works
Self-citationExtracellular matrix alterations in brains lacking four of its components
Rauch, U., Zhou, X.-H., & Roos, G. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.01.026 · Cited by 88 · see citing works
Lambert, N. A., & Wilson, W. A. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021294 · Cited by 71 · see citing works
Gurevicius, K., Gureviciene, I., Valjakka, A., Schachner, M., & Tanila, H. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2003.12.001 · Cited by 58 · see citing works
Self-citationBrevican isoforms associate with neural membranes
Seidenbecher, C. I., Smalla, K., Fischer, N., Gundelfinger, E. D., & Kreutz, M. R. (2002) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2002.01183.x · Cited by 55 · see citing works
Rapid and efficient electroporation-based gene transfer into primary dissociated neurons
Dityatev, A. E., Hammond, M. S. L., Thiel, C., Ruonala, M. O., Delling, M., Siebenkotten, G., Nix, M., & Dityatev, A. E. (2003) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(03)00202-4 · Cited by 51 · see citing works
Self-citationGrosche, J., & Br�ckner, G. (2001) · Experimental Brain Research · doi:10.1007/s002210000617 · Cited by 50 · see citing works
Self-citationPerineuronal nets in the rhesus monkey and human basal forebrain including basal ganglia
Adams, I., Brauer, K., Arélin, C., Härtig, W., Fine, A., Mäder, M., Arendt, T., & Brückner, G. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00419-5 · Cited by 48 · see citing works
Self-citationKannenberg, K., Sieghart, W., & REUTER, H. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00533.x · Cited by 48 · see citing works
Hobohm, C., Härtig, W., Brauer, K., & Brückner, G. (1998) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(98)00044-1 · Cited by 41 · see citing works
Self-citationBrückner, G., Kacza, J., & Grosche, J. (2004) · Journal of Molecular Histology · doi:10.1023/b:hijo.0000023374.22298.50 · Cited by 33 · see citing works
Self-citationEssin, K., Nistri, A., & Magazanik, L. G. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02045.x · Cited by 25 · see citing works
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
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Dityatev, A., Schachner, M., & Sonderegger, P. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2898 · Cited by 559 · see citing works
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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 · see citing works
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Casting a Wide Net: Role of Perineuronal Nets in Neural Plasticity
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Molecular signals of plasticity at the tetrapartite synapse
Dityatev, A., & Rusakov, D. A. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.12.006 · Cited by 267 · see citing works
Self-citationSteullet, P., Cabungcal, J. H., Monin, A., Dwir, D., O'Donnell, P., Cuenod, M., & Do, K. Q. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2014.06.021 · Cited by 262 · see citing works
Crosstalk between glia, extracellular matrix and neurons
Song, I., & Dityatev, A. E. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.03.003 · Cited by 263 · see citing works
Self-citationTargeting the neural extracellular matrix in neurological disorders
Soleman, S., Filippov, M. A., Dityatev, A., & Fawcett, J. W. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.050 · Cited by 244 · see citing works
Self-citationEnwright, J. F., Sanapala, S., Foglio, A., Berry, R., Fish, K. N., & Lewis, D. A. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2016.24 · Cited by 223 · see citing works
Dityatev, A. E., Seidenbecher, C. I., & Schachner, M. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.08.003 · Cited by 229 · see citing works
Self-citationAdult neurogenesis, glia, and the extracellular matrix
Cope, E. C., & Gould, E. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.03.023 · Cited by 236 · see citing works
Cabungcal, J.-H., Steullet, P., Kraftsik, R., Cuenod, M., & Do, K. Q. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.09.020 · Cited by 232 · see citing works
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 · see citing works
Self-citationPerineuronal 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
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 · 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
Lam, D., Enright, H. A., Cadena, J., Peters, S. K. G., Sales, A. P., Osburn, J. J., Soscia, D. A., Kulp, K. S., Wheeler, E. K., & Fischer, N. O. (2019) · Scientific Reports · doi:10.1038/s41598-019-40128-1 · Cited by 205 · see citing works
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
Glia as drivers of abnormal neuronal activity
Robel, S., & Sontheimer, H. W. (2015) · Nature Neuroscience · doi:10.1038/nn.4184 · Cited by 199 · see citing works
Microglia regulate synaptic development and plasticity
Andoh, M., & Koyama, R. (2021) · Developmental Neurobiology · doi:10.1002/dneu.22814 · Cited by 188 · see citing works
Recent advances in quantitative colocalization analysis: Focus on neuroscience
Zinchuk, V. S., & Grossenbacher‐Zinchuk, O. (2009) · Progress in Histochemistry and Cytochemistry · doi:10.1016/j.proghi.2009.03.001 · Cited by 184 · see citing works
The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders
Wen, T. H., Binder, D. K., Ethell, I. M., & Razak, K. A. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00270 · Cited by 170 · see citing works
Modulation 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 · 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
Wen, T. H., Afroz, S., Reinhard, S. M., Palacios, A. R., Tapia, K., Binder, D. K., Razak, K. A., & Ethell, I. M. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhx258 · Cited by 165 · see citing works
Integrins as receptor targets for neurological disorders
Wu, X., & Reddy, D. S. (2012) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.12.008 · Cited by 175 · see citing works
“LN, VN, reelin and chondroitin sulfates are reported to be involved in neuronal development (Heinrich et al., 2006; Dityatev et al., 2007).”
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 · see citing works
Miyata, S., & Kitagawa, H. (2017) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2017.06.010 · Cited by 171 · see citing works
Kwok, J. C. F., Carulli, D., & Fawcett, J. W. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06878.x · Cited by 170 · see citing works
Microglia Elimination Increases Neural Circuit Connectivity and Activity in Adult Mouse Cortex
Liu, Y., Spangenberg, E. E., Tang, B., Holmes, T. C., Green, K. N., & Xu, X. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2140-20.2020 · Cited by 163 · see citing works
Shaping Synapses by the Neural Extracellular Matrix
Ferrer-Ferrer, M., & Dityatev, A. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00040 · Cited by 169 · see citing works
Self-citationCellot, G., Toma, F. M., Kasap Varley, Z., Laishram, J., Villari, A., Quintana, M., Cipollone, S., Prato, M., & Ballerini, L. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.1332-11.2011 · 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
Pantazopoulos, H., Markota, M., Jaquet, F., Ghosh, D., Wallin, A., Santos, A., Caterson, B., & Berretta, S. (2015) · Translational Psychiatry · doi:10.1038/tp.2014.128 · Cited by 153 · see citing works
Orlando, C., Ster, J., Gerber, U., Fawcett, J. W., & Raineteau, O. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.2406-12.2012 · Cited by 153 · see citing works
The Brain’s Extracellular Matrix and Its Role in Synaptic Plasticity
Frischknecht, R., & Gundelfinger, E. D. (2012) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-7091-0932-8_7 · Cited by 156 · see citing works
Berretta, S., Pantazopoulos, H., Markota, M., Brown, C., & Batzianouli, E. T. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2014.12.040 · Cited by 152 · 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
Perineuronal nets in brain physiology and disease
Testa, D., Prochiantz, A., & Nardo, A. A. D. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.09.011 · Cited by 141 · see citing works
Geissler, M., Gottschling, C., Aguado, A., Rauch, U., Wetzel, C. H., Hatt, H., & Faissner, A. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3275-12.2013 · Cited by 140 · see citing works
Riga, D., Kramvis, I., Koskinen, M. K., van Bokhoven, P., van der Harst, J. E., Heistek, T. S., Jaap Timmerman, A., van Nierop, P., van der Schors, R. C., Pieneman, A. W., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aai8753 · Cited by 128 · see citing works
Giamanco, K. A., & Matthews, R. T. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.05.055 · Cited by 138 · see citing works
Wingert, J. C., & Sorg, B. A. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.673210 · Cited by 129 · 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
Dzyubenko, E., Gottschling, C., & Faissner, A. (2016) · Neural Plasticity · doi:10.1155/2016/5214961 · Cited by 134 · see citing works
Extracellular matrix protein expression is brain region dependent
Dauth, S., Grevesse, T., Pantazopoulos, H., Campbell, P. H., Maoz, B. M., Berretta, S., & Parker, K. K. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.23965 · Cited by 134 · see citing works
Oohashi, T., Edamatsu, M., Bekku, Y., & Carulli, D. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.09.010 · Cited by 131 · see citing works
A ‘GAG’ reflex prevents repair of the damaged CNS
Sherman, L. S., & Back, S. A. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2007.11.001 · Cited by 116 · see citing works
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 · see citing works
Extracellular matrix molecules, their receptors, and secreted proteases in synaptic plasticity
Włodarczyk, J., Mukhina, I. V., Kaczmarek, L., & Dityatev, A. E. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20958 · Cited by 123 · see citing works
Self-citationGottschling, C., Wegrzyn, D., Denecke, B., & Faissner, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-50404-9 · Cited by 111 · see citing works
In Sickness and in Health: Perineuronal Nets and Synaptic Plasticity in Psychiatric Disorders
Pantazopoulos, H., & Berretta, S. (2015) · Neural Plasticity · doi:10.1155/2016/9847696 · Cited by 118 · see citing works
Nowicka, 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
Extracellular matrix in plasticity and epileptogenesis
Dityatev, A. E., & Fellin, T. (2008) · Neuron Glia Biology · doi:10.1017/s1740925x09000118 · Cited by 116 · see citing works
Self-citationChondroitin sulphate proteoglycans: Key modulators of spinal cord and brain plasticity
Bartus, K., James, N. D., Bosch, K. D., & Bradbury, E. J. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.08.008 · Cited by 117 · see citing works
Seizure-like activity in hyaluronidase-treated dissociated hippocampal cultures
Vedunova, M., Sakharnova, T., Mitroshina, E., Perminova, M., Pimashkin, A., Zakharov, Y., Dityatev, A., & Mukhina, I. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00149 · Cited by 107 · see citing works
Self-citationMorawski, 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
Self-citationChloride Dysregulation, Seizures, and Cerebral Edema: A Relationship with Therapeutic Potential
Glykys, J. C., Dzhala, V. I., Egawa, K., Kahle, K. T., Delpire, E. J., & Staley, K. J. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.03.006 · Cited by 109 · see citing works
Tewari, B. P., Chaunsali, L., Prim, C. E., & Sontheimer, H. W. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1022754 · Cited by 107 · see citing works
Yamada, J., Ohgomori, T., & Jinno, S. (2015) · European Journal of Neuroscience · doi:10.1111/ejn.12792 · Cited by 99 · see citing works
Andrews, E. M., Richards, R. J., Yin, F. Q., Viapiano, M. S., & Jakeman, L. B. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.09.008 · Cited by 102 · see citing works
Brain extracellular matrix retains connectivity in neuronal networks
Bikbaev, A., Frischknecht, R., & Heine, M. (2015) · Scientific Reports · doi:10.1038/srep14527 · Cited by 88 · 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
Fretham, S. J. B., Carlson, E. S., Wobken, J. D., Tran, P. V., Petryk, A., & Georgieff, M. K. (2012) · Hippocampus · doi:10.1002/hipo.22004 · Cited by 95 · see citing works
Gildawie, K. R., Honeycutt, J. A., & Brenhouse, H. C. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.12.010 · Cited by 90 · see citing works
Neural ECM molecules in synaptic plasticity, learning, and memory
Senkov, O., Anđjus, P. R., Radenović, L., Soriano, E., & Dityatev, A. E. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63486-3.00003-7 · Cited by 94 · see citing works
Self-citationForostyak, S., Homola, A., Turnovcová, K., Svítil, P., Jendelová, P., & Syková, E. (2014) · Stem Cells · doi:10.1002/stem.1812 · Cited by 92 · see citing works
Hayani, H., Song, I., & Dityatev, A. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00149 · Cited by 84 · see citing works
Self-citationBozzelli, 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
Aggrecan-based extracellular matrix is an integral part of the human basal ganglia circuit
Brückner, G., Morawski, M., & Arendt, T. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.10.033 · Cited by 90 · see citing works
Self-citationJiang, Z., Cowell, R. M., & Nakazawa, K. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00116 · Cited by 89 · see citing works
Recognition molecules and neural repair
Loers, G., & Schachner, M. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04409.x · Cited by 88 · see citing works
Self-citationMurase, S., Lantz, C. L., & Quinlan, E. M. (2017) · eLife · doi:10.7554/elife.27345 · Cited by 87 · see citing works
Shah, A., & Lodge, D. J. (2013) · Translational Psychiatry · doi:10.1038/tp.2012.145 · Cited by 87 · see citing works
Remodeling of extracellular matrix and epileptogenesis
Dityatev, A. E. (2010) · Epilepsia · doi:10.1111/j.1528-1167.2010.02612.x · Cited by 86 · see citing works
Self-citationThe crosstalk of hyaluronan-based extracellular matrix and synapses
Frischknecht, R., & Seidenbecher, C. I. (2008) · Neuron Glia Biology · doi:10.1017/s1740925x09990226 · Cited by 84 · see citing works
Hippocampal Metaplasticity Induced by Deficiency in the Extracellular Matrix Glycoprotein Tenascin-R
Bukalo, O., Schachner, M., & Dityatev, A. E. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1022-07.2007 · Cited by 80 · see citing works
Self-citationDiverse 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
Extracellular Matrix in Neural Plasticity and Regeneration
Chelyshev, Y. A., Kabdesh, I. M., & Mukhamedshina, Y. O. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00986-0 · Cited by 76 · see citing works
Repeated Binge Drinking Increases Perineuronal Nets in the Insular Cortex
Chen, H., He, D., & Lasek, A. W. (2015) · Alcoholism: Clinical and Experimental Research · doi:10.1111/acer.12847 · Cited by 77 · see citing works
Mirzadeh, Z., Alonge, K. M., Cabrales, E., Herranz‐Pérez, V., Scarlett, J. M., Brown, J. M., Hassouna, R., Matsen, M. E., Hồng, N. T., García‐Verdugo, J. M., et al. (2019) · Nature Metabolism · doi:10.1038/s42255-018-0029-0 · Cited by 76 · see citing works
Regulation of Perineuronal Nets in the Adult Cortex by the Activity of the Cortical Network
Devienne, G. F., Picaud, S., Cohen, I., Piquet, J., Tricoire, L., Testa, D., Nardo, A. A. D., Rossier, J., Cauli, B., & Lambolez, B. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0434-21.2021 · Cited by 78 · see citing works
Miyata, S., & Kitagawa, H. (2016) · Neural Plasticity · doi:10.1155/2016/1305801 · Cited by 70 · see citing works
Beebe, N. L., Young, J. W., Mellott, J. G., & Schofield, B. R. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0217-16.2016 · Cited by 71 · see citing works
Releasing Addiction Memories Trapped in Perineuronal Nets
Lasek, A. W., Chen, H., & Chen, W.-Y. (2018) · Trends in Genetics · doi:10.1016/j.tig.2017.12.004 · Cited by 71 · see citing works
Perineuronal nets control visual input via thalamic recruitment of cortical PV interneurons
Faini, G., Aguirre, A., Landi, S., Lamers, D., Pizzorusso, T., Ratto, G. M., Deleuze, C., & Bacci, A. (2018) · eLife · doi:10.7554/elife.41520 · Cited by 64 · see citing works
Sato, T., Kudo, T., Ikehara, Y., Ogawa, H., Hirano, T., Kiyohara, K., Hagiwara, K., Togayachi, A., Ema, M., Takahashi, S., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.159244 · Cited by 68 · see citing works
Training and anti-CSPG combination therapy for spinal cord injury
García‐Alías, G., & Fawcett, J. W. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.09.009 · Cited by 67 · see citing works
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 67 · see citing works
Horii‐Hayashi, N., Sasagawa, T., Matsunaga, W., & Nishi, M. (2015) · Neural Plasticity · doi:10.1155/2015/256389 · Cited by 66 · see citing works
Fossati, G., Pozzi, D., Canzi, A., Mirabella, F., Valentino, S., Morini, R., Ghirardini, E., Filipello, F., Moretti, M., Gotti, C., et al. (2018) · The EMBO Journal · doi:10.15252/embj.201899529 · Cited by 65 · see citing works
Berezin, V., Walmod, P. S., Filippov, M. A., & Dityatev, A. E. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63486-3.00015-3 · Cited by 62 · see citing works
Self-citation
- Authors
- Dityatev, A., Brückner, G., Dityateva, G., Grosche, J., Kleene, R., & Schachner, M.
- Affiliations
- Leipzig University (DE)
- University Medical Center Hamburg-Eppendorf (DE)
- Corresponding author
- Schachner, Melitta
- Venue
- Developmental Neurobiology
- Publisher
- Wiley
- Published
- 2007-02-09
- Volume
- 67
- Issue
- 5
- Pages
- 570-588
- ISSN
- 1932-8451 (ISSN-L)
- 1932-846X
- OpenAlex
- W2106489369
- Cited by
- 365
- References
- 59
- Citations by year
- 2026: 13 · 2025: 27 · 2024: 21 · 2023: 20 · 2022: 24 · 2021: 24 · 2020: 25 · 2019: 29 · 2018: 27 · 2017: 24 · 2016: 19 · 2015: 19 · 2014: 18 · 2013: 13 · 2012: 13
- FWCI
- 4.89
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Developmental Neurobiology (publishedVersion)
- PubMed (publishedVersion)
- Rutgers University Community Repository (Rutgers University) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- perineuronal nets, chondroitin sulfate proteoglycans, extracellular matrix, parvalbumin interneurons, basket cells, fast-spiking interneurons, AMPA receptors, L-type calcium channels, chondroitinase ABC, GABAergic synapses, interneuron excitability, hippocampus, postnatal development
- MeSH terms
- Animals, Cell Count, Cells, Cultured, Chondroitin Sulfates, Electrophysiology, Extracellular Matrix, Hippocampus, Immunohistochemistry, Interneurons, Mice, Inbred C57BL, Proteoglycans, Synapses, Blotting, Western, Receptors, GABA, Chondroitin ABC Lyase, Satellite Cells, Perineuronal, Mice
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