The DOI matches its Crossref record; 86 of the 86 references it cites were found in a registry or an index.
Primary Hippocampal Neurons, Which Lack Four Crucial Extracellular Matrix Molecules, Display Abnormalities of Synaptic Structure and Function and Severe Deficits in Perineuronal Net Formation
Open accessAbstract
The extracellular matrix (ECM) of the brain plays crucial roles during the development, maturation, and regeneration of the CNS. In a subpopulation of neurons, the ECM condenses to superstructures called perineuronal nets (PNNs) that surround synapses. Camillo Golgi described PNNs a century ago, yet their biological functions remain elusive. Here, we studied a mouse mutant that lacks four ECM components highly enriched in the developing brain: the glycoproteins tenascin-C and tenascin-R and the chondroitin sulfate proteoglycans brevican and neurocan. Primary embryonic hippocampal neurons and astrocytes were cultivated using a cell insert system that allows for co-culture of distinct cell populations in the absence of direct membrane contacts. The wild-type and knock-out cells were combined in the four possible permutations. Using this approach, neurons cultivated in the presence of mutant astrocytes displayed a transient increase of synapses after 2 weeks. However, after a period of 3 weeks or longer, synapse formation and stabilization were compromised when either neuron or astrocyte cell populations or both were of mutant origin. The development of PNN structures was observed, but their size was substantially reduced on knock-out neurons. The synaptic activity of both wild-type and knock-out neurons was monitored using whole-cell patch clamping. The salient observation was a reduced frequency of IPSCs and EPSCs, whereas the amplitudes were not modified. Remarkably, the knock-out neuron phenotypes could not be rescued by wild-type astrocytes. We conclude that the elimination of four ECM genes compromises neuronal function.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“In a previous study our laboratory investigated hippocampal neurons of the quadruple knockout mouse in vitro and found diminished PNNs and an altered expression of synaptic proteins that were accompanied by a decreased frequency of mEPSCs and mIPSCs after 14 and 21 DIV29.”
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 [29]
In the citing paper
“This may be due in part to the degradation of the PNNs in which synapses are embedded, as the genetic ablation of one or more PNN structural components and consequent loss of neuronal PNN integrity can induce the loss of synapses [28, 80] and impaired synaptic colocalization/expression of neurotransmitter receptor subunits [29], potentially manifesting as deficits in synaptic plasticity (e.g. LTP)”
From Microglia facilitate loss of perineuronal nets in the Alzheimer's disease brain (2020) · cites this paper as [80]
In the citing paper
“PNNs are autonomously constructed by neurons (Miyata et al. , 2005; Geissler et al. , 2013; Fowke et al. , 2017)”
From Microglial depletion prevents extracellular matrix changes and striatal volume reduction in a model of Huntington's disease (2020) · cites this paper as Geissler et al. , 2013
In the citing paper
“The results found for the in vivo PNN formation fit perfectly with the in vitro findings29, both demonstrating a diminished PNN formation in the postnatal quadruple knockout mouse.”
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 [29]
In the citing paper
“The loss of TnC, TnR, brevican and neurocan resulted in a significant increase of synaptic density within 14 DIV that transited to a decremented synapse number after 21 DIV.”
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 [29]
In the citing paper
“Neurons coated with PNNs were characterized by an attenuated synapse number after both 14 and 21 DIV29.”
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 [29]
In the citing paper
“In this model hippocampal neurons lacking neurocan, brevican, TN-R and TN-C display rudimentary PNNs and reduced synapse number, suggesting that PNNs are important for synapse formation/stabilization (Geissler et al., 2013).”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Geissler et al., 2013
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Cahoy, J. D., Emery, B., Kaushal, A., Foo, L. C., Zamanian, J. L., Christopherson, K. S., Xing, Y., Lubischer, J. L., Krieg, P. A., Krupenko, S. A., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-07.2008 · Cited by 3,129
Tripartite synapses: astrocytes process and control synaptic information
Perea, G., Navarrete, M., & Araque, A. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.05.001 · Cited by 1,820
Kaech, S., & Banker, G. A. (2006) · Nature Protocols · doi:10.1038/nprot.2006.356 · Cited by 1,766
CNS synaptogenesis promoted by glia-derived cholesterol
Mauch, D. H., Nägler, K., Schumacher, S., Göritz, C., Müller, E.-C., Otto, A., & Pfrieger, F. W. (2001) · Science · doi:10.1126/science.294.5545.1354 · Cited by 1,711
Thrombospondins are astrocyte-secreted proteins that promote CNS synaptogenesis
Christopherson, K. S., Ullian, E. M., Stokes, C. C. A., Mullowney, C. E., Hell, J. W., Agah, A., Lawler, J., Mosher, D. F., Bornstein, P., & Barres, B. A. (2005) · Cell · doi:10.1016/j.cell.2004.12.020 · Cited by 1,688
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
Glia: listening and talking to the synapse
Haydon, P. G. (2001) · Nature reviews. Neuroscience · doi:10.1038/35058528 · Cited by 1,454
Control of Synaptic Strength by Glial TNFα
Beattie, E. C., Stellwagen, D., Morishita, W., Bresnahan, J. C., Ha, B. K., Von Zastrow, M., Beattie, M. S., & Malenka, R. C. (2002) · Science · doi:10.1126/science.1067859 · Cited by 1,344
Culturing hippocampal neurons.
Tanaka, H. (2002) · Folia Pharmacologica Japonica · doi:10.1254/fpj.119.163 · Cited by 1,141
Sommer, I., & Schachner, M. (1981) · Developmental Biology · doi:10.1016/0012-1606(81)90477-2 · Cited by 1,136
Cited by
Sorted by citations
The roles of perineuronal nets and the perinodal extracellular matrix in neuronal function
Fawcett, J. W., Oohashi, T., & Pizzorusso, T. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0196-3 · Cited by 589
Bioprinting: From Tissue and Organ Development to in Vitro Models
Mota, C., Camarero‐Espinosa, S., Baker, M. B., Wieringa, P. A., & Moroni, L. (2020) · Chemical Reviews · doi:10.1021/acs.chemrev.9b00789 · Cited by 359
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
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 270
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
Miyata, S., & Kitagawa, H. (2017) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2017.06.010 · Cited by 171
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
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
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
Wingert, J. C., & Sorg, B. A. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.673210 · Cited by 129
Kim, S. Y., Senatorov, V. V., Morrissey, C. S., Lippmann, K., Vazquez, O. N., Milikovsky, D. Z., Gu, F., Parada, I., Prince, D. A., Becker, A. J., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-07394-3 · Cited by 141
Dzyubenko, E., Gottschling, C., & Faissner, A. (2016) · Neural Plasticity · doi:10.1155/2016/5214961 · Cited by 134
Self-citationOohashi, T., Edamatsu, M., Bekku, Y., & Carulli, D. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.09.010 · Cited by 131
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
Gottschling, C., Wegrzyn, D., Denecke, B., & Faissner, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-50404-9 · Cited by 111
Self-citation“GAG-ing with the neuron”: The role of glycosaminoglycan patterning in the central nervous system
Smith, P. D., Coulson‐Thomas, V. J., Foscarin, S., Kwok, J. C. F., & Fawcett, J. W. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.08.004 · Cited by 114
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
Cell adhesion and matricellular support by astrocytes of the tripartite synapse
Hillen, A. E. J., Burbach, J. P. H., & Hol, E. M. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.02.002 · Cited by 108
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
Avram, S., Shaposhnikov, S. A., Buiu, C., & Mernea, M. (2014) · BioMed Research International · doi:10.1155/2014/642798 · Cited by 111
Quraishe, S., Forbes, L. H., & Andrews, M. R. (2018) · Neural Plasticity · doi:10.1155/2018/2952386 · Cited by 108
Luca, C. D., Colangelo, A. M., Virtuoso, A., Alberghina, L., & Papa, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21041539 · Cited by 107
Molecular mechanisms of scar-sourced axon growth inhibitors
Ohtake, Y., & Li, S. (2014) · Brain Research · doi:10.1016/j.brainres.2014.08.064 · Cited by 105
Dzyubenko, E., Rozenberg, A., Hermann, D. M., & Faissner, A. (2016) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2016.09.001 · Cited by 98
Self-citationMechanotransduction in neuronal cell development and functioning
Chighizola, M., Dini, T., Lenardi, C., Milani, P., Podestà, A., & Schulte, C. (2019) · Biophysical Reviews · doi:10.1007/s12551-019-00587-2 · Cited by 101
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
A Sweet Talk: The Molecular Systems of Perineuronal Nets in Controlling Neuronal Communication
Spijker, H. M. V. ‘., & Kwok, J. C. F. (2017) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2017.00033 · Cited by 89
Duncan, B. W., Murphy, K. E., & Maness, P. F. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.625340 · Cited by 85
Human neuronal maturation comes of age: cellular mechanisms and species differences
Wallace, J. L., & Pollen, A. A. (2024) · Nature Reviews Neuroscience · doi:10.1038/s41583-023-00760-3 · Cited by 82
Marcette, J., Chen, J. J., & Nonet, M. L. (2014) · eLife · doi:10.7554/elife.01637 · Cited by 79
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
Circadian Rhythms of Perineuronal Net Composition
Pantazopoulos, H., Gisabella, B., Rexrode, L., Benefield, D., Yıldız, E., Seltzer, P., Valeri, J., Chelini, G., Reich, A., Ardelt, M., et al. (2020) · eNeuro · doi:10.1523/eneuro.0034-19.2020 · Cited by 77
Signaling pathways regulating neuron–glia interaction and their implications in Alzheimer's disease
Lian, H., & Zheng, H. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13424 · Cited by 77
Blosa, M., Sonntag, M., Jäger, C., Weigel, S., Seeger, J., Frischknecht, R., Seidenbecher, C. I., Matthews, R. T., Arendt, T., Rübsamen, R., et al. (2015) · The Journal of Physiology · doi:10.1113/jp270849 · Cited by 74
Yamada, J., & Jinno, S. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.061 · Cited by 71
Mechanisms for modulation of neural plasticity and axon regeneration by chondroitin sulphate
Miyata, S., & Kitagawa, H. (2014) · The Journal of Biochemistry · doi:10.1093/jb/mvu067 · Cited by 73
Bres, E. E., & Faissner, A. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00031 · Cited by 73
Self-citationThe Role of Chondroitin Sulfate Proteoglycans in Nervous System Development
Mencio, C. P., Hussein, R. K., Yu, P., & Geller, H. M. (2020) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155420959147 · Cited by 72
Extracellular matrix remodeling through endocytosis and resurfacing of Tenascin-R
Dankovich, T. M., Kaushik, R., Olsthoorn, L. H. M., Petersen, G. C., Giro, P. E., Kluever, V., Agüi‐Gonzalez, P., Grewe, K., Bao, G., Beuermann, S., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-27462-7 · Cited by 64
Modulation of semaphorin3A in perineuronal nets during structural plasticity in the adult cerebellum
Carulli, D., Foscarin, S., Faralli, A., Pajaj, E., & Rossi, F. (2013) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2013.08.003 · Cited by 59
Apóstolo, N., Smukowski, S. N., Vanderlinden, J., Condomitti, G., Rybakin, V., ten Bos, J., Trobiani, L., Portegies, S., Vennekens, K. M., Gounko, N. V., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-18956-x · Cited by 63
Influence of the extracellular matrix on endogenous and transplanted stem cells after brain damage
Roll, L., & Faissner, A. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00219 · Cited by 54
Self-citationRoll, L., & Faissner, A. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.09.012 · Cited by 54
Self-citationPerineuronal Nets: Subtle Structures with Large Implications
Carceller, H., Gramuntell, Y., Klimczak, P., & Nácher, J. (2022) · The Neuroscientist · doi:10.1177/10738584221106346 · Cited by 54
Role of immune responses for extracellular matrix remodeling in the ischemic brain
Dzyubenko, E., Manrique‐Castano, D., Kleinschnitz, C., Faissner, A., & Hermann, D. M. (2018) · Therapeutic Advances in Neurological Disorders · doi:10.1177/1756286418818092 · Cited by 55
Self-citationIn vitro models for neurotoxicology research
Barbosa, D. J., Capela, J. P., Bastos, M. D. L., & Carvalho, F. D. (2015) · Toxicology Research · doi:10.1039/c4tx00043a · Cited by 49
Hyaluronan synthesis by developing cortical neurons in vitro
Fowke, T. M., Karunasinghe, R. N., Bai, J.-Z., Jordan, S., Gunn, A. J., & Dean, J. M. (2017) · Scientific Reports · doi:10.1038/srep44135 · Cited by 47
A potential role for glia‐derived extracellular matrix remodeling in postinjury epilepsy
Kim, S. Y., Porter, B. E., Friedman, A., & Kaufer, D. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23758 · Cited by 47
Schulte, C., Ripamonti, M., Maffioli, E., Cappelluti, M. A., Nonnis, S., Puricelli, L., Lamanna, J., Piazzoni, C., Podestà, A., Lenardi, C., et al. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00267 · Cited by 44
Diverse roles for glycosaminoglycans in neural patterning
Saied‐Santiago, K., & Bülow, H. E. (2017) · Developmental Dynamics · doi:10.1002/dvdy.24555 · Cited by 51
Neural ECM in laminar organization and connectivity development in healthy and diseased human brain
Milošević, N. J., Judáš, M., Aronica, E., & Kostović, I. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63486-3.00007-4 · Cited by 43
Blacktop, J. M., Todd, R. P., & Sorg, B. A. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.03.018 · Cited by 43
Heikkinen, A., Pihlajaniemi, T., Faissner, A., & Yuzaki, M. (2014) · Progress in Brain Research · doi:10.1016/b978-0-444-63486-3.00002-5 · Cited by 42
Self-citationFine structure analysis of perineuronal nets in the ketamine model of schizophrenia
Kaushik, R., Lipachev, N., Matuszko, G., Kochneva, A., Dvoeglazova, A., Becker, A., Paveliev, M., & Dityatev, A. E. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14853 · Cited by 43
Perineuronal Net Protein Neurocan Inhibits NCAM/EphA3 Repellent Signaling in GABAergic Interneurons
Sullivan, C. S., Gotthard, I., Wyatt, E. V., Bongu, S., Mohan, V., Weinberg, R. J., & Maness, P. F. (2018) · Scientific Reports · doi:10.1038/s41598-018-24272-8 · Cited by 37
AbouElhassan, K. M., Sarhan, H. A., Hussein, A. K., Taye, A., Ahmed, Y. M., & Safwat, M. A. (2022) · International Journal of Nanomedicine · doi:10.2147/ijn.s381353 · Cited by 40
Dzyubenko, E., Manrique‐Castano, D., Kleinschnitz, C., Faissner, A., & Hermann, D. M. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.08.001 · Cited by 40
Self-citationLi, Y., Li, Z., Jin, T., Wang, Z., & Zhao, P. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-160804 · Cited by 38
The potential of memory enhancement through modulation of perineuronal nets
Duncan, J. A., Foster, R., & Kwok, J. C. F. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14672 · Cited by 41
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
Self-citationKaretko, M., Skangiel-Kramska, J., & Nowicka, D. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.07.049 · Cited by 37
Mueller-Buehl, C., Reinhard, J., Roll, L., Bader, V., Winklhofer, K. F., & Faissner, A. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.886527 · Cited by 37
Self-citationFrom 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
The role of extracellular matrix in spinal cord development
Wiese, S., & Faissner, A. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.05.018 · Cited by 36
Self-citationRegulation of the E/I-balance by the neural matrisome
Mueller-Buehl, C., Wegrzyn, D., Bauch, J., & Faissner, A. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1102334 · Cited by 35
Self-citationRaum, H., Dietsche, B., Nagels, A., Witt, S. H., Rietschel, M., Kircher, T. T. J., & Krug, A. (2014) · Human Brain Mapping · doi:10.1002/hbm.22635 · Cited by 32
Biology of Tenascin C and its Role in Physiology and Pathology
Abedsaeidi, M., Hojjati, F., Tavassoli, A., & Sahebkar, A. (2023) · Current Medicinal Chemistry · doi:10.2174/0929867330666230404124229 · Cited by 28
Yang, X. (2020) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0117 · Cited by 31
Glia activation and its role in oxidative stress
Ogundele, O. M., Omoaghe, A. O., Ajonijebu, D. C., Ojo, A. A., Fabiyi-Edebor, T. D., Olajide, O. J., Falode, D. T., & Adeniyi, P. A. (2013) · Metabolic Brain Disease · doi:10.1007/s11011-013-9446-7 · Cited by 28
Ueno, H., Suemitsu, S., Murakami, S., Kitamura, N., Wani, K., Matsumoto, Y., Okamoto, M., & Ishihara, T. (2018) · IBRO Reports · doi:10.1016/j.ibror.2018.11.006 · Cited by 26
NPY-Y1 receptor signaling controls spatial learning and perineuronal net expression
Bertocchi, I., Mele, P., Ferrero, G., Oberto, A., Carulli, D., & Eva, C. (2021) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108425 · Cited by 26
Jansen, S., Gottschling, C., Faissner, A., & Manahan‐Vaughan, D. (2017) · Hippocampus · doi:10.1002/hipo.22742 · Cited by 26
Self-citationPrice, J. C., Levett, S. J., Radu, V., Simpson, D., Barcons, A. M., Adams, C. F., & Mather, M. L. (2019) · Small · doi:10.1002/smll.201900455 · Cited by 26
Li, X., Wu, X., Lu, T., Kuang, C., Si, Y., Zheng, W., Li, Z., & Xue, Y.-X. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25063412 · Cited by 28
Quattromani, M. J., Hakon, J., Rauch, U., Bauer, A. Q., & Wieloch, T. W. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.01.011 · Cited by 25
Self-citationGottschling, C., Dzyubenko, E., Geißler, M., & Faissner, A. (2016) · Journal of Visualized Experiments · doi:10.3791/54757 · Cited by 25
Self-citationFaralli, A., Dagna, F., Albera, A., Bekku, Y., Oohashi, T., Albera, R., Rossi, F., & Carulli, D. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1095-7 · Cited by 24
Ulc, A., Gottschling, C., Schäfer, I., Wegrzyn, D., van Leeuwen, S., Luft, V., Reinhard, J., & Faissner, A. (2017) · Biological Chemistry · doi:10.1515/hsz-2016-0275 · Cited by 25
Self-citationSinha, A., Kawakami, J., Cole, K. S., Ladutska, A., Nguyen, M. Y., Zalmai, M. S., Holder, B. L., Broerman, V. M., Matthews, R. T., & Bouyain, S. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.104952 · Cited by 24
Balsara, R. D., Dang, A. T., Donahue, D. L., Snow, T., & Castellino, F. (2015) · PLoS ONE · doi:10.1371/journal.pone.0122840 · Cited by 23
Gottschling, C., Geißler, M., Springer, G., Wolf, R. J., Juckel, G., & Faissner, A. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.08.055 · Cited by 22
Self-citationCarstens, K. E., Gloss, B. R., Alexander, G. M., & Dudek, S. M. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.15050 · Cited by 19
Briones, B. A., Pisano, T. J., Pitcher, M. N., Haye, A. E., Diethorn, E. J., Engel, E. A., Cameron, H. A., & Gould, E. (2021) · Hippocampus · doi:10.1002/hipo.23296 · Cited by 20
Illa, M., Brito, V., Plà, L., Eixarch, E., Arbat‐Plana, A., Batallé, D., Muñoz‐Moreno, E., Crispi, F., Udina, E., Figueras, F., et al. (2017) · Fetal Diagnosis and Therapy · doi:10.1159/000481171 · Cited by 16
Carbohydrate based biomaterials for neural interface applications
Dhawan, V., & Cui, X. T. (2022) · Journal of Materials Chemistry B · doi:10.1039/d2tb00584k · Cited by 17
Woo, A. M., & Sontheimer, H. W. (2023) · Frontiers in Molecular Medicine · doi:10.3389/fmmed.2023.1198021 · Cited by 17
Spatial patterns and cell surface clusters in perineuronal nets
Arnst, N., Kuznetsova, S., Lipachev, N., Shaikhutdinov, N., Melnikova, A., Олегович, М. М., Uvarov, P., Baltina, T., Rauvala, H., Osin, Y. N., et al. (2016) · Brain Research · doi:10.1016/j.brainres.2016.07.020 · Cited by 15
Reorganization of the Brain Extracellular Matrix in Hippocampal Sclerosis
Sitaš, B., Bobić‐Rasonja, M., Mrak, G., Trnski, S., Skorić, M. K., Orešković, D., Knezović, V., Gadže, Ž. P., Petanjek, Z., Šimić, G., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23158197 · Cited by 16
Wegrzyn, D., Manitz, M. P., Kostka, M., Freund, N., Juckel, G., & Faissner, A. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14934 · Cited by 16
Self-citationHyaluronic Acid and Regenerative Medicine: New Insights into the Stroke Therapy
Shahi, M., Mohammadnejad, D., Karimipour, M., Rasta, S. H., Rahbarghazi, R., & Abedelahi, A. (2020) · Current Molecular Medicine · doi:10.2174/1566524020666200326095837 · Cited by 14
Critical functions of extracellular matrix in brain metastasis seeding
Yuzhalin, A. E., & Yu, D. (2023) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-04944-z · Cited by 15
Gisabella, B., Babu, J., Valeri, J., Rexrode, L., & Pantazopoulos, H. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.646678 · Cited by 16
González-Calvo, I., Cizeron, M., Bessereau, J., & Selimi, F. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.866444 · Cited by 12
Aberrant perineuronal nets alter spinal circuits, impair motor function, and increase plasticity
Sánchez-Ventura, J., Canal, C., Hidalgo, J., Penas, C., Navarro, X., Espin, A. T., Fouad, K., & Udina, E. (2022) · Experimental Neurology · doi:10.1016/j.expneurol.2022.114220 · Cited by 12
Parallels between the extracellular matrix roles in developmental biology and cancer biology
Yuzhalin, A. E. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.09.010 · Cited by 11
Disease-specific glycosaminoglycan patterns in the extracellular matrix of human lung and brain
Ennemoser, M., Pum, A., & Kungl, A. J. (2021) · Carbohydrate Research · doi:10.1016/j.carres.2021.108480 · Cited by 11
Fasulo, L., Brandi, R., Arisi, I., Regina, F. L., Berretta, N., Capsoni, S., D’Onofrio, M., & Cattaneo, A. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00020 · Cited by 10
Patel, D. C., Swift, N. A., Tewari, B. P., Browning, J. L., Prim, C. E., Chaunsali, L., Kimbrough, I. F., Olsen, M. L., & Sontheimer, H. W. (2023) · Brain · doi:10.1093/brain/awad430 · Cited by 10
Mueller-Buehl, C., Pakusch, J., Bader, V., Winklhofer, K. F., Mark, M. D., & Faissner, A. (2025) · Scientific Reports · doi:10.1038/s41598-025-89580-2 · Cited by 10
Self-citationMolecular mechanisms mediating involvement of glial cells in brain plastic remodeling in epilepsy
Хаспеков, Л. Г., & Frumkina, L. E. (2017) · Biochemistry (Moscow) · doi:10.1134/s0006297917030178 · Cited by 10
Metadata
- Authors
- Geissler, M., Gottschling, C., Aguado, A., Rauch, U., Wetzel, C. H., Hatt, H., & Faissner, A.
- Affiliations
- Ruhr University Bochum (DE)
- Lund University (SE)
- University of Regensburg (DE)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2013-05-01
- Volume
- 33
- Issue
- 18
- Pages
- 7742-7755
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6618965
- OpenAlex
- W2012448906
- Cited by
- 140
- References
- 86
- Citations by year
- 2026: 5 · 2025: 4 · 2024: 7 · 2023: 13 · 2022: 12 · 2021: 15 · 2020: 18 · 2019: 10 · 2018: 11 · 2017: 16 · 2016: 7 · 2015: 8 · 2014: 11 · 2013: 3
- FWCI
- 4.74
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Lund University Publications (Lund University) (submittedVersion, other-oa)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Keywords
- perineuronal nets, extracellular matrix, hippocampal neurons, astrocytes, tenascin-C, tenascin-R, brevican, neurocan, chondroitin sulfate proteoglycans, synaptogenesis, synapse stabilization, inhibitory postsynaptic currents, excitatory postsynaptic currents, co-culture, embryonic neurons
- MeSH terms
- Animals, Astrocytes, Cell Count, Cells, Cultured, Embryo, Mammalian, Female, Hippocampus, Male, Mice, Inbred C57BL, Nerve Net, Neurons, Synapses, Extracellular Matrix Proteins, Mice, Knockout, Gene Expression Regulation, Developmental, Coculture Techniques, Tenascin, Excitatory Postsynaptic Potentials, Mice, Inhibitory Postsynaptic Potentials, Neurocan, Brevican
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