Extracellular matrix of the central nervous system: from neglect to challenge
Open accessAbstract
The basic concept, that specialized extracellular matrices rich in hyaluronan, chondroitin sulfate proteoglycans (aggrecan, versican, neurocan, brevican, phosphacan), link proteins and tenascins (Tn-R, Tn-C) can regulate cellular migration and axonal growth and thus, actively participate in the development and maturation of the nervous system, has in recent years gained rapidly expanding experimental support. The swift assembly and remodeling of these matrices have been associated with axonal guidance functions in the periphery and with the structural stabilization of myelinated fiber tracts and synaptic contacts in the maturating central nervous system. Particular interest has been focused on the putative role of chondroitin sulfate proteoglycans in suppressing central nervous system regeneration after lesions. The axon growth inhibitory properties of several of these chondroitin sulfate proteoglycans in vitro, and the partial recovery of structural plasticity in lesioned animals treated with chondroitin sulfate degrading enzymes in vivo have significantly contributed to the increased awareness of this long time neglected structure.
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
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?
During development, the ECM and CSPGs regulate neuronal migration, axon outgrowth, synaptogenesis and synaptic maturation.
“During development, the ECM, and CSPGs in particular, regulate neuronal migration, axon outgrowth, synaptogenesis and synaptic maturation.23, 27, 28, 29, 30, 31”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [29]
PNNs are mainly composed of hyaluronan, chondroitin sulfate proteoglycans, tenascins, and link proteins.
“The main components are hyaluronan (Figure 1), chondroitin sulfate proteoglycans (CSPGs) (i.e. aggrecan, brevican, neurocan, versican and phosphocan) (Figure 2), tenascins (Figure 3), and link proteins”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Zimmermann and Dours-Zimmermann, 2008
The perinodal net, a PNN-like structure, is commonly associated with the node of Ranvier.
“the perinodal-matrix or peridonal net, a PNN-like structure (Dours-Zimmermann et al., 2009; Zimmermann and Dours-Zimmermann, 2008), is commonly associated with the node of Ranvier”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Zimmermann and Dours-Zimmermann, 2008
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Genome-wide atlas of gene expression in the adult mouse brain
Lein, E. S., Hawrylycz, M. J., Ao, N., Ayres, M., Bensinger, A., Bernard, A., Boe, A. F., Boguski, M. S., Brockway, K. S., Byrnes, E. J., et al. (2007) · Nature · doi:10.1038/nature05453 · Cited by 5,572 · see citing works
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 · 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
PROTEOGLYCANS: STRUCTURES AND INTERACTIONS
Kjellén, L., & Lindahl, U. (1991) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.60.070191.002303 · Cited by 1,724 · see citing works
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 · 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
Proteoglycans: Structures And Interactions
Kjellén, L. (1991) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.60.1.443 · Cited by 1,602 · see citing works
Extracellular space structure revealed by diffusion analysis
Nicholson, C., & Syková, E. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01261-2 · Cited by 914 · see citing works
Camenisch, T. D., Spicer, A. P., Brehm-Gibson, T., Biesterfeldt, J., Augustine, M. L., Calabro, A., Kubalak, S., Klewer, S. E., & McDonald, J. A. (2000) · Journal of Clinical Investigation · doi:10.1172/jci10272 · Cited by 901 · see citing works
PORTER, S., CLARK, I. M., KEVORKIAN, L., & EDWARDS, D. R. (2005) · Biochemical Journal · doi:10.1042/bj20040424 · Cited by 779 · see citing works
Sulfated proteoglycans in astroglial barriers inhibit neurite outgrowth in vitro
Snow, D. M., Lemmon, V., Carrino, D. A., Caplan, A. I., & Silver, J. (1990) · Experimental Neurology · doi:10.1016/s0014-4886(05)80013-5 · Cited by 776 · see citing works
Tissir, F., & Goffinet, A. M. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1113 · Cited by 748 · see citing works
Purification and Cloning of Aggrecanase-1: A Member of the ADAMTS Family of Proteins
Tortorella, M. D., Burn, T. C., Pratta, M. A., Abbaszade, I., Hollis, J. M., Liu, R., Rosenfeld, S. A., Copeland, R. A., Decicco, C. P., Wynn, R., et al. (1999) · Science · doi:10.1126/science.284.5420.1664 · Cited by 686 · see citing works
The local differentiation of myelinated axons at nodes of Ranvier
Poliak, S., & Peles, E. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1253 · Cited by 673 · see citing works
Multiple domains of the large fibroblast proteoglycan, versican.
Zimmermann, D., & Ruoslahti, E. I. (1989) · The EMBO Journal · doi:10.1002/j.1460-2075.1989.tb08447.x · Cited by 652 · see citing works
Self-citationIozzo, R. V., & Murdoch, A. D. (1996) · The FASEB Journal · doi:10.1096/fasebj.10.5.8621059 · Cited by 647 · 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
Proteoglycans in the Developing Brain: New Conceptual Insights for Old Proteins
Bandtlow, C. E., & Zimmermann, D. R. (2000) · Physiological Reviews · doi:10.1152/physrev.2000.80.4.1267 · Cited by 632 · see citing works
Self-citationWeigel, P. H., Hascall, V., & Tammi, M. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.22.13997 · Cited by 629 · see citing works
Mice develop normally without tenascin.Preprint
Saga, Y., Yagi, T., Ikawa, Y., Sakakura, T., & Aizawa, S. (1992) · Genes & Development · doi:10.1101/gad.6.10.1821 · Cited by 582 · see citing works
Galtrey, C. M., & Fawcett, J. W. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2006.09.006 · Cited by 575 · see citing works
Toole, B. P. (2001) · Seminars in Cell and Developmental Biology · doi:10.1006/scdb.2000.0244 · Cited by 571 · see citing works
Hyaluronan-binding Proteins: Tying Up the Giant
Day, A. J., & Prestwich, G. D. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.r100036200 · Cited by 567 · see citing works
Moon, L. D. F., Asher, R. A., Rhodes, K. E., & Fawcett, J. W. (2001) · Nature Neuroscience · doi:10.1038/87415 · Cited by 563 · see citing works
Determination of protease cleavage site motifs using mixture-based oriented peptide libraries
Turk, B. E., Huang, L. L., Piro, E. T., & Cantley, L. C. (2001) · Nature Biotechnology · doi:10.1038/90273 · Cited by 560 · see citing works
Tenascins: regulation and putative functions during pathological stress
Chiquet-Ehrismann, R., & Chiquet, M. (2003) · Journal of Pathology · doi:10.1002/path.1415 · Cited by 557 · see citing works
Jones, L. L., Margolis, R. U., & Tuszynski, M. H. (2003) · Experimental Neurology · doi:10.1016/s0014-4886(03)00087-6 · Cited by 545 · see citing works
Extracellular Matrix Molecules that Influence Neural Development
Sanes, J. R. (1989) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.12.030189.002423 · Cited by 532 · see citing works
Reelin, lipoprotein receptors and synaptic plasticity
Herz, J., & Chen, Y. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn2009 · Cited by 524 · 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
Cloning and Characterization of ADAMTS11 , an Aggrecanase from the ADAMTS Family
Abbaszade, I. G., Liu, R., Yang, F., Rosenfeld, S. A., Ross, O. H., Link, J. R., Ellis, D. M., Tortorella, M. D., Pratta, M. A., Hollis, J. M., et al. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.33.23443 · Cited by 490 · see citing works
Neurocan Is Upregulated in Injured Brain and in Cytokine-Treated Astrocytes
Asher, R. A., Morgenstern, D. A., Fidler, P. S., Adcock, K. H., Oohira, A., Braistead, J. E., Levine, J. M., Margolis, R. U., ROGERS, J. H., & Fawcett, J. W. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02427.2000 · Cited by 482 · see citing works
Synthesis and sorting of proteoglycans
Prydz, K., & Dalen, K. T. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.2.193 · Cited by 481 · see citing works
McKeon, R. J., Jurynec, M. J., & Buck, C. R. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-24-10778.1999 · Cited by 480 · see citing works
Ruoslahti, E. (1996) · Glycobiology · doi:10.1093/glycob/6.5.489 · Cited by 467 · see citing works
Sandy, J. D., Westling, J., Kenagy, R. D., Iruela‐Arispe, M. L., Verscharen, C., Rodrı́guez-Manzaneque, J. C., Zimmermann, D. R., Lemire, J. M., Fischer, J. W., Wight, T. N., et al. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m009737200 · Cited by 454 · see citing works
Self-citationMammalian Hyaluronan Synthases
Itano, N., & Kimata, K. (2002) · IUBMB Life · doi:10.1080/15216540214929 · Cited by 428 · see citing works
Chapter 22 Chondroitin sulphate proteoglycans in the CNS injury response
Morgenstern, D. A., Asher, R. A., & Fawcett, J. W. (2002) · Progress in brain research · doi:10.1016/s0079-6123(02)37024-9 · Cited by 419 · see citing works
Chondroitinase ABC Promotes Sprouting of Intact and Injured Spinal Systems after Spinal Cord Injury
Barritt, A. W., Davies, M., Marchand, F., Hartley, R., Grist, J., Yip, P., McMahon, S. B., & Bradbury, E. J. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2980-06.2006 · Cited by 413 · see citing works
Polarized Domains of Myelinated Axons
Salzer, J. L. (2003) · Neuron · doi:10.1016/s0896-6273(03)00628-7 · Cited by 399 · see citing works
Peles, E., Nativ, M., Campbell, P. L., Sakurai, T., Martinez, R., Lev, S., Clary, D. O., Schilling, J., Barnea, G., Plowman, G. D., et al. (1995) · Cell · doi:10.1016/0092-8674(95)90312-7 · Cited by 397 · see citing works
Tang, X., Davies, J. E., & Davies, S. J. A. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10523 · Cited by 387 · see citing works
Perineuronal nets — a specialized form of extracellular matrix in the adult nervous system
Celio, M. R., & Blümcke, I. (1994) · Brain Research Reviews · doi:10.1016/0165-0173(94)90006-x · Cited by 386 · see citing works
Matrix metalloproteinases in brain development and remodeling: Synaptic functions and targets
Ethell, I. M., & Ethell, D. W. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21273 · Cited by 378 · see citing works
Structural and functional recovery from early monocular deprivation in adult rats
Pizzorusso, T., Medini, P., Landi, S., Baldini, S., Berardi, N., & Maffei, L. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602657103 · Cited by 367 · see citing works
Composition of Perineuronal Net Extracellular Matrix in Rat Brain
Deepa, S. S., Carulli, D., Galtrey, C., Rhodes, K., Fukuda, J., Mikami, T., Sugahara, K., & Fawcett, J. W. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m600544200 · Cited by 367 · 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
Spinal cord repair strategies: why do they work?
Bradbury, E. J., & McMahon, S. B. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1964 · Cited by 352 · see citing works
Aggrecan 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
New insights into the roles of agrin
Bezáková, G., & Rüegg, M. A. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1074 · 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
The Molecular Diversity of Glycosaminoglycans Shapes Animal Development
Bülow, H. E., & Hobert, O. (2006) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010605.093433 · Cited by 340 · see citing works
Characterization and Molecular Evolution of a Vertebrate Hyaluronan Synthase Gene Family
Spicer, A. P., & McDonald, J. A. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.4.1923 · Cited by 339 · see citing works
Milev, P., Friedlander, D. R., Sakurai, T., Karthikeyan, L., Flad, M., Margolis, R. K., Grumet, M., & Margolis, R. U. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.127.6.1703 · Cited by 328 · see citing works
Somerville, R. P. T., Longpré, J., Jungers, K. A., Engle, J. M., Ross, M., Evanko, S. P., Wight, T. N., Leduc, R., & Apte, S. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m211009200 · Cited by 324 · see citing works
Mjaatvedt, C. H., Yamamura, H., Capehart, A. A., Turner, D., & Markwald, R. R. (1998) · Developmental Biology · doi:10.1006/dbio.1998.9001 · Cited by 321 · see citing works
Hyaluronate binding properties of versican.
LeBaron, R. G., Zimmermann, D., & Ruoslahti, E. I. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)50191-0 · Cited by 317 · see citing works
Self-citationSulfotransferases in glycosaminoglycan biosynthesis
Kusche‐Gullberg, M. (2003) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2003.08.002 · Cited by 314 · see citing works
The extracellular matrix of the central and peripheral nervous systems: structure and function
Rutka, J. T., Apodaca, G., Stern, R., & Rosenblum, M. L. (1988) · Journal of neurosurgery · doi:10.3171/jns.1988.69.2.0155 · Cited by 307 · see citing works
Maurel, P., Rauch, U., Flad, M., Margolis, R. K., & Margolis, R. U. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.7.2512 · Cited by 305 · see citing works
Site-restricted expression of cytotactin during development of the chicken embryo.
Crossin, K. L., Hoffman, S., Grumet, M., Thiery, J. P., & Edelman, G. M. (1986) · The Journal of Cell Biology · doi:10.1083/jcb.102.5.1917 · Cited by 300 · see citing works
Chondroitin sulphate proteoglycans: preventing plasticity or protecting the CNS?
Rhodes, K. E., & Fawcett, J. W. (2003) · Journal of Anatomy · doi:10.1111/j.1469-7580.2004.00261.x · Cited by 296 · see citing works
Laywell, E. D., Dörries, U., Bartsch, U., Faissner, A., Schachner, M., & Steindler, D. A. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.7.2634 · Cited by 293 · see citing works
Hyaluronan-dependent pericellular matrix☆
Evanko, S. P., Tammi, M., Tammi, R., & Wight, T. N. (2007) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2007.08.008 · Cited by 286 · see citing works
Epidermal growth factor (EGF)-like repeats of human tenascin-C as ligands for EGF receptor
Swindle, C. S., Tran, K. T., Johnson, T. D., Banerjee, P., Mayes, A. M., Griffith, L., & Wells, A. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.200103103 · Cited by 286 · see citing works
Mechanisms involved in cartilage proteoglycan catabolism
Caterson, B., Flannery, C. R., Hughes, C., & Little, C. B. (2000) · Matrix Biology · doi:10.1016/s0945-053x(00)00078-0 · Cited by 285 · see citing works
Cellular 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
Extracellular matrix and the brain: components and function
Novak, U., & Kaye, A. H. (2000) · Journal of Clinical Neuroscience · doi:10.1054/jocn.1999.0212 · Cited by 279 · 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
ADAMTS‐1 cleaves a cartilage proteoglycan, aggrecan
Kuno, K., Okada, Y., Kawashima, H., Nakamura, H., Miyasaka, M., Ohno, H., & Matsushima, K. (2000) · FEBS Letters · doi:10.1016/s0014-5793(00)01854-8 · Cited by 273 · see citing works
Zimmermann, D., Dours-Zimmermann, M. T., Schubert, M., & Bruckner‐Tuderman, L. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.124.5.817 · Cited by 271 · 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 1× · see citing works
“In addition, the establishment of perineuronal nets seems to stabilize the neuronal circuitry by suppressing the formation of new synaptic contacts (Galtrey and Fawcett 2007; HockWeld et al. 1990; Rauch 2004; Yamaguchi 2000).”
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
Gates, M. A., Thomas, L. B., Howard, E. M., Laywell, E. D., Sajin, B., Faissner, A., Götz, B., Silver, J., & Steindler, D. A. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903610205 · Cited by 268 · see citing works
Neurofascin assembles a specialized extracellular matrix at the axon initial segment
Hedstrom, K. L., Xu, X., Ogawa, Y., Frischknecht, R., Seidenbecher, C. I., Shrager, P., & Rasband, M. N. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200705119 · Cited by 268 · see citing works
Rauch, U., Gao, P., Janetzko, A., Flaccus, A., Hilgenberg, L., Tekotte, H., Margolis, R. K., & Margolis, R. U. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)98755-7 · Cited by 267 · see citing works
Versican Is Upregulated in CNS Injury and Is a Product of Oligodendrocyte Lineage Cells
Asher, R. A., Morgenstern, D. A., Shearer, M. C., Adcock, K. H., Pesheva, P., & Fawcett, J. W. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-06-02225.2002 · Cited by 265 · see citing works
Steindler, D. A., Cooper, N. G. F., Faissner, A., & Schachner, M. (1989) · Developmental Biology · doi:10.1016/s0012-1606(89)80056-9 · Cited by 264 · see citing works
Brakebusch, C., Seidenbecher, C. I., Asztely, F., Rauch, U., Matthies, H., Meyer, H., Krug, M., Böckers, T. M., Zhou, X., Kreutz, M. R., et al. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.21.7417-7427.2002 · Cited by 264 · see citing works
Oakley, R. A., & Tosney, K. W. (1991) · Developmental Biology · doi:10.1016/s0012-1606(05)80017-x · Cited by 260 · see citing works
Landolt, R., Vaughan, L., Winterhalter, K. H., & Zimmermann, D. R. (1995) · Development · doi:10.1242/dev.121.8.2303 · Cited by 260 · see citing works
Self-citationCritical Periods in the Visual System: Changing Views for a Model of Experience-Dependent Plasticity
Hooks, B. M., & Chen, C. (2007) · Neuron · doi:10.1016/j.neuron.2007.10.003 · Cited by 254 · see citing works
Pindzola, R. R., Doller, C. M., & Silver, J. (1993) · Developmental Biology · doi:10.1006/dbio.1993.1057 · Cited by 251 · see citing works
Dours-Zimmermann, M. T., & Zimmermann, D. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)30089-2 · Cited by 249 · see citing works
Self-citationNiederöst, B. P., Zimmermann, D. R., Schwab, M. E., & Bandtlow, C. E. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-20-08979.1999 · Cited by 249 · see citing works
Self-citationWeber, 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
Perineuronal nets potentially protect against oxidative stress
Morawski, M., Brückner, M. K., Riederer, P., Brückner, G., & Arendt, T. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.04.017 · Cited by 246 · see citing works
Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan gene
Watanabe, H., Kimata, K., Line, S. R. P., Strong, D., Gao, L., Kozak, C. A., & Yamada, Y. (1994) · Nature Genetics · doi:10.1038/ng0694-154 · Cited by 245 · see citing works
Skin wounds and severed nerves heal normally in mice lacking tenascin-C.
Forsberg, E., Hirsch, E., Fröhlich, L., Meyer, M., Ekblom, P., Aszódi, A., Werner, S., & Fässler, R. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.13.6594 · Cited by 235 · see citing works
Tenascin-R mediates activity-dependent recruitment of neuroblasts in the adult mouse forebrain
Saghatelyan, A., de Chevigny, A., Schachner, M., & Lledo, P. (2004) · Nature Neuroscience · doi:10.1038/nn1211 · Cited by 229 · see citing works
Yamada, H., Fredette, B. J., Shitara, K., Hagihara, K., Miura, R., Ranscht, B., Stallcup, W. B., & Yamaguchi, Y. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-20-07784.1997 · Cited by 228 · see citing works
MMPs in the central nervous system: Where the good guys go bad
AGRAWAL, S., LAU, L., & Yong, V. W. (2007) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2007.06.003 · Cited by 226 · see citing works
Isogai, Z., Aspberg, A., Keene, D. R., Ono, R. N., Reinhardt, D. P., & Sakai, L. Y. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m110583200 · Cited by 222 · see citing works
Milev, P., Maurel, P., Chiba, A., Mevissen, M., Popp, S., Yamaguchi, Y., Margolis, R. K., & Margolis, R. U. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.8759 · Cited by 219 · see citing works
Milev, P., Maurel, P., Häring, M., Margolis, R. K., & Margolis, R. U. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.26.15716 · Cited by 210 · see citing works
Fibulin-1 Is a Ligand for the C-type Lectin Domains of Aggrecan and Versican
Aspberg, A., Adam, S., Kostka, G., Timpl, R., & Heinegård, D. K. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.29.20444 · Cited by 207 · see citing works
DeAngelis, P. L. (1999) · Cellular and Molecular Life Sciences CMLS · doi:10.1007/s000180050461 · Cited by 207 · 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
Extracellular matrix components associated with remodeling processes in brain
Rauch, U. (2004) · Cellular and Molecular Life Sciences (CMLS) · doi:10.1007/s00018-004-4043-x · Cited by 205 · see citing works
Olin, A. I., Mörgelin, M., Sasaki, T., Timpl, R., Heinegård, D. K., & Aspberg, A. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m006783200 · Cited by 204 · 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
Spicer, A. P., Joo, A., & Bowling, R. A. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m213100200 · Cited by 201 · see citing works
Matthews, R. T., Gary, S. C., Zerillo, C. A., Pratta, M. A., Solomon, K. A., Arner, E. C., & Hockfield, S. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m909764199 · Cited by 197 · see citing works
Brain derived versican V2 is a potent inhibitor of axonal growth
Schmalfeldt, M., Bandtlow, C. E., Dours-Zimmermann, M. T., Winterhalter, K. H., & Zimmermann, D. R. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.5.807 · Cited by 197 · see citing works
Self-citationLander, 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
Mice lacking link protein develop dwarfism and craniofacial abnormalities
Watanabe, H., & Yamada, Y. (1999) · Nature Genetics · doi:10.1038/6016 · Cited by 190 · see citing works
Milev, P., Chiba, A., Häring, M., Rauvala, H., Schachner, M., Ranscht, B., Margolis, R. K., & Margolis, R. U. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.12.6998 · Cited by 190 · see citing works
A sodium channel signaling complex: modulation by associated receptor protein tyrosine phosphatase β
Ratcliffe, C. F., Qu, Y., McCormick, K. A., Tibbs, V. C., Dixon, J. E., Scheuer, T., & Catterall, W. A. (2000) · Nature Neuroscience · doi:10.1038/74805 · Cited by 182 · see citing works
Barnea, G., Grumet, M., Milev, P., Silvennoinen, O., Levy, J. B., Sap, J., & Schlessinger, J. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)36625-5 · Cited by 182 · see citing works
Activation of the Proteolytic Activity of ADAMTS4 (Aggrecanase-1) by C-terminal Truncation
Gao, G., Westling, J., Thompson, V. P., Howell, T. D., Gottschall, P. E., & Sandy, J. D. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m107443200 · Cited by 178 · see citing works
Fuss, B., Wintergerst, E. S., Bartsch, U., & Schachner, M. (1993) · The Journal of Cell Biology · doi:10.1083/jcb.120.5.1237 · Cited by 177 · see citing works
Meet the Tenascins: Multifunctional and Mysterious
Hsia, H. C., & Schwarzbauer, J. E. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.r500005200 · Cited by 176 · see citing works
The extracellular matrix of the nervous system
Carbonetto, S. (1984) · Trends in Neurosciences · doi:10.1016/s0166-2236(84)80061-2 · Cited by 176 · see citing works
Prieto, A. L., Jones, F. S., Cunningham, B. A., Crossin, K. L., & Edelman, G. M. (1990) · The Journal of Cell Biology · doi:10.1083/jcb.111.2.685 · Cited by 175 · see citing works
The distribution of tenascin-X is distinct and often reciprocal to that of tenascin-C.
Matsumoto, K., Saga, Y., Ikemura, T., Sakakura, T., & Chiquet‐Ehrismann, R. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.125.2.483 · Cited by 174 · see citing works
Role of ADAMTS-1 in Atherosclerosis
Jönsson‐Rylander, A., Nilsson, T., Fritsche‐Danielson, R., Hammarström, A., Behrendt, M., Andersson, J.-O., Lindgren, K., Andersson, A., Wallbrandt, P., Rosengren, B. E., et al. (2004) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000150045.27127.37 · Cited by 173 · see citing works
Evers, M. R., Salmen, B., Bukalo, O., Rollenhagen, A., Bösl, M. R., Morellini, F., Bartsch, U., Dityatev, A., & Schachner, M. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-16-07177.2002 · Cited by 172 · see citing works
Brevican Is Degraded by Matrix Metalloproteinases and Aggrecanase-1 (ADAMTS4) at Different Sites
Nakamura, H., Fujii, Y., Inoki, I., Sugimoto, K., Tanzawa, K., Matsuki, H., Miura, R., Yamaguchi, Y., & Okada, Y. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m003875200 · Cited by 168 · see citing works
The structure and function of tenascins in the nervous system
Joester, A., & Faissner, A. (2001) · Matrix Biology · doi:10.1016/s0945-053x(00)00136-0 · Cited by 165 · see citing works
Extracellular Matrix and Visual Cortical Plasticity
Berardi, N., Pizzorusso, T., & Maffei, L. (2004) · Neuron · doi:10.1016/j.neuron.2004.12.008 · Cited by 163 · see citing works
Toole, B. P. (2000) · Journal of Clinical Investigation · doi:10.1172/jci10706 · Cited by 161 · see citing works
Neurocan 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
Carulli, D., Rhodes, K. E., & Fawcett, J. W. (2007) · Journal of Comparative Neurology · doi:10.1002/cne.21231 · Cited by 158 · see citing works
Spicer, A. P., & Tien, J. (2004) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.20006 · Cited by 156 · see citing works
ADAMTS-8 exhibits aggrecanase activity and is expressed in human articular cartilage
Collins‐Racie, L. A., Flannery, C. R., Zeng, W., Corcoran, C., Annis-Freeman, B., Agostino, M. J., Arai, M., DiBlasio-Smith, E. A., Dorner, A. J., Georgiadis, K. E., et al. (2004) · Matrix Biology · doi:10.1016/j.matbio.2004.05.004 · Cited by 154 · see citing works
Distinct interaction of versican/PG-M with hyaluronan and link protein
Matsumoto, K., Shionyu, M., Go, M., Shimizu, K., Shinomura, T., Kimata, K., & Watanabe, H. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m305060200 · Cited by 153 · see citing works
Haas, C. A., Rauch, U., Thon, N., Merten, T., & Deller, T. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-22-09953.1999 · Cited by 151 · see citing works
Characterization of METH-1/ADAMTS1 Processing Reveals Two Distinct Active Forms
Rodrı́guez-Manzaneque, J. C., Milchanowski, A. B., Dufour, E. K., Leduc, R., & Iruela‐Arispe, M. L. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m002599200 · Cited by 151 · see citing works
Seidenbecher, C. I., Richter, K., Rauch, U., Fässler, R., Garner, C. C., & Gundelfinger, E. D. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.45.27206 · Cited by 149 · see citing works
Neame, P. J., & Barry, F. (1993) · Cellular and Molecular Life Sciences · doi:10.1007/bf01923584 · Cited by 146 · see citing works
Held‐Feindt, J., Paredes, E. B., Blömer, U., Seidenbecher, C. I., Stark, A. M., Mehdorn, H. M., & Mentlein, R. (2005) · International Journal of Cancer · doi:10.1002/ijc.21258 · Cited by 144 · see citing works
The versican C-type lectin domain recognizes the adhesion protein tenascin-R.
Aspberg, A., Binkert, C., & Ruoslahti, E. I. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.23.10590 · Cited by 142 · see citing works
Harroch, S., Furtado, G. C., Brück, W., D, J. R. M., Lafaille, J. J., Chao, M. V., Buxbaum, J. D., & Schlessinger, J. (2002) · Nature Genetics · doi:10.1038/ng1004 · Cited by 140 · see citing works
Maeda, N., Hamanaka, H., Oohira, A., & Noda, M. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00069-h · Cited by 134 · see citing works
The Secreted Metalloprotease ADAMTS20 Is Required for Melanoblast Survival
Silver, D. L., Hou, L., Somerville, R. P. T., Young, M. E., Apte, S., & Pavan, W. J. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000003 · Cited by 132 · see citing works
Hyaluronan Synthesis Induces Microvillus-like Cell Surface Protrusions
Kultti, A. H., Rilla, K. J., Tiihonen, R., Spicer, A. P., Tammi, R., & Tammi, M. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m512840200 · Cited by 132 · 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
Structural Basis for Interactions between Tenascins and Lectican C-Type Lectin Domains
Lundell, A., Olin, A. I., Mörgelin, M., al-Karadaghi, S., Aspberg, A., & Logan, D. T. (2004) · Structure · doi:10.1016/j.str.2004.05.021 · Cited by 127 · see citing works
Delpech, B., & Halavent, C. (1981) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1981.tb01672.x · Cited by 127 · see citing works
Zako, M., Shinomura, T., Ujita, M., Ito, K., & Kimata, K. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.8.3914 · Cited by 127 · see citing works
The Role of Hyaluronan Synthase 3 in Ventilator-induced Lung Injury
Bai, K., Spicer, A. P., Mascarenhas, M. M., Yu, L., Ochoa, C. D., Garg, H. G., & Quinn, D. A. (2005) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200405-652oc · Cited by 126 · see citing works
Disinhibition of neurite growth to repair the injured adult CNS: Focusing on Nogo
Gonzenbach, R. R., & Schwab, M. E. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-007-7170-3 · Cited by 125 · see citing works
Oohashi, T., Hirakawa, S., Bekku, Y., Rauch, U., Zimmermann, D. R., Su, W.-D., Ohtsuka, A., Murakami, T., & Ninomiya, Y. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2001.1061 · Cited by 124 · see citing works
Self-citationMeyer‐Puttlitz, B., Milev, P., Junker, E., Zimmer, I., Margolis, R. U., & Margolis, R. K. (1995) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1995.65052327.x · Cited by 124 · 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 3× · see citing works
“are in vitro primarily astrocyte-derived (John et al. 2006), although perineuronal net-like structures develop apparently also in the virtual absence of glial cells (Miyata et al.”
BackgroundMaeda, N., & Noda, M. (1996) · Development · doi:10.1242/dev.122.2.647 · Cited by 120 · see citing works
Tenascin knockout mice: barrels, boundary molecules, and glial scars
Steindler, D. A., Settles, D. L., Erickson, H. P., Laywell, E. D., Yoshiki, A., Faissner, A., & Kusakabe, M. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-03-01971.1995 · Cited by 119 · see citing works
The Proteoglycan Lectin Domain Binds Sulfated Cell Surface Glycolipids and Promotes Cell Adhesion
Miura, R., Aspberg, A., Ethell, I. M., Hagihara, K., Schnaar, R. L., Ruoslahti, E. I., & Yamaguchi, Y. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.16.11431 · Cited by 119 · see citing works
Margolis, R. K., Margolis, R. U., Preti, C., & Lai, D. (1975) · Biochemistry · doi:10.1021/bi00693a004 · Cited by 118 · see citing works
Versican V2 Is a Major Extracellular Matrix Component of the Mature Bovine Brain
Schmalfeldt, M., Dours-Zimmermann, M. T., Winterhalter, K. H., & Zimmermann, D. R. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.25.15758 · Cited by 118 · see citing works
Self-citationNo Obvious Abnormality in Mice Deficient in Receptor Protein Tyrosine Phosphatase β
Harroch, S., Palmeri, M., Rosenbluth, J. M., Custer, A., Okigaki, M., Shrager, P., Blum, M., Buxbaum, J. D., & Schlessinger, J. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.20.7706-7715.2000 · Cited by 115 · see citing works
Rilla, K. J., Tiihonen, R., Kultti, A. H., Tammi, M., & Tammi, R. (2008) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.2008.951665 · Cited by 114 · see citing works
Miller, B., Sheppard, A. M., Bicknese, A. R., & Pearlman, A. L. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903550410 · Cited by 114 · see citing works
Axon 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
Bekku, Y., Su, W.-D., Hirakawa, S., Fässler, R., Ohtsuka, A., Kang, J. S., Sanders, J., Murakami, T., Ninomiya, Y., & Oohashi, T. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00133-7 · Cited by 114 · see citing works
Human glioblastomas overexpress ADAMTS-5 that degrades brevican
Nakada, M., Miyamori, H., Kita, D., Takahashi, T., Yamashita, J., Sato, H., Miura, R., Yamaguchi, Y., & Okada, Y. (2005) · Acta Neuropathologica · doi:10.1007/s00401-005-1032-6 · Cited by 113 · see citing works
Isolation and Partial Characterization of a Glial Hyaluronate-binding Protein
Perides, G., Lane, W. S., Andrews, D. M., Dahl, D. R., & Bignami, A. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)83646-8 · Cited by 112 · see citing works
Bignami, A., Perides, G., & Rahemtulla, F. G. (1993) · Journal of Neuroscience Research · doi:10.1002/jnr.490340110 · Cited by 109 · see citing works
Yuan, W., Matthews, R. T., Sandy, J. D., & Gottschall, P. E. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00347-0 · Cited by 109 · see citing works
Adamts9 is widely expressed during mouse embryo development
Jungers, K. A., Goff, C. L., Somerville, R. P. T., & Apte, S. (2005) · Gene Expression Patterns · doi:10.1016/j.modgep.2005.03.004 · Cited by 108 · see citing works
Mörgelin, M., Paulsson, M., Malmström, A., & Heinegård, D. K. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)80176-4 · Cited by 105 · see citing works
Westling, J., Gottschall, P. E., Thompson, V. P., Cockburn, A., Perides, G., Zimmermann, D. R., & Sandy, J. D. (2004) · Biochemical Journal · doi:10.1042/bj20030896 · Cited by 104 · see citing works
Self-citationMilev, P., Fischer, D., Häring, M., Schulthess, T., Margolis, R. K., Chiquet‐Ehrismann, R., & Margolis, R. U. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.24.15501 · Cited by 102 · see citing works
Zeng, W., Corcoran, C., Collins‐Racie, L. A., LaVallie, E. R., Morris, E. A., & Flannery, C. R. (2006) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2006.01.013 · Cited by 102 · see citing works
Immunohistological Localization of Tenascin in the Developing and Lesioned Adult Mouse Optic Nerve
Bartsch, U., Bartsch, S., Dörries, U., & Schachner, M. (1992) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1992.tb00881.x · Cited by 102 · see citing works
Molecular evidence for early activity-dependent development of hamster motor neurons
Kalb, R., & Hockfield, S. (1988) · The Journal of Neuroscience · doi:10.1523/jneurosci.08-07-02350.1988 · Cited by 102 · see citing works
Perineuronal nets protect against amyloid β-protein neurotoxicity in cultured cortical neurons
Miyata, S., Nishimura, Y., & Nakashima, T. (2007) · Brain Research · doi:10.1016/j.brainres.2007.02.066 · Cited by 101 · see citing works
On the existence of a cartilage‐like proteoglycan and link proteins in the central nervous system
Asher, R. A., Scheibe, R. J., Keiser, H. D., & Bignami, A. (1995) · Glia · doi:10.1002/glia.440130406 · Cited by 100 · see citing works
Ripellino, J. A., Bailo, M., Margolis, R. U., & Margolis, R. K. (1988) · The Journal of Cell Biology · doi:10.1083/jcb.106.3.845 · Cited by 100 · see citing works
Yamagata, M., Shinomura, T., & Kimata, K. (1993) · Anatomy and Embryology · doi:10.1007/bf00174419 · Cited by 96 · see citing works
Milev, P., Monnerie, H., Popp, S., Margolis, R. K., & Margolis, R. U. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.34.21439 · Cited by 95 · see citing works
Abnormal Behavior and Neurotransmissions of Tenascin Gene Knockout Mouse
Fukamauchi, F., Mataga, N., Wang, Y., Sato, S., Yoshiki, A., & Kusakabe, M. (1996) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1996.0561 · Cited by 95 · see citing works
Versican V0 and V1 Guide Migratory Neural Crest Cells
Dutt, S., Kléber, M., Matasci, M., Sommer, L., & Zimmermann, D. R. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m510834200 · Cited by 94 · see citing works
Self-citationSeyfried, N. T., McVey, G. F., Almond, A., Mahoney, D. J., Dudhia, J., & Day, A. J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m411297200 · Cited by 94 · see citing works
Behavioral alterations in mice deficient for the extracellular matrix glycoprotein tenascin-R
Freitag, S., Schachner, M., & Morellini, F. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(03)00109-8 · Cited by 93 · see citing works
Neame, P. J., Christner, J. E., & Baker, J. R. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)45445-2 · Cited by 91 · see citing works
Scherberich, A., Tucker, R. P., Samandari, E., Brown-Luedi, M., Martin, D., & Chiquet-Ehrismann, R. (2004) · Journal of Cell Science · doi:10.1242/jcs.00867 · Cited by 90 · see citing works
Joester, A., & Faissner, A. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.24.17144 · Cited by 89 · see citing works
Lemons, M. L., Sandy, J. D., Anderson, D. K., & Howland, D. R. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-13-04772.2001 · Cited by 89 · see citing works
Proteoglycans in brain development
Schwartz, N. B., & Domowicz, M. S. (2004) · Glycoconjugate Journal · doi:10.1023/b:glyc.0000046278.34016.36 · Cited by 88 · see citing works
Extracellular 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
MMPs and ADAMTSs: functional studies
Carl, R. F. (2006) · Frontiers in bioscience · doi:10.2741/1818 · Cited by 85 · see citing works
Mapping of a Defined Neurocan Binding Site to Distinct Domains of Tenascin-C
Rauch, U., Clement, A. B., Retzler, C., Fröhlich, L. F., Fässler, R., Göhring, W., & Faissner, A. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.43.26905 · Cited by 84 · see citing works
Brevican: a major proteoglycan in adult brain.
Yamaguchi, Y. (1996) · PubMed · Cited by 84 · see citing works
Boundaries and Wounds, Glia and Glycoconjugates
Laywell, E. D., & Steindler, D. A. (1991) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1991.tb15603.x · Cited by 83 · see citing works
Isolation of a Tenascin-R Binding Protein from Mouse Brain Membranes
Xiao, Z., Bartsch, U., Margolis, R. K., Rougon, G. N., Montag, D., & Schachner, M. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.51.32092 · Cited by 80 · see citing works
Severe cognitive and motor coordination deficits in Tenascin‐R‐deficient mice
Sallaz, M., & Montag, D. (2003) · Genes Brain & Behavior · doi:10.1034/j.1601-183x.2003.00003.x · Cited by 80 · see citing works
Expression of ADAMTS1 during murine development
Thai, S. N.-M., & Iruela‐Arispe, M. L. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(02)00115-6 · Cited by 75 · see citing works
Construction of perineuronal net-like structure by cortical neurons in culture
Miyata, S., Nishimura, Y., Hayashi, N., & Oohira, A. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.07.031 · Cited by 75 · see citing works
In vivo characterization of endogenous proliferating cells in adult rat subcortical white matter
Gensert, J. M., & Goldman, J. E. (1996) · Glia · doi:10.1002/(sici)1098-1136(199605)17:1 · Cited by 75 · see citing works
Niisato, K., Fujikawa, A., Komai, S., Shintani, T., Watanabe, E., Sakaguchi, G., Katsuura, G., Manabe, T., & Noda, M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2565.04.2005 · Cited by 71 · see citing works
Neidhardt, J., Fehr, S., Kutsche, M., Löhler, J., & Schachner, M. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00012-5 · Cited by 70 · see citing works
Hirakawa, S., Oohashi, T., Su, W.-D., Yoshioka, H., MURAKAMI, T., Arata, J., & Ninomiya, Y. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.3583 · Cited by 70 · see citing works
Rauch, U. (1997) · Cell and Tissue Research · doi:10.1007/s004410050940 · Cited by 69 · see citing works
Cross, A. K., Haddock, G., Stock, C. J., Allan, S. M., Surr, J., Bunning, R. A. D., Buttle, D. J., & Woodroofe, M. N. (2006) · Brain Research · doi:10.1016/j.brainres.2006.02.136 · Cited by 68 · see citing works
Intrinsic and extrinsic determinants of ion channel localization in neurons
Hedstrom, K. L., & Rasband, M. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04001.x · Cited by 67 · see citing works
Myelination and behaviour of tenascin‐C null transgenic mice
Kiernan, B. W., Garcion, E., Ferguson, J., Frost, E. E., Torres, E. M., Dunnett, S. B., Saga, Y., Aizawa, S., Faissner, A., Kaur, R., et al. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00729.x · Cited by 67 · see citing works
Miguel, R. F., Pollak, A., & Lubec, G. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.09.008 · Cited by 64 · see citing works
The matrix metalloproteinases and CNS plasticity: An overview
Milward, E. A., Fitzsimmons, C., Szklarczyk, A., & Conant, K. E. (2007) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2007.04.010 · Cited by 63 · see citing works
Kalb, R. G., & Hockfield, S. J. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90148-w · Cited by 62 · see citing works
Flagged first, then by citations
1 of the 240 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Extracellular Matrix Degradation and Remodeling in Development and Disease
Lu, P., Takai, K., Weaver, V. M., & Werb, Z. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005058 · Cited by 2,265 · see citing works
Proteoglycan form and function: A comprehensive nomenclature of proteoglycans
Iozzo, R. V., & Schaefer, L. (2015) · Matrix Biology · doi:10.1016/j.matbio.2015.02.003 · Cited by 1,264 · see citing works
The extracellular matrix: tools and insights for the "omics" era
Naba, A., Clauser, K. R., Ding, H., Whittaker, C. A., Carr, S. A., & Hynes, R. O. (2016) · Matrix Biology · doi:10.1016/j.matbio.2015.06.003 · Cited by 1,037 · see citing works
A neurocentric perspective on glioma invasion
Cuddapah, V. A., Robel, S., Watkins, S., & Sontheimer, H. W. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3765 · Cited by 826 · see citing works
The blood-brain barrier: an engineering perspective
Wong, A. D., Ye, M., Levy, A. F., Rothstein, J. D., Bergles, D. E., & Searson, P. C. (2013) · Frontiers in Neuroengineering · doi:10.3389/fneng.2013.00007 · Cited by 662 · see citing works
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 · see citing works
Engineered In Vitro Disease Models
Benam, K. H., Dauth, S., Hassell, B., Herland, A., Jain, A., Jang, K.-J., Karalis, K., Kim, H. J., MacQueen, L., Mahmoodian, R., et al. (2015) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev-pathol-012414-040418 · Cited by 554 · see citing works
Extracellular Matrix: Functions in the Nervous System
Barros, C. S., Franco, S. J., & Muller, U. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005108 · Cited by 506 · see citing works
Animals lacking link protein have attenuated perineuronal nets and persistent plasticity
Carulli, D., Pizzorusso, T., Kwok, J. C. F., Putignano, E., Poli, A., Forostyak, S., Andrews, M. R., Deepa, S. S., Glant, T. T., & Fawcett, J. W. (2010) · Brain · doi:10.1093/brain/awq145 · Cited by 495 · see citing works
Formation of the Ovarian Follicular Antrum and Follicular Fluid1
Rodgers, R. J., & Irving‐Rodgers, H. F. (2010) · Biology of Reproduction · doi:10.1095/biolreprod.109.082941 · Cited by 453 · see citing works
Extracellular matrix and perineuronal nets in CNS repair
Kwok, J. C. F., Dick, G., Wang, D., & Fawcett, J. W. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20974 · Cited by 395 · see citing works
Miroshnikova, Y. A., Mouw, J. K., Barnes, J. M., Pickup, M. W., Lakins, J. N., Kim, Y., Lobo, K. A., Persson, A. I., Reis, G. F., McKnight, T. R., et al. (2016) · Nature Cell Biology · doi:10.1038/ncb3429 · Cited by 380 · see citing works
The perineuronal net and the control of CNS plasticity
Wang, D., & Fawcett, J. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1375-y · Cited by 373 · see citing works
Interstitial guidance of cancer invasion
Gritsenko, P. G., Ilina, O., & Friedl, P. (2011) · The Journal of Pathology · doi:10.1002/path.3031 · Cited by 347 · see citing works
Tissue mechanics regulate brain development, homeostasis and disease
Barnes, J. M., Przybyla, L., & Weaver, V. M. (2017) · Journal of Cell Science · doi:10.1242/jcs.191742 · Cited by 313 · see citing works
Regenerative Therapies for Central Nervous System Diseases: a Biomaterials Approach
Tam, R. Y., Führmann, T., Mitrousis, N., & Shoichet, M. S. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.237 · Cited by 292 · see citing works
Current advances in electrospun gelatin-based scaffolds for tissue engineering applications
Aldana, A. A., & Abraham, G. A. (2016) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2016.09.044 · Cited by 286 · see citing works
How the extracellular matrix shapes neural development
Long, K. R., & Huttner, W. Β. (2019) · Open Biology · doi:10.1098/rsob.180216 · Cited by 263 · see citing works
Tumor Cell Invasion in Glioblastoma
Vollmann‐Zwerenz, A., Leidgens, V., Feliciello, G., Klein, C. A., & Hau, P. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21061932 · Cited by 256 · see citing works
Targeting 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
The Medium of Haptic Perception: A Tensegrity Hypothesis
Turvey, M. T., & Fonseca, S. T. (2014) · Journal of Motor Behavior · doi:10.1080/00222895.2013.798252 · Cited by 235 · see citing works
Drug and gene delivery across the blood–brain barrier with focused ultrasound
Timbie, K. F., Mead, B. P., & Price, R. J. (2015) · Journal of Controlled Release · doi:10.1016/j.jconrel.2015.08.059 · Cited by 230 · see citing works
Glioma infiltration and extracellular matrix: key players and modulators
Ferrer, V. P., Moura‐Neto, V., & Mentlein, R. (2018) · Glia · doi:10.1002/glia.23309 · Cited by 223 · see citing works
Provisional matrix: A role for versican and hyaluronan
Wight, T. N. (2016) · Matrix Biology · doi:10.1016/j.matbio.2016.12.001 · Cited by 220 · see citing works
Baiguera, S., Gaudio, C. D., Lucatelli, E., Kuevda, E. V., Boieri, M., Mazzanti, B., Bianco, A., & Macchiarini, P. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.10.060 · Cited by 211 · see citing works
The brain interstitial system: Anatomy, modeling, in vivo measurement, and applications
Lei, Y., Han, H., Yuan, F., Javeed, A., & Zhao, Y. L. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.12.007 · Cited by 215 · 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
Bioprinting for Neural Tissue Engineering
Knowlton, S. M., Anand, S., Shah, T., & Taşoğlu, S. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.11.001 · Cited by 201 · see citing works
Three mechanisms assemble central nervous system nodes of Ranvier
Susuki, K., Chang, K.-J., Zollinger, D. R., Liu, Y., Ogawa, Y., Eshed-Eisenbach, Y., Dours-Zimmermann, M. T., Oses-Prieto, J. A., Burlingame, A. L., Seidenbecher, C. I., et al. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.005 · Cited by 186 · see citing works
Self-citationProteoglycans and their roles in brain cancer
Wade, A., Robinson, A. E., Engler, J. R., Petritsch, C. K., James, C. D., & Phillips, J. J. (2013) · FEBS Journal · doi:10.1111/febs.12109 · Cited by 193 · see citing works
The 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 189 · see citing works
Nandadasa, S., Foulcer, S. J., & Apte, S. (2014) · Matrix Biology · doi:10.1016/j.matbio.2014.01.005 · Cited by 182 · 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
Hyaluronic Acid: Incorporating the Bio into the Material
Wolf, K. J., & Kumar, S. (2019) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.8b01268 · Cited by 178 · see citing works
Hemphill, M. A., Dauth, S., Yu, C. J., Dabiri, B. E., & Parker, K. K. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.041 · Cited by 173 · see citing works
The performance of laminin-containing cryogel scaffolds in neural tissue regeneration
Jurga, M., Dainiak, M. B., Sarnowska, A., Jabłońska, A., Tripathi, A., Plieva, F. M., Savina, I. N., Strojek, L., Jungvid, H., Kumar, A., et al. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.01.049 · Cited by 170 · 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
Coleman, L. G., Liu, W., Oguz, I., Styner, M., & Crews, F. T. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.11.021 · Cited by 170 · see citing works
Human astrocytes develop physiological morphology and remain quiescent in a novel 3D matrix
Placone, A. L., McGuiggan, P. M., Bergles, D. E., Guerrero‐Cazares, H., Quiñones‐Hinojosa, A., & Searson, P. C. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.11.046 · Cited by 162 · see citing works
Morawski, M., Brückner, G., Jäger, C., Seeger, G., & Arendt, T. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.05.022 · Cited by 156 · see citing works
Dissecting and rebuilding the glioblastoma microenvironment with engineered materials
Wolf, K. J., Chen, J., Coombes, J. D., Aghi, M. K., & Kumar, S. (2019) · Nature Reviews Materials · doi:10.1038/s41578-019-0135-y · Cited by 159 · 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
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
Mechanical and Biological Interactions of Implants with the Brain and Their Impact on Implant Design
Prodanov, D., & Delbeke, J. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00011 · Cited by 148 · see citing works
Benchmarking in vitro tissue-engineered blood–brain barrier models
DeStefano, J. G., Jamieson, J. J., Linville, R. M., & Searson, P. C. (2018) · Fluids and Barriers of the CNS · doi:10.1186/s12987-018-0117-2 · Cited by 142 · see citing works
Fong, A. H., Romero-López, M., Heylman, C. M., Keating, M., Tran, D. D., Sobrino, A., Tran, A. Q., Pham, H. H., Fimbres, C., Gershon, P. D., et al. (2016) · Tissue Engineering Part A · doi:10.1089/ten.tea.2016.0027 · Cited by 140 · see citing works
Aggrecan: Beyond cartilage and into the brain
Morawski, M., Brückner, G., Arendt, T., & Matthews, R. T. (2012) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2012.01.010 · Cited by 136 · 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
Pyka, M., Wetzel, C., Aguado, A., Geissler, M., Hatt, H., & Faissner, A. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07690.x · Cited by 131 · see citing works
Said, N. A., Sänchez‐Carbayo, M., Smith, S. C., & Theodorescu, D. (2012) · Journal of Clinical Investigation · doi:10.1172/jci61392 · Cited by 133 · 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
3D brain angiogenesis model to reconstitute functional human blood–brain barrier in vitro
Lee, S., Chung, M., Lee, B., & Jeon, N. L. (2019) · Biotechnology and Bioengineering · doi:10.1002/bit.27224 · Cited by 129 · see citing works
Versican and the regulation of cell phenotype in disease
Wight, T. N., Kinsella, M. G., Evanko, S. P., Potter‐Perigo, S., & Merrilees, M. J. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.12.028 · Cited by 129 · see citing works
An Experimenter’s Guide to Glioblastoma Invasion Pathways
de Gooijer, M. C., Navarro, M. G., Bernards, R., Würdinger, T., & van Tellingen, O. (2018) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2018.07.003 · Cited by 123 · see citing works
Versican V2 Assembles the Extracellular Matrix Surrounding the Nodes of Ranvier in the CNS
Dours-Zimmermann, M. T., Maurer, K., Rauch, U., Stoffel, W., Fassler, R., & Zimmermann, D. R. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4158-08.2009 · Cited by 123 · see citing works
Self-citationSood, D., Chwalek, K., Stuntz, E., Pouli, D., Du, C., Tang‐Schomer, M. D., Georgakoudi, I., Black, L. D., & Kaplan, D. L. (2015) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.5b00446 · Cited by 123 · see citing works
Advancing models of neural development with biomaterials
Roth, J. G., Huang, M. S., Li, T. L., Feig, V. R., Jiang, Y., Cui, B., Greely, H. T., Bao, Z., Pașca, S. P., & Heilshorn, S. C. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00496-y · Cited by 120 · see citing works
Tunable hydrogel viscoelasticity modulates human neural maturation
Roth, J. G., Huang, M. S., Navarro, R. S., Akram, J., LeSavage, B. L., & Heilshorn, S. C. (2023) · Science Advances · doi:10.1126/sciadv.adh8313 · Cited by 121 · see citing works
Role of Microenvironment in Glioma Invasion: What We Learned from In Vitro Models
Manini, I., Caponnetto, F., Bartolini, A., Ius, T., Mariuzzi, L., Loreto, C. D., Beltrami, A. P., & Cesselli, D. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19010147 · Cited by 119 · 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
The extracellular matrix compartment of neural stem and glial progenitor cells
Faissner, A., & Reinhard, J. (2015) · Glia · doi:10.1002/glia.22839 · Cited by 117 · see citing works
Novel enzymatically cross-linked hyaluronan hydrogels support the formation of 3D neuronal networks
Broguière, N., Isenmann, L., & Zenobi‐Wong, M. (2016) · Biomaterials · doi:10.1016/j.biomaterials.2016.04.036 · Cited by 116 · see citing works
Chondroitin 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
Grifno, G. N., Farrell, A. M., Linville, R. M., Arevalo, D., Kim, J. H., Gu, L., & Searson, P. C. (2019) · Scientific Reports · doi:10.1038/s41598-019-50193-1 · Cited by 112 · see citing works
Role of the Microenvironment in Glioma Pathogenesis
Jayaram, M. A., & Phillips, J. J. (2023) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-051122-110348 · Cited by 112 · see citing works
Gottschling, C., Wegrzyn, D., Denecke, B., & Faissner, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-50404-9 · Cited by 111 · see citing works
Protective Properties of Neural Extracellular Matrix
Suttkus, A., Morawski, M., & Arendt, T. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8990-4 · Cited by 108 · see citing works
Matrix Metalloproteinase 9 in Epilepsy: The Role of Neuroinflammation in Seizure Development
Bronisz, E., & Kurkowska‐Jastrzębska, I. (2016) · Mediators of Inflammation · doi:10.1155/2016/7369020 · Cited by 105 · see citing works
Li, H., Koenig, A. M., Sloan, P., & Leipzig, N. D. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.07.038 · Cited by 104 · see citing works
Mechanosensation in traumatic brain injury
Keating, C. E., & Cullen, D. K. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105210 · Cited by 103 · see citing works
Katt, M. E., Linville, R. M., Mayo, L. N., Xu, Z. S., & Searson, P. C. (2018) · Fluids and Barriers of the CNS · doi:10.1186/s12987-018-0092-7 · Cited by 102 · see citing works
ADAMTS expression and function in central nervous system injury and disorders
Gottschall, P. E., & Howell, M. D. (2015) · Matrix Biology · doi:10.1016/j.matbio.2015.01.014 · Cited by 100 · see citing works
Hoffmann, C. J., Harms, U., Rex, A., Szulzewsky, F., Wolf, S. A., Grittner, U., Lättig-Tünnemann, G., Sendtner, M., Kettenmann, H., Dirnagl, U., et al. (2015) · Circulation · doi:10.1161/circulationaha.114.013003 · Cited by 96 · 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
Krishnaswamy, V. R., Benbenishty, A., Blinder, P., & Sagi, I. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03182-6 · Cited by 92 · see citing works
Hasanzadeh, E., Seifalian, A. M., Mellati, A., Saremi, J., Asadpour, S., Enderami, S. E., Nekounam, H., & Mahmoodi, N. (2023) · Materials Today Bio · doi:10.1016/j.mtbio.2023.100614 · Cited by 93 · see citing works
Astrocyte-secreted neurocan controls inhibitory synapse formation and function
Irala, D., Wang, S., Sakers, K., Nagendren, L., Severino, F. P. U., Bindu, D. S., Savage, J. T., & Eroğlu, Ç. (2024) · Neuron · doi:10.1016/j.neuron.2024.03.007 · Cited by 93 · see citing works
Seidlits, S. K., Liang, J., Bierman, R. D., Sohrabi, A., Karam, J., Holley, S. M., Cepeda, C., & Walthers, C. M. (2019) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.36603 · Cited by 87 · see citing works
(2012) · Europe PMC (PubMed Central) · Cited by 88 · see citing works
Delbeke, J., Hoffman, L., Mols, K., Braeken, D., & Prodanov, D. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00663 · Cited by 87 · see citing works
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 87 · see citing works
The 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
Lost in disruption: Role of proteases in glioma invasion and progression
Mentlein, R., Hattermann, K., & Held-Feindt, J. (2012) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2011.12.001 · Cited by 85 · see citing works
An advanced glioma cell invasion assay based on organotypic brain slice cultures
Eisemann, T., Costa, B., Strelau, J., Mittelbronn, M. G. A., Angel, P. E., & Peterziel, H. (2018) · BMC Cancer · doi:10.1186/s12885-018-4007-4 · Cited by 83 · see citing works
Inhibitors of myelination: ECM changes, CSPGs and PTPs
Harlow, D. E., & Macklin, W. B. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.10.017 · Cited by 78 · see citing works
Diverse functions of perineuronal nets
Karetko, M., & Skangiel-Kramska, J. (2009) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2009-1766 · Cited by 76 · see citing works
Molecular Neuropathology of Astrocytes and Oligodendrocytes in Alcohol Use Disorders
Miguel-Hidalgo, J. J. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00078 · Cited by 77 · see citing works
Gritsenko, P. G., Leenders, W. P. J., & Friedl, P. (2017) · Histochemistry and Cell Biology · doi:10.1007/s00418-017-1604-2 · Cited by 77 · see citing works
Schneider, C. S., Perez, J. G., Cheng, E., Zhang, C., Mastorakos, P., Hanes, J. S., Winkles, J. A., Woodworth, G. F., & Kim, A. J. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.11.054 · Cited by 76 · see citing works
Mentlein, R., Hattermann, K., Hemion, C., Jungbluth, A. A., & Held‐Feindt, J. (2010) · Biological Chemistry · doi:10.1515/bc.2010.119 · Cited by 76 · see citing works
Model systems for studying the blood-brain barrier: Applications and challenges
Jackson, S., Meeks, C., Vézina, A., Robey, R. W., Tanner, K., & Gottesman, M. M. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2019.05.028 · Cited by 74 · see citing works
Extracellular matrix and biomimetic engineering microenvironment for neuronal differentiation
Yim, E. K. F., Jain, D., Mattiassi, S., & Goh, E. K. (2019) · Neural Regeneration Research · doi:10.4103/1673-5374.266907 · Cited by 76 · see citing works
Integration of neurogenesis and angiogenesis models for constructing a neurovascular tissue
Uwamori, H., Higuchi, T., Arai, K., & Sudo, R. (2017) · Scientific Reports · doi:10.1038/s41598-017-17411-0 · Cited by 75 · see citing works
Miyata, S., & Kitagawa, H. (2016) · Neural Plasticity · doi:10.1155/2016/1305801 · Cited by 70 · see citing works
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 72 · see citing works
Nanotherapeutic treatment of the invasive glioblastoma tumor microenvironment
Pandey, N., Anastasiadis, P., Carney, C. P., Kanvinde, P. P., Woodworth, G. F., Winkles, J. A., & Kim, A. J. (2022) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2022.114415 · Cited by 72 · see citing works
Highly PEGylated DNA Nanoparticles Provide Uniform and Widespread Gene Transfer in the Brain
Mastorakos, P., Zhang, C., Berry, S., Oh, Y., Lee, S., Eberhart, C. G., Woodworth, G. F., Suk, J. S., & Hanes, J. (2015) · Advanced Healthcare Materials · doi:10.1002/adhm.201400800 · Cited by 80 · see citing works
Glioblastoma: To Target the Tumor Cell or the Microenvironment?
Vleeschouwer, S. D., & Bergers, G. (2017) · Codon Publications eBooks · doi:10.15586/codon.glioblastoma.2017.ch16 · Cited by 70 · see citing works
- Authors
- Zimmermann, D. R., & Dours-Zimmermann, M. T.
- Affiliations
- University Hospital Zurich (CH)
- Corresponding author
- Zimmermann, Dieter R.
- Venue
- Histochemistry and Cell Biology
- Published
- 2008-08-12
- Volume
- 130
- Issue
- 4
- Pages
- 635-653
- ISSN
- 0948-6143 (ISSN-L)
- 1432-119X
- OpenAlex
- W2146369085
- Cited by
- 465
- References
- 240
- Citations by year
- 2026: 16 · 2025: 20 · 2024: 29 · 2023: 27 · 2022: 31 · 2021: 30 · 2020: 30 · 2019: 31 · 2018: 35 · 2017: 18 · 2016: 28 · 2015: 27 · 2014: 42 · 2013: 22 · 2012: 18
- FWCI
- 1.63
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Histochemistry and Cell Biology (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Zurich Open Repository and Archive (University of Zurich) (acceptedVersion, other-oa)
- reroDoc Digital Library (submittedVersion)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion, other-oa)
- Zurich Open Repository and Archive (University of Zurich)
- Funders
- National Science Foundation
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Universität Zürich
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- extracellular matrix, central nervous system, hyaluronic acid, chondroitin sulfate proteoglycans, aggrecan, versican, neurocan, brevican, phosphacan, tenascin, axon guidance, axon growth, myelination, synapse maturation, central nervous system regeneration, lesion recovery, structural plasticity
- MeSH terms
- Animals, Axons, Central Nervous System, Extracellular Matrix, Humans, Chondroitin Sulfate Proteoglycans
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