Influence of glial‐derived matrix molecules, especially chondroitin sulfates, on neurite growth and survival of cultured mouse embryonic motoneurons
Abstract
Mechanisms controlling neuronal survival and regeneration play an important role during development, after birth, and under lesion conditions. Isolated embryonic mouse motoneurons have been a useful tool for studying such basic mechanisms. These cultured motoneurons depend on extracellular matrix (ECM) molecules, which are potent mediators of survival and axonal growth and guidance in the CNS and in vitro, exhibiting either attractive or repellent guidance cues. Additionally, ECM proteoglycans and glycoproteins are components of the glial scar acting as a growth barrier for regenerating axons. Compared with CNS axon outgrowth, less is known about the cues that guide motoneurons toward their peripheral targets. Because we are interested in the effects of glial‐derived chondroitin sulfate proteoglycans (CSPGs), we have worked out a model system for investigating the influences of glial‐derived matrix molecules on motoneuron outgrowth and survival. We used cultured embryonic mouse motoneurons to investigate axon growth effects of matrix molecules produced by the glial‐derived cell lines A7, Neu7, and Oli‐neu primary astrocytes as wellas the immortalized Schwann cell line IMS32. The results indicate that molecules of the ECM, especially chondroitin sulfates, play an important role as axon growth‐promoting cues. We could demonstrate a modifying effect of the matrix components on motoneuron survival and caspase3‐induced apoptosis. © 2010 Wiley‐Liss, Inc.
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PNN formation is critically dependent on glial cells, which secrete and organize CSPGs and other ECM molecules.
“This process is critically dependent on glial cells, which secrete and organize CSPGs and other ECM molecules.35, 36, 37”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [36]
Glial cells are a major source of CSPGs and critically contribute to PNN formation and maintenance.
“Glial cells are a main source of chondroitin sulfate proteoglycans (abbreviated here as CSPGs), and have been shown to critically contribute to the formation and maintenance of PNNs (Faissner et al., 2010; John et al., 2006; Klausmeyer et al., 2011; Wiese et al., 2012).”
From Losing the sugar coating: Potential impact of perineuronal net abnormalities on interneurons in schizophrenia (2015) · cites this paper as Klausmeyer et al., 2011
Cites
Fitch, M. T., & Silver, J. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2007.05.014 · Cited by 1,007 · cited 2× · see citing works
“Chondroitin sulfates exhibit inhibitory properties (Davies et al., 1997; Fawcett, 2006; Fitch and Silver, 2008), but there are also examples of neurite outgrowthpromoting effects (Brittis et al.”
BackgroundSulfated 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
Regeneration of adult axons in white matter tracts of the central nervous system
Davies, S. J. A., Fitch, M. T., Memberg, S. P., Hall, A. K., Raisman, G., & Silver, J. (1997) · Nature · doi:10.1038/37776 · Cited by 737 · see citing works
Cell death in the development of the lateral motor column of the chick embryo
Hamburger, V. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901600408 · Cited by 660 · 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
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
Riad, M., Garcia, S., Watkins, K. C., Jodoin, N., Doucet, �., Langlois, X., Mestikawy, S. E., Hamon, M., & Descarries, L. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000207)417:2 · Cited by 502 · 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
Chondroitin Sulfate as a Regulator of Neuronal Patterning in the Retina
Brittis, P. A., Canning, D. R., & Silver, J. (1992) · Science · doi:10.1126/science.1738848 · Cited by 416 · 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
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
Isolation of a neural chondroitin sulfate proteoglycan with neurite outgrowth promoting properties.
Faissner, A., Clement, A. M., Lochter, A., Streit, A., Mandl, C., & Schachner, M. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.126.3.783 · Cited by 354 · see citing works
Self-citationCarulli, 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
Laminin‐immunoreactive glia distinguish regenerative adult CNS systems from non‐regenerative ones.
Liesi, P. (1985) · The EMBO Journal · doi:10.1002/j.1460-2075.1985.tb03963.x · Cited by 297 · see citing works
Jones, L. L., Sajed, D. R., & Tuszynski, M. H. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-28-09276.2003 · Cited by 283 · 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
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
J1-160 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
Fidler, P. S., Schütte, K., Asher, R. A., Dobbertin, A., Thornton, S. R., Calle, Y., Muir, E. M., Levine, J. M., Geller, H. M., ROGERS, J. H., et al. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-20-08778.1999 · Cited by 261 · see citing works
Self-citation[Chondroitin sulfate proteoglycans in neural development and regeneration].
Gu, W.-L., & Lu, P. (2007) · PubMed · Cited by 255 · see citing works
Do neurons in the vertebrate CNS migrate on laminin?
Liesi, P. (1985) · The EMBO Journal · doi:10.1002/j.1460-2075.1985.tb03755.x · Cited by 245 · see citing works
Developmental axon pruning mediated by BDNF-p75NTR–dependent axon degeneration
Singh, K. K., Park, K. J., Hong, E. J., Kramer, B. M., Greenberg, M. E., Kaplan, D. R., & Miller, F. D. (2008) · Nature Neuroscience · doi:10.1038/nn.2114 · Cited by 237 · 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
Is astrocyte laminin involved in axon guidance in the mammalian CNS?
Liesi, P., & Silver, J. (1988) · Developmental Biology · doi:10.1016/0012-1606(88)90366-1 · Cited by 218 · 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
An inhibitor of neurite outgrowth produced by astrocytes
Smith‐Thomas, L. C., Fok‐Seang, J., Stevens, J., Du, J., Muir, E. M., Faissner, A., Geller, H. M., ROGERS, J. H., & Fawcett, J. W. (1994) · Journal of Cell Science · doi:10.1242/jcs.107.6.1687 · Cited by 203 · see citing works
Self-citationGaltrey, 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
Nervous system proteoglycans as modulators of neurite outgrowth
Bovolenta, P., & Fernaud-Espinosa, I. (2000) · Progress in Neurobiology · doi:10.1016/s0301-0082(99)00044-1 · Cited by 189 · see citing works
Davies, J. E., Tang, X., Denning, J. W., Archibald, S. J., & Davies, S. J. A. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03184.x · Cited by 188 · see citing works
Glial Boundaries in the Developing Nervous System
Steindler, D. A. (1993) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.16.030193.002305 · Cited by 179 · see citing works
Sakurai, T., Lustig, M., Nativ, M., Hemperly, J., Schlessinger, J., Peles, E., & Grumet, M. (1997) · Journal of Cell Biology · doi:10.1083/jcb.136.4.907 · Cited by 176 · see citing works
Clement, A. M., Nadanaka, S., Masayama, K., Mandl, C., Sugahara, K., & Faissner, A. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.43.28444 · Cited by 175 · see citing works
Self-citationThe tenascin gene family in axon growth and guidance
Faissner, A. (1997) · Cell and Tissue Research · doi:10.1007/s004410050938 · Cited by 170 · see citing works
Self-citationGarwood, J., Schnädelbach, O., Clement, A. M., Schütte, K., Bach, A., & Faissner, A. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-10-03888.1999 · Cited by 168 · see citing works
Self-citationChondroitin sulfate proteoglycans as mediators of axon growth and pathfinding
Margolis, R. U., & Margolis, R. K. (1997) · Cell and Tissue Research · doi:10.1007/s004410050939 · Cited by 167 · 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
Self-citationDohrmann, U., Edgar, D., Sendtner, M., & Thoenen, H. (1986) · Developmental Biology · doi:10.1016/0012-1606(86)90089-8 · Cited by 154 · see citing works
Chondroitin sulfate proteoglycans in neural development and regeneration
Carulli, D., Laabs, T. L., Geller, H. M., & Fawcett, J. W. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.03.018 · Cited by 154 · see citing works
Biosynthesis and membrane topography of the neural cell adhesion molecule L1.
Faissner, A., Teplow, D. B., Kübler, H.-D., et al. (1985) · The EMBO Journal · doi:10.1002/j.1460-2075.1985.tb04052.x · Cited by 154 · see citing works
Self-citationAxon guidance at the midline choice point
Kaprielian, Z., Runko, E., & Imondi, R. (2001) · Developmental Dynamics · doi:10.1002/dvdy.1143 · Cited by 151 · see citing works
Astrocytes in culture synthesize and secrete a variant form of fibronectin
Price, J., & Hynes, R. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-08-02205.1985 · Cited by 143 · see citing works
Axon guidance at choice points
Stoeckli, E. T., & Landmesser, L. T. (1998) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(98)80010-x · Cited by 139 · see citing works
Developmental motoneuron cell death and neurotrophic factors
Sendtner, M., Pei, G., Beck, M., et al. (2000) · Cell and Tissue Research · doi:10.1007/s004410000217 · Cited by 136 · see citing works
Emerling, D. E., & Lander, A. D. (1996) · Neuron · doi:10.1016/s0896-6273(00)80242-1 · Cited by 129 · see citing works
Fibronectin is expressed by astrocytes cultured from embryonic and early postnatal rat brain
Liesi, P., Kirkwood, T. B. L., & Vaheri, A. I. (1986) · Experimental Cell Research · doi:10.1016/0014-4827(86)90570-7 · Cited by 127 · see citing works
von Holst, A., Sirko, S., & Faissner, A. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0422-06.2006 · Cited by 124 · see citing works
Self-citationVincent, V. A. M., Tilders, F. J. H., & van Dam, A.-M. (1997) · Glia · doi:10.1002/(sici)1098-1136(199703)19:3 · Cited by 123 · 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 2× · see citing works
“…isoforms of phosphacan/RPTPb (rabbit polyclonal 1:50; Klausmeyer et al., 2007); pAb NC-2 antineurocan (rabbit polyclonal 1:200; Retzler et al., 1996); pAb antibrevican (guinea pig polyclonal 1:200; John et al., 2006); and pAb KAF14 anti-tenascin-C (rabbit polyclonal 1:200; Faissner et al., 1990).”
BackgroundWatabe, K., Fukuda, T., Tanaka, J., et al. (1995) · Journal of Neuroscience Research · doi:10.1002/jnr.490410215 · Cited by 119 · see citing works
Wiese, S., Herrmann, T., Drepper, C., Jablonka, S., Funk, N., Klausmeyer, A., Rogers, M., Rush, R. A., & Sendtner, M. (2009) · Nature Protocols · doi:10.1038/nprot.2009.193 · Cited by 118 · see citing works
Self-citationAxon routing at the optic chiasm after enzymatic removal of chondroitin sulfate in mouse embryos
Chung, K. Y., Taylor, J. S. H., Shum, D. K., & Chan, S. O. (2000) · Development · doi:10.1242/dev.127.12.2673 · Cited by 117 · see citing works
Ito, Y., Hikino, M., Yajima, Y., Mikami, T., Sirko, S., von Holst, A., Faissner, A., Fukui, S., & Sugahara, K. (2004) · Glycobiology · doi:10.1093/glycob/cwi036 · Cited by 114 · see citing works
Self-citationThe role of p75NTR in modulating neurotrophin survival effects in developing motoneurons
Wiese, S., Metzger, F., Holtmann, B., & Sendtner, M. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00585.x · Cited by 109 · see citing works
Self-citationGarwood, J., Garcion, E., Dobbertin, A., Heck, N., Calco, V., ffrench‐Constant, C., & Faissner, A. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03727.x · Cited by 104 · see citing works
Self-citationGarwood, J., Heck, N., Reichardt, F., & Faissner, A. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m211721200 · Cited by 94 · see citing works
Self-citationGeller, H. M., & Dubois-Dalcq, M. E. (1988) · The Journal of Cell Biology · doi:10.1083/jcb.107.5.1977 · Cited by 93 · see citing works
Matthiessen, H. P., Schmalenbach, C., & Müller, H. W. (1989) · Glia · doi:10.1002/glia.440020307 · Cited by 93 · see citing works
Bao, X., Mikami, T., Yamada, S., Faissner, A., Muramatsu, T., & Sugahara, K. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m413423200 · Cited by 89 · see citing works
Self-citationMapping 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
Self-citationSakurai, T., Friedlander, D. R., & Grumet, M. (1996) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19960315)43:6 · Cited by 84 · see citing works
Zebrafish unplugged reveals a role for muscle-specific kinase homologs in axonal pathway choice
Zhang, J., Lefebvre, J. L., Zhao, S., & Granato, M. (2004) · Nature Neuroscience · doi:10.1038/nn1350 · Cited by 84 · see citing works
Dobbertin, A., Rhodes, K. E., Garwood, J., Properzi, G., Heck, N., ROGERS, J. H., Fawcett, J. W., & Faissner, A. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00257-4 · Cited by 82 · see citing works
Self-citationPurification of axonin‐1, a protein that is secreted from axons during neurogenesis.
Rüegg, M. A., Stoeckli, E. T., Kuhn, T. B., et al. (1989) · The EMBO Journal · doi:10.1002/j.1460-2075.1989.tb03348.x · Cited by 79 · see citing works
An analysis of astrocytic cell lines with different abilities to promote axon growth
Fok‐Seang, J., Smith‐Thomas, L. C., Meiners, S. A., et al. (1995) · Brain Research · doi:10.1016/0006-8993(95)00575-b · Cited by 70 · see citing works
Streit, A., Faissner, A., Gehrig, B., & Schachner, M. (1990) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1990.tb04931.x · Cited by 66 · see citing works
Self-citationPesheva, P., Probstmeier, R., Skubitz, A. P. N., et al. (1994) · Journal of Cell Science · doi:10.1242/jcs.107.8.2323 · Cited by 66 · see citing works
Binding of the J 1 Adhesion Molecules to Extracellular Matrix Constituents
Faissner, A., Kruse, J., Kühn, K., & Schachner, M. (1990) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1990.tb02350.x · Cited by 62 · see citing works
Self-citationChondroitin Sulfates Affect the Formation of the Segmental Motor Nerves in Zebrafish Embryos
Bernhardt, R. R., & Schachner, M. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9673 · Cited by 58 · see citing works
Garwood, J., Rigato, F., Heck, N., & Faissner, A. (2001) · PubMed · Cited by 57 · see citing works
Self-citationLocalization of aggrecan and versican in the developing rat central nervous system.
Popp, S., Andersen, J. S., Maurel, P., & Margolis, R. U. (2003) · Developmental Dynamics · doi:10.1002/dvdy.10282 · Cited by 55 · see citing works
Guntinas‐Lichius, O., Angelov, D. N., Morellini, F., Lenzen, M., Skouras, E., Schachner, M., & Irintchev, A. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04424.x · Cited by 55 · see citing works
Proteoglycans as Modulators of Axon Guidance Cue Function
de Wit, J., & Verhaagen, J. (2007) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-70956-7_7 · Cited by 54 · see citing works
Glial cells assemble hyaluronan-based pericellular matrices in vitro
Maleski, M. P., & Hockfield, S. J. (1997) · Glia · doi:10.1002/(sici)1098-1136(199707)20:3 · Cited by 48 · see citing works
Proteoglycans Provide Neurite Guidance at an Astrocyte Boundary
Powell, E. M., Fawcett, J. W., & Geller, H. M. (1997) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1997.0629 · Cited by 47 · see citing works
Tenascin‐C is involved in motor axon outgrowth in the trunk of developing zebrafish
Schweitzer, J., Becker, T., Lefebvre, J. L., Granato, M., Schachner, M., & Becker, C. G. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20525 · Cited by 47 · see citing works
The Glial Response to Injury and Its Role in the Inhibition of CNS Repair
Fawcett, J. W. (2007) · Springer eBooks · doi:10.1007/0-387-30128-3_2 · Cited by 46 · see citing works
Neuron–glia interactions during axon guidance in Drosophila
Hidalgo, A. (2003) · Biochemical Society Transactions · doi:10.1042/bst0310050 · Cited by 45 · see citing works
Butowt, R., & von Bartheld, C. S. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02497.x · Cited by 42 · see citing works
Glia as mediators of growth cone guidance: studies from insect nervous systems
Auld, V. J. (1999) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050378 · Cited by 41 · see citing works
Krull, C. E., Oland, L. A., Faissner, A., Schachner, M., & Tolbert, L. P. (1994) · Journal of Neurobiology · doi:10.1002/neu.480250808 · Cited by 40 · see citing works
Self-citationChan, C. C. M., Roberts, C. R., Steeves, J. D., & Tetzlaff, W. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21522 · Cited by 37 · see citing works
Structural and Electron Microscopic Analysis of Neurocan and Recombinant Neurocan Fragments
Retzler, C., Wiedemann, H., Kulbe, G., & Rauch, U. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.29.17107 · Cited by 34 · see citing works
Siddiqui, S., Horvat-Bröcker, A., & Faissner, A. (2008) · Neuron Glia Biology · doi:10.1017/s1740925x09990020 · Cited by 30 · see citing works
Self-citationMotor axon migration: a long way to go
Schneider, V., & Granato, M. (2003) · Developmental Biology · doi:10.1016/s0012-1606(03)00329-4 · Cited by 28 · see citing works
Differential expression of phosphacan/RPTPβ isoforms in the developing mouse visual system
Klausmeyer, A., Garwood, J., & Faissner, A. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21479 · Cited by 28 · see citing works
Self-citationKatoh‐Semba, R., Matsuda, M., Watanabe, E., Maeda, N., & Oohira, A. (1998) · Neuroscience Research · doi:10.1016/s0168-0102(98)00047-9 · Cited by 28 · see citing works
Astrocyte and Muscle-Derived Secreted Factors Differentially Regulate Motoneuron Survival
Taylor, A. R., Gifondorwa, D. J., Newbern, J. M., Robinson, M., Strupe, J. L., Prevette, D. M., Oppenheim, R. W., & Milligan, C. E. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4947-06.2007 · Cited by 27 · see citing works
Siddiqui, S., Horvat‐Broecker, A., & Faissner, A. (2009) · Glia · doi:10.1002/glia.20860 · Cited by 26 · see citing works
Self-citationJung, M., Crang, A. J., Blackemore, W. F., et al. (1994) · Journal of Neuroscience Research · doi:10.1002/jnr.490370204 · Cited by 23 · see citing works
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Astrocytes as a Source for Extracellular Matrix Molecules and Cytokines
Wiese, S., Karus, M., & Faissner, A. (2012) · Frontiers in Pharmacology · doi:10.3389/fphar.2012.00120 · Cited by 262 · see citing works
Self-citationPantazopoulos, 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
Berretta, S., Pantazopoulos, H., Markota, M., Brown, C., & Batzianouli, E. T. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2014.12.040 · Cited by 152 · see citing works
Córdova-Palomera, A., Fatjó-Vilas, M., Gastó, C., Navarro, V, Krebs, M.-O., & Fañanás, L. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.49 · Cited by 117 · see citing works
Proteoglycan abnormalities in olfactory epithelium tissue from subjects diagnosed with schizophrenia
Pantazopoulos, H., Boyer-Boiteau, A., Holbrook, E. H., Jang, W., Hahn, C.-G., Arnold, S. E., & Berretta, S. (2013) · Schizophrenia Research · doi:10.1016/j.schres.2013.08.013 · Cited by 47 · see citing works
“CSPGs, and versican in particular, promote axon outgrowth (Wu et al., 2004; Maeda, 2010; Klausmeyer et al., 2011).”
Background
- Authors
- Klausmeyer, A., Conrad, R., Faissner, A., & Wiese, S.
- Affiliations
- Ruhr University Bochum (DE)
- Corresponding author
- Wiese, Stefan
- ORCID
- Wiese, Stefan
- Venue
- Journal of Neuroscience Research
- Publisher
- Wiley
- Published
- 2010-12-08
- Volume
- 89
- Issue
- 2
- Pages
- 127-141
- ISSN
- 0360-4012 (ISSN-L)
- 1097-4547
- OpenAlex
- W2062696235
- Cited by
- 24
- References
- 90
- Citations by year
- 2025: 1 · 2024: 1 · 2022: 2 · 2021: 1 · 2020: 1 · 2019: 1 · 2018: 1 · 2017: 1 · 2016: 2 · 2015: 6 · 2014: 1 · 2013: 3 · 2012: 2
- FWCI
- 0.77
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neuroscience Research (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Keywords
- chondroitin sulfate proteoglycans, extracellular matrix, neurite outgrowth, motoneuron survival, glial scar, axon guidance, Schwann cells, astrocytes, caspase-3, apoptosis, peripheral nerve regeneration
- MeSH terms
- Animals, Cell Differentiation, Cell Line, Cell Survival, Chondroitin Sulfates, Embryo, Mammalian, Extracellular Matrix, Fluorescent Antibody Technique, Motor Neurons, Neuroglia, Neurites, Mice
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 ›
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