Leukocyte common antigen-related phosphatase is a functional receptor for chondroitin sulfate proteoglycan axon growth inhibitors
Open accessAbstract
Chondroitin sulfate proteoglycans (CSPGs) are a family of extracellular matrix molecules with various functions in regulating tissue morphogenesis, cell division, and axon guidance. A number of CSPGs are highly upregulated by reactive glial scar tissues after injuries and form a strong barrier for axonal regeneration in the adult vertebrate CNS. Although CSPGs may negatively regulate axonal growth via binding and altering activity of other growth-regulating factors, the molecular mechanisms by which CSPGs restrict axonal elongation are not well understood. Here, we identified a novel receptor mechanism whereby CSPGs inhibit axonal growth via interactions with neuronal transmembrane leukocyte common antigen-related phosphatase (LAR). CSPGs bind LAR with high affinity in transfected COS-7 cells and coimmunoprecipitate with LAR expressed in various tissues including the brain and spinal cord. CSPG stimulation enhances activity of LAR phosphatase in vitro. Deletion of LAR in knock-out mice or blockade of LAR with sequence-selective peptides significantly overcomes neurite growth restrictions of CSPGs in neuronal cultures. Intracellularly, CSPG–LAR interaction mediates axonal growth inhibition of neurons partially via inactivating Akt and activating RhoA signals. Systemic treatments with LAR-targeting peptides in mice with thoracic spinal cord transection injuries induce significant axon growth of descending serotonergic fibers in the vicinity of the lesion and beyond in the caudal spinal cord and promote locomotor functional recovery. Identification of LAR as a novel CSPG functional receptor provides a therapeutic basis for enhancing axonal regeneration and functional recovery after CNS injuries in adult mammals.
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Treatments with LAR-targeting peptides or LAR knockout significantly improve axonal growth and behavioral recovery after spinal cord injury.
“LAR deletion in knock-out mice overcomes growth restriction of CSPGs on neurites in neuronal cultures, and treatments with LAR-targeting peptides or LAR knockout significantly improve axonal growth and behavioral recovery after spinal cord injury (Fisher et al., 2011;Xu et al., 2015).”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Fisher et al., 2011
LAR deletion in knockout mice overcomes growth restriction of CSPGs on neurites in neuronal cultures.
“LAR deletion in knock-out mice overcomes growth restriction of CSPGs on neurites in neuronal cultures, and treatments with LAR-targeting peptides or LAR knockout significantly improve axonal growth and behavioral recovery after spinal cord injury (Fisher et al., 2011;Xu et al., 2015).”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Fisher et al., 2011
LAR interacts with high levels of extracellular CSPGs, including versican, in both normal and injured CNS.
“LAR interacts with high levels of extracellular CSPGs, including versican, in both the normal and injured CNS.”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Fisher et al., 2011
Known CS/CSPG receptors include contactin-1, RPTPσ, LAR, and NgR1 and NgR3.
“Known CS/CSPG receptors are: contactin-1 (Mikami et al., 2009), receptor protein tyrosine phosphatase sigma (RPTPσ; Shen et al., 2009), leukocyte common antigen-related phosphatase (LAR; Fisher et al., 2011) and Nogo receptor (NgR) 1 and 3 (Dickendesher et al., 2012).”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Fisher et al., 2011
CSPGs, especially their GAG moieties, may inhibit growth by binding to a specific receptor.
“Specifically, CSPGs, and particularly their GAG moieties, may act by i) binding to a specific receptor; ii) blocking the growth-promoting activity of integrins; iii) presenting growth-inhibitory proteins.”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Fisher et al., 2011
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Cites
Regeneration beyond the glial scar
Silver, J., & Miller, J. H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1326 · Cited by 3,090 · see citing works
Self-citationIn Vivo Protein Transduction: Delivery of a Biologically Active Protein into the Mouse
Schwarze, S. R., Ho, A. L., Vocero-Akbani, A. M., & Dowdy, S. F. (1999) · Science · doi:10.1126/science.285.5433.1569 · Cited by 2,418 · 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
Protein tyrosine phosphatases: from genes, to function, to disease
Tonks, N. K. (2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2039 · Cited by 1,685 · see citing works
Futaki, S., Suzuki, T. W., Ohashi, W., Yagami, T., Tanaka, S., Ueda, K., & Sugiura, Y. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m007540200 · Cited by 1,667 · see citing works
Basso, D., Fisher, L., Anderson, A., Jakeman, L., McTigue, D. M., & Popovich, P. (2006) · Journal of Neurotrauma · doi:10.1089/neu.2006.23.635 · Cited by 1,615 · see citing works
McKeon, R., Schreiber, R., Rudge, J., & Silver, J. (1991) · The Journal of Neuroscience · doi:10.1523/jneurosci.11-11-03398.1991 · Cited by 1,188 · see citing works
Self-citationGSK-3β Regulates Phosphorylation of CRMP-2 and Neuronal Polarity
Yoshimura, T., Kawano, Y., Arimura, N., Kawabata, S., Kikuchi, A., & Kaibuchi, K. (2005) · Cell · doi:10.1016/j.cell.2004.11.012 · Cited by 877 · 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
Self-citationCRMP-2 binds to tubulin heterodimers to promote microtubule assembly
Fukata, Y., Itoh, T. J., Kimura, T., Ménager, C., Nishimura, T., Shiromizu, T., Watanabe, H., Inagaki, N., Iwamatsu, A., Hotani, H., et al. (2002) · Nature Cell Biology · doi:10.1038/ncb825 · Cited by 761 · see citing works
Courtine, G., Song, B., Roy, R. R., Zhong, H., Herrmann, J. E., Ao, Y., Qi, J., Edgerton, V. R., & Sofroniew, M. V. (2007) · Nature Medicine · doi:10.1038/nm1682 · Cited by 730 · see citing works
Nogo-66 receptor antagonist peptide promotes axonal regeneration
GrandPré, T., Li, S., & Strittmatter, S. M. (2002) · Nature · doi:10.1038/417547a · Cited by 712 · see citing works
Self-citationPTPσ Is a Receptor for Chondroitin Sulfate Proteoglycan, an Inhibitor of Neural Regeneration
Shen, Y., Tenney, A. P., Busch, S. A., Horn, K. P., Cuascut, F. X., Liu, K., He, Z., Silver, J., & Flanagan, J. G. (2009) · Science · doi:10.1126/science.1178310 · Cited by 682 · see citing works
Self-citationMoon, 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
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
Zhou, F., Zhou, J., Dedhar, S., Wu, Y.-H., & Snider, W. D. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.011 · Cited by 528 · see citing works
Fouad, K., Schnell, L., Bunge, M. B., Schwab, M. E., Liebscher, T., & Pearse, D. D. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3562-04.2005 · Cited by 473 · 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
Schnell, L., Fearn, S., Klassen, H. J., Schwab, M. E., & Perry, V. H. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00792.x · Cited by 410 · see citing works
Monnier, P. P., Sierra, A., Schwab, J. M., Henke‐Fahle, S., & Mueller, B. K. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(02)00035-0 · Cited by 400 · see citing works
Functional regeneration of respiratory pathways after spinal cord injury
Alilain, W. J., Horn, K. P., Hu, H., Dick, T. E., & Silver, J. (2011) · Nature · doi:10.1038/nature10199 · Cited by 393 · see citing works
Self-citationKantor, D. B., Chivatakarn, O., Thompson-Peer, K. L., Oster, S. F., Inatani, M., Hansen, M. J., Flanagan, J. G., Yamaguchi, Y., Sretavan, D. W., Giger, R. J., et al. (2004) · Neuron · doi:10.1016/j.neuron.2004.12.002 · Cited by 380 · see citing works
Eph/ephrin signaling in morphogenesis, neural development and plasticity
Klein, R. (2004) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2004.07.002 · Cited by 314 · see citing works
Manipulating the glial scar: Chondroitinase ABC as a therapy for spinal cord injury
Bradbury, E. J., & Carter, L. M. (2010) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2010.06.015 · Cited by 314 · see citing works
Efficient testing of motor function in spinal cord injured rats
Metz, G. A. S., Merkler, D., Dietz, V., Schwab, M. E., & Fouad, K. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02778-5 · Cited by 312 · see citing works
Houlé, J. D., Tom, V. J., Mayes, D. A., Wagoner, G., Phillips, N., & Silver, J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1166-06.2006 · Cited by 311 · see citing works
Self-citationLi, S., Liu, B. P., Budel, S., Li, M., Ji, B., Walus, L. R., Li, W., Jirik, A., Rabacchi, S. A., Choi, E., et al. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2828-04.2004 · Cited by 306 · see citing works
Self-citationDelayed Systemic Nogo-66 Receptor Antagonist Promotes Recovery from Spinal Cord Injury
Li, S., & Strittmatter, S. M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-10-04219.2003 · Cited by 305 · see citing works
Self-citationLiprins, a Family of LAR Transmembrane Protein-tyrosine Phosphatase-interacting Proteins
Serra‐Pages, C., Medley, Q. G., Tang, M., Hart, A. C., & Streuli, M. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.25.15611 · Cited by 292 · see citing works
Phosphorylation by Rho Kinase Regulates CRMP-2 Activity in Growth Cones
Arimura, N., Ménager, C., Kawano, Y., Yoshimura, T., Kawabata, S., Hattori, A., Fukata, Y., Amano, M., Goshima, Y., Inagaki, M., et al. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.22.9973-9984.2005 · Cited by 260 · see citing works
[Chondroitin sulfate proteoglycans in neural development and regeneration].
Gu, W.-L., & Lu, P. (2007) · PubMed · Cited by 255 · see citing works
Johnson, K. G., Tenney, A. P., Ghose, A., Duckworth, A. M., Higashi, M., Parfitt, K. D., Marcu, O., Heslip, T. R., Marsh, J., Schwarz, T. L., et al. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.026 · Cited by 254 · see citing works
LAR receptor protein tyrosine phosphatases in the development and maintenance of excitatory synapses
Dunah, A. W., Hueske, E., Wyszynski, M. W., Hoogenraad, C. C., Jaworski, J., Pak, D. T. S., Simonetta, A., Liu, G., & Sheng, M. (2005) · Nature Neuroscience · doi:10.1038/nn1416 · Cited by 244 · see citing works
Self-citationChondroitin-4-sulfation negatively regulates axonal guidance and growth
Wang, H., Katagiri, Y., McCann, T. E., Unsworth, E., Goldsmith, P., Yu, Z.-X., Tan, F., Santiago, L., Mills, E. M., Wang, Y., et al. (2008) · Journal of Cell Science · doi:10.1242/jcs.032649 · Cited by 243 · see citing works
Inactivation of Glycogen Synthase Kinase 3 Promotes Axonal Growth and Recovery in the CNS
Dill, J., Wang, H., Zhou, F., & Li, S. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1178-08.2008 · Cited by 229 · see citing works
Self-citationCafferty, W. B. J., Yang, S., Duffy, P. J., Li, S., & Strittmatter, S. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5176-06.2007 · Cited by 223 · see citing works
Self-citationChondroitin sulfate proteoglycans in neural development and regeneration
Laabs, T. L., Carulli, D., Geller, H. M., & Fawcett, J. W. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.01.014 · Cited by 211 · see citing works
Petratos, S., Li, Q.-X., George, A. J., Hou, X., Kerr, M. L., Unabia, S. E., Hatzinisiriou, I., Maksel, D., Aguilar, M.-I., & Small, D. H. (2008) · Brain · doi:10.1093/brain/awm260 · Cited by 197 · see citing works
Lander, C., Kind, P., Maleski, M., & Hockfield, S. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-06-01928.1997 · Cited by 195 · see citing works
Extracellular regulators of axonal growth in the adult central nervous system
Liu, B. P., Cafferty, W. B. J., Budel, S., & Strittmatter, S. M. (2006) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2006.1891 · Cited by 188 · see citing works
Grimpe, B., & Silver, J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4986-03.2004 · Cited by 184 · see citing works
Self-citationNonsteroidal Anti-Inflammatory Drugs Promote Axon Regeneration via RhoA Inhibition
Fu, Q., Hue, J., & Li, S. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4353-06.2007 · Cited by 183 · see citing works
Self-citationKwok, J. C. F., Afshari, F. T., García‐Alías, G., & Fawcett, J. W. (2008) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-2008-00439 · Cited by 170 · see citing works
Evidence That Collapsin Response Mediator Protein-2 Is Involved in the Dynamics of Microtubules
Gu, Y., & Ihara, Y. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.c000179200 · Cited by 169 · see citing works
CS-4,6 is differentially upregulated in glial scar and is a potent inhibitor of neurite extension
Gilbert, R. J., McKeon, R. J., Darr, A., Calabro, A. R., Hascall, V., & Bellamkonda, R. V. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.04.006 · Cited by 168 · see citing works
Multiple Regions of the NG2 Proteoglycan Inhibit Neurite Growth and Induce Growth Cone Collapse
Ughrin, Y., Chen, Z. J., & Levine, J. M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-01-00175.2003 · Cited by 165 · see citing works
The G3 Domain of Versican Enhances Cell Proliferation via Epidermial Growth Factor-like Motifs
Zhang, Y., Cao, L., Yang, B., & Yang, B. B. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.33.21342 · Cited by 156 · see citing works
Fry, E. J., Chagnon, M. J., López‐Vales, R., Tremblay, M. L., & David, S. (2010) · Glia · doi:10.1002/glia.20934 · Cited by 152 · see citing works
Chagnon, M. J., Uetani, N., & Tremblay, M. L. (2004) · Biochemistry and Cell Biology · doi:10.1139/o04-120 · Cited by 152 · see citing works
Fox, A. N., & Zinn, K. (2005) · Current Biology · doi:10.1016/j.cub.2005.08.035 · Cited by 151 · see citing works
Tom, V. J., Sandrow-Feinberg, H. R., Miller, K., Santi, L., Connors, T. M., Lemay, M. A., & Houlé, J. D. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3641-09.2009 · Cited by 141 · see citing works
PTEN couples Sema3A signalling to growth cone collapse
Chadborn, N., Ahmed, A. I., Holt, M., Prinjha, R. K., Dunn, G., Jones, G. E., & Eickholt, B. J. (2006) · Journal of Cell Science · doi:10.1242/jcs.02801 · Cited by 136 · see citing works
Protein tyrosine phosphatases: regulatory mechanisms
den Hertog, J., Östman, A., & Böhmer, F. (2008) · FEBS Journal · doi:10.1111/j.1742-4658.2008.06247.x · Cited by 135 · see citing works
O'Grady, P., Thai, T. C., & Saito, H. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.141.7.1675 · Cited by 132 · see citing works
Heparan sulfate proteoglycans and the emergence of neuronal connectivity
Vactor, D. V., Wall, D. P., & Johnson, K. G. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.01.011 · Cited by 124 · see citing works
Laabs, T. L., Wang, H., Katagiri, Y., McCann, T. E., Fawcett, J. W., & Geller, H. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2807-07.2007 · Cited by 117 · see citing works
A ‘GAG’ reflex prevents repair of the damaged CNS
Sherman, L. S., & Back, S. A. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2007.11.001 · Cited by 116 · see citing works
Chondroitinase ABC improves basic and skilled locomotion in spinal cord injured cats
Tester, N. J., & Howland, D. R. (2007) · Experimental Neurology · doi:10.1016/j.expneurol.2007.07.019 · Cited by 115 · see citing works
Receptor and nonreceptor protein tyrosine phosphatases in the nervous system
Paul, S., & Lombroso, P. (2003) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-003-3123-7 · Cited by 108 · see citing works
Therapeutic time window for the application of chondroitinase ABC after spinal cord injury
García‐Alías, G., Lin, R., Akrimi, S. F., Story, D., Bradbury, E. J., & Fawcett, J. W. (2007) · Experimental Neurology · doi:10.1016/j.expneurol.2007.11.002 · Cited by 105 · see citing works
A Molecular Mechanism for Ibuprofen-Mediated RhoA Inhibition in Neurons
Dill, J., Patel, A., Yang, X., Bachoo, R. M., Powell, C. M., & Li, S. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5045-09.2010 · Cited by 90 · see citing works
Self-citationTAT-based drug delivery system – new directions in protein delivery for new hopes?
Rapoport, M., & Lorberboum‐Galski, H. (2009) · Expert Opinion on Drug Delivery · doi:10.1517/17425240902887029 · Cited by 87 · see citing works
Zai, L. J., Ferrari, C., Dice, C., Subbaiah, S., Havton, L. A., Coppola, G., Geschwind, D. H., Irwin, N., Huebner, E. A., Strittmatter, S. M., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4498-10.2011 · Cited by 82 · see citing works
Jefferson, S. C., Tester, N. J., & Howland, D. R. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4459-10.2011 · Cited by 80 · see citing works
Xie, Y., Yeo, T. T. S., Zhang, C., Yang, T., Tisi, M. A., Massa, S. M., & Longo, F. M. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05130.2001 · Cited by 79 · see citing works
Self-citationA Chondroitin Sulfate Chain Attached to the Bone Dentin Matrix Protein 1 NH2-Terminal Fragment
Qin, C., Huang, B., Wygant, J. N., McIntyre, B. W., McDonald, C. H., Cook, R. G., & Butler, W. T. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m512964200 · Cited by 71 · see citing works
Protein-tyrosine Phosphatase (PTP) Wedge Domain Peptides
Xie, Y., Massa, S. M., Craig, S., Major, D. L., Yang, T., Tisi, M. A., Derevyanny, V. D., Runge, W. O., Mehta, B., Moore, L. A., et al. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m603131200 · Cited by 70 · see citing works
Self-citationHeparan sulfate regulates ephrin-A3/EphA receptor signaling
Irie, F., Okuno, M., Matsumoto, K., Pasquale, E. B., & Yamaguchi, Y. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801302105 · Cited by 67 · see citing works
Expression of mutant amyloid precursor proteins induces apoptosis in PC12 cells
Zhao, B., Chrest, F. J., Horton, W. E., Sisodia, S. S., & Kusiak, J. W. (1997) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19970201)47:3 · Cited by 65 · see citing works
Self-citationKim, B. G., Dai, H., Lynskey, J. V., McAtee, M., & Bregman, B. S. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.20980 · Cited by 62 · see citing works
Yang, T., Bernabeu, R., Xie, Y., Zhang, J. S., Massa, S. M., Rempel, H. C., & Longo, F. M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03353.2003 · Cited by 55 · see citing works
Self-citationHaapasalo, A., Kim, D. Y., Carey, B. W., Turunen, M. K., Pettingell, W. H., & Kovacs, D. M. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611324200 · Cited by 52 · see citing works
Zhang, J. S., Honkaniemi, J., Yang, T., Yeo, T. T. S., & Longo, F. M. (1998) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1998.0663 · Cited by 46 · see citing works
Self-citationYang, T., Yin, W., Derevyanny, V. D., Moore, L. A., & Longo, F. M. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04403.x · Cited by 46 · see citing works
Self-citationKolkman, M. J. M., Streijger, F., Linkels, M., Bloemen, M., Heeren, D. J., Hendriks, W. J. A. J., & der Zee, C. E. E. M. V. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.02.006 · Cited by 43 · see citing works
Tsujikawa, K., Kawakami, N., Uchino, Y., Ichijo, T., Furukawa, T., Saito, H., & Yamamoto, H. (2001) · Molecular Endocrinology · doi:10.1210/mend.15.2.0592 · Cited by 42 · see citing works
Selective changes in GABAA receptor subtypes in white matter neurons of patients with focal epilepsy
Loup, F., Picard, F., Yonekawa, Y., Wieser, H. G., & Fritschy, J. (2009) · Brain · doi:10.1093/brain/awp178 · Cited by 41 · see citing works
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Alizadeh, A., Dyck, S. M., & Karimi‐Abdolrezaee, S. (2019) · Frontiers in Neurology · doi:10.3389/fneur.2019.00282 · Cited by 1,447 · see citing works
The Biology of Regeneration Failure and Success After Spinal Cord Injury
Tran, A. P., Warren, P. M., & Silver, J. (2018) · Physiological Reviews · doi:10.1152/physrev.00017.2017 · Cited by 883 · see citing works
Self-citationFrom basics to clinical: A comprehensive review on spinal cord injury
Silva, N. A., Sousa, N., Reis, R. L., & Salgado, A. J. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.11.002 · Cited by 814 · see citing works
Moving beyond the glial scar for spinal cord repair
Bradbury, E. J., & Burnside, E. R. (2019) · Nature Communications · doi:10.1038/s41467-019-11707-7 · Cited by 748 · see citing works
Functional regeneration beyond the glial scar
Cregg, J. M., DePaul, M. A., Filous, A. R., Lang, B. T., Tran, A. P., & Silver, J. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2013.12.024 · Cited by 664 · see citing works
Self-citationPathophysiology of the brain extracellular matrix: a new target for remyelination
Lau, L. W., Cua, R., Keough, M. B., Haylock-Jacobs, S., & Yong, V. W. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3550 · Cited by 549 · see citing works
Biosynthesis and function of chondroitin sulfate
Mikami, T., & Kitagawa, H. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.06.006 · Cited by 505 · see citing works
Modulation of the proteoglycan receptor PTPσ promotes recovery after spinal cord injury
Lang, B. T., Cregg, J. M., DePaul, M. A., Tran, A. P., Xu, K., Dyck, S. M., Madalena, K. M., Brown, B. P., Weng, Y.-L., Li, S., et al. (2015) · Nature · doi:10.1038/nature13974 · Cited by 465 · see citing works
Self-citationNgR1 and NgR3 are receptors for chondroitin sulfate proteoglycans
Dickendesher, T. L., Baldwin, K. T., Mironova, Y. A., Koriyama, Y., Raiker, S. J., Askew, K. L., Wood, A., Geoffroy, C. G., Zheng, B., Liepmann, C. D., et al. (2012) · Nature Neuroscience · doi:10.1038/nn.3070 · Cited by 449 · 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
Reactive Astrogliosis after Spinal Cord Injury—Beneficial and Detrimental Effects
Karimi-Abdolrezaee, S., & Billakanti, R. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8287-4 · Cited by 331 · see citing works
Axon growth inhibition by RhoA/ROCK in the central nervous system
Fujita, Y., & Yamashita, T. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00338 · Cited by 271 · 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
Contrasting the Glial Response to Axon Injury in the Central and Peripheral Nervous Systems
Lutz, A. B., & Barres, B. A. (2014) · Developmental Cell · doi:10.1016/j.devcel.2013.12.002 · Cited by 229 · see citing works
Glial Cells Shape Pathology and Repair After Spinal Cord Injury
Gaudet, A. D., & Fonken, L. K. (2018) · Neurotherapeutics · doi:10.1007/s13311-018-0630-7 · Cited by 232 · see citing works
Reaching the brain: Advances in optic nerve regeneration
Benowitz, L. I., He, Z., & Goldberg, J. L. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.12.015 · Cited by 223 · see citing works
The glial scar in spinal cord injury and repair
Yuan, Y., & He, C. (2013) · Neuroscience Bulletin · doi:10.1007/s12264-013-1358-3 · Cited by 212 · see citing works
Regeneration of Spinal Cord Connectivity Through Stem Cell Transplantation and Biomaterial Scaffolds
Katoh, H., Yokota, K., & Fehlings, M. G. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00248 · Cited by 199 · see citing works
Mizumoto, S., Yamada, S., & Sugahara, K. (2015) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2015.06.004 · Cited by 199 · see citing works
Dyck, S. M., & Karimi‐Abdolrezaee, S. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.04.006 · Cited by 189 · see citing works
Scar-mediated inhibition and CSPG receptors in the CNS
Sharma, K., Selzer, M. E., & Li, S. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.07.009 · Cited by 189 · see citing works
Self-citationCombinatorial Therapies After Spinal Cord Injury: How Can Biomaterials Help?
Führmann, T., Anandakumaran, P. N., & Shoichet, M. S. (2017) · Advanced Healthcare Materials · doi:10.1002/adhm.201601130 · Cited by 188 · 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
New insights into glial scar formation after spinal cord injury
Tran, A. P., Warren, P. M., & Silver, J. (2021) · Cell and Tissue Research · doi:10.1007/s00441-021-03477-w · Cited by 186 · see citing works
Self-citationProteoglycans and neuronal migration in the cerebral cortex during development and disease
Maeda, N. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00098 · Cited by 181 · see citing works
Microglia as hackers of the matrix: sculpting synapses and the extracellular space
Crapser, J. D., Arreola, M. A., Tsourmas, K. I., & Green, K. N. (2021) · Cellular & Molecular Immunology · doi:10.1038/s41423-021-00751-3 · Cited by 178 · see citing works
Miyata, S., & Kitagawa, H. (2017) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2017.06.010 · Cited by 171 · see citing works
LAR-RPTPs: synaptic adhesion molecules that shape synapse development
Um, J. W., & Ko, J. (2013) · Trends in Cell Biology · doi:10.1016/j.tcb.2013.07.004 · Cited by 164 · see citing works
Semaphorin 3A Binds to the Perineuronal Nets via Chondroitin Sulfate Type E Motifs in Rodent Brains
Dick, G., Tan, C. L., Alves, J. N., Ehlert, E. M. E., Miller, G. M., Hsieh-Wilson, L. C., Sugahara, K., Oosterhof, A., van Kuppevelt, T. H., Verhaagen, J., et al. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.310029 · Cited by 160 · see citing works
Crapser, J. D., Ochaba, J., Soni, N., Reidling, J. C., Thompson, L. M., & Green, K. N. (2020) · Brain · doi:10.1093/brain/awz363 · Cited by 157 · see citing works
Burnside, E. R., & Bradbury, E. J. (2013) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12114 · Cited by 153 · see citing works
Ye, Q., & Miao, Q.-L. (2013) · Matrix Biology · doi:10.1016/j.matbio.2013.04.001 · Cited by 146 · see citing works
Chondroitin Sulfate Proteoglycans in the Nervous System: Inhibitors to Repair
Siebert, J. R., Conta, A. C., & Osterhout, D. J. (2014) · BioMed Research International · doi:10.1155/2014/845323 · Cited by 151 · see citing works
A sulfated carbohydrate epitope inhibits axon regeneration after injury
Brown, J. M., Xia, J., Zhuang, B., Cho, K.-S., Rogers, C. J., Gama, C. I., Rawat, M., Tully, S. E., Uetani, N., Mason, D. E., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1121318109 · Cited by 154 · see citing works
“Targeting astrocytes in CNS injury and disease: A translational research approach”
Filous, A. R., & Silver, J. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.03.009 · Cited by 149 · see citing works
Self-citationChondroitin sulfates and their binding molecules in the central nervous system
Djerbal, L., Lortat-Jacob, H., & Kwok, J. (2017) · Glycoconjugate Journal · doi:10.1007/s10719-017-9761-z · Cited by 144 · see citing works
Chondroitin sulfate proteoglycans inhibit oligodendrocyte myelination through PTPσ
Pendleton, J. C., Shamblott, M. J., Gary, D. S., Belegu, V., Hurtado, A., Malone, M. L., & McDonald, J. W. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.04.003 · Cited by 134 · see citing works
Oohashi, T., Edamatsu, M., Bekku, Y., & Carulli, D. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.09.010 · Cited by 131 · see citing works
Filous, A. R., Tran, A. P., Howell, C., Busch, S. A., Evans, T. A., Stallcup, W. B., Kang, S. H., Bergles, D. E., Lee, S.-I., Levine, J. M., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1309-14.2014 · Cited by 129 · see citing works
Self-citationExtracellular matrix and traumatic brain injury
George, N., & Geller, H. M. (2018) · Journal of Neuroscience Research · doi:10.1002/jnr.24151 · Cited by 128 · see citing works
Silver, D. J., Siebzehnrübl, F. A., Schildts, M. J., Yachnis, A. T., Smith, G. M., Smith, A., Scheffler, B., Reynolds, B. A., Silver, J., & Steindler, D. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3004-12.2013 · Cited by 125 · see citing works
Self-citationAn Extracellular Perspective on CNS Maturation: Perineuronal Nets and the Control of Plasticity
Carulli, D., & Verhaagen, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052434 · Cited by 123 · see citing works
C ell therapy for spinal cord injury with olfactory ensheathing glia cells ( OEC s)
Gómez, R. M., Sánchez, M. Y., Portela-Lomba, M., Ghotme, K. A., Barreto, G. E., Sierra, J., & Moreno-Flores, M. T. (2018) · Glia · doi:10.1002/glia.23282 · Cited by 115 · see citing works
“GAG-ing with the neuron”: The role of glycosaminoglycan patterning in the central nervous system
Smith, P. D., Coulson‐Thomas, V. J., Foscarin, S., Kwok, J. C. F., & Fawcett, J. W. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.08.004 · Cited by 112 · see citing works
Robust Axonal Regeneration Occurs in the Injured CAST/Ei Mouse CNS
Omura, T., Omura, K., Tedeschi, A., Riva, P., Painter, M. W., Rojas, L., Martin, J., Lisi, V., Huebner, E. A., Latrémolière, A., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.005 · Cited by 110 · see citing works
Self-citationDyck, S. M., Kataria, H., Alizadeh, A., Santhosh, K. T., Lang, B. T., Silver, J., & Karimi‐Abdolrezaee, S. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1128-2 · Cited by 110 · see citing works
Self-citationGlial scar and immune cell involvement in tissue remodeling and repair following acute CNS injuries
Rapôso, C., & Schwartz, M. (2014) · Glia · doi:10.1002/glia.22676 · Cited by 107 · see citing works
Integrins promote axonal regeneration after injury of the nervous system
Nieuwenhuis, B., Haenzi, B., Andrews, M. R., Verhaagen, J., & Fawcett, J. W. (2018) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.12398 · Cited by 104 · see citing works
Using extracellular matrix for regenerative medicine in the spinal cord
Volpato, F. Z., Führmann, T., Migliaresi, C., Hutmacher, D. W., & Dalton, P. D. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.03.057 · Cited by 103 · see citing works
Glycogen Synthase Kinase 3 Beta (GSK3β) at the Tip of Neuronal Development and Regeneration
Seira, O., & del Rı́o, J. A. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8571-y · Cited by 103 · see citing works
Molecular mechanisms of scar-sourced axon growth inhibitors
Ohtake, Y., & Li, S. (2014) · Brain Research · doi:10.1016/j.brainres.2014.08.064 · Cited by 102 · see citing works
Self-citationMiller, G. M., & Hsieh‐Wilson, L. C. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.08.015 · Cited by 98 · see citing works
Proteoglycans in brain development and pathogenesis
Schwartz, N. B., & Domowicz, M. S. (2018) · FEBS Letters · doi:10.1002/1873-3468.13026 · Cited by 99 · see citing works
Ohtake, Y., Park, D., Muneer, P. M. A., Li, H., Xu, B., Sharma, K., Smith, G. M., Selzer, M. E., & Li, S. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.02.037 · Cited by 96 · see citing works
Self-citationPTEN inhibition and axon regeneration and neural repair
Li, S., Ohtake, Y., & Hayat, U. (2015) · Neural Regeneration Research · doi:10.4103/1673-5374.165496 · Cited by 95 · see citing works
Self-citationGlycan sulfation patterns define autophagy flux at axon tip via PTPRσ-cortactin axis
Sakamoto, K., Ozaki, T., Ko, Y., Tsai, C.-F., Gong, Y., Morozumi, M., Ishikawa, Y., Uchimura, K., Nadanaka, S., Kitagawa, H., et al. (2019) · Nature Chemical Biology · doi:10.1038/s41589-019-0274-x · Cited by 95 · see citing works
Valverde, P., Ardá, A., Reichardt, N., Jiménez‐Barbero, J., & Gimeno, A. (2019) · MedChemComm · doi:10.1039/c9md00292h · Cited by 92 · see citing works
Repair of spinal cord injury with neuronal relays: From fetal grafts to neural stem cells
Bonner, J. F., & Steward, O. (2015) · Brain Research · doi:10.1016/j.brainres.2015.01.006 · Cited by 92 · see citing works
Hayani, H., Song, I., & Dityatev, A. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00149 · Cited by 84 · see citing works
Microenvironmental regulation of oligodendrocyte replacement and remyelination in spinal cord injury
Alizadeh, A., & Karimi‐Abdolrezaee, S. (2016) · The Journal of Physiology · doi:10.1113/jp270895 · Cited by 89 · see citing works
Spinal cord regeneration: where fish, frogs and salamanders lead the way, can we follow?
Quiroz, J. D. D., & Echeverri, K. (2013) · Biochemical Journal · doi:10.1042/bj20121807 · Cited by 85 · see citing works
Wang, X., Yang, C., Wang, X., Miao, J., Chen, W., Zhou, Y., Xu, Y., An, Y., Cheng, A., Ye, W., et al. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.028 · Cited by 84 · see citing works
Contributions of chondroitin sulfate proteoglycans to neurodevelopment, injury, and cancer
Silver, D. J., & Silver, J. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.03.016 · Cited by 84 · see citing works
Self-citationDyck, S. M., Alizadeh, A., Santhosh, K. T., Proulx, E. H., Wu, C., & Karimi‐Abdolrezaee, S. (2015) · Stem Cells · doi:10.1002/stem.1979 · Cited by 84 · see citing works
Recent insights on astrocyte mechanisms in CNS homeostasis, pathology, and repair
Hart, C. G., & Karimi‐Abdolrezaee, S. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24922 · Cited by 85 · see citing works
Luo, F., Tran, A. P., Li, X., Sanapala, C., Lang, B. T., Silver, J., & Yang, Y. (2018) · Nature Communications · doi:10.1038/s41467-018-06505-6 · Cited by 81 · see citing works
Self-citationRaspa, A., Carminati, L., Pugliese, R., Fontana, F., & Gelain, F. (2020) · Journal of Controlled Release · doi:10.1016/j.jconrel.2020.11.027 · Cited by 80 · 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
Structural basis for extracellular cis and trans RPTPσ signal competition in synaptogenesis
Coles, C. H., Mitakidis, N., Zhang, P., Elegheert, J., Lu, W., Stoker, A. W., Nakagawa, T., Craig, A. M., Jones, E. Y., & Aricescu, A. R. (2014) · Nature Communications · doi:10.1038/ncomms6209 · Cited by 78 · see citing works
Where no synapses go: gatekeepers of circuit remodeling and synaptic strength
Mironova, Y. A., & Giger, R. J. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.04.003 · Cited by 75 · see citing works
Ran, N., Li, W., Zhang, R., Lin, C., Zhang, J., Wei, Z., Li, Z. C., Yuan, Z., Wang, M., Fan, B., et al. (2022) · Bioactive Materials · doi:10.1016/j.bioactmat.2022.07.002 · Cited by 75 · see citing works
Advances in the Signaling Pathways Downstream of Glial-Scar Axon Growth Inhibitors
Sami, A., Selzer, M. E., & Li, S. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00174 · Cited by 74 · see citing works
Self-citationThe Chemorepulsive Protein Semaphorin 3A and Perineuronal Net-Mediated Plasticity
de Winter, F., Kwok, J. C. F., Fawcett, J. W., Vo, T. T., Carulli, D., & Verhaagen, J. (2016) · Neural Plasticity · doi:10.1155/2016/3679545 · Cited by 84 · see citing works
Wilems, T. S., Pardieck, J., Iyer, N. R., & Sakiyama‐Elbert, S. E. (2015) · Acta Biomaterialia · doi:10.1016/j.actbio.2015.09.018 · Cited by 71 · see citing works
Hatano, S., & Watanabe, H. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00232 · Cited by 72 · see citing works
Role of CSPG receptor LAR phosphatase in restricting axon regeneration after CNS injury
Xu, B., Park, D., Ohtake, Y., Li, H., Hayat, U., Liu, J., Selzer, M. E., Longo, F. M., & Li, S. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.08.030 · Cited by 73 · see citing works
Self-citationReorganization of Intact Descending Motor Circuits to Replace Lost Connections After Injury
Fink, K. L., & Cafferty, W. B. J. (2016) · Neurotherapeutics · doi:10.1007/s13311-016-0422-x · Cited by 71 · see citing works
Mechanisms for modulation of neural plasticity and axon regeneration by chondroitin sulphate
Miyata, S., & Kitagawa, H. (2014) · The Journal of Biochemistry · doi:10.1093/jb/mvu067 · Cited by 70 · see citing works
Melrose, J. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14652 · Cited by 72 · see citing works
Gulati, K., & Poluri, K. M. (2015) · Glycoconjugate Journal · doi:10.1007/s10719-015-9642-2 · Cited by 70 · see citing works
Howell, M. D., & Gottschall, P. E. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.05.034 · Cited by 66 · see citing works
Sustained dual drug delivery of anti-inhibitory molecules for treatment of spinal cord injury
Wilems, T. S., & Sakiyama‐Elbert, S. E. (2015) · Journal of Controlled Release · doi:10.1016/j.jconrel.2015.06.031 · Cited by 68 · see citing works
Intra-Axonal Translation of RhoA Promotes Axon Growth Inhibition by CSPG
Walker, B. A., Ji, S., & Jaffrey, S. R. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0176-12.2012 · Cited by 67 · see citing works
NG2/CSPG4 and progranulin in the posttraumatic glial scar
Schäfer, M. K. E., & Tegeder, I. (2017) · Matrix Biology · doi:10.1016/j.matbio.2017.10.002 · Cited by 67 · see citing works
Flexible Roles for Proteoglycan Sulfation and Receptor Signaling
Yu, P., Pearson, C. S., & Geller, H. M. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2017.10.005 · Cited by 67 · see citing works
Gardner, R. T., & Habecker, B. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5866-12.2013 · Cited by 66 · see citing works
Insights into the physiological role of CNS regeneration inhibitors
Baldwin, K. T., & Giger, R. J. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00023 · Cited by 65 · see citing works
Remyelination Therapy for Multiple Sclerosis
Keough, M. B., & Yong, V. W. (2012) · Neurotherapeutics · doi:10.1007/s13311-012-0152-7 · Cited by 63 · see citing works
Yuan, J., Zou, M., Xiang, X., Zhu, H., Chu, W., Liu, W., Chen, F., & Lin, J. (2015) · Journal of Surgical Research · doi:10.1016/j.jss.2014.12.055 · Cited by 63 · see citing works
Wu, D., Klaw, M. C., Connors, T. M., Kholodilov, N. G., Burke, R. E., & Tom, V. J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0719-15.2015 · Cited by 62 · see citing works
Elias, P. Z., Liu, G. W., Wei, H., Jensen, M. C., Horner, P. J., & Pun, S. H. (2015) · Journal of Controlled Release · doi:10.1016/j.jconrel.2015.03.003 · Cited by 62 · see citing works
Chondroitin Sulfate Impairs Neural Stem Cell Migration Through ROCK Activation
Galindo, L. T., Mundim, M. V., Pinto, A. A. S., Chiarantin, G. M. D., de Almeida, M. E. S., Lamers, M. L., Horwitz, A. R., dos Santos, M. F., & Porcionatto, M. A. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0565-8 · Cited by 62 · see citing works
Modulation of semaphorin3A in perineuronal nets during structural plasticity in the adult cerebellum
Carulli, D., Foscarin, S., Faralli, A., Pajaj, E., & Rossi, F. (2013) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2013.08.003 · Cited by 59 · see citing works
Two PTP receptors mediate CSPG inhibition by convergent and divergent signaling pathways in neurons
Ohtake, Y., Wong, D., Abdul-Muneer, P. M., Selzer, M. E., & Li, S. (2016) · Scientific Reports · doi:10.1038/srep37152 · Cited by 59 · see citing works
Self-citationTargeting phosphatase-dependent proteoglycan switch for rheumatoid arthritis therapy
Doody, K. M., Stanford, S. M., Sacchetti, C., Svensson, M. N. D., Coles, C. H., Mitakidis, N., Kiosses, W. B., Bartók, B., Fos, C., Cory, E., et al. (2015) · Science Translational Medicine · doi:10.1126/scitranslmed.aaa4616 · Cited by 61 · see citing works
Receptor protein tyrosine phosphatase sigma regulates synapse structure, function and plasticity
Horn, K. E., Xu, B., Gobert, D., Hamam, B. N., Thompson, K. M., Wu, C., Bouchard, J., Uetani, N., Racine, R. J., Tremblay, M. L., et al. (2012) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2012.07762.x · Cited by 56 · see citing works
Involvement of Rho-family GTPases in axon branching
Spillane, M., & Gallo, G. (2014) · Small GTPases · doi:10.4161/sgtp.27974 · Cited by 60 · see citing works
Sulfated glycosaminoglycans: their distinct roles in stem cell biology
Mikami, T., & Kitagawa, H. (2016) · Glycoconjugate Journal · doi:10.1007/s10719-016-9732-9 · Cited by 60 · see citing works
Stephenson, E. L., & Yong, V. W. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.04.010 · Cited by 60 · see citing works
Determinants of Axon Growth, Plasticity, and Regeneration in the Context of Spinal Cord Injury
Filous, A. R., & Schwab, J. M. (2017) · American Journal Of Pathology · doi:10.1016/j.ajpath.2017.09.005 · Cited by 59 · see citing works
- Authors
- Fisher, D., Xing, B., Dill, J., Li, H., Hoang, H. H., Zhao, Z., Yang, X.-L., Bachoo, R., Cannon, S., Longo, F. M., Sheng, M., Silver, J., & Li, S.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- Stanford University (US)
- Howard Hughes Medical Institute (US)
- Case Western Reserve University (US)
- ORCID
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2011-10-05
- Volume
- 31
- Issue
- 40
- Pages
- 14051-14066
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC3220601
- OpenAlex
- W2086085796
- Cited by
- 312
- References
- 77
- Citations by year
- 2026: 9 · 2025: 12 · 2024: 7 · 2023: 13 · 2022: 23 · 2021: 22 · 2020: 15 · 2019: 19 · 2018: 28 · 2017: 24 · 2016: 14 · 2015: 36 · 2014: 39 · 2013: 32 · 2012: 17
- FWCI
- 11.80
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc)
- Funders
- Christopher and Dana Reeve Foundation
- Morton Cure Paralysis Fund
- Paralyzed Veterans of America
- National Institutes of Health (NS025713)
- National Institute of Neurological Disorders and Stroke (R37NS025713, NS025713, R01NS025713, R21NS066114)
- 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, axon growth inhibition, neurite outgrowth, glial scar, spinal cord transection, axon regeneration, Akt signaling, RhoA signaling, locomotor recovery, central nervous system injury
- MeSH terms
- Animals, Axons, Cells, Cultured, Chlorocebus aethiops, Female, Growth Inhibitors, Humans, Mice, Inbred C57BL, Mice, Mutant Strains, Protein Binding, Chondroitin Sulfate Proteoglycans, Mice, Knockout, COS Cells, Mice, Receptor-Like Protein Tyrosine Phosphatases, Class 2
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