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Increased chondroitin sulfate proteoglycan expression in denervated brainstem targets following spinal cord injury creates a barrier to axonal regeneration overcome by chondroitinase ABC and neurotrophin-3.
Open accessAbstract
Increased chondroitin sulfate proteoglycan (CSPG) expression in the vicinity of a spinal cord injury (SCI) is a primary participant in axonal regeneration failure. However, the presence of similar increases of CSPG expression in denervated synaptic targets well away from the primary lesion and the subsequent impact on regenerating axons attempting to approach deafferented neurons have not been studied. Constitutively expressed CSPGs within the extracellular matrix and perineuronal nets of the adult rat dorsal column nuclei (DCN) were characterized using real-time PCR, Western blot analysis and immunohistochemistry. We show for the first time that by 2 days and through 3 weeks following SCI, the levels of NG2, neurocan and brevican associated with reactive glia throughout the DCN were dramatically increased throughout the DCN despite being well beyond areas of trauma-induced blood brain barrier breakdown. Importantly, regenerating axons from adult sensory neurons microtransplanted 2 weeks following SCI between the injury site and the DCN were able to regenerate rapidly within white matter (as shown previously by Davies et al. [Davies, S.J., Goucher, D.R., Doller, C., Silver, J., 1999. Robust regeneration of adult sensory axons in degenerating white matter of the adult rat spinal cord. J. Neurosci. 19, 5810-5822]) but were unable to enter the denervated DCN. Application of chondroitinase ABC or neurotrophin-3-expressing lentivirus in the DCN partially overcame this inhibition. When the treatments were combined, entrance by regenerating axons into the DCN was significantly augmented. These results demonstrate both an additional challenge and potential treatment strategy for successful functional pathway reconstruction after SCI.
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“In rat spinal cord injury models, increased concentrations of CSPGs and PNN expression were found at injury sites and surrounding secondary dorsal column relay neurons (Massey et al., 2008).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Massey et al., 2008
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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 3,151
Self-citationTrk Receptors: Roles in Neuronal Signal Transduction
Huang, E. J., & Reichardt, L. F. (2003) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.72.121801.161629 · Cited by 2,537 · cited 1×
“NT-3 through activation of axonal Trk receptors and subsequent intracellular signaling (for review see Huang and Reichardt, 2003) stimulate regeneration despite the presence of CSPGs and other inhibitory molecules (Oudega and Hagg, 1996; Bradbury et al., 1999; Oudega and Hagg, 1999; Lu et al.,…”
BackgroundChondroitinase 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
Wong‐Riley, M. T. T. (1979) · Brain Research · doi:10.1016/0006-8993(79)90728-5 · Cited by 1,853
Self-Inactivating Lentivirus Vector for Safe and Efficient In Vivo Gene Delivery
Zufferey, R., Dull, T., Mandel, R. J., Bukovsky, A., Quiroz, D., Naldini, L., & Trono, D. (1998) · Journal of Virology · doi:10.1128/jvi.72.12.9873-9880.1998 · Cited by 1,815
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
Purification and Properties of Bacterial Chondroitinases and Chondrosulfatases
Yamagata, T., Saito, H., Habuchi, O., & Suzuki, S. (1968) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)93574-x · Cited by 1,238
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
Self-citationMassive Cortical Reorganization After Sensory Deafferentation in Adult Macaques
Pons, T. P., Garraghty, P. E., Ommaya, A. K., Kaas, J. H., Taub, E., & Mishkin, M. (1991) · Science · doi:10.1126/science.1843843 · Cited by 1,081
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
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Fitch, M. T., & Silver, J. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2007.05.014 · Cited by 1,007
Self-citationThe 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 903
Self-citationAnimals 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
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Kwok, J. C. F., Dick, G., Wang, D., & Fawcett, J. W. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20974 · Cited by 395
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Manipulating the glial scar: Chondroitinase ABC as a therapy for spinal cord injury
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Astrocytes as a Source for Extracellular Matrix Molecules and Cytokines
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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
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Alizadeh, A., Dyck, S. M., & Karimi‐Abdolrezaee, S. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00035 · Cited by 246
Bonner, J. F., Connors, T. M., Silverman, W. F., Kowalski, D. P., Lemay, M. A., & Fischer, I. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4130-10.2011 · Cited by 219
Keough, M. B., Rogers, J. A., Zhang, P., Jensen, S. K., Stephenson, E. L., Chen, T., Hurlbert, M. G., Lau, L. W., Rawji, K. S., Plemel, J. R., et al. (2016) · Nature Communications · doi:10.1038/ncomms11312 · Cited by 217
Kaas, J. H., Qi, H.-X., Burish, M. J., Gharbawie, O. A., Onifer, S. M., & Massey, J. M. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2007.06.014 · Cited by 191
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Kanno, H., Pressman, Y., Moody, A., Berg, R., Muir, E. M., ROGERS, J. H., Ozawa, H., Itoi, E., Pearse, D. D., & Bunge, M. B. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2661-13.2014 · Cited by 170
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Plasticity After Spinal Cord Injury: Relevance to Recovery and Approaches to Facilitate It
Onifer, S. M., Smith, G. M., & Fouad, K. (2011) · Neurotherapeutics · doi:10.1007/s13311-011-0034-4 · Cited by 151
Self-citationThe role of astrocyte‐mediated plasticity in neural circuit development and function
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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 143
Kwon, B. K., & Tetzlaff, W. (2001) · Spine · doi:10.1097/00007632-200112151-00003 · Cited by 116
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 121
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Kwon, B. K., Okon, E. B., Plunet, W. T., Baptiste, D. C., Fouad, K., Hillyer, J. E., Weaver, L. C., Fehlings, M. G., & Tetzlaff, W. (2010) · Journal of Neurotrauma · doi:10.1089/neu.2009.1150 · Cited by 114
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Takeuchi, K., Yoshioka, N., Onaga, S. H., Watanabe, Y., Miyata, S., Wada, Y., Kudo, C., Okada, M., Ohko, K., Oda, K., et al. (2013) · Nature Communications · doi:10.1038/ncomms3740 · Cited by 110
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Carter, L. M., Starkey, M. L., Akrimi, S. F., Davies, M., McMahon, S. B., & Bradbury, E. J. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2217-08.2008 · Cited by 107
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Young, W. (2014) · Cell Transplantation · doi:10.3727/096368914x678427 · Cited by 106
Zhao, R., Andrews, M. R., Wang, D., Warren, P. M., Gullo, M., Schnell, L., Schwab, M. E., & Fawcett, J. W. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12276 · Cited by 109
Andrews, E. M., Richards, R. J., Yin, F. Q., Viapiano, M. S., & Jakeman, L. B. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.09.008 · Cited by 104
Self-citationLiu, T., Xu, J., Chan, B. P., & Chew, S. Y. (2011) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.33271 · Cited by 100
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Zhao, R., & Fawcett, J. W. (2013) · Neuroscience Bulletin · doi:10.1007/s12264-013-1359-2 · Cited by 104
Hu, B., Kong, L., Matthews, R. T., & Viapiano, M. S. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m801433200 · Cited by 98
Self-citationYi, J., Katagiri, Y., Susarla, B., Figge, D., Symes, A. J., & Geller, H. M. (2012) · Journal of Comparative Neurology · doi:10.1002/cne.23156 · Cited by 93
Li, X., Yang, Z., & Zhang, A. (2009) · Biomaterials · doi:10.1016/j.biomaterials.2009.05.047 · Cited by 91
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Kusindarta, D. L., & Wihadmadyatami, H. (2018) · InTech eBooks · doi:10.5772/intechopen.75728 · Cited by 95
Hyatt, A. J. T., Wang, D., Kwok, J. C. F., Fawcett, J. W., & Martin, K. R. G. (2010) · Journal of Controlled Release · doi:10.1016/j.jconrel.2010.06.026 · Cited by 92
Aggrecan-based extracellular matrix is an integral part of the human basal ganglia circuit
Brückner, G., Morawski, M., & Arendt, T. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.10.033 · Cited by 90
Starkey, M. L., Bartus, K., Barritt, A. W., & Bradbury, E. J. (2012) · European Journal of Neuroscience · doi:10.1111/ejn.12017 · Cited by 93
Immature astrocytes promote CNS axonal regeneration when combined with chondroitinase ABC
Filous, A. R., Miller, J. H., Coulson‐Thomas, Y. M., Horn, K. P., Alilain, W. J., & Silver, J. (2010) · Developmental Neurobiology · doi:10.1002/dneu.20820 · Cited by 93
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Lukáčová, N., Kisucká, A., Bimbová, K., Bačová, M., Ileninová, M., Kuruc, T., & Gálik, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222413577 · Cited by 94
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Dyck, 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 85
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Harlow, D. E., & Macklin, W. B. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.10.017 · Cited by 79
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Karetko, M., & Skangiel-Kramska, J. (2009) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2009-1766 · Cited by 76
Shang, A., Hong, S.-Q., Xu, Q., Wang, H., Yang, Y., Wang, Z., Xu, B., Jiang, X., & Xu, R. (2011) · Brain Research · doi:10.1016/j.brainres.2011.03.019 · Cited by 75
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Whitaker, C. M., Beaumont, É., Wells, M. J., Magnuson, D. S. K., Hetman, M., & Onifer, S. M. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.03.087 · Cited by 68
Self-citationTraining and anti-CSPG combination therapy for spinal cord injury
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Wang, X., Hasan, O., Arzeno, A. H., Benowitz, L. I., Cafferty, W. B. J., & Strittmatter, S. M. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.06.009 · Cited by 68
Gardner, R. T., & Habecker, B. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5866-12.2013 · Cited by 66
Wang, L., Zhang, R., & Li, J. (2014) · Acta Neurochirurgica · doi:10.1007/s00701-014-2089-6 · Cited by 65
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GDNF selectively promotes regeneration of injury-primed sensory neurons in the lesioned spinal cord
Mills, C. D., Allchorne, A. J., Griffin, R. S., Woolf, C. J., & Costigan, M. (2007) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2007.06.011 · Cited by 65
Petrosyan, H. A., Hunanyan, A. S., Alessi, V., Schnell, L., Levine, J. M., & Arvanian, V. L. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4702-12.2013 · Cited by 61
Bowes, C., Massey, J. M., Burish, M. J., Cerkevich, C. M., & Kaas, J. H. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1121604109 · Cited by 54
Self-citationCarter, L. M., McMahon, S. B., & Bradbury, E. J. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2010.12.023 · Cited by 55
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Ibrahim, A. G.-E., Kirkwood, P., Raisman, G., & Li, Y. (2009) · Brain · doi:10.1093/brain/awp030 · Cited by 46
Ong, W., Pinese, C., & Chew, S. Y. (2019) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2019.03.004 · Cited by 46
Karetko-Sysa, M., Skangiel-Kramska, J., & Nowicka, D. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.05.022 · Cited by 45
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Noble, M., Davies, J. E., Mayer-Pröschel, M., Pröschel, C., & Davies, S. J. A. (2011) · Neurotherapeutics · doi:10.1007/s13311-011-0071-z · Cited by 44
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Reier, P. J., Lane, M. A., Hall, E. D., Teng, Y. D., & Howland, D. R. (2012) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52137-8.00026-7 · Cited by 44
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Sirko, S., Akita, K., von Holst, A., & Faissner, A. (2010) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(10)79003-0 · Cited by 40
Cheng, C.-H., Lin, C.-T., Lee, M.-J., Tsai, M., Huang, W.-H., Huang, M.-C., Lin, Y.-L., Chen, C.-J., Huang, W., & Cheng, H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0138705 · Cited by 43
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Tran, K. A., DeOre, B. J., Ikejiani, D., Means, K., Paone, L. S., Marchi, L. D., Suprewicz, Ł., Koziol, K., Bouyer, J., Byfield, F. J., et al. (2023) · Biomaterials · doi:10.1016/j.biomaterials.2023.122061 · Cited by 37
Onifer, S. M., Nunn, C. D., Decker, J. A., Payne, B. N., Wagoner, M. R., Puckett, A. H., Massey, J. M., Armstrong, J. E., Kaddumi, E. G., Fentress, K. G., et al. (2007) · Experimental Neurology · doi:10.1016/j.expneurol.2007.06.012 · Cited by 35
Self-citationWong, R., Chen, X., Wang, Y., Hu, X., & Jin, M. M. (2011) · Annals of Biomedical Engineering · doi:10.1007/s10439-011-0482-3 · Cited by 31
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Reis, A. V., Guilherme, M. R., Mattoso, L. H. C., Rubira, A. F., Tambourgi, E. B., & Muniz, E. C. (2008) · Pharmaceutical Research · doi:10.1007/s11095-008-9732-y · Cited by 27
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Swarup, V. P., Mencio, C. P., Hlady, V., & Kuberan, B. (2013) · BioMolecular Concepts · doi:10.1515/bmc-2012-0042 · Cited by 27
Rezaei, S., Dabirmanesh, B., Zare, L., Golestani, A., Javan, M., & Khajeh, K. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.12.258 · Cited by 28
Baer, M. L., Henderson, S. C., & Colello, R. J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0142740 · Cited by 26
Donnelly, E. M., Strappe, P., McGinley, L. M., Madigan, N. N., Geurts, E., Rooney, G. E., Windebank, A. J., Fraher, J., Dockery, P., O’Brien, T., et al. (2010) · The Journal of Gene Medicine · doi:10.1002/jgm.1509 · Cited by 26
Oudega, M., Bradbury, E. J., & Ramer, M. S. (2012) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52137-8.00038-3 · Cited by 25
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Ghosh, B., Nong, J., Wang, Z., Urban, M. W., Heinsinger, N. M., Trovillion, V. A., Wright, M. C., Lepore, A. C., & Zhong, Y. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.04.014 · Cited by 22
Guilherme, M. R., Reis, A. V., Alves, B. R., Kunita, M. H., Rubira, A. F., & Tambourgi, E. B. (2010) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2010.08.051 · Cited by 24
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Unal, D. B., Caliari, S. R., & Lampe, K. J. (2019) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2019.07.013 · Cited by 24
Donnelly, E. M., Madigan, N. N., Rooney, G. E., Knight, A., Chen, B., Ball, B. G., Kinnavane, L., Garcia, Y., Dockery, P., Fraher, J., et al. (2012) · Cytotherapy · doi:10.3109/14653249.2012.714865 · Cited by 24
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Beller, J. A., Kulengowski, B., Kobraei, E. M., Curinga, G., Calulot, C. M., Bahrami, A., Hering, T. M., & Snow, D. M. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.02.012 · Cited by 24
Metadata
- Authors
- Massey, J. M., Amps, J., Viapiano, M. S., Matthews, R. T., Wagoner, M. R., Whitaker, C. M., Alilain, W., Yonkof, A. L., Khalyfa, A., Cooper, N. G. F., Silver, J., & Onifer, S. M.
- Affiliations
- University of Louisville (US)
- Case Western Reserve University (US)
- Yale University (US)
- Corresponding author
- Onifer, Stephen M.
- ORCID
- Venue
- Experimental Neurology
- Publisher
- Elsevier BV
- Published
- 2008-02
- Volume
- 209
- Issue
- 2
- Pages
- 426-445
- ISSN
- 0014-4886 (ISSN-L)
- PMC
- PMC2270474
- OpenAlex
- W1998297893
- Cited by
- 185
- References
- 114
- Citations by year
- 2026: 7 · 2025: 3 · 2024: 4 · 2023: 8 · 2022: 7 · 2021: 10 · 2020: 6 · 2019: 8 · 2018: 9 · 2017: 3 · 2016: 5 · 2015: 7 · 2014: 15 · 2013: 15 · 2012: 15
- FWCI
- 5.29
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Experimental Neurology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (NS25713, NS40411, RR15576, RR16481)
- Office of Experimental Program to Stimulate Competitive Research (EPS-9874764)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Health Sciences › Medicine › Clinical Neurology › Spinal Cord Injury Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Keywords
- chondroitin sulfate proteoglycans, spinal cord injury, axon regeneration, denervation, dorsal column nuclei, chondroitinase ABC, neurotrophin-3, NG2, neurocan, brevican, perineuronal nets, sensory neurons, white matter, reactive glia
- MeSH terms
- Chondroitin Sulfate Proteoglycan 4, Animals, Antigens, Brain Stem, Cholera Toxin, Disease Models, Animal, Extracellular Matrix, Ganglia, Spinal, Gene Expression Regulation, Genetic Vectors, Male, Nerve Tissue Proteins, Chondroitin Sulfate Proteoglycans, Proteoglycans, Random Allocation, Spinal Cord Injuries, Time Factors, Genetic Therapy, Rats, Sprague-Dawley, Cell Transplantation, Chondroitin ABC Lyase, Neurotrophin 3, Rats
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