The DOI matches its Crossref record; 77 of the 77 references it cites were found in a registry or an index.
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.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“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
In the citing paper
“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
In the citing paper
“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
In the citing paper
“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
In the citing paper
“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
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Regeneration beyond the glial scar
Silver, J., & Miller, J. H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1326 · Cited by 3,151
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
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
Protein tyrosine phosphatases: from genes, to function, to disease
Tonks, N. K. (2006) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2039 · Cited by 1,712
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
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
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-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 903
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
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
Research works printed but not linked: 1
- 10.1210/me.15.2.271 · DOI
Cited by
Sorted by citations
Items 101–200 of 313
Role of Chondroitin Sulfation Following Spinal Cord Injury
Hussein, R. K., Mencio, C. P., Katagiri, Y., Brake, A., & Geller, H. M. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00208 · Cited by 60
Axon plasticity in the mammalian central nervous system after injury
Chen, M., & Zheng, B. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2014.08.008 · Cited by 63
Pantazaka, E., & Papadimitriou, Ε. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2014.01.009 · Cited by 57
RhoA/Rho kinase in spinal cord injury
Xu, X., & Wu, X. (2015) · Neural Regeneration Research · doi:10.4103/1673-5374.169601 · Cited by 57
A Molecular Mechanism Regulating the Timing of Corticogeniculate Innervation
Brooks, J. M., Su, J., Levy, C., Wang, J. S., Seabrook, T. A., Guido, W., & Fox, M. A. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.09.041 · Cited by 55
Dyck, S. M., Kataria, H., Akbari‐Kelachayeh, K., Silver, J., & Karimi‐Abdolrezaee, S. (2018) · Glia · doi:10.1002/glia.23533 · Cited by 61
Self-citationCooke, P., Janowitz, H. N., & Dougherty, S. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.872501 · Cited by 61
An in vitro assay to study induction of the regenerative state in sensory neurons
Frey, E. N., Valakh, V., Karney-Grobe, S., Shi, Y., Milbrandt, J., & DiAntonio, A. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.10.012 · Cited by 52
In vitro models of axon regeneration
Al‐Ali, H., Beckerman, S. R., Bixby, J. L., & Lemmon, V. (2016) · Experimental Neurology · doi:10.1016/j.expneurol.2016.01.020 · Cited by 60
LAR Receptor Tyrosine Phosphatase Family in Healthy and Diseased Brain
Cornejo, F., Cortés, B. I., Findlay, G. M., & Cancino, G. I. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.659951 · Cited by 54
Luo, D., Zhang, Y., Yuan, X., Pan, Y., Yang, L., Zhao, Y., Zhuo, R., Chen, C., Peng, L., Li, W., et al. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.01.027 · Cited by 54
Gwak, S., Macks, C. P., Jeong, D. U., Kindy, M. S., Lynn, M., Webb, K., & Lee, J. S. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2017.01.003 · Cited by 51
Li, H., Ghorbani, S., Ling, C., Yong, V. W., & Xue, M. (2023) · Neurobiology of Disease · doi:10.1016/j.nbd.2023.106282 · Cited by 52
Self-citationKim, Y., Kang, H., Powathil, G., Kim, H., Trucu, D., Lee, W., Lawler, S. E., & Chaplain, M. A. J. (2018) · PLoS ONE · doi:10.1371/journal.pone.0204865 · Cited by 51
Sun, X., Liu, H., Tan, Z., Hou, Y., Pang, M., Chen, S., Xiao, L., Yuan, Q., Liu, B., Rong, L., et al. (2022) · Small · doi:10.1002/smll.202205012 · Cited by 50
Yu, P., Jin, J., Tilve, S. M., Huang, Z., Zhou, L., & Geller, H. M. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.226398 · Cited by 48
de Lima, S., Habboub, G., & Benowitz, L. I. (2012) · International review of neurobiology · doi:10.1016/b978-0-12-407178-0.00007-7 · Cited by 47
Li, H., Wong, C. W., Li, W., Ruven, C., He, L., Wu, X., Lang, B. T., Silver, J., & Wu, W. (2015) · Scientific Reports · doi:10.1038/srep14923 · Cited by 47
Self-citationYu, P., Santiago, L. Y., Katagiri, Y., & Geller, H. M. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07638.x · Cited by 45
The role of RhoA in retrograde neuronal death and axon regeneration after spinal cord injury
Hu, J., Zhang, G., Rodemer, W., Jin, L., Shifman, M. I., & Selzer, M. E. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.11.006 · Cited by 45
The roles of neuronal and glial precursors in overcoming chondroitin sulfate proteoglycan inhibition
Ketschek, A., Haas, C., Gallo, G., & Fischer, I. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.03.017 · Cited by 44
Jahan, N., & Hannila, S. S. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.10.023 · Cited by 44
Fink, K. L., Strittmatter, S. M., & Cafferty, W. B. J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3165-15.2015 · Cited by 43
Dermatan 4-O-sulfotransferase1 ablation accelerates peripheral nerve regeneration
Akyüz, N., Rost, S., Mehanna, A., Bian, S., Loers, G., Oezen, I., Mishra, B., Hoffmann, K., Guseva, D., Laczynska, E., et al. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.01.025 · Cited by 46
Wiersma, A. M., Fouad, K., & Winship, I. R. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0770-17.2017 · Cited by 44
Cell Therapeutic Strategies for Spinal Cord Injury
Zhou, P., Guan, J., Xu, P., Zhao, J., Zhang, C., Zhang, B., Mao, Y., & Cui, W. (2019) · Advances in Wound Care · doi:10.1089/wound.2019.1046 · Cited by 42
Mechanisms and repair strategies for white matter degeneration in CNS injury and diseases
Shahsavani, N., Kataria, H., & Karimi‐Abdolrezaee, S. (2021) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2021.166117 · Cited by 43
Vajn, K., Plunkett, J. A., Tapanes-Castillo, A., & Oudega, M. (2013) · Neuroscience Bulletin · doi:10.1007/s12264-013-1361-8 · Cited by 43
Regulation of oligodendrocyte precursor maintenance by chondroitin sulphate glycosaminoglycans
Karus, M., Ulc, A., Ehrlich, M., Czopka, T., Hennen, E., Fischer, J., Mizhorova, M., Qamar, N., Brüstle, O., & Faissner, A. (2015) · Glia · doi:10.1002/glia.22928 · Cited by 45
Sainath, R., Ketschek, A., Grandi, L., & Gallo, G. (2016) · Developmental Neurobiology · doi:10.1002/dneu.22420 · Cited by 42
Inhibition of Semaphorin3A Promotes Ocular Dominance Plasticity in the Adult Rat Visual Cortex
Boggio, E. M., Ehlert, E. M., Lupori, L., Moloney, E. B., De Winter, F., Vander Kooi, C. W., Baroncelli, L., Mecollari, V., Blits, B., Fawcett, J. W., et al. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1499-0 · Cited by 41
Hart, C. G., & Karimi‐Abdolrezaee, S. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113455 · Cited by 45
Hegvik, T., Waløen, K., Pandey, S. K., Faraone, S. V., Haavik, J., & Zayats, T. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0540-z · Cited by 39
Luo, F., Wang, J., Zhang, Z., You, Z., Bedolla, A., Okwubido-Williams, F. V., Huang, L. F., Silver, J., & Luo, Y. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111137 · Cited by 39
Self-citationZou, Y., Stagi, M., Wang, X., Yiğitkanlı, K., Siegel, C., Nakatsu, F., Cafferty, W. B. J., & Strittmatter, S. M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1718-15.2015 · Cited by 38
Poly(ADP-ribose) polymerase 1 is a novel target to promote axonal regeneration
Brochier, C., Jones, J. I., Willis, D. E., & Langley, B. C. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1509754112 · Cited by 39
Environmental cues determine the fate of astrocytes after spinal cord injury
Li, S., & Nathan, F. M. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.221144 · Cited by 39
Self-citationKatano, T., Takao, K., Abe, M., Yamazaki, M., Watanabe, M., Miyakawa, T., Sakimura, K., & Ito, S. (2018) · Molecular Brain · doi:10.1186/s13041-018-0407-2 · Cited by 39
Extrinsic and intrinsic regulation of axon regeneration at a crossroads
Kaplan, A., Tone, S. O., & Fournier, A. E. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00027 · Cited by 40
The potential of memory enhancement through modulation of perineuronal nets
Duncan, J. A., Foster, R., & Kwok, J. C. F. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14672 · Cited by 41
Strategies to neutralize RhoA/ROCK pathway after spinal cord injury
Roy, A., Pathak, Z., & Kumar, H. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113794 · Cited by 39
Farrugia, B. L., & Melrose, J. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241814101 · Cited by 39
Siebert, J. R., Eade, A. M., & Osterhout, D. J. (2015) · BioMed Research International · doi:10.1155/2015/752572 · Cited by 40
Diverse functions of protein tyrosine phosphatase σ in the nervous and immune systems
Ohtake, Y., Saito, A., & Li, S. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.01.014 · Cited by 39
Self-citationLogun, M. T., Bisel, N. S., Tanasse, E. A., Zhao, W., Gunasekera, B., Mao, L., & Karumbaiah, L. (2016) · Journal of Materials Chemistry B · doi:10.1039/c6tb01083k · Cited by 37
Rewiring the spinal cord: Direct and indirect strategies
Dell’Anno, M. T., & Strittmatter, S. M. (2016) · Neuroscience Letters · doi:10.1016/j.neulet.2016.12.002 · Cited by 36
Molecular approaches for spinal cord injury treatment
Martinez, A. B., de Almeida, F. M., Marques, S. A., dos Santos, A. R., Prins, C. A., Cardoso, F. S. D. S., Heringer, L. D. S., & Mendonça, H. R. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.344830 · Cited by 43
Rho Signaling and Axon Regeneration
McKerracher, L. J., Ferraro, G. B., & Fournier, A. E. (2012) · International review of neurobiology · doi:10.1016/b978-0-12-398309-1.00007-x · Cited by 35
Coles, C. H., Jones, E. Y., & Aricescu, A. R. (2014) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2014.09.007 · Cited by 37
Promoting Axon Regeneration in Adult CNS by Targeting Liver Kinase B1
Ohtake, Y., Sami, A., Jiang, X., Horiuchi, M., Slattery, K., Ma, L., Smith, G. M., Selzer, M. E., Muramatsu, S., & Li, S. (2018) · Molecular Therapy · doi:10.1016/j.ymthe.2018.10.019 · Cited by 33
Self-citationPTPσ inhibitors promote hematopoietic stem cell regeneration
Zhang, Y., Roos, M. M., Himburg, H. A., Termini, C. M., Quarmyne, M., Li, M., Zhao, L., Kan, J., Fang, T., Xiao, Y., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11490-5 · Cited by 33
Mimicking Extracellular Matrix via Engineered Nanostructured Biomaterials for Neural Repair
Raspa, A., & Gelain, F. (2020) · Current Neuropharmacology · doi:10.2174/1570159x18666201111111102 · Cited by 36
Chambel, S. S., & Cruz, C. D. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.373674 · Cited by 36
Logun, M. T., Wynens, K. E., Simchick, G. A., Zhao, W., Mao, L., Zhao, Q. C., Mukherjee, S., Brat, D. J., & Karumbaiah, L. (2019) · The FASEB Journal · doi:10.1096/fj.201802610rr · Cited by 32
Nakamura, F., Okada, T., Shishikura, M., Uetani, N., Taniguchi, M., Yagi, T., Iwakura, Y., Ohshima, T., Goshima, Y., & Strittmatter, S. M. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2519-16.2017 · Cited by 31
Shida, M., Mikami, T., Tamura, J.-I., & Kitagawa, H. (2019) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2019.06.004 · Cited by 31
Chondroitinase ABC Promotes Axon Regeneration and Reduces Retrograde Apoptosis Signaling in Lamprey
Hu, J., Rodemer, W., Zhang, G., Jin, L., Li, S., & Selzer, M. E. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.653638 · Cited by 32
Self-citationLi, H., Park, D., Muneer, P. M. A., Xu, B., Wang, H., Xing, B., Wu, D. W., & Li, S. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.051 · Cited by 31
Self-citationHosseini, S. M., Alizadeh, A., Shahsavani, N., Chopek, J. W., Ahlfors, J.-E., & Karimi‐Abdolrezaee, S. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.2177-21.2022 · Cited by 35
Sulfated glycans in network rewiring and plasticity after neuronal injuries
Kadomatsu, K., & Sakamoto, K. (2013) · Neuroscience Research · doi:10.1016/j.neures.2013.10.005 · Cited by 30
Pleiotropic molecules in axon regeneration and neuroinflammation
Lang, B. T., Wang, J., Filous, A. R., Au, N. P. B., Ma, C. H. E., & Shen, Y. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.04.031 · Cited by 32
Emerging molecular therapeutic targets for spinal cord injury
Wang, S., Smith, G. M., Selzer, M. E., & Li, S. (2019) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2019.1661381 · Cited by 31
Self-citationYang, X. (2020) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0117 · Cited by 31
Self-citationThe use of viral vectors to promote repair after spinal cord injury
Islam, A., & Tom, V. J. (2022) · Experimental Neurology · doi:10.1016/j.expneurol.2022.114102 · Cited by 29
Mueller, A. L., Davis, A., Sovich, S., Carlson, S. S., & Robinson, F. R. (2016) · Neural Plasticity · doi:10.1155/2016/6021428 · Cited by 29
Chemistry and Function of Glycosaminoglycans in the Nervous System
Schwartz, N. B., & Domowicz, M. S. (2014) · Advances in Neurobiology · doi:10.1007/978-1-4939-1154-7_5 · Cited by 25
Sugar glues for broken neurons
Swarup, V. P., Mencio, C. P., Hlady, V., & Kuberan, B. (2013) · BioMolecular Concepts · doi:10.1515/bmc-2012-0042 · Cited by 27
Global Analysis of Neuronal Phosphoproteome Regulation by Chondroitin Sulfate Proteoglycans
Yu, P., Pisitkun, T., Wang, G., Wang, R., Katagiri, Y., Guček, M., Knepper, M. A., & Geller, H. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0059285 · Cited by 25
Liu, Y., Zhao, C., Zhang, R., Pang, Y., Li, L., & Feng, S. (2024) · Stem Cell Research & Therapy · doi:10.1186/s13287-024-03914-x · Cited by 25
Blockade of chondroitin sulfate proteoglycans-induced axonal growth inhibition by LOTUS
Kurihara, Y., Saito, Y., & Takei, K. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.034 · Cited by 25
Zhang, G., Hu, J., Li, S., Huang, L. A., & Selzer, M. E. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23529 · Cited by 25
Self-citationA Drosophila ‐centric view of protein tyrosine phosphatases
Hatzihristidis, T., Desai, N., Hutchins, A. P., Meng, T., Tremblay, M. L., & Miranda‐Saavedra, D. (2015) · FEBS Letters · doi:10.1016/j.febslet.2015.03.005 · Cited by 23
Protein Tyrosine Phosphatase σ in Proteoglycan-Mediated Neural Regeneration Regulation
Chien, P. N., & Ryu, S. E. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8346-x · Cited by 26
Mechanisms of axon regeneration and its inhibition: Roles of sulfated glycans
Kadomatsu, K., & Sakamoto, K. (2014) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2014.06.009 · Cited by 24
Zhou, H., Li, X., Li, F., Liu, C., Liang, Z., Liu, S., Zhang, B., Wang, T., Chu, T., Lu, L., et al. (2014) · Brain Research · doi:10.1016/j.brainres.2014.08.048 · Cited by 24
Cheng, L., Sami, A., Ghosh, B., Urban, M. W., Heinsinger, N. M., Liang, S. S., Smith, G. M., Wright, M. C., Li, S., & Lepore, A. C. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105153 · Cited by 26
Self-citationCatabolism of chondroitin sulfate
Yamada, S. (2015) · Cellular & Molecular Biology Letters · doi:10.1515/cmble-2015-0011 · Cited by 23
Silver, L. D., Michael, J. V., Goldfinger, L. E., & Gallo, G. (2014) · Developmental Neurobiology · doi:10.1002/dneu.22174 · Cited by 23
ADAMTS‐4 in oligodendrocytes contributes to myelination with an impact on motor function
Pruvost, M., Lépine, M., Leonetti, C., Etard, O., Naveau, M., Agin, V., Docagne, F., Maubert, E., Ali, C., Emery, É., et al. (2017) · Glia · doi:10.1002/glia.23207 · Cited by 30
Letko-Khait, N., Zuccaro, S., Abdo, D., Cui, H., Siu, R., Ho, E., Morshead, C. M., & Shoichet, M. S. (2024) · Biomaterials · doi:10.1016/j.biomaterials.2024.122818 · Cited by 25
Katagiri, Y., Morgan, A. A., Yu, P., Bangayan, N. J., Junka, R., & Geller, H. M. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.003081 · Cited by 22
Bäumer, B. E., Kurz, A., Borrie, S. C., Sickinger, S., Dours-Zimmermann, M. T., Zimmermann, D. R., & Bandtlow, C. E. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3094-13.2014 · Cited by 22
Sainath, R., Armijo‐Weingart, L., Ketschek, A., Xu, Z., Li, S., & Gallo, G. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22535 · Cited by 22
Self-citationYao, M., Fang, J., Li, J., Ng, A. C. K., Liu, J., Leung, G., Song, F., Zhang, J., & Chang, C. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02561-4 · Cited by 22
McCullough, B. S., Batsomboon, P., Hutchinson, K. B., Dudley, G. B., & Barrios, A. M. (2019) · Journal of Natural Products · doi:10.1021/acs.jnatprod.9b00663 · Cited by 21
Orlando, C., & Raineteau, O. (2014) · Brain Structure and Function · doi:10.1007/s00429-013-0701-9 · Cited by 22
James, G., Foster, S. R., Key, B., & Beverdam, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074115 · Cited by 21
Loers, G., Liao, Y., Hu, C., Xue, W., Shen, H., Zhao, W., & Schachner, M. (2019) · Scientific Reports · doi:10.1038/s41598-018-37685-2 · Cited by 21
Traffic lights for axon growth: proteoglycans and their neuronal receptors
Shen, Y. (2014) · Neural Regeneration Research · doi:10.4103/1673-5374.128236 · Cited by 19
Zhu, Z., Li, R., Guo, W.-L., Qi, Z., Yu, L., Sun, T., Qu, W., & Liu, Q. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.244796 · Cited by 18
Type IIa RPTPs and Glycans: Roles in Axon Regeneration and Synaptogenesis
Sakamoto, K., Ozaki, T., Suzuki, Y., & Kadomatsu, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115524 · Cited by 18
Shijo, T., Warita, H., Suzuki, N., Kitajima, Y., Ikeda, K., Akiyama, T., Ono, H., Mitsuzawa, S., Nishiyama, A., Izumi, R., et al. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24127 · Cited by 18
Niknam, P., Raoufy, M. R., Fathollahi, Y., & Javan, M. (2019) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2019.103391 · Cited by 20
Milton, A. J., Kwok, J. C. F., McClellan, J., Randall, S., Lathia, J. D., Warren, P. M., Silver, D. J., & Silver, J. (2023) · Journal of Neurotrauma · doi:10.1089/neu.2023.0117 · Cited by 19
Self-citationAxonal Regeneration by Glycosaminoglycan
Sakamoto, K., Ozaki, T., & Kadomatsu, K. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.702179 · Cited by 17
Sensory Axon Regeneration: A Review from an in vivo Imaging Perspective
Han, S. B., Kim, H., Skuba, A., Tessler, A. R., Ferguson, T. A., & Son, Y. (2012) · Experimental Neurobiology · doi:10.5607/en.2012.21.3.83 · Cited by 17
Recovery after spinal cord injury by modulation of the proteoglycan receptor PTPσ
Rink, S., Arnold, D., Wöhler, A., Bendella, H., Meyer, C., Μanthou, M. E., Papamitsou, T., Sarıkçıoğlu, L., & Angelov, D. N. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.08.003 · Cited by 17
Chemistry and Function of Glycosaminoglycans in the Nervous System
Schwartz, N. B., & Domowicz, M. S. (2022) · Advances in neurobiology · doi:10.1007/978-3-031-12390-0_5 · Cited by 17
Paxillin phosphorylation counteracts proteoglycan-mediated inhibition of axon regeneration
Kuboyama, T., Luo, X., Park, K. K., Blackmore, M. G., Tojima, T., Tohda, C., Bixby, J. L., Lemmon, V., & Kamiguchi, H. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.06.011 · Cited by 17
Mikami, T., & Kitagawa, H. (2023) · The Journal of Biochemistry · doi:10.1093/jb/mvac110 · Cited by 15
Metadata
- 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
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