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Astrocyte scar formation aids central nervous system axon regeneration
Open accessAbstract
Transected axons fail to regrow in the mature central nervous system. Astrocytic scars are widely regarded as causal in this failure. Here, using three genetically targeted loss-of-function manipulations in adult mice, we show that preventing astrocyte scar formation, attenuating scar-forming astrocytes, or ablating chronic astrocytic scars all failed to result in spontaneous regrowth of transected corticospinal, sensory or serotonergic axons through severe spinal cord injury (SCI) lesions. By contrast, sustained local delivery via hydrogel depots of required axon-specific growth factors not present in SCI lesions, plus growth-activating priming injuries, stimulated robust, laminin-dependent sensory axon regrowth past scar-forming astrocytes and inhibitory molecules in SCI lesions. Preventing astrocytic scar formation significantly reduced this stimulated axon regrowth. RNA sequencing revealed that astrocytes and non-astrocyte cells in SCI lesions express multiple axon-growth-supporting molecules. Our findings show that contrary to the prevailing dogma, astrocyte scar formation aids rather than prevents central nervous system axon regeneration.
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“Such transcriptomic profiling specifically shows that reactive astrocytes adopt distinct molecular states in different disease models48,66–70, in different CNS regions70, and in brain tumors71.”
From Reactive astrocyte nomenclature, definitions, and future directions (2021) · cites this paper as [48]
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“Likewise, reactive astrocytes are also diverse, as unequivocally demonstrated by microarray-based66–68 and RNAseq-based48,69–71 transcriptomic profiling of mouse bulk astrocytes48,66–70 or of astrocyte populations preselected according to cell-surface markers71.”
From Reactive astrocyte nomenclature, definitions, and future directions (2021) · cites this paper as [48]
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“For example, activation of STAT3-dependent transcription is beneficial in neonatal white matter injury47, traumatic brain injury30, spinal cord injury48,49, and motor neuron injury50, but detrimental in AD models42,43.”
From Reactive astrocyte nomenclature, definitions, and future directions (2021) · cites this paper as [48]
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Cites
Faul, F., Erdfelder, E., Lang, A.-G., & Buchner, A. (2007) · Behavior Research Methods · doi:10.3758/bf03193146 · Cited by 65,971
STAR: ultrafast universal RNA-seq aligner
Dobin, A., Davis, C. A., Schlesinger, F., Drenkow, J., Zaleski, C., Jha, S., Batut, P., Chaisson, M., & Gingeras, T. R. (2013) · Bioinformatics · doi:10.1093/bioinformatics/bts635 · Cited by 51,709
Robinson, M. D., McCarthy, D. J., & Smyth, G. K. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btp616 · Cited by 41,364
HTSeq—a Python framework to work with high-throughput sequencing data
Anders, S., Pyl, P. T., & Huber, W. (2015) · Bioinformatics · doi:10.1093/bioinformatics/btu638 · Cited by 21,464
A robust and high-throughput Cre reporting and characterization system for the whole mouse brain
Madisen, L., Zwingman, T. A., Sunkin, S. M., Oh, S. W., Zariwala, H. A., Gu, H., Ng, L. L., Palmiter, R. D., Hawrylycz, M. J., Jones, A. R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2467 · Cited by 6,907
Zhang, Y., Chen, K., Sloan, S. A., Bennett, M. L., Scholze, A. R., O'Keeffe, S., Phatnani, H. P., Guarnieri, P., Caneda, C., Ruderisch, N., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.1860-14.2014 · Cited by 4,875
Regeneration beyond the glial scar
Silver, J., & Miller, J. H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1326 · Cited by 3,151
Degeneration and Regeneration of the Nervous System.
(1929) · JAMA · doi:10.1001/jama.1929.02710220063037 · Cited by 2,908
Genomic analysis of reactive astrogliosis
Zamanian, J. L., Xu, L., Foo, L. C., Nouri, N., Zhou, L., Giffard, R. G., & Barres, B. A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.6221-11.2012 · Cited by 2,404
David, S., & Aguayo, A. J. (1981) · Science · doi:10.1126/science.6171034 · Cited by 1,698
Flagged first, then by citations
Cited by
Sorted by citations
Items 501–600 of 1,002
Regulatory Role of Mesenchymal Stem Cells on Secondary Inflammation in Spinal Cord Injury
Pang, Q.-M., Chen, S.-Y., Fu, S.-P., Zhou, H., Zhang, Q., Ao, J., Luo, X.-P., & Zhang, T. (2022) · Journal of Inflammation Research · doi:10.2147/jir.s349572 · Cited by 48
In vivo spatiotemporal dynamics of astrocyte reactivity following neural electrode implantation
Savya, S. P., Li, F., Lam, S., Wellman, S. M., Stieger, K. C., Chen, K., Eles, J. R., & Kozai, T. D. Y. (2022) · Biomaterials · doi:10.1016/j.biomaterials.2022.121784 · Cited by 46
Potassium and glutamate transport is impaired in scar-forming tumor-associated astrocytes
Campbell, S. C., Muñoz‐Ballester, C., Chaunsali, L., Mills, W. A., Yang, J. H., Sontheimer, H. W., & Robel, S. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.104628 · Cited by 50
Novel innovations in cell and gene therapies for spinal cord injury
Zavvarian, M.-M., Toossi, A., Khazaei, M., Hong, J., & Fehlings, M. G. (2020) · F1000Research · doi:10.12688/f1000research.21989.1 · Cited by 47
Song, P., Han, T., Xiang, X., Wang, Y., Fang, H., Niu, Y., & Shen, C. (2020) · Stem Cell Research & Therapy · doi:10.1186/s13287-020-01691-x · Cited by 49
Zhang, J., Li, Y., Xiong, J., Xu, H., Xiang, G., Fan, M., Zhou, K., Lin, Y., Chen, X., Xie, L., et al. (2021) · Bioactive Materials · doi:10.1016/j.bioactmat.2021.03.001 · Cited by 48
Han, T., Song, P., Wu, Z., Xiang, X., Liu, Y., Wang, Y., Fang, H., Niu, Y., & Shen, C. (2021) · Stem Cell Reviews and Reports · doi:10.1007/s12015-021-10219-6 · Cited by 50
Koupourtidou, C., Schwarz, V., Aliee, H., Frerich, S., Fischer-Sternjak, J., Bocchi, R., Simon-Ebert, T., Bai, X., Sirko, S., Kirchhoff, F., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-46625-w · Cited by 48
Villarreal, A., Vidos, C., Busso, M. M., Cieri, M. B., & Ramos, A. J. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.689346 · Cited by 48
Heterogeneity and Molecular Markers for CNS Glial Cells Revealed by Single-Cell Transcriptomics
Sun, J., Song, Y., Chen, Z., Qiu, J., Zhu, S., Wu, L., & Xing, L. (2021) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-021-01159-3 · Cited by 52
Lee, B., Lee, S. M., Song, J. W., & Choi, J. W. (2024) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2024.009 · Cited by 49
Thelin, E. P., Hall, C. E., Gupta, K., Carpenter, K. L. H., Chandran, S., Hutchinson, P. J., Patani, R., & Helmy, A. E. (2017) · Journal of Neurotrauma · doi:10.1089/neu.2017.5155 · Cited by 47
TGF-β Secretion by M2 Macrophages Induces Glial Scar Formation by Activating Astrocytes In Vitro
Song, G., Yang, R., Zhang, Q., Chen, L., Huang, D., Zeng, J., Yang, C., & Zhang, T. (2019) · Journal of Molecular Neuroscience · doi:10.1007/s12031-019-01361-5 · Cited by 48
Role of astrocyte purinergic signaling in epilepsy
Nikolic, L. M., Nobili, P., Shen, W., & Audinat, É. (2019) · Glia · doi:10.1002/glia.23747 · Cited by 51
Biomaterial Approaches to Modulate Reactive Astroglial Response
Zuidema, J. M., Gilbert, R. J., & Gottipati, M. K. (2018) · Cells Tissues Organs · doi:10.1159/000494667 · Cited by 46
Extrinsic and Intrinsic Regulation of Axon Regeneration by MicroRNAs after Spinal Cord Injury
Li, P., Teng, Z., & Liu, C. (2016) · Neural Plasticity · doi:10.1155/2016/1279051 · Cited by 45
Jin, Z., Tian, L., Zhang, Y., Zhang, X., Kang, J., Dong, H., Huang, N., Pan, L., & Ning, B. (2022) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13929 · Cited by 46
Glial aging and its impact on central nervous system myelin regeneration
Rawji, K. S., Neumann, B., & Franklin, R. J. M. (2022) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14933 · Cited by 47
Role of CXCL10 in Spinal Cord Injury
Qiao, X.-Y., Zhang, W. Y., & Zhao, W. (2022) · International Journal of Medical Sciences · doi:10.7150/ijms.76694 · Cited by 47
Teh, D. B. L., Prasad, A., Jiang, W., Ariffin, M. Z., Khanna, S., Belorkar, A., Wong, L., Liu, X., & All, A. H. (2017) · Scientific Reports · doi:10.1038/s41598-017-13174-w · Cited by 50
Haindl, M. T., Köck, U., Adzemovic, M. Z., Fazekas, F., & Hochmeister, S. (2018) · Glia · doi:10.1002/glia.23556 · 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
Lin, P. H., Dong, Q., & Chew, S. Y. (2021) · Materials Advances · doi:10.1039/d0ma00732c · Cited by 46
Updated Understanding of the Glial-Vascular Unit in Central Nervous System Disorders
Yao, D., Zhang, R., Xie, M., Ding, F., Wang, M., & Wang, W. (2022) · Neuroscience Bulletin · doi:10.1007/s12264-022-00977-9 · Cited by 47
Yoo, H.-S., Shanmugalingam, U., & Smith, P. D. (2021) · Cells · doi:10.3390/cells10061339 · Cited by 48
Wang, J., Kong, X., Li, Q., Li, C., Yu, H., Ning, G., Xiang, Z., Liu, Y., & Feng, S. (2021) · Biofabrication · doi:10.1088/1758-5090/ac0c5f · Cited by 45
Comparison of subacute and chronic scar tissues after complete spinal cord transection
Li, X., Yang, B., Xiao, Z., Zhao, Y., Han, S., Yin, Y., Chen, B., & Dai, J. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.05.008 · Cited by 46
Wu, R., Mao, S., Wang, Y., Zhou, S., Liu, Y., Liu, M., Gu, X., & Yu, B. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01303 · Cited by 45
Progress toward finding the perfect match: hydrogels for treatment of central nervous system injury
Hlavac, N., Kasper, M., & Schmidt, C. E. (2020) · Materials Today Advances · doi:10.1016/j.mtadv.2019.100039 · Cited by 45
Zhang, X., Guo, X., Kang, X., Yang, H. Y., Guo, W., Guan, L., Wu, H., & Du, L. (2020) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.9b00368 · Cited by 45
Cholesterol Dysmetabolism in Alzheimer’s Disease: A Starring Role for Astrocytes?
Staurenghi, E., Giannelli, S., Testa, G., Sottero, B., Leonarduzzi, G., & Gamba, P. (2021) · Antioxidants · doi:10.3390/antiox10121890 · Cited by 44
Function of Glia in Aging and the Brain Diseases
Vallés, S. L., Iradi, A., Aldasoro, M., Vila, J. M., Aldasoro, C., de la Torre, J., Campos-Campos, J., & Jorda, A. (2019) · International Journal of Medical Sciences · doi:10.7150/ijms.37769 · Cited by 45
Abdel‐Aty, A., Khater, M. M. A., Bǎleanu, D., Khalil, E. M., Bouslimi, J., & Omri, M. (2020) · Advances in Difference Equations · doi:10.1186/s13662-020-02852-1 · Cited by 44
Yang, X. Y., Geng, K., Zhang, J., Zhang, Y., Shao, J., & Xia, W. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00943 · Cited by 44
Thornton, M. A., Mehta, M. D., Morad, T. T., Dixie, K. L. I., Khankan, R. R., Griffis, K. G., Yeung, A. K., Zhong, H., Roy, R. R., Edgerton, V. R., et al. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.07.015 · Cited by 44
Pathology of inflammatory diseases of the nervous system: Human disease versus animal models
Lassmann, H. (2019) · Glia · doi:10.1002/glia.23726 · Cited by 44
Pentraxin 3 contributes to neurogenesis after traumatic brain injury in mice
Zhou, C., Chen, H., Zheng, J., Guo, Z.-D., Huang, Z., Wu, Y., Zhong, J.-J., Sun, X.-C., & Cheng, C.-J. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.285001 · Cited by 37
Murata, Y., Sugimoto, K., Yang, C., Harada, K., Gono, R., Harada, T., Miyashita, Y., Higashisaka, K., Katada, R., Tanaka, J., et al. (2020) · Neurochemistry International · doi:10.1016/j.neuint.2020.104848 · Cited by 44
Bai, Q., Teng, L., Zhang, X., & Dong, C. (2021) · Advanced Healthcare Materials · doi:10.1002/adhm.202101809 · Cited by 44
Interface astrogliosis in contact sport head impacts and military blast exposure
Babcock, K. J., Abdolmohammadi, B., Kiernan, P. T., Mahar, I., Cherry, J. D., Alvarez, V. E., Goldstein, L. E., Stein, T. D., McKee, A. C., & Huber, B. R. (2022) · Acta Neuropathologica Communications · doi:10.1186/s40478-022-01358-z · Cited by 46
Wang, Y., Liu, W.-C., Geng, P., Du, W., Guo, C., Wang, Q., Zheng, G., & Jin, X. (2023) · Aging and Disease · doi:10.14336/ad.2023.1010 · Cited by 45
Quan, H., & Zhang, R. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1320271 · Cited by 48
Pu, H., Jiang, X., Hu, X., Xia, J., Hong, D., Zhang, W., Gao, Y., Chen, J., & Shi, Y. (2016) · Translational Stroke Research · doi:10.1007/s12975-016-0498-y · Cited by 45
Adult NSC diversity and plasticity: the role of the niche
Llorens-Bobadilla, E., & Martín-Villalba, A. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.11.008 · Cited by 45
Axonal regeneration in zebrafish spinal cord
Ghosh, S., & Hui, S. P. (2018) · Regeneration · doi:10.1002/reg2.99 · Cited by 46
Zarei‐Kheirabadi, M., Hesaraki, M., Kiani, S., & Baharvand, H. (2019) · Stem Cell Research & Therapy · doi:10.1186/s13287-019-1448-x · Cited by 43
Assinck, P., Sparling, J. S., Dworski, S., Duncan, G. J., Wu, D., Liu, J., Kwon, B. K., Biernaskie, J. A., Miller, F. D., & Tetzlaff, W. (2020) · Stem Cell Reports · doi:10.1016/j.stemcr.2020.05.017 · Cited by 43
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
Foster, V. S., Rash, L. D., King, G. F., & Rank, M. M. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.738043 · Cited by 44
Is Graphene Shortening the Path toward Spinal Cord Regeneration?
Girão, A. F., Serrano, M. C., Completo, A., & Marques, P. A. A. P. (2022) · ACS Nano · doi:10.1021/acsnano.2c04756 · Cited by 44
SIRT1 inactivation switches reactive astrocytes to an antiinflammatory phenotype in CNS autoimmunity
Zhang, W., Xiao, D., Li, X., Zhang, Y., Rasouli, J., Casella, G., Boehm, A., Hwang, D., Ishikawa, L. L. W., Thomé, R., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci151803 · Cited by 44
Mode of action of astrocytes in pain: From the spinal cord to the brain
Chen, Y.-L., Feng, X., Cheung, C., & Liu, J. A. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102365 · Cited by 44
Infliximab Can Improve Traumatic Brain Injury by Suppressing the Tumor Necrosis Factor Alpha Pathway
Zhou, Y., Fan, R., Botchway, B. O. A., Zhang, Y., & Liu, X. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02293-1 · Cited by 42
The structural and functional evidence for vesicular release from astrocytes in situ
Bohmbach, K., Schwarz, M. K., Schoch, S., & Henneberger, C. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.01.015 · Cited by 47
Inhibition and enhancement of neural regeneration by chondroitin sulfate proteoglycans
Rauvala, H., Paveliev, M., Kuja‐Panula, J., & Kulesskaya, N. (2017) · Neural Regeneration Research · doi:10.4103/1673-5374.206630 · Cited by 45
A role for ErbB signaling in the induction of reactive astrogliosis
Chen, J., He, W., Hu, X., Shen, Y., Cao, J., Wei, Z., Luan, Y., He, L., Jiang, F., & Tao, Y. (2017) · Cell Discovery · doi:10.1038/celldisc.2017.44 · Cited by 42
Petrova, V., & Eva, R. (2018) · Developmental Neurobiology · doi:10.1002/dneu.22608 · Cited by 42
Kamermans, A., Planting, K. E., Jalink, K., van Horssen, J., & de Vries, H. E. (2018) · Glia · doi:10.1002/glia.23526 · Cited by 42
Li, L., Ni, L., Eugenín, E. A., Heary, R. F., & Elkabes, S. (2019) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.04.010 · Cited by 42
de Jong, C. G. H. M., Gabius, H., & Baron, W. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03327-7 · Cited by 44
Scar Tissue‐Targeting Polymer Micelle for Spinal Cord Injury Treatment
Wang, J., Li, D., Liang, C., Wang, C., Zhou, X., Ying, L., Tao, Y., Xu, H., Shu, J., Huang, X., et al. (2020) · Small · doi:10.1002/smll.201906415 · Cited by 41
Complex roles for reactive astrocytes in the triple transgenic mouse model of Alzheimer disease
Guillemaud, O., Ceyzériat, K., Saint-Georges, T., Cambon, K., Petit, F., Haim, L. B., Sauvage, M.-A. C.-D., Guillermier, M., Bernier, S., Hérard, A., et al. (2019) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.02.010 · Cited by 40
Neuroimmune System as a Driving Force for Plasticity Following CNS Injury
O’Reilly, M. L., & Tom, V. J. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00187 · Cited by 44
Michalski, D., Spielvogel, E., Puchta, J., Reimann, W., Barthel, H., Nitzsche, B., Mages, B., Jäger, C., Martens, H., Horn, A. K. E., et al. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.575598 · Cited by 44
Role of Astrocytes in Major Neuropsychiatric Disorders
Zhang, X., Alnafisah, R. S., Hamoud, A.-R. A., Shukla, R., Wen, Z., McCullumsmith, R. E., & O'Donovan, S. M. (2021) · Neurochemical Research · doi:10.1007/s11064-020-03212-x · Cited by 43
Chun, H., Lim, J., Park, K. D., & Lee, C. J. (2021) · Glia · doi:10.1002/glia.24110 · Cited by 42
Potential neurotoxic activity of diverse molecules released by astrocytes
Murray, T. E., Richards, C. M., Robert-Gostlin, V. N., Bernath, A. K., Lindhout, I. A., & Klegeris, A. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.08.015 · Cited by 40
Wu, J., Lu, B., Yang, R., Chen, Y., Chen, X., & Li, Y. (2021) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13641 · Cited by 41
Dynamic modulation of the blood–brain barrier in the healthy brain
Friedman, A., Prager, O., Serlin, Y., & Kaufer, D. (2025) · Nature reviews. Neuroscience · doi:10.1038/s41583-025-00976-5 · Cited by 48
Biomaterial strategies for limiting the impact of secondary events following spinal cord injury
Ham, T. R., & Leipzig, N. D. (2017) · Biomedical Materials · doi:10.1088/1748-605x/aa9bbb · Cited by 41
Kaushik, R., Morkovin, E. I., Schneeberg, J., Confettura, A. D., Kreutz, M. R., Senkov, O., & Dityatev, A. E. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00411 · Cited by 38
Lien, B. V., Tuszynski, M. H., & Lu, P. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.01.006 · Cited by 41
Role of Astrocytes in Post-traumatic Epilepsy
Xu, S., Sun, Q., Fan, J., Jiang, Y., Yang, W., Cui, Y., Yu, Z., Jiang, H., & Li, B. (2019) · Frontiers in Neurology · doi:10.3389/fneur.2019.01149 · Cited by 44
Medina‐Ceja, L., Salazar‐Sánchez, J. C., Ortega‐Ibarra, J., & Morales‐Villagrán, A. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20235976 · Cited by 41
Functional rewiring across spinal injuries via biomimetic nanofiber scaffolds
Usmani, S., Biagioni, A. F., Medelin, M., Scaini, D., Casani, R., Aurand, E. R., Padró, D., Egimendia, A., Ramos‐Cabrer, P., Scarselli, M., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2005708117 · Cited by 41
Functionalized nanogel for treating activated astrocytes in spinal cord injury
Papa, S., Veneruso, V., Mauri, E., Cremonesi, G., Mingaj, X., Mariani, A., Paola, M. D., Rossetti, A., Sacchetti, A., Rossi, F., et al. (2020) · Journal of Controlled Release · doi:10.1016/j.jconrel.2020.12.006 · Cited by 42
Pericytes for Therapeutic Approaches to Ischemic Stroke
Cao, L., Zhou, Y., Chen, M., Li, L., & Zhang, W. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.629297 · Cited by 41
Tamaru, T., Kobayakawa, K., Saiwai, H., Konno, D., Kijima, K., Yoshizaki, S., Hata, K., Iura, H., Ono, G., Haruta, Y., et al. (2022) · Experimental Neurology · doi:10.1016/j.expneurol.2022.114264 · Cited by 40
Lane, M. A., Lepore, A. C., & Fischer, I. (2016) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2017.1270206 · Cited by 40
Maclean, F. L., Wang, Y., Walker, R., Horne, M. K., Williams, R. J., & Nisbet, D. R. (2017) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.7b00524 · Cited by 41
Wang, W., Su, Y., Tang, S., Li, H., Xie, W., Chen, J., Shen, L., Pan, X., & Ning, B. (2019) · Aging · doi:10.18632/aging.101919 · Cited by 40
Griffin, J. M., Fackelmeier, B., Clemett, C. A., Fong, D. M., Mouravlev, A., Young, D., & O’Carroll, S. J. (2020) · Experimental Neurology · doi:10.1016/j.expneurol.2020.113232 · Cited by 43
Wang, Y., Xie, C., Wang, P., Wang, X., Wang, C., Xun, X., Lin, C., Huang, Z., Cheng, Y., Li, L., et al. (2020) · Journal of Controlled Release · doi:10.1016/j.jconrel.2020.04.042 · Cited by 40
Smith, B. C., Sinyuk, M., Jenkins, J. E., Psenicka, M. W., & Williams, J. L. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01861-x · Cited by 41
Advances in immunotherapy for the treatment of spinal cord injury
Mamun, A. A., Monalisa, I., Kubra, K. T., Akter, A., Akter, J., Sarker, T., Munir, F., Wu, Y., Jia, C., Taniya, M. A., et al. (2020) · Immunobiology · doi:10.1016/j.imbio.2020.152033 · Cited by 40
Extracellular Vesicles: Novel Roles in Neurological Disorders
Jin, Q., Wu, P., Zhou, X., Qian, H., & Xu, W. (2021) · Stem Cells International · doi:10.1155/2021/6640836 · Cited by 40
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Cordella, F., Sanchini, C., Rosito, M., Ferrucci, L., Pediconi, N., Cortese, B., Guerrieri, F., Pascucci, G. R., Antonangeli, F., Peruzzi, G., et al. (2021) · Cells · doi:10.3390/cells10102648 · Cited by 38
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Metadata
- Authors
- Anderson, M. A., Burda, J. E., Ren, Y., Ao, Y., O’Shea, T. M., Kawaguchi, R., Coppola, G., Khakh, B. S., Deming, T. J., & Sofroniew, M. V.
- Affiliations
- Tongji University (CN)
- University of California, Los Angeles (US)
- Corresponding author
- Sofroniew, Michael V.
- ORCID
- Venue
- Nature
- Published
- 2016-03-30
- Volume
- 532
- Issue
- 7598
- Pages
- 195-200
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5243141
- OpenAlex
- W2335534790
- Cited by
- 1,851
- References
- 104
- Citations by year
- 2026: 116 · 2025: 163 · 2024: 180 · 2023: 159 · 2022: 234 · 2021: 250 · 2020: 224 · 2019: 159 · 2018: 162 · 2017: 136 · 2016: 62
- FWCI
- 97.34
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
- Funders
- National Institute of Mental Health (R01MH099559, MH104069, MH099559A, DP1MH104069)
- National Institute of Neurological Disorders and Stroke (NS084030, NS057624, NS060677, R01NS060677, R01NS057624, P30NS062691, R01NS084030)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Health Sciences › Medicine › Clinical Neurology › Spinal Cord Injury Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- axon regeneration, spinal cord injury, central nervous system injury, corticospinal axons, sensory axons, serotonergic axons, hydrogel delivery, laminin, axon growth inhibition, astrocytes
- MeSH terms
- Animals, Astrocytes, Axons, Central Nervous System, Cicatrix, Female, Models, Biological, Nerve Regeneration, Chondroitin Sulfate Proteoglycans, Spinal Cord Injuries, Reproducibility of Results, Genomics, Mice
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