The DOI matches its Crossref record; 104 of the 104 references it cites were found in a registry or an index.
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.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“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]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“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]
The cited source says what the claim attributes to it.
In the citing paper
“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]
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
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
Cited by
Sorted by citations
Items 901–1,000 of 1,002
The role of astrocyte metabolic reprogramming in ischemic stroke (Review)
Chen, W., Mao, T., Ma, R., Xiong, Y., Han, R., & Wang, L. (2025) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2025.5490 · Cited by 18
Pradhan, L. K., & Das, S. K. (2020) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-020-00893-4 · Cited by 21
Glutamate Carrier Involvement in Mitochondrial Dysfunctioning in the Brain White Matter
Hillen, A. E. J., & Heine, V. M. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.00151 · Cited by 18
Differential Regenerative Capacity of the Optic Tectum of Adult Medaka and Zebrafish
Shimizu, Y., & Kawasaki, T. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.686755 · Cited by 19
Xiao, X., Zhao, T., Miyagishima, K. J., Chen, S., Li, W., & Nadal-Nicolás, F. M. (2021) · Laboratory Investigation · doi:10.1038/s41374-021-00637-y · Cited by 19
Tong, K., Li, S., Chen, G., Ma, C., Liu, X., Liu, S., & Chen, N. (2023) · Molecular Neurobiology · doi:10.1007/s12035-022-03156-z · Cited by 18
Chen, R., Routh, B. N., Gaudet, A. D., & Fonken, L. K. (2023) · Journal of Biological Rhythms · doi:10.1177/07487304231178950 · Cited by 21
Gao, P., Ding, X., Khan, T. M., Rong, W., Franke, H., & Illés, P. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.02.030 · Cited by 19
Correlation of mRNA Expression and Signal Variability in Chronic Intracortical Electrodes
Falcone, J., Carroll, S. L., Saxena, T. K., Mandavia, D., Clark, A., Yarabarla, V., & Bellamkonda, R. V. (2018) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2018.00026 · Cited by 19
Kim, C., Canavero, S., Sikkema, W. K. A., Kim, J., Kim, J., Walter, J. W., Dieter, R. A., Chung, H.-M., Mana, A., & Tour, J. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.235301 · Cited by 19
Yu, B., & Gu, X. (2018) · Frontiers of Medicine · doi:10.1007/s11684-018-0642-z · Cited by 20
Zanuzzi, C. N., Nishida, F., Sisti, M. S., Barbeito, C. G., & Portiansky, E. L. (2018) · Tissue and Cell · doi:10.1016/j.tice.2018.11.007 · Cited by 19
Astrocytes: Initiators of and Responders to Inflammation
Soung, A., & Klein, R. S. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.89760 · Cited by 19
Xue, W., Zhang, H., Fan, Y., Xiao, Z., Zhao, Y., Liu, W., Bai, X., Yin, Y., Chen, B., Li, J., et al. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02375-w · Cited by 19
Comparing axon regeneration in male and female mice after peripheral nerve injury
Jang, E., Bae, Y., Yang, E. M., Gim, Y., Suh, H., Kim, S., Park, S., Park, J. B., & Hur, E. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24955 · Cited by 19
Axonal outgrowth stimulation after alginate/mesenchymal stem cell therapy in injured rat spinal cord
Blaško, J., Székiová, E., Slovinská, L., Kafka, J., & Čı́žková, D. (2017) · Acta Neurobiologiae Experimentalis · doi:10.21307/ane-2017-066 · Cited by 19
Xu, J., Shi, C., Ding, Y., Qin, T., Li, C., Yuan, F., Liu, Y., Xie, Y., Qin, Y., Cao, Y., et al. (2024) · Advanced Science · doi:10.1002/advs.202406398 · Cited by 18
Qin, T., Qin, Y., Wen, H., Wu, T., Duan, C., Cao, Y. B., Sun, Y. X., Zhou, H., Lü, H., Jiang, L., et al. (2025) · Journal of Extracellular Vesicles · doi:10.1002/jev2.70126 · Cited by 18
de Amorim, V. C. M., Oliveira, M. S., da Silva, A. B., David, J. M., David, J. P. L., Costa, M. D. F. D., Butt, A. M., da Silva, V. D. A., & Costa, S. L. (2020) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-020-01905-2 · Cited by 18
Repetitive injury and absence of monocytes promote astrocyte self‐renewal and neurological recovery
Canhos, L. L., Chen, M., Falk, S., Popper, B., Straub, T., Götz, M., & Sirko, S. (2020) · Glia · doi:10.1002/glia.23893 · Cited by 19
Neuroinflammation: Breaking barriers and bridging gaps
Estera, L. A., Walsh, S. P., Headen, J. A., Williamson, R. E., & Kalinski, A. L. (2021) · Neuroscience Research · doi:10.1016/j.neures.2021.11.001 · Cited by 18
Kabdesh, I. M., Mukhamedshina, Y. O., Arkhipova, S. S., Sabirov, D., Kuznecov, M. S., Vyshtakalyuk, A. B., Rizvanov, A. A., James, V. H., & Chelyshev, Y. A. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.817752 · Cited by 18
Astrocytes-Derived Small Extracellular Vesicles Hinder Glioma Growth
Serpe, C., Michelucci, A., Monaco, L., Rinaldi, A., Luca, M. D., Familiari, P., Relucenti, M., Pietro, E. D., Castro, M. A. D., D’Agnano, I., et al. (2022) · Biomedicines · doi:10.3390/biomedicines10112952 · Cited by 17
Liu, A., Yu, L., Li, X., Zhang, K., Zhang, W., So, K., Tissir, F., Qu, Y., & Zhou, L. (2023) · Glia · doi:10.1002/glia.24378 · Cited by 18
PJA1 mediates the effects of astrocytic GPR30 on learning and memory in female mice
Wang, X., Jiang, Y., Feng, B., Ma, X., Zhang, K., Yang, F., Liu, Z., Yang, L., Jiao, Y., Lu, L., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci165812 · Cited by 18
Zhao, H., Zong, X., Li, L., Li, N., Liu, C., Zhang, W., Li, J., Yang, C., & Huang, S. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03650-y · Cited by 21
Mutual regulation of microglia and astrocytes after Gas6 inhibits spinal cord injury
Chen, J., Zeng, X., Wang, L., Zhang, W., Li, G., Cheng, X., Su, P., Wan, Y., & Li, X. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-23-01130 · Cited by 19
Augmenting fibronectin levels in injured adult CNS promotes axon regeneration in vivo
Łukomska, A., Rheaume, B. A., Frost, M. P., Theune, W. C., Xing, J., Damania, A., & Trakhtenberg, E. F. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.114877 · Cited by 17
The Potential of Targeting Brain Pathology with Ascl1/Mash1
Tang, B. L. (2017) · Cells · doi:10.3390/cells6030026 · Cited by 18
Syntheses of Bis(N-heterocyclic carbene)s and their application in main-group chemistry
Röther, A., & Kretschmer, R. (2020) · Journal of Organometallic Chemistry · doi:10.1016/j.jorganchem.2020.121289 · Cited by 18
Lu, T., Wang, P., Liang, Y., Li, M., Li, D., Du, K.-H., Zhu, J., & Wu, J. (2020) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2020.08.085 · Cited by 18
Pons-Espinal, M., Blasco-Agell, L., & Consiglio, A. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03700-x · Cited by 18
Schmidt, E. K. A., Raposo, P. J. F., Vavrek, R., & Fouad, K. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.12.013 · Cited by 19
Response of Astrocyte Subpopulations Following Spinal Cord Injury
Allahyari, R. V., Heinsinger, N. M., Hwang, D. H., Jaffe, D. A., Rasouli, J., Shiers, S. I., Thomas, S. J., Price, T. J., Rostami, A. M., & Lepore, A. C. (2022) · Cells · doi:10.3390/cells11040721 · Cited by 18
Activation of Nrf2 to Optimise Immune Responses to Intracerebral Haemorrhage
Loan, J. J., Salman, R. A., McColl, B. W., & Hardingham, G. E. (2022) · Biomolecules · doi:10.3390/biom12101438 · Cited by 17
Network Analysis Reveals TNF as a Major Hub of Reactive Inflammation Following Spinal Cord Injury
Zhu, W., Chen, X., Ning, L., & Jin, K. (2019) · Scientific Reports · doi:10.1038/s41598-018-37357-1 · Cited by 18
Targeting astrocytes in brain injuries: A translational research approach
Barreto, G. E. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.09.001 · Cited by 18
CRISPRi screens in human astrocytes elucidate regulators of distinct inflammatory reactive statesPreprint
Leng, K., Rose, I. V. L., Kim, H., Xia, W., Romero‐Fernandez, W., Rooney, B., Koontz, M., Li, E., Ao, Y., Wang, S., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.08.23.457400 · Cited by 18
Self-citationWu, L., Pandey, V., Hull, V. L., Qu, Z., Jami‐Alahmadi, Y., Gradinaru, V., Wohlschlegel, J. A., & Khakh, B. S. (2025) · Neuron · doi:10.1016/j.neuron.2025.05.019 · Cited by 19
Self-citationBiosensors for Studies on Adhesion-Mediated Cellular Responses to Their Microenvironment
Saffioti, N. A., Cavalcanti‐Adam, E. A., & Pallarola, D. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.597950 · Cited by 18
Using MS induced pluripotent stem cells to investigate MS aetiology
Fortune, A. J., Fletcher, J. L., Blackburn, N. B., & Young, K. M. (2022) · Multiple Sclerosis and Related Disorders · doi:10.1016/j.msard.2022.103839 · Cited by 17
Continual Deletion of Spinal Microglia Reforms Astrocyte Scar Favoring Axonal Regeneration
Xia, L., Qi, J., Tang, M., Liu, J., Zhang, D., Zhu, Y., & Hu, B. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.881195 · Cited by 18
Hypergravity Attenuates Reactivity in Primary Murine Astrocytes
Lichterfeld, Y., Kalinski, L., Schunk, S., Schmakeit, T., Feles, S., Frett, T., Herrmann, H. O., Hemmersbach, R., & Liemersdorf, C. (2022) · Biomedicines · doi:10.3390/biomedicines10081966 · Cited by 17
Spreading of alpha-synuclein between different cell types
Ruf, W. P., Meirelles, J. L., & Danzer, K. M. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2022.114059 · Cited by 19
IRES-mediated Wnt2 translation in apoptotic neurons triggers astrocyte dedifferentiation
Fan, H., Yang, J., Zhang, K., Xing, J.-L., Guo, B., Mao, H., Wang, W., Hu, Y., Lin, W., Huang, Y., et al. (2022) · npj Regenerative Medicine · doi:10.1038/s41536-022-00248-1 · Cited by 17
Astrocyte Responses to Complement Peptide C3a are Highly Context-Dependent
Pekna, M., Siqin, S., de Pablo, Y., Stokowska, A., Naluai, Å. T., & Pekny, M. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03743-5 · Cited by 17
Lu, Y., Chen, C., Wang, H., Du, R., Ji, J., Xu, T., Yang, C., & Chen, X. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.109322 · Cited by 17
Huang, L., Sun, X., Pan, H., Wang, L., He, C., & Wei, Q. (2023) · World Journal of Stem Cells · doi:10.4252/wjsc.v15.i5.385 · Cited by 17
Nakamura, K., & Ago, T. (2023) · Journal of Atherosclerosis and Thrombosis · doi:10.5551/jat.rv22007 · Cited by 17
Kijima, C., Inaba, T., Hira, K., Miyamoto, N., Yamashiro, K., Urabe, T., Hattori, N., & Ueno, Y. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03629-9 · Cited by 18
Forston, M. D., Wei, G. Z., Chariker, J. H., Stephenson, T., Andres, K. R., Glover, C., Rouchka, E. C., Whittemore, S. R., & Hetman, M. (2023) · Scientific Reports · doi:10.1038/s41598-023-48425-6 · Cited by 17
Huang, J., Hu, X., Chen, Z., Ouyang, F., Li, J., Hu, Y., Zhao, Y., Wang, J., Yao, F., Jing, J., et al. (2024) · Journal of Neuroinflammation · doi:10.1186/s12974-024-03089-5 · Cited by 18
Mao, Q., Liang, B., Leng, Z., Ma, W., Chen, Y., & Xie, Y. (2024) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2024.111086 · Cited by 18
Li, Y., Yang, C., Fang, S., Zhou, Y., Li, M., Liu, Z., Zhang, X., Duan, L., Liu, K., & Sun, F. (2024) · Advanced Materials · doi:10.1002/adma.202413957 · Cited by 17
The Paper that Restarted Modern Central Nervous System Axon Regeneration Research
Fawcett, J. W. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.02.012 · Cited by 17
Spinal Cord Injury — Healing from Within
Monje, M. (2021) · New England Journal of Medicine · doi:10.1056/nejmcibr2030836 · Cited by 17
CXCL12 promotes spinal nerve regeneration and functional recovery after spinal cord injury
Li, J., Wu, Y., Chen, P., Huang, X., Liu, Y., Peng, M., & Wu, R. (2021) · Neuroreport · doi:10.1097/wnr.0000000000001613 · Cited by 17
Non-Cell-Autonomous Regulation of Optic Nerve Regeneration by Amacrine Cells
Sergeeva, E. G., Rosenberg, P. A., & Benowitz, L. I. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.666798 · Cited by 18
Respiratory axon regeneration in the chronically injured spinal cord
Cheng, L., Sami, A., Ghosh, B., Goudsward, H. J., Smith, G. M., Wright, M. C., Li, S., & Lepore, A. C. (2021) · Neurobiology of Disease · doi:10.1016/j.nbd.2021.105389 · Cited by 17
Axonal 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
Wang, Y., Zhang, X., Chen, F., Song, N., & Xie, J. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.689276 · Cited by 18
Therapeutic Potential of Astrocyte Purinergic Signalling in Epilepsy and Multiple Sclerosis
Nobili, P., Shen, W., Milicevic, K. D., Pristov, J. B., Audinat, É., & Nikolic, L. M. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.900337 · Cited by 17
Koehn, L. M., Noor, N. M., Dong, Q., Er, S. Y., Rash, L. D., King, G. F., Dzięgielewska, K. M., Saunders, N. R., & Habgood, M. D. (2016) · F1000Research · doi:10.12688/f1000research.9094.1 · Cited by 17
Heimann, G., Canhos, L. L., Frik, J., Jäger, G., Lepko, T., Ninkovic, J., Götz, M., & Sirko, S. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx112 · Cited by 18
Nanomedicine-enabled next-generation therapeutics for spinal cord injury
Ge, M., Ding, Y., Hu, T., Chen, Y., Shahin, V., Li, B., Huang, T., Qian, Y., Zhou, Z., Tao, Y., et al. (2025) · Materials Today · doi:10.1016/j.mattod.2025.04.001 · Cited by 17
Nascimento, D., Ferreira, A. M. F., & Cruz, C. D. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26199624 · Cited by 18
Glial Cells in the Early Stages of Neurodegeneration: Pathogenesis and Therapeutic Targets
Ahremenko, E. A., Andreev, A., Apushkin, D., & Korkotian, E. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262411995 · Cited by 20
Dynamic glial response and crosstalk in demyelination-remyelination and neurodegeneration processes
Shields, C. B., Cai, J., Chu, T., Shields, L. B. E., Zeng, W., Zhang, Y., Wang, Y., & Barnes, G. N. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.300975 · Cited by 21
Post-Traumatic Seizures: A Deep-Dive Into Pathogenesis
Anwer, F., Oliveri, F., Fotios, K., Panday, P., Franchini, A. P. A., Iskander, B., & Hamid, P. (2021) · Cureus · doi:10.7759/cureus.14395 · Cited by 16
Astrocyte-secreted chordin-like 1 regulates spine density after ischemic injury
Blanco‐Suárez, E., & Allen, N. J. (2022) · Scientific Reports · doi:10.1038/s41598-022-08031-4 · Cited by 17
N6-methyladenosine modification: A potential regulatory mechanism in spinal cord injury
Liu, D., Fan, B., Li, J., Sun, T., Ma, J., Zhou, X., & Feng, S. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.989637 · Cited by 16
Chen, L., Xiong, L., Yao, L., Pan, J., Arzola, E. P., Zhu, X., Mei, L., & Xiong, W. (2023) · Alzheimer s Research & Therapy · doi:10.1186/s13195-023-01202-z · Cited by 17
Franklin, M. E., Bennett, C., Arboite, M., Álvarez-Ciara, A., Corrales, N., Verdelus, J., Dietrich, W. D., Keane, R. W., Vaccari, J. P. D. R., & Prasad, A. (2023) · Biomaterials · doi:10.1016/j.biomaterials.2023.122102 · Cited by 17
Cullen, P., & Sun, D. (2023) · Frontiers in Ophthalmology · doi:10.3389/fopht.2023.1217137 · Cited by 20
Shang, Z., Liu, Z., Han, M. H., Fan, H., Lu, D., Zhou, Z., Wang, Z., Li, Y., Wang, X., Wang, B., et al. (2023) · Composites Part B Engineering · doi:10.1016/j.compositesb.2023.111146 · Cited by 16
Recent Advances in the Treatment of Spinal Cord Injury.
Yari, D., Saberi, A., Salmasi, Z., Ghoreishi, S. A., Etemad, L., Movaffagh, J., & Ganjeifar, B. (2024) · PubMed Central · doi:10.22038/abjs.2023.73944.3424 · Cited by 16
Fu, Y. Q., Zheng, Y., Li, Z. L., Huang, X. Y., Wang, X. W., Cui, M. Y., Zhang, Y. Q., Gao, B. R., Zhang, C., Fan, X. X., et al. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.106873 · Cited by 16
ADAMTS‐4 in central nervous system pathologies
Lemarchant, S., Wojciechowski, S., Vivien, D., & Koıstınaho, J. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24021 · Cited by 19
Pei, D., Liu, N., Li, D., Yan, H., Wang, Q., Fang, Y., Xie, L., & Li, H.-P. (2017) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2017.06.020 · Cited by 16
Wang, Z., Huang, J. Y., Liu, C., Liu, L., Shen, Y., Shen, C., & Liu, C. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01151 · Cited by 16
Sardari, M., Dzyubenko, E., Schmermund, B., Yin, D., Qi, Y., Kleinschnitz, C., & Hermann, D. M. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00026 · Cited by 17
A mouse model of complete-crush transection spinal cord injury made by two operations
Li, C., Zhu, X., Lee, C.-M. J., Wu, Z., & Cheng, L. (2020) · Annals of Translational Medicine · doi:10.21037/atm.2020.01.58 · Cited by 16
Calcium Dynamics in Astrocytes During Cell Injury
Wakida, N. M., Gomez‐Godinez, V., Li, H., Nguyen, J., Kim, E. K., Dynes, J. L., Othy, S., Lau, A., Ding, P., Shi, L. Z., et al. (2020) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2020.00912 · Cited by 16
Gage, M., Gard, M., & Thippeswamy, T. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.867949 · Cited by 18
Astrocyte-Neuronal Communication and Its Role in Stroke
Yao, Z., Sun, X., Huang, J., Chen, L., & Dong, S. (2023) · Neurochemical Research · doi:10.1007/s11064-023-03966-0 · Cited by 16
Depletion of astrocytic transglutaminase 2 improves injury outcomes
Monteagudo, A., Feola, J., Natola, H., Ji, C., Pröschel, C., & Johnson, G. V. W. (2018) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2018.06.007 · Cited by 16
Combinatorial therapies for spinal cord injury: strategies to induce regeneration
Salgado, A., Gomes, E., & Silva, N. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.243705 · Cited by 16
Singhal, G., Morgan, J., Jawahar, M. C., Corrigan, F., Jaehne, E. J., Toben, C. G., Manavis, J., Hannan, A. J., & Baune, B. T. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00057 · Cited by 16
Reversing Glial Scar Back To Neural Tissue Through NeuroD1-Mediated Astrocyte-To-Neuron ConversionPreprint
Zhang, L., Lei, Z., Guo, Z., Pei, Z., Chen, Y.-C., Zhang, F., Cai, A., Mok, Y.-K., Lee, G., Swaminnathan, V., et al. (2018) · bioRxiv · doi:10.1101/261438 · Cited by 18
Temporal and spatial analysis of astrocytes following stroke identifies novel drivers of reactivityPreprint
Kim, R. D., Marchildon, A. E., Frazel, P. W., Hasel, P., Guo, A. X., & Liddelow, S. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.12.566710 · Cited by 18
Isaković, J., Gorup, D., & Mitrečić, D. (2019) · Croatian Medical Journal · doi:10.3325/cmj.2019.60.127 · Cited by 14
Relationships Among Gut Microbiota, Ischemic Stroke and Its Risk Factors: Based on Research Evidence
Huang, Q., Cai, G., Liu, T., & Liu, Z. (2022) · International Journal of General Medicine · doi:10.2147/ijgm.s353276 · Cited by 15
Regulation of Oxidative Stress by Long Non-coding RNAs in Central Nervous System Disorders
Xu, X., & Zhang, Y. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.931704 · Cited by 15
Li, H., He, B., Zhang, X., Hao, H., Yang, T., Sun, C., Song, H., Wang, Y., Zhu, Z., Hu, Y., et al. (2022) · Cell & Bioscience · doi:10.1186/s13578-022-00867-7 · Cited by 17
Liu, S., Lin, G., Yang, Q. L., Wang, P., Ma, C., Qian, X., He, X., Dong, Z., Liu, Y., Liu, M., et al. (2022) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13998 · Cited by 15
The role of purinergic receptors in neural repair and regeneration after spinal cord injury
Cheng, R., Ren, W., Luo, B., & Ye, X. (2022) · Neural Regeneration Research · doi:10.4103/1673-5374.363186 · Cited by 15
Zhang, W., Jia, M., Lian, J., Lu, S., Zhou, J., Fan, Z., Zhu, Z., He, Y., Huang, C., Zhu, M., et al. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14170 · Cited by 16
Models and approaches to comprehend and address glial inflammation following spinal cord injury
Patil, V., Bohara, R. A., Kanala, V. K., McMahon, S. S., & Pandit, A. S. (2023) · Drug Discovery Today · doi:10.1016/j.drudis.2023.103722 · Cited by 16
New role of astrocytes in neuroprotective mechanisms after ischemic stroke
Xie, X., & Liu, J. (2023) · Arquivos de Neuro-Psiquiatria · doi:10.1055/s-0043-1770352 · Cited by 16
Michalski, D., Pitsch, R., Pillai, D. R., Mages, B., Aleithe, S., Grosche, J., Martens, H., Schlachetzki, F., & Härtig, W. (2017) · PLOS ONE · doi:10.1371/journal.pone.0174996 · Cited by 15
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
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