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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Transcriptomic profiling shows that reactive astrocytes adopt distinct molecular states in different disease models, in different CNS regions, and in brain tumors.
“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]
The Extended Data compare RNA-seq profiles of spinal-cord-injury reactive astrocytes with previously reported forebrain stroke-reactive astrocytes; only 58.5% of the top elevated forebrain genes were also significantly elevated after spinal cord injury. This supports molecular differences between those contexts, but disease model and CNS region change together, so the paper does not establish distinct states attributable to region independently. The brain-tumor clause is attached to a different citation. (LLM, conf=0.83)
Experimental — accuracy not yet measuredReactive astrocytes are diverse, as demonstrated by transcriptomic profiling of mouse bulk astrocytes or preselected astrocyte populations.
“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]
Activation of STAT3-dependent transcription is beneficial in neonatal white matter injury, traumatic brain injury, spinal cord injury, and motor neuron injury, but detrimental in AD models.
“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 · see citing works
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 · see citing works
Robinson, M. D., McCarthy, D. J., & Smyth, G. K. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btp616 · Cited by 41,364 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Regeneration beyond the glial scar
Silver, J., & Miller, J. H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1326 · Cited by 3,090 · see citing works
Degeneration and Regeneration of the Nervous System.
(1929) · JAMA · doi:10.1001/jama.1929.02710220063037 · Cited by 2,920 · see citing works
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 · see citing works
David, S., & Aguayo, A. J. (1981) · Science · doi:10.1126/science.6171034 · Cited by 1,698 · see citing works
Reactive Astrocytes Protect Tissue and Preserve Function after Spinal Cord Injury
Faulkner, J., Herrmann, J., Woo, M. J., Tansey, K., Doan, N., & Sofroniew, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3547-03.2004 · Cited by 1,600 · see citing works
Self-citationMolecular Mechanisms of Axon Guidance
Dickson, B. J. (2002) · Science · doi:10.1126/science.1072165 · Cited by 1,431 · see citing works
Reactive Gliosis and the Multicellular Response to CNS Damage and Disease
Burda, J. E., & Sofroniew, M. V. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.034 · Cited by 1,431 · see citing works
Self-citationAstrocyte barriers to neurotoxic inflammation
Sofroniew, M. V. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3898 · Cited by 1,202 · see citing works
Self-citationNeuropilin Is a Receptor for the Axonal Chemorepellent Semaphorin III
He, Z., & Tessier‐Lavigne, M. (1997) · Cell · doi:10.1016/s0092-8674(00)80534-6 · Cited by 1,137 · see citing works
Bush, T. G., Puvanachandra, N., Horner, C. H., Polito, A., Ostenfeld, T., Svendsen, C. N., Mucke, L., Johnson, M. H., & Sofroniew, M. V. (1999) · Neuron · doi:10.1016/s0896-6273(00)80781-3 · Cited by 1,116 · see citing works
Self-citationDeleted in Colorectal Cancer (DCC) Encodes a Netrin Receptor
Keino‐Masu, K., Masu, M., Hinck, L., Leonardo, E. D., Chan, S. S.-Y., Culotti, J. G., & Tessier‐Lavigne, M. (1996) · Cell · doi:10.1016/s0092-8674(00)81336-7 · Cited by 1,013 · see citing works
Cell-type-specific isolation of ribosome-associated mRNA from complex tissues
Sanz, E., Yang, L., Su, T., Morris, D. R., McKnight, G. S., & Amieux, P. S. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0907143106 · Cited by 982 · see citing works
STAT3 is a Critical Regulator of Astrogliosis and Scar Formation after Spinal Cord Injury
Herrmann, J. E., Imura, T., Song, B., Qi, J., Ao, Y., Nguyen, T. K., Korsak, R. A., Takeda, K., Akira, S., & Sofroniew, M. V. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1709-08.2008 · Cited by 958 · see citing works
Self-citationAxons from CNS neurones regenerate into PNS grafts
Richardson, P. M., Mcguinness, U. M., & Aguayo, A. J. (1980) · Nature · doi:10.1038/284264a0 · Cited by 938 · see citing works
A Cre-inducible diphtheria toxin receptor mediates cell lineage ablation after toxin administration
Buch, T., Heppner, F. L., Tertilt, C., Heinen, T. J. A. J., Kremer, M., Wunderlich, F. T., Jung, S., & Waisman, A. (2005) · Nature Methods · doi:10.1038/nmeth762 · Cited by 922 · see citing works
Wanner, I. B., Anderson, M. A., Song, B., Levine, J., Fernandez, A., Gray-Thompson, Z., Ao, Y., & Sofroniew, M. V. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2121-13.2013 · Cited by 839 · see citing works
Self-citationRapidly recovering hydrogel scaffolds from self-assembling diblock copolypeptide amphiphiles
Nowak, A. P., Breedveld, V., Pakstis, L., Ozbas, B., Pine, D. J., Pochan, D. J., & Deming, T. J. (2002) · Nature · doi:10.1038/417424a · Cited by 809 · see citing works
Self-citationReversible Ponceau staining as a loading control alternative to actin in Western blots
Romero-Calvo, I., Ocón, B., Martínez-Moya, P., Suárez, M. D., Zarzuelo, A., Martínez-Augustin, O., & de Medina, F. S. (2010) · Analytical Biochemistry · doi:10.1016/j.ab.2010.02.036 · Cited by 771 · see citing works
Sustained axon regeneration induced by co-deletion of PTEN and SOCS3
Sun, F., Park, K. K., Belin, S., Wang, D., Lu, T., Chen, G., Zhang, K., Yeung, C., Feng, G., Yankner, B. A., et al. (2011) · Nature · doi:10.1038/nature10594 · Cited by 754 · see citing works
Neumann, S., & Woolf, C. J. (1999) · Neuron · doi:10.1016/s0896-6273(00)80755-2 · Cited by 659 · see citing works
Lecticans: organizers of the brain extracellular matrix
Yamaguchi, Y. (2000) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000690 · Cited by 642 · see citing works
Grill, R., Murai, K. K., Blesch, A., Gage, F. H., & Tuszynski, M. H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-14-05560.1997 · Cited by 619 · see citing works
Takeda, K., Kaisho, T., Yoshida, N., Takeda, J., Kishimoto, T., & Akira, S. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1500168 · Cited by 616 · see citing works
Kang, S. H., Li, Y., Fukaya, M., Lorenzini, I., Cleveland, D. W., Ostrow, L. W., Rothstein, J. D., & Bergles, D. E. (2013) · Nature Neuroscience · doi:10.1038/nn.3357 · Cited by 599 · see citing works
Tong, X., Ao, Y., Faas, G. C., Nwaobi, S. E., Xu, J., Haustein, M. D., Anderson, M. A., Mody, I., Olsen, M. L., Sofroniew, M. V., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3691 · Cited by 592 · see citing works
Self-citationFulminant Jejuno-Ileitis following Ablation of Enteric Glia in Adult Transgenic Mice
Bush, T. G., Savidge, T., Freeman, T. C., Cox, H. J., Campbell, E. A., Mucke, L., Johnson, M. H., & Sofroniew, M. V. (1998) · Cell · doi:10.1016/s0092-8674(00)81571-8 · Cited by 590 · see citing works
Self-citationTakeda, K., Kaisho, T., Yoshida, N., Takeda, J., Kishimoto, T., & Akira, S. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.161.9.4652 · Cited by 584 · see citing works
The netrin receptor UNC5B mediates guidance events controlling morphogenesis of the vascular system
Lu, X., le Noble, F. A. C., Li, Y., Jiang, Q., de Lafarge, B., Sugiyama, D., Bréant, C., Claes, F., Smet, F. D., Thomas, J., et al. (2004) · Nature · doi:10.1038/nature03080 · Cited by 550 · see citing works
Biosynthesis and function of chondroitin sulfate
Mikami, T., & Kitagawa, H. (2013) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.06.006 · Cited by 505 · see citing works
Peripheral injury enhances central regeneration of primary sensory neurones
Richardson, P. M., & Issa, V. M. K. (1984) · Nature · doi:10.1038/309791a0 · Cited by 494 · see citing works
NEURAL CELL ADHESION MOLECULES OF THE IMMUNOGLOBULIN SUPERFAMILY: Role in Axon Growth and Guidance
Walsh, F. S., & Doherty, P. (1997) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.13.1.425 · Cited by 476 · see citing works
Plexin A Is a Neuronal Semaphorin Receptor that Controls Axon Guidance
Winberg, M. L., Noordermeer, J. N., Tamagnone, L., Comoglio, P. M., Spriggs, M. K., Tessier‐Lavigne, M., & Goodman, C. S. (1998) · Cell · doi:10.1016/s0092-8674(00)81715-8 · Cited by 470 · see citing works
Modulation of the proteoglycan receptor PTPσ promotes recovery after spinal cord injury
Lang, B. T., Cregg, J. M., DePaul, M. A., Tran, A. P., Xu, K., Dyck, S. M., Madalena, K. M., Brown, B. P., Weng, Y.-L., Li, S., et al. (2015) · Nature · doi:10.1038/nature13974 · Cited by 465 · see citing works
Neuronal Intrinsic Mechanisms of Axon Regeneration
Liu, K., Tedeschi, A., Park, K. K., & He, Z. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113723 · Cited by 458 · see citing works
Friedlander, D. R., Milev, P., Karthikeyan, L., Margolis, R. K., Margolis, R. U., & Grumet, M. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.125.3.669 · Cited by 454 · see citing works
Retinal Ganglion Cells Do Not Extend Axons by Default
Goldberg, J. L., Espinosa, J. S., Xu, Y., Davidson, N., Kovacs, G. T. A., & Barres, B. A. (2002) · Neuron · doi:10.1016/s0896-6273(02)00602-5 · Cited by 452 · see citing works
Systemic administration of epothilone B promotes axon regeneration after spinal cord injury
Ruschel, J., Hellal, F., Flynn, K. C., Dupraz, S., Elliott, D. A., Tedeschi, A., Bates, M., Sliwinski, C., Brook, G. A., Dobrindt, K., et al. (2015) · Science · doi:10.1126/science.aaa2958 · Cited by 433 · see citing works
Astrocytes Block Axonal Regeneration in Mammals by Activating the Physiological Stop Pathway
Liuzzi, F. J., & Lasek, R. J. (1987) · Science · doi:10.1126/science.3603044 · Cited by 401 · see citing works
Functions of Nogo proteins and their receptors in the nervous system
Schwab, M. E. (2010) · Nature reviews. Neuroscience · doi:10.1038/nrn2936 · Cited by 378 · see citing works
Shigetomi, E., Bushong, E. A., Haustein, M. D., Tong, X., Jackson‐Weaver, O., Kracun, S., Xu, J. P., Sofroniew, M. V., Ellisman, M. H., & Khakh, B. S. (2013) · The Journal of General Physiology · doi:10.1085/jgp.201210949 · Cited by 378 · see citing works
Self-citationBDNF-expressing marrow stromal cells support extensive axonal growth at sites of spinal cord injury
Lu, P., JONES, L., & Tuszynski, M. H. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.09.018 · Cited by 375 · see citing works
IGF-I specifically enhances axon outgrowth of corticospinal motor neurons
Özdinler, P. H., & Macklis, J. D. (2006) · Nature Neuroscience · doi:10.1038/nn1789 · Cited by 341 · see citing works
Concepts and Methods for the Study of Axonal Regeneration in the CNS
Tuszynski, M. H., & Steward, O. (2012) · Neuron · doi:10.1016/j.neuron.2012.05.006 · Cited by 305 · see citing works
Can regenerating axons recapitulate developmental guidance during recovery from spinal cord injury?
Harel, N. Y., & Strittmatter, S. M. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1957 · Cited by 297 · see citing works
RGM is a repulsive guidance molecule for retinal axons
Monnier, P. P., Sierra, A., Macchi, P., Deitinghoff, L., Andersen, J., Mann, M., Flad, M., Hornberger, M. R., Stahl, B., Bonhoeffer, F., et al. (2002) · Nature · doi:10.1038/nature01041 · Cited by 293 · see citing works
Zukor, K., Belin, S., Wang, C., Keelan, N., Wang, X., & He, Z. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2510-13.2013 · Cited by 281 · see citing works
Neogenin mediates the action of repulsive guidance molecule
Rajagopalan, S., Deitinghoff, L., Davis, D., Conrad, S., Skutella, T., Chédotal, A., Mueller, B. K., & Strittmatter, S. M. (2004) · Nature Cell Biology · doi:10.1038/ncb1156 · Cited by 276 · see citing works
Avnur, Z., & Geiger, B. (1984) · Cell · doi:10.1016/0092-8674(84)90276-9 · Cited by 265 · see citing works
Herde, A. M., Hauk, T. G., & Fischer, D. (2007) · Brain · doi:10.1093/brain/awm257 · Cited by 249 · see citing works
Contrasting the Glial Response to Axon Injury in the Central and Peripheral Nervous Systems
Lutz, A. B., & Barres, B. A. (2014) · Developmental Cell · doi:10.1016/j.devcel.2013.12.002 · Cited by 229 · see citing works
Chemotropic guidance facilitates axonal regeneration and synapse formation after spinal cord injury
Alto, L. T., Havton, L. A., Conner, J. M., Hollis, E. R., II, Blesch, A., & Tuszynski, M. H. (2009) · Nature Neuroscience · doi:10.1038/nn.2365 · Cited by 212 · see citing works
Hu, H., Marton, T. F., & Goodman, C. S. (2001) · Neuron · doi:10.1016/s0896-6273(01)00453-6 · Cited by 207 · see citing works
Regeneration of Axons in the Vertebrate Central Nervous System
Windle, W. F. (1956) · Physiological Reviews · doi:10.1152/physrev.1956.36.4.427 · Cited by 200 · see citing works
Leukemia Inhibitory Factor Determines the Growth Status of Injured Adult Sensory Neurons
Cafferty, W. B. J., Gardiner, N. J., Gavazzi, I., Powell, J., McMahon, S. B., Heath, J. K., Munson, J. B., Cohen, J., & Thompson, S. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-18-07161.2001 · Cited by 199 · see citing works
Astrocyte-Associated Fibronectin Is Critical for Axonal Regeneration in Adult White Matter
Tom, V. J., Doller, C. M., Malouf, A. T., & Silver, J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2120-04.2004 · Cited by 189 · see citing works
Kawaja, M. D., & Gage, F. H. (1991) · Neuron · doi:10.1016/0896-6273(91)90346-2 · Cited by 185 · see citing works
Local translation and directional steering in axons
Lin, A. C., & Holt, C. E. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601808 · Cited by 184 · see citing works
Blesch, A., & Tuszynski, M. H. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10934 · Cited by 179 · see citing works
Busch, S. A., Horn, K. P., Cuascut, F. X., Hawthorne, A. L., Bai, L., Miller, R. H., & Silver, J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3705-09.2010 · Cited by 179 · see citing works
Draxin, a Repulsive Guidance Protein for Spinal Cord and Forebrain Commissures
Islam, S. M., Shinmyo, Y., Okafuji, T., Su, Y., Naser, I. B., Ahmed, G., Zhang, S., Chen, S., Ohta, K., Kiyonari, H., et al. (2009) · Science · doi:10.1126/science.1165187 · Cited by 179 · see citing works
Collagen Matrix in Spinal Cord Injury
Klapka, N., & Müller, H. W. (2006) · Journal of Neurotrauma · doi:10.1089/neu.2006.23.422 · Cited by 173 · see citing works
α9 Integrin Promotes Neurite Outgrowth on Tenascin-C and Enhances Sensory Axon Regeneration
Andrews, M. R., Czvitkovich, S., Dassie, E., Vogelaar, C. F., Faissner, A., Blits, B., Gage, F. H., ffrench‐Constant, C., & Fawcett, J. W. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0759-09.2009 · Cited by 161 · see citing works
Axon regeneration through scars and into sites of chronic spinal cord injury
Lu, P., Jones, L. L., & Tuszynski, M. H. (2006) · Experimental Neurology · doi:10.1016/j.expneurol.2006.07.030 · Cited by 155 · see citing works
Blesch, A., Uy, H. S., Grill, R., Cheng, J.-G., Patterson, P. H., & Tuszynski, M. H. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-09-03556.1999 · Cited by 154 · see citing works
Axonal growth therapeutics: regeneration or sprouting or plasticity?
Cafferty, W. B. J., McGee, A. W., & Strittmatter, S. M. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.02.004 · Cited by 151 · see citing works
Windle, W. F., Clemente, C., & Chambers, W. W. (1952) · The Journal of Comparative Neurology · doi:10.1002/cne.900960207 · Cited by 146 · see citing works
Götz, B., Scholze, A., Clement, A. M., Joester, A., Schütte, K., Wigger, F., Frank, R. W., Spieß, E., Ekblom, P., & Faissner, A. (1996) · The Journal of Cell Biology · doi:10.1083/jcb.132.4.681 · Cited by 140 · see citing works
Biocompatibility of amphiphilic diblock copolypeptide hydrogels in the central nervous system
Yang, C.-Y., Song, B., Ao, Y., Nowak, A. P., Abelowitz, R. B., Korsak, R. A., Havton, L. A., Deming, T. J., & Sofroniew, M. V. (2009) · Biomaterials · doi:10.1016/j.biomaterials.2009.01.056 · Cited by 139 · see citing works
Self-citationSzebenyi, G., Dent, E. W., Callaway, J. L., Seys, C. W., Lueth, H., & Kalil, K. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-11-03932.2001 · Cited by 136 · see citing works
NG2 Glial Cells Provide a Favorable Substrate for Growing Axons
Yang, Z., Suzuki, R., Daniels, S. B., Brunquell, C. B., Sala, C. J., & Nishiyama, A. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4247-05.2006 · Cited by 123 · see citing works
Galectin-1 Regulates Initial Axonal Growth in Peripheral Nerves after Axotomy
Horie, H., Inagaki, Y., Sohma, Y., Nozawa, R., Okawa, K., Hasegawa, M., Muramatsu, N., Kawano, H., Horie, M., Koyama, H., et al. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-22-09964.1999 · Cited by 120 · see citing works
Integrin-laminin interactions controlling neurite outgrowth from adult DRG neurons in vitro
Plantman, S., Patarroyo, M. E., Fried, K., Domogatskaya, A., Tryggvason, K., Hammarberg, H., & Cullheim, S. (2008) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2008.05.015 · Cited by 117 · see citing works
Hawthorne, A. L., Hu, H., Kundu, B., Steinmetz, M. P., Wylie, C. J., Deneris, E. S., & Silver, J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6663-10.2011 · Cited by 113 · see citing works
Robust Axonal Regeneration Occurs in the Injured CAST/Ei Mouse CNS
Omura, T., Omura, K., Tedeschi, A., Riva, P., Painter, M. W., Rojas, L., Martin, J., Lisi, V., Huebner, E. A., Latrémolière, A., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.005 · Cited by 110 · see citing works
Self-citationHill, J. J., Jin, K., Mao, X., Xie, L., & Greenberg, D. A. (2012) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1205697109 · Cited by 99 · see citing works
Miller, G. M., & Hsieh‐Wilson, L. C. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.08.015 · Cited by 98 · see citing works
Draxin Inhibits Axonal Outgrowth through the Netrin Receptor DCC
Ahmed, G., Shinmyo, Y., Ohta, K., Islam, S. M., Hossain, M., Naser, I. B., Riyadh, M. A., Su, Y., Zhang, S., Tessier‐Lavigne, M., et al. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0943-11.2011 · Cited by 97 · see citing works
Song, B., Song, J., Zhang, S., Anderson, M. A., Ao, Y., Yang, C.-Y., Deming, T. J., & Sofroniew, M. V. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.08.060 · Cited by 94 · see citing works
Self-citationMason, C. A., Edmondson, J., & Hatten, M. E. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-09-03124.1988 · Cited by 93 · see citing works
Lee, J. K., Chow, R., Xie, F., Chow, S. Y., Tolentino, K. E., & Zheng, B. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2269-10.2010 · Cited by 77 · see citing works
Where no synapses go: gatekeepers of circuit remodeling and synaptic strength
Mironova, Y. A., & Giger, R. J. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.04.003 · Cited by 75 · see citing works
SLITRK1 Binds 14-3-3 and Regulates Neurite Outgrowth in a Phosphorylation-Dependent Manner
Kajiwara, Y., Buxbaum, J. D., & Grice, D. E. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.05.033 · Cited by 73 · see citing works
White, R., Yin, F. Q., & Jakeman, L. B. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2008.06.012 · Cited by 71 · see citing works
Astroglial-Derived Periostin Promotes Axonal Regeneration after Spinal Cord Injury
Shih, C., Lacagnina, M., Leuer-Bisciotti, K., & Pröschel, C. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2947-13.2014 · Cited by 70 · see citing works
Decorin promotes robust axon growth on inhibitory CSPGs and myelin via a direct effect on neurons
Minor, K. H., Tang, X., Kahrilas, G. A., Archibald, S. J., Davies, J. E., & Davies, S. J. A. (2008) · Neurobiology of Disease · doi:10.1016/j.nbd.2008.06.009 · Cited by 64 · see citing works
Nakanishi, K., Aono, S., Hirano, K., Kuroda, Y., Ida‐Eto, M., Tokita, Y., Matsui, F., & Oohira, A. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m601498200 · Cited by 58 · see citing works
Syndecan Promotes Axon Regeneration by Stabilizing Growth Cone Migration
Edwards, T. J., & Hammarlund, M. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.06.008 · Cited by 57 · see citing works
Netrin-1 Acts as a Repulsive Guidance Cue for Sensory Axonal Projections toward the Spinal Cord
Masuda, T., Watanabe, K., Sakuma, C., Ikenaka, K., Ono, K., & Yaginuma, H. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1926-08.2008 · Cited by 57 · see citing works
Sango, K., Oohira, A., Ajiki, K., Tokashiki, A., Horie, M., & Kawano, H. (2003) · Experimental Neurology · doi:10.1016/s0014-4886(03)00090-6 · Cited by 55 · see citing works
The extracellular-matrix protein matrilin 2 participates in peripheral nerve regeneration
Malin, D., Sonnenberg-Riethmacher, E., Guseva, D., Wagener, R., Aszódi, A., Irintchev, A., & Riethmacher, D. (2009) · Journal of Cell Science · doi:10.1242/jcs.040378 · Cited by 54 · see citing works
Tenascin-R as a Repellent Guidance Molecule for Developing Optic Axons in Zebrafish
Becker, C. G., Schweitzer, J., Feldner, J., Becker, T., & Schachner, M. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-15-06232.2003 · Cited by 51 · see citing works
Hossain-Ibrahim, M. K., Rezajooi, K., Stallcup, W. B., Lieberman, A. R., & Anderson, P. N. (2007) · BMC Neuroscience · doi:10.1186/1471-2202-8-80 · Cited by 50 · see citing works
Zhang, S., Anderson, M. A., Ao, Y., Khakh, B. S., Fan, J. H., Deming, T. J., & Sofroniew, M. V. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.11.005 · Cited by 48 · see citing works
Self-citationThermoresponsive Copolypeptide Hydrogel Vehicles for Central Nervous System Cell Delivery
Zhang, S., Burda, J. E., Anderson, M. A., Zhao, Z., Ao, Y., Cheng, Y., Sun, Y. E., Deming, T. J., & Sofroniew, M. V. (2015) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.5b00153 · Cited by 40 · see citing works
Self-citationHurtado, A., Podinin, H., Oudega, M., & Grimpe, B. (2008) · Brain · doi:10.1093/brain/awn206 · Cited by 37 · see citing works
Perlecan Antagonizes Collagen IV and ADAMTS9/GON-1 in Restricting the Growth of Presynaptic Boutons
Qin, J., Liang, J., & Ding, M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.5128-13.2014 · Cited by 36 · see citing works
Farhy-Tselnicker, I., Boisvert, M., & Allen, N. J. (2014) · Biochemical Society Transactions · doi:10.1042/bst20140166 · Cited by 34 · see citing works
Jiang, R., Haustein, M. D., Sofroniew, M. V., & Khakh, B. S. (2014) · Journal of Visualized Experiments · doi:10.3791/51972 · Cited by 25 · see citing works
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- [47]Zhang S Thermoresponsive copolypeptide hydrogel vehicles for CNS cell delivery ACS Biomat Sci Eng 1 705 717 2015 PMC4991036 27547820
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Neurotoxic reactive astrocytes are induced by activated microglia
Liddelow, S. A., Guttenplan, K. A., Clarke, L. E., Bennett, F. C., Bohlen, C. J., Schirmer, L., Bennett, M. L., Münch, A. E., Chung, W.-S., Peterson, T. C., et al. (2017) · Nature · doi:10.1038/nature21029 · Cited by 7,971 · see citing works
Reactive astrocyte nomenclature, definitions, and future directions
Escartin, C., Galea, E., Lakatos, A., O’Callaghan, J. P., Petzold, G. C., Serrano-Pozo, A., Steinhäuser, C., Volterra, A., Carmignoto, G., Agarwal, A., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-020-00783-4 · Cited by 2,533 · see citing works
Self-citationAhuja, C. S., Wilson, J. R., Nori, S., Kotter, M. R. N., Druschel, C., Curt, A., & Fehlings, M. G. (2017) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2017.18 · Cited by 2,441 · see citing works
Reactive Astrocytes: Production, Function, and Therapeutic Potential
Liddelow, S. A., & Barres, B. A. (2017) · Immunity · doi:10.1016/j.immuni.2017.06.006 · Cited by 2,336 · see citing works
Traumatic Spinal Cord Injury: An Overview of Pathophysiology, Models and Acute Injury Mechanisms
Alizadeh, A., Dyck, S. M., & Karimi‐Abdolrezaee, S. (2019) · Frontiers in Neurology · doi:10.3389/fneur.2019.00282 · Cited by 1,447 · see citing works
Normal aging induces A1-like astrocyte reactivity
Clarke, L. E., Liddelow, S. A., Chakraborty, C., Münch, A. E., Heiman, M., & Barres, B. A. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1800165115 · Cited by 1,237 · see citing works
Microglial control of astrocytes in response to microbial metabolites
Rothhammer, V., Borucki, D. M., Tjon, E. C., Takenaka, M. C., Chao, C.-C., Ardura-Fabregat, A., de Lima, K. A., Gutiérrez-Vázquez, C., Hewson, P., Staszewski, O., et al. (2018) · Nature · doi:10.1038/s41586-018-0119-x · Cited by 1,051 · see citing works
Confronting false discoveries in single-cell differential expression
Squair, J. W., Gautier, M., Kathe, C., Anderson, M. A., James, N. D., Hutson, T. H., Hudelle, R., Qaiser, T., Matson, K. J. E., Barraud, Q., et al. (2021) · doi:10.1101/2021.03.12.435024 · Cited by 1,017 · see citing works
Self-citationAstrocyte Crosstalk in CNS Inflammation
Linnerbauer, M., Wheeler, M. A., & Quintana, F. J. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.012 · Cited by 989 · see citing works
Cell transplantation therapy for spinal cord injury
Assinck, P., Duncan, G. J., Hilton, B. J., Plemel, J. R., & Tetzlaff, W. (2017) · Nature Neuroscience · doi:10.1038/nn.4541 · Cited by 941 · see citing works
Astrocytes: Key Regulators of Neuroinflammation
Colombo, E., & Farina, C. (2016) · Trends in Immunology · doi:10.1016/j.it.2016.06.006 · Cited by 901 · see citing works
The Biology of Regeneration Failure and Success After Spinal Cord Injury
Tran, A. P., Warren, P. M., & Silver, J. (2018) · Physiological Reviews · doi:10.1152/physrev.00017.2017 · Cited by 883 · see citing works
Spinal cord injury: molecular mechanisms and therapeutic interventions
Hu, X., Xu, W., Ren, Y., Wang, Z., He, X., Huang, R., Ma, B., Zhao, J., Zhu, R., & Cheng, L. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01477-6 · Cited by 823 · see citing works
Self-citationBrain regulatory T cells suppress astrogliosis and potentiate neurological recovery
Ito, M., Komai, K., Mise-Omata, S., Iizuka-Koga, M., Noguchi, Y., Kondo, T., Sakai, R., Matsuo, K., Nakayama, T., Yoshie, O., et al. (2019) · Nature · doi:10.1038/s41586-018-0824-5 · Cited by 784 · see citing works
Moving beyond the glial scar for spinal cord repair
Bradbury, E. J., & Burnside, E. R. (2019) · Nature Communications · doi:10.1038/s41467-019-11707-7 · Cited by 748 · see citing works
Astrocyte Reactivity: Subtypes, States, and Functions in CNS Innate Immunity
Sofroniew, M. V. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.07.004 · Cited by 721 · see citing works
Self-citationBiomimetic 3D-printed scaffolds for spinal cord injury repair
Koffler, J. Y., Zhu, W. Z., Qu, X., Platoshyn, O., Dulin, J. N., Brock, J., Graham, L., Lu, P., Sakamoto, J. S., Maršala, M., et al. (2019) · Nature Medicine · doi:10.1038/s41591-018-0296-z · Cited by 715 · see citing works
Function and therapeutic value of astrocytes in neurological diseases
Lee, H.-G., Wheeler, M. A., & Quintana, F. J. (2022) · Nature Reviews Drug Discovery · doi:10.1038/s41573-022-00390-x · Cited by 662 · see citing works
The Role of Astrocytes in CNS Inflammation
Giovannoni, F., & Quintana, F. J. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.07.007 · Cited by 651 · see citing works
Neuronal vulnerability and multilineage diversity in multiple sclerosis
Schirmer, L., Velmeshev, D., Holmqvist, S., Kaufmann, M., Werneburg, S., Jung, D., Vistnes, S., Stockley, J. H., Young, A., Steindel, M., et al. (2019) · Nature · doi:10.1038/s41586-019-1404-z · Cited by 638 · see citing works
Functional diversity of astrocytes in neural circuit regulation
Haim, L. B., & Rowitch, D. H. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.159 · Cited by 618 · see citing works
Cell biology of spinal cord injury and repair
O’Shea, T. M., Burda, J. E., & Sofroniew, M. V. (2017) · Journal of Clinical Investigation · doi:10.1172/jci90608 · Cited by 590 · see citing works
Self-citationInteraction of Microglia and Astrocytes in the Neurovascular Unit
Liu, L., Liu, J., Bao, J.-S., Bai, Q.-Q., & Wang, G. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01024 · Cited by 591 · see citing works
Spinal Cord Injury Scarring and Inflammation: Therapies Targeting Glial and Inflammatory Responses
Orr, M. B., & Gensel, J. C. (2018) · Neurotherapeutics · doi:10.1007/s13311-018-0631-6 · Cited by 584 · see citing works
Microglia-Astrocyte Crosstalk: An Intimate Molecular Conversation
Jha, M. K., Jo, M., Kim, J.-H., & Suk, K. (2019) · The Neuroscientist · doi:10.1177/1073858418783959 · Cited by 579 · see citing works
Hara, M., Kobayakawa, K., Ohkawa, Y., Kumamaru, H., Yokota, K., Saito, T., Kijima, K., Yoshizaki, S., Harimaya, K., Nakashima, Y., et al. (2017) · Nature Medicine · doi:10.1038/nm.4354 · Cited by 539 · see citing works
Microenvironment Imbalance of Spinal Cord Injury
Fan, B., Wei, Z., Yao, X. X., Shi, G., Cheng, X., Zhou, X., Zhou, H., Ning, G., Kong, X., & Feng, S. (2018) · Cell Transplantation · doi:10.1177/0963689718755778 · Cited by 538 · see citing works
Inflammation: the link between comorbidities, genetics, and Alzheimer’s disease
Newcombe, E. A., Camats-Perna, J., Silva, M. L., Valmas, N., Huat, T. J., & Medeiros, R. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1313-3 · Cited by 532 · see citing works
Required growth facilitators propel axon regeneration across complete spinal cord injury
Anderson, M. A., O’Shea, T. M., Burda, J. E., Ao, Y., Barlatey, S. L., Bernstein, A. M., Kim, J. H., James, N. D., Rogers, A. D., Kato, B., et al. (2018) · Nature · doi:10.1038/s41586-018-0467-6 · Cited by 528 · see citing works
Self-citationFunctional roles of reactive astrocytes in neuroinflammation and neurodegeneration
Patani, R., Hardingham, G. E., & Liddelow, S. A. (2023) · Nature Reviews Neurology · doi:10.1038/s41582-023-00822-1 · Cited by 531 · see citing works
Neuroinflammation in the central nervous system: Symphony of glial cells
Yang, Q., & Zhou, J. (2018) · Glia · doi:10.1002/glia.23571 · Cited by 520 · see citing works
Spinal cord repair: advances in biology and technology
Courtine, G., & Sofroniew, M. V. (2019) · Nature Medicine · doi:10.1038/s41591-019-0475-6 · Cited by 508 · see citing works
Self-citationMAFG-driven astrocytes promote CNS inflammation
Wheeler, M. A., Clark, I. C., Tjon, E. C., Li, Z., Zandee, S. E. J., Couturier, C. P., Watson, B. R., Scalisi, G., Alkwai, S., Rothhammer, V., et al. (2020) · Nature · doi:10.1038/s41586-020-1999-0 · Cited by 501 · see citing works
Molecular characterization of selectively vulnerable neurons in Alzheimer’s disease
Leng, K., Li, E., Eser, R., Piergies, A., Sit, R., Tan, M., Neff, N., Li, S. H., Rodriguez, R. D., Suemoto, C. K., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-020-00764-7 · Cited by 485 · see citing works
STAT3 labels a subpopulation of reactive astrocytes required for brain metastasis
Priego, N., Zhu, L., Monteiro, C., Mulders, M., Wasilewski, D., Bindeman, W., Doglio, L., Martínez, L., Martínez-Saez, E., Ramón y Cajal, S., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0044-4 · Cited by 452 · see citing works
Crosstalk Between Astrocytes and Microglia: An Overview
Matejuk, A., & Ransohoff, R. M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01416 · Cited by 445 · see citing works
Henrik Heiland, D., Ravi, V. M., Behringer, S. P., Frenking, J. H., Wurm, J., Joseph, K., Garrelfs, N. W. C., Strähle, J., Heynckes, S., Grauvogel, J., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-10493-6 · Cited by 437 · see citing works
Oligodendrocyte, Astrocyte, and Microglia Crosstalk in Myelin Development, Damage, and Repair
Domingues, H. S., Portugal, C. C., Socodato, R., & Relvas, J. B. (2016) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2016.00071 · Cited by 438 · see citing works
Roles of neuropathology-associated reactive astrocytes: a systematic review
Lawrence, J. M., Schardien, K., Wigdahl, B., & Nonnemacher, M. R. (2023) · Acta Neuropathologica Communications · doi:10.1186/s40478-023-01526-9 · Cited by 433 · see citing works
Astrocytes in human central nervous system diseases: a frontier for new therapies
Verkhratsky, A., Butt, A., Li, B., Illes, P., Zorec, R., Semyanov, A., Tang, Y., & Sofroniew, M. V. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01628-9 · Cited by 428 · see citing works
Self-citationThe diversity and disparity of the glial scar
Adams, K. L., & Gallo, V. (2017) · Nature Neuroscience · doi:10.1038/s41593-017-0033-9 · Cited by 423 · see citing works
Reactive astrocytes function as phagocytes after brain ischemia via ABCA1-mediated pathway
Morizawa, Y. M., Hirayama, Y., Ohno, N., Shibata, S., Shigetomi, E., Sui, Y., Nabekura, J., Sato, K., Okajima, F., Takebayashi, H., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00037-1 · Cited by 411 · see citing works
Synthetic polypeptides: from polymer design to supramolecular assembly and biomedical application
Song, Z., Han, Z., Lv, S., Chen, C., Chen, L., Yin, L., & Cheng, J. (2017) · Chemical Society Reviews · doi:10.1039/c7cs00460e · Cited by 407 · see citing works
The soft mechanical signature of glial scars in the central nervous system
Moeendarbary, E., Weber, I. P., Sheridan, G. K., Koser, D. E., Soleman, S., Haenzi, B., Bradbury, E. J., Fawcett, J. W., & Franze, K. (2017) · Nature Communications · doi:10.1038/ncomms14787 · Cited by 408 · see citing works
Rat models of spinal cord injury: from pathology to potential therapies
Kjell, J., & Olson, L. (2016) · Disease Models & Mechanisms · doi:10.1242/dmm.025833 · Cited by 408 · see citing works
Immune cell regulation of glia during CNS injury and disease
Greenhalgh, A. D., David, S., & Bennett, F. C. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-0263-9 · Cited by 398 · see citing works
Reducing Pericyte-Derived Scarring Promotes Recovery after Spinal Cord Injury
Dias, D. O., Kim, H., Holl, D., Solnestam, B. W., Lundeberg, J., Carlén, M., Göritz, C., & Frisén, J. (2018) · Cell · doi:10.1016/j.cell.2018.02.004 · Cited by 396 · see citing works
High complement levels in astrocyte‐derived exosomes of Alzheimer disease
Goetzl, E. J., Schwartz, J. B., Abner, E. L., Jicha, G. A., & Kapogiannis, D. (2018) · Annals of Neurology · doi:10.1002/ana.25172 · Cited by 369 · see citing works
Astrocyte Heterogeneity: Impact to Brain Aging and Disease
Matias, I., Morgado, J., & Gomes, F. C. A. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00059 · Cited by 387 · see citing works
Dissecting spinal cord regeneration
Sofroniew, M. V. (2018) · Nature · doi:10.1038/s41586-018-0068-4 · Cited by 358 · see citing works
Self-citationShinozaki, Y., Shibata, K., Yoshida, K., Shigetomi, E., Gachet, C., Ikenaka, K., Tanaka, K. F., & Koizumi, S. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.04.047 · Cited by 341 · see citing works
Hyperactivity with Disrupted Attention by Activation of an Astrocyte Synaptogenic Cue
Nagai, J., Rajbhandari, A. K., Gangwani, M. R., Hachisuka, A., Coppola, G., Masmanidis, S. C., Fanselow, M. S., & Khakh, B. S. (2019) · Cell · doi:10.1016/j.cell.2019.03.019 · Cited by 322 · see citing works
Self-citationHe, X., Li, Y., Deng, B., Lin, A., Zhang, G., Ma, M., Wang, Y., Yang, Y., & Kang, X. (2022) · Cell Proliferation · doi:10.1111/cpr.13275 · Cited by 329 · see citing works
Regulation of axonal regeneration after mammalian spinal cord injury
Zheng, B., & Tuszynski, M. H. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00562-y · Cited by 328 · see citing works
Dual-function injectable angiogenic biomaterial for the repair of brain tissue following stroke
Nih, L. R., Gojgini, S., Carmichael, S. T., & Segura, T. (2018) · Nature Materials · doi:10.1038/s41563-018-0083-8 · Cited by 325 · see citing works
An update on reactive astrocytes in chronic pain
Li, T., Chen, X., Zhang, C., Zhang, Y., & Yao, W. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1524-2 · Cited by 318 · see citing works
Central nervous system regeneration
Varadarajan, S. G., Hunyara, J. L., Hamilton, N. R., Kolodkin, A. L., & Huberman, A. D. (2022) · Cell · doi:10.1016/j.cell.2021.10.029 · Cited by 312 · see citing works
Cahill, T. J., Choudhury, R. P., & Riley, P. R. (2017) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2017.106 · Cited by 309 · see citing works
Inflammation after Ischemic Stroke: The Role of Leukocytes and Glial Cells
Kim, J. Y., Park, J., Chang, J. Y., Kim, S.-H., & Lee, J. E. (2016) · Experimental Neurobiology · doi:10.5607/en.2016.25.5.241 · Cited by 311 · see citing works
The Evolving Landscape of Brain Metastasis
Valiente, M., Ahluwalia, M. S., Boire, A. A., Brastianos, P. K., Goldberg, S. B., Lee, E. Q., Rhun, É. L., Preusser, M., Winkler, F., & Soffietti, R. (2018) · Trends in cancer · doi:10.1016/j.trecan.2018.01.003 · Cited by 310 · see citing works
A1/A2 astrocytes in central nervous system injuries and diseases: Angels or devils?
Fan, Y., & Huo, J. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105080 · Cited by 310 · see citing works
The translational landscape in spinal cord injury: focus on neuroplasticity and regeneration
Hutson, T. H., & Giovanni, S. D. (2019) · Nature Reviews Neurology · doi:10.1038/s41582-019-0280-3 · Cited by 305 · see citing works
Improved tools to study astrocytes
Yu, X., Nagai, J., & Khakh, B. S. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-0264-8 · Cited by 298 · see citing works
Self-citationLoría, F., Vargas, J., Bousset, L., Syan, S., Salles, A., Melki, R., & Zurzolo, C. (2017) · Acta Neuropathologica · doi:10.1007/s00401-017-1746-2 · Cited by 278 · see citing works
Single-cell analysis of the cellular heterogeneity and interactions in the injured mouse spinal cord
Milich, L. M., Choi, J. S., Ryan, C. B., Cerqueira, S. R., Benavides, S., Yahn, S. L., Tsoulfas, P., & Lee, J. K. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20210040 · Cited by 285 · see citing works
Barcoded viral tracing of single-cell interactions in central nervous system inflammation
Clark, I. C., Gutiérrez-Vázquez, C., Wheeler, M. A., Li, Z., Rothhammer, V., Linnerbauer, M., Sanmarco, L. M., Guo, L., Blain, M., Zandee, S. E. J., et al. (2021) · Science · doi:10.1126/science.abf1230 · Cited by 285 · see citing works
Li, L., Acioglu, C., Heary, R. F., & Elkabes, S. (2021) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2020.10.007 · Cited by 283 · see citing works
Astrocyte senescence: Evidence and significance
Cohen, J., & Torres, C. (2019) · Aging Cell · doi:10.1111/acel.12937 · Cited by 281 · see citing works
Questions and (some) answers on reactive astrocytes
Escartin, C., Guillemaud, O., & Carrillo‐de Sauvage, M. (2019) · Glia · doi:10.1002/glia.23687 · Cited by 275 · see citing works
Zhou, X., Wahane, S., Friedl, M.-S., Kluge, M., Friedel, C. C., Avrampou, K., Zachariou, V., Guo, L., Zhang, B., He, X., et al. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0597-7 · Cited by 275 · see citing works
Cell type prioritization in single-cell data
Skinnider, M. A., Squair, J. W., Kathe, C., Anderson, M. A., Gautier, M., Matson, K. J. E., Milano, M., Hutson, T. H., Barraud, Q., Phillips, A. A., et al. (2021) · Nature Biotechnology · doi:10.1038/s41587-020-0605-1 · Cited by 274 · see citing works
Self-citationInjury-induced ctgfa directs glial bridging and spinal cord regeneration in zebrafish
Mokalled, M. H., Patra, C., Dickson, A. L., Endo, T., Stainier, D. Y. R., & Poss, K. D. (2016) · Science · doi:10.1126/science.aaf2679 · Cited by 266 · see citing works
Li, C., Wu, Z., Zhou, L., Shao, J., Hu, X., Xu, W., Ren, Y., Zhu, X., Ge, W., Zhang, K., et al. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-00885-4 · Cited by 266 · see citing works
Self-citationAstrocytes are necessary for blood–brain barrier maintenance in the adult mouse brain
Heithoff, B. P., George, K. K., Phares, A. N., Zuidhoek, I. A., Muñoz‐Ballester, C., & Robel, S. (2020) · Glia · doi:10.1002/glia.23908 · Cited by 256 · see citing works
Ceyzériat, K., Ben Haim, L., Denizot, A., Pommier, D., Matos, M., Guillemaud, O., Palomares, M.-A., Abjean, L., Petit, F., Gipchtein, P., et al. (2018) · Acta Neuropathologica Communications · doi:10.1186/s40478-018-0606-1 · Cited by 256 · see citing works
Environmental Control of Astrocyte Pathogenic Activities in CNS Inflammation
Wheeler, M. A., Jaronen, M., Covacu, R., Zandee, S., Scalisi, G., Rothhammer, V., Tjon, E. C., Chao, C., Kenison, J. E., Blain, M., et al. (2019) · Cell · doi:10.1016/j.cell.2018.12.012 · Cited by 250 · see citing works
Dissecting the Dual Role of the Glial Scar and Scar-Forming Astrocytes in Spinal Cord Injury
Yang, T., Dai, Y., Chen, G., & Cui, S. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00078 · Cited by 257 · see citing works
Itoh, N., Itoh, Y., Tassoni, A., Ren, E., Kaito, M., Ohno, A., Ao, Y., Farkhondeh, V., Johnsonbaugh, H., Burda, J., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1716032115 · Cited by 253 · see citing works
Self-citationLiu, W.-Z., Ma, Z.-J., Li, J.-R., & Kang, X.-W. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02153-8 · Cited by 252 · see citing works
Brambilla, R. (2019) · Acta Neuropathologica · doi:10.1007/s00401-019-01980-7 · Cited by 246 · see citing works
Progression in translational research on spinal cord injury based on microenvironment imbalance
Fan, B., Wei, Z., & Feng, S. (2022) · Bone Research · doi:10.1038/s41413-022-00199-9 · Cited by 248 · see citing works
Targeting pericytes for therapeutic approaches to neurological disorders
Cheng, J., Korte, N., Nortley, R., Sethi, H., Tang, Y., & Attwell, D. (2018) · Acta Neuropathologica · doi:10.1007/s00401-018-1893-0 · Cited by 242 · see citing works
Restoring brain function after stroke — bridging the gap between animals and humans
Ward, N. (2017) · Nature Reviews Neurology · doi:10.1038/nrneurol.2017.34 · Cited by 242 · see citing works
Brain Microvascular Pericytes in Vascular Cognitive Impairment and Dementia
Uemura, M. T., Maki, T., Ihara, M., Lee, V. M. ‐., & Trojanowski, J. Q. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.00080 · Cited by 239 · see citing works
Neuroinflammation: An astrocyte perspective
Lee, H., Lee, J.-H., Flausino, L. E., & Quintana, F. J. (2023) · Science Translational Medicine · doi:10.1126/scitranslmed.adi7828 · Cited by 241 · see citing works
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Díaz-Castro, B., Robel, S., & Mishra, A. (2023) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-091922-031205 · Cited by 238 · see citing works
3D printing nano conductive multi-walled carbon nanotube scaffolds for nerve regeneration
Lee, S., Zhu, W., Nowicki, M. A., Lee, G., Heo, D. N., Kim, J., Zuo, Y. Y., & Zhang, L. G. (2017) · Journal of Neural Engineering · doi:10.1088/1741-2552/aa95a5 · Cited by 238 · see citing works
Stratification of astrocytes in healthy and diseased brain
Verkhratsky, A., Zorec, R., & Parpura, V. (2017) · Brain Pathology · doi:10.1111/bpa.12537 · Cited by 236 · see citing works
Application of neural network algorithm in fault diagnosis of mechanical intelligence
Xu, X., Cao, D. T. N., Zhou, Y., & Gao, J. Y. (2020) · Mechanical Systems and Signal Processing · doi:10.1016/j.ymssp.2020.106625 · Cited by 230 · see citing works
Glial Cells Shape Pathology and Repair After Spinal Cord Injury
Gaudet, A. D., & Fonken, L. K. (2018) · Neurotherapeutics · doi:10.1007/s13311-018-0630-7 · Cited by 232 · see citing works
Microglia and Astrocytes in Disease: Dynamic Duo or Partners in Crime?
Liddelow, S. A., Marsh, S. E., & Stevens, B. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.07.006 · Cited by 226 · see citing works
Han, Q., Xie, Y., Ordaz, J. D., Huh, A., Huang, N., Wu, W., Liu, N., Chamberlain, K. A., Sheng, Z., & Xu, X. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.02.002 · Cited by 221 · see citing works
Schiweck, J., Eickholt, B. J., & Murk, K. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00261 · Cited by 223 · see citing works
Astrocyte-immune cell interactions in physiology and pathology
Han, R. T., Kim, R. D., Molofsky, A. V., & Liddelow, S. A. (2021) · Immunity · doi:10.1016/j.immuni.2021.01.013 · Cited by 223 · see citing works
Protective Functions of Reactive Astrocytes Following Central Nervous System Insult
Linnerbauer, M., & Rothhammer, V. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.573256 · Cited by 221 · see citing works
Neurotoxic Reactive Astrocytes Drive Neuronal Death after Retinal Injury
Guttenplan, K. A., Stafford, B. K., El-Danaf, R. N., Adler, D. I., Münch, A. E., Weigel, M. K., Huberman, A. D., & Liddelow, S. A. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107776 · Cited by 221 · see citing works
Molecular mechanisms of astrocyte-induced synaptogenesis
Baldwin, K. T., & Eroğlu, Ç. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.05.006 · Cited by 214 · see citing works
Stroke subtype-dependent synapse elimination by reactive gliosis in mice
Shi, X., Luo, L., Wang, J., Shen, H., Li, Y., Mamtilahun, M., Liu, C., Shi, R., Lee, J.-H., Tian, H., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-27248-x · Cited by 218 · see citing works
Narayanaswami, V., Dahl, K., Bernard‐Gauthier, V., Josephson, L., Cumming, P. D., & Vasdev, N. (2018) · Molecular Imaging · doi:10.1177/1536012118792317 · Cited by 215 · see citing works
Astrocyte Activation in Neurovascular Damage and Repair Following Ischaemic Stroke
Patabendige, A., Singh, A., Jenkins, S. I., Sen, J., & Chen, R. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084280 · Cited by 216 · see citing works
- 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 › Pathology and Forensic Medicine › 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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