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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
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Items 101–200 of 1,002
Axon Regeneration in the Central Nervous System: Facing the Challenges from the Inside
Curcio, M., & Bradke, F. (2018) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100617-062508 · Cited by 213
Astrocytes: Integrative Regulators of Neuroinflammation in Stroke and Other Neurological Diseases
Cekanaviciute, E., & Buckwalter, M. S. (2016) · Neurotherapeutics · doi:10.1007/s13311-016-0477-8 · Cited by 229
Metabolic Control of Astrocyte Pathogenic Activity via cPLA2-MAVS
Chao, C., Gutiérrez‐Vázquez, C., Rothhammer, V., Mayo, L., Wheeler, M. A., Tjon, E. C., Zandee, S., Blain, M., de Lima, K. A., Takenaka, M. C., et al. (2019) · Cell · doi:10.1016/j.cell.2019.11.016 · Cited by 207
de Pins, B., Cifuentes-Díaz, C., Farah, A. T., López-Molina, L., Montalban, E., Sancho‐Balsells, A., López, A. V., Ginés, S., Delgado-Garcia, J. M., Alberch, J., et al. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2121-18.2019 · Cited by 197
Current Advancements in Spinal Cord Injury Research—Glial Scar Formation and Neural Regeneration
Clifford, T., Finkel, Z., Rodriguez, B., Joseph, A., & Cai, L. (2023) · Cells · doi:10.3390/cells12060853 · Cited by 211
Chedly, J., Soares, S., Montembault, A., von Boxberg, Y., Ravaille‐Veron, M., Mouffle, C., Benassy, M., Taxi, J., David, L., & Nothias, F. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2017.05.024 · Cited by 205
CNS fibroblasts form a fibrotic scar in response to immune cell infiltration.
Dorrier, C. E., Aran, D., Haenelt, E. A., Sheehy, R. N., Hoi, K. K., Pintarić, L., Chen, Y., Lizama, C. O., Cautivo, K. M., Weiner, G. A., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-020-00770-9 · Cited by 199
Regeneration of Spinal Cord Connectivity Through Stem Cell Transplantation and Biomaterial Scaffolds
Katoh, H., Yokota, K., & Fehlings, M. G. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00248 · Cited by 204
Emerging roles for CNS fibroblasts in health, injury and disease
Dorrier, C., Jones, H. E., Pintarić, L., Siegenthaler, J. A., & Daneman, R. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00525-w · Cited by 204
Helical polymers for biological and medical applications
Leigh, T., & Fernández‐Trillo, F. (2020) · Nature Reviews Chemistry · doi:10.1038/s41570-020-0180-5 · Cited by 199
Park, J.-S., Kam, T.-I., Lee, S., Park, H., Oh, Y., Kwon, S.-H., Song, J.-J., Kim, D., Kim, H., Jhaldiyal, A., et al. (2021) · Acta Neuropathologica Communications · doi:10.1186/s40478-021-01180-z · Cited by 192
Minimally Invasive and Regenerative Therapeutics
Ashammakhi, N. A., Ahadian, S., Darabi, M. A., Tahchi, M. R. E., Lee, J., Suthiwanich, K., Sheikhi, A., Dokmeci, M. R., Öklü, R., & Khademhosseini, A. (2018) · Advanced Materials · doi:10.1002/adma.201804041 · Cited by 194
Astrocytes and Microglia as Major Players of Myelin Production in Normal and Pathological Conditions
Traiffort, É., Kassoussi, A., Zahaf, A., & Laouarem, Y. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00079 · Cited by 202
Reactive Astrocytes Facilitate Vascular Repair and Remodeling after Stroke
Williamson, M. R., Fuertes, C. J. A., Dunn, A. K., Drew, M. R., & Jones, T. A. (2020) · Cell Reports · doi:10.1016/j.celrep.2021.109048 · Cited by 200
Li, J., Pan, L., Pembroke, W. G., Rexach, J. E., Godoy, M. I., Condro, M. C., Alvarado, A. G., Harteni, M., Chen, Y., Stiles, L., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-24232-3 · Cited by 196
Combinatorial Therapies After Spinal Cord Injury: How Can Biomaterials Help?
Führmann, T., Anandakumaran, P. N., & Shoichet, M. S. (2017) · Advanced Healthcare Materials · doi:10.1002/adhm.201601130 · Cited by 190
Wang, L., Pei, S., Han, L., Guo, B., Li, Y., Duan, R., Yao, Y., Xue, B., Chen, X., & Jia, Y. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000494652 · Cited by 191
The complex STATes of astrocyte reactivity: How are they controlled by the JAK-STAT3 pathway?
Ceyzériat, K., Abjean, L., Carrillo-de Sauvage, M.-A., Ben Haim, L., & Escartin, C. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.05.043 · Cited by 185
Microglia Are Irrelevant for Neuronal Degeneration and Axon Regeneration after Acute Injury
Hilla, A. M., Diekmann, H., & Fischer, D. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0584-17.2017 · Cited by 176
New insights into glial scar formation after spinal cord injury
Tran, A. P., Warren, P. M., & Silver, J. (2021) · Cell and Tissue Research · doi:10.1007/s00441-021-03477-w · Cited by 188
CNS remyelination and inflammation: From basic mechanisms to therapeutic opportunities
Franklin, R. J. M., & Simons, M. (2022) · Neuron · doi:10.1016/j.neuron.2022.09.023 · Cited by 184
Schmidt, B. Z., Lehmann, M., Gutbier, S., Nembo, E. N., Noël, S., Smirnova, L., Forsby, A., Hescheler, J., Avci, H. X., Härtung, T., et al. (2016) · Archives of Toxicology · doi:10.1007/s00204-016-1805-9 · Cited by 191
Axon Regeneration in the Mammalian Optic Nerve
Williams, P. R., Benowitz, L. I., Goldberg, J. L., & He, Z. (2020) · Annual Review of Vision Science · doi:10.1146/annurev-vision-022720-094953 · Cited by 177
Microglia as hackers of the matrix: sculpting synapses and the extracellular space
Crapser, J. D., Arreola, M. A., Tsourmas, K. I., & Green, K. N. (2021) · Cellular & Molecular Immunology · doi:10.1038/s41423-021-00751-3 · Cited by 178
Zhao, Y., Tang, F., Xiao, Z., Han, G. Z., Wang, N., Yin, N., Chen, B., Jiang, X., Yun, C., Han, W., et al. (2017) · Cell Transplantation · doi:10.3727/096368917x695038 · Cited by 180
In Vivo Reprogramming for CNS Repair: Regenerating Neurons from Endogenous Glial Cells
Li, H., & Chen, G. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.004 · Cited by 176
Regenerating optic pathways from the eye to the brain
Laha, B., Stafford, B. K., & Huberman, A. D. (2017) · Science · doi:10.1126/science.aal5060 · Cited by 172
Aberrant Calcium Signals in Reactive Astrocytes: A Key Process in Neurological Disorders
Shigetomi, E., Saito, K., Sano, F., & Koizumi, S. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20040996 · Cited by 181
Significant roles of neuroinflammation in Parkinson’s disease: therapeutic targets for PD prevention
Lee, Y., Lee, S., Chang, S., & Lee, J. (2019) · Archives of Pharmacal Research · doi:10.1007/s12272-019-01133-0 · Cited by 171
Divergent transcriptional regulation of astrocyte reactivity across disorders
Burda, J. E., O’Shea, T. M., Ao, Y., Suresh, K. B., Wang, S., Bernstein, A. M., Chandra, A., Deverasetty, S., Kawaguchi, R., Kim, J. H., et al. (2022) · Nature · doi:10.1038/s41586-022-04739-5 · Cited by 164
Self-citationRedox Trimetallic Nanozyme with Neutral Environment Preference for Brain Injury
Mu, X., Wang, J., Li, Y., Xu, F., Long, W., Ouyang, L., Liu, H., Jing, Y., Wang, J., Dai, H., et al. (2019) · ACS Nano · doi:10.1021/acsnano.8b08045 · Cited by 166
Polypeptide-based self-healing hydrogels: Design and biomedical applications
Cai, L., Liu, S., Guo, J., & Jia, Y. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.07.001 · Cited by 166
Tezel, G. (2021) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2021.100998 · Cited by 175
Mechanisms of Endogenous Neuroprotective Effects of Astrocytes in Brain Injury
Bylicky, M. A., Mueller, G. P., & Day, R. M. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/6501031 · Cited by 170
Regenerative Therapies for Spinal Cord Injury
Ashammakhi, N. A., Kim, H., Ehsanipour, A., Bierman, R. D., Kaarela, O. I., Xue, C., Khademhosseini, A., & Seidlits, S. K. (2019) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2019.0182 · Cited by 170
Voskuhl, R. R., Itoh, N., Tassoni, A., Matsukawa, M. A., Ren, E., Tse, V., Jang, E., Suen, T. T., & Itoh, Y. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1821306116 · Cited by 162
Molecular and cellular mechanisms underlying brain metastasis of breast cancer
Hosonaga, M., Saya, H., & Arima, Y. (2020) · Cancer and Metastasis Reviews · doi:10.1007/s10555-020-09881-y · Cited by 163
Cells of the Blood–Brain Barrier: An Overview of the Neurovascular Unit in Health and Disease
McConnell, H., & Mishra, A. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2289-6_1 · Cited by 174
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. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01180-9 · Cited by 158
Self-citationDysfunction of Cerebrovascular Endothelial Cells: Prelude to Vascular Dementia
Wang, F., Cao, Y., Ma, L., Pei, H., Rausch, W., & Li, H. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00376 · Cited by 163
Astrocytes and microglia: Models and tools
Guttenplan, K. A., & Liddelow, S. A. (2018) · The Journal of Experimental Medicine · doi:10.1084/jem.20180200 · Cited by 162
Crapser, J. D., Ochaba, J., Soni, N., Reidling, J. C., Thompson, L. M., & Green, K. N. (2020) · Brain · doi:10.1093/brain/awz363 · Cited by 157
The role of astrocyte structural plasticity in regulating neural circuit function and behavior
Lawal, O., Ulloa Severino, F. P., & Eroglu, C. (2022) · Glia · doi:10.1002/glia.24191 · Cited by 142
Ma, N., He, T., Johnston, L. J., & Ma, X. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1758008 · Cited by 162
Oxidative stress and regeneration
Jaganjac, M., Milković, L., Žarković, N., & Žarković, K. (2022) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2022.02.004 · Cited by 162
Tao, G., Dingfei, Q., Li, L., Xiaowei, W., Zhou, Z., Liu, W., Zhu, T., Ning, B., Yan-ning, Q., Wei, Z., et al. (2020) · Cell Death Discovery · doi:10.1038/s41420-020-00333-8 · Cited by 154
Chandrasekaran, A., Avci, H. X., Leist, M., Kobolák, J., & Dinnyés, A. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00215 · Cited by 159
The aryl hydrocarbon receptor and the gut–brain axis
Barroso, A., Mahler, J. V., Fonseca-Castro, P. H., & Quintana, F. J. (2021) · Cellular & Molecular Immunology · doi:10.1038/s41423-020-00585-5 · Cited by 152
Tedeschi, A., & Bradke, F. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.12.005 · Cited by 157
Ren, Y., Ao, Y., O’Shea, T. M., Burda, J. E., Bernstein, A. M., Brumm, A. J., Muthusamy, N., Ghashghaei, H. T., Carmichael, S. T., Cheng, L., et al. (2017) · Scientific Reports · doi:10.1038/srep41122 · Cited by 152
Self-citationThe Important Interface Between Apolipoprotein E and Neuroinflammation in Alzheimer’s Disease
Kloske, C. M., & Wilcock, D. M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00754 · Cited by 152
Fibrotic scarring following lesions to the central nervous system
Dias, D. O., & Göritz, C. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.02.009 · Cited by 148
RhoA drives actin compaction to restrict axon regeneration and astrocyte reactivity after CNS injury
Stern, S., Hilton, B. J., Burnside, E. R., Dupraz, S., Handley, E. E., Gonyer, J. M., Brakebusch, C., & Bradke, F. (2021) · Neuron · doi:10.1016/j.neuron.2021.08.014 · Cited by 152
Nagappan, P. G., Chen, H., & Wang, D. Y. (2020) · Military Medical Research · doi:10.1186/s40779-020-00259-3 · Cited by 152
Squair, J. W., Milano, M., de Coucy, A., Gautier, M., Skinnider, M. A., James, N. D., Cho, N., Lasne, A., Kathe, C., Hutson, T. H., et al. (2023) · Science · doi:10.1126/science.adi6412 · Cited by 149
Self-citationAstrocytes, Microglia, and Parkinson’s Disease
Joe, E.-H., Choi, D., An, J., Eun, J.-H., Jou, I., & Park, S.-M. (2018) · Experimental Neurobiology · doi:10.5607/en.2018.27.2.77 · Cited by 142
Two-photon calcium imaging of neuronal activity
Grienberger, C., Giovannucci, A., Zeiger, W., & Portera‐Cailliau, C. (2022) · Nature Reviews Methods Primers · doi:10.1038/s43586-022-00147-1 · Cited by 159
Astroglial atrophy in Alzheimer’s disease
Verkhratsky, A., Rodriguez, J. J., Pivoriūnas, A., Zorec, R., & Semyanov, A. V. (2019) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-019-02310-2 · Cited by 150
Li, F., Sami, A., Noristani, H. N., Slattery, K., Qiu, J., Groves, T., Wang, S., Veerasammy, K., Chen, Y. X., Morales, J., et al. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.08.015 · Cited by 147
Zhang, Q., Liu, C., Shi, R., Zhou, S., Shan, H., Deng, L., Chen, T., Guo, Y., Zhang, Z., Yang, G., et al. (2022) · Aging and Disease · doi:10.14336/ad.2021.1029 · Cited by 138
Hartmann, K., Sepulveda-Falla, D., Rose, I. V. L., Madore, C., Muth, C., Matschke, J., Butovsky, O., Liddelow, S., Glatzel, M., & Krasemann, S. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-019-0735-1 · Cited by 141
The Struggle to Make CNS Axons Regenerate: Why Has It Been so Difficult?
Fawcett, J. W. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02844-y · Cited by 137
Fu, H., Zhao, Y., Hu, D., Wang, S., Yu, T., & Zhang, L. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2733-4 · Cited by 141
Li, W., Chen, J., Zhao, S., Huang, T., Ying, H., Trujillo, C., Molinaro, G., Zhou, Z., Jiang, T., Liu, W., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-28787-7 · Cited by 143
Dual extra-retinal origins of microglia in the model of retinal microglia repopulation
Huang, Y., Xu, Z., Xiong, S., Qin, G., Sun, F., Yang, J. F., Yuan, T., Zhao, L., Wang, K., Liang, Y.-X., et al. (2018) · Cell Discovery · doi:10.1038/s41421-018-0011-8 · Cited by 134
Liu, X., Sui, B., & Sun, J. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2017.01.006 · Cited by 140
Post-stroke remodeling processes in animal models and humans
Cirillo, C., Brihmat, N., Castel-Lacanal, E., Friec, A. L., Barbieux‐Guillot, M., Raposo, N., Pariente, J., Viguier, A., Simonetta‐Moreau, M., Albucher, J., et al. (2019) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x19882788 · Cited by 144
Yao, M., Ventura, P. B., Jiang, Y., Rodriguez, F. J., Wang, L., Perry, J. S. A., Yang, Y., Wahl, K., Crittenden, R. B., Bennett, M. L., et al. (2020) · Cell · doi:10.1016/j.cell.2019.12.024 · Cited by 133
Mechanobiology of the brain in ageing and Alzheimer's disease
Hall, C. M., Moeendarbary, E., & Sheridan, G. K. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14766 · Cited by 140
Selective Modulation of A1 Astrocytes by Drug-Loaded Nano-Structured Gel in Spinal Cord Injury
Vismara, I., Papa, S., Veneruso, V., Mauri, E., Mariani, A., Paola, M. D., Affatato, R., Rossetti, A., Sponchioni, M., Moscatelli, D., et al. (2019) · ACS Nano · doi:10.1021/acsnano.9b05579 · Cited by 136
Miyamoto, N., Magami, S., Inaba, T., Ueno, Y., Hira, K., Kijima, C., Nakajima, S., Yamashiro, K., Urabe, T., & Hattori, N. (2020) · Glia · doi:10.1002/glia.23814 · Cited by 138
A molecular switch for neuroprotective astrocyte reactivity
Cameron, E. G., Nahmou, M. M., Toth, A. B., Heo, L., Tanasă, B., Dalal, R., Yan, W., Nallagatla, P., Xia, X., Hay, S., et al. (2023) · Nature · doi:10.1038/s41586-023-06935-3 · Cited by 137
Can injured adult CNS axons regenerate by recapitulating development?
Hilton, B. J., & Bradke, F. (2017) · Development · doi:10.1242/dev.148312 · Cited by 139
Biodegradation of ECM hydrogel promotes endogenous brain tissue restoration in a rat model of stroke
Ghuman, H., Mauney, C., Donnelly, J., Massensini, A. R., Badylak, S. F., & Modo, M. (2018) · Acta Biomaterialia · doi:10.1016/j.actbio.2018.09.020 · Cited by 131
Qian, D., Li, L., Rong, Y., Liu, W., Wang, Q., Zhou, Z., Gu, C., Huang, Y., Zhao, X., Chen, J., et al. (2019) · Cell Cycle · doi:10.1080/15384101.2019.1667189 · Cited by 133
Reactive Astrogliosis: Implications in Spinal Cord Injury Progression and Therapy
Li, X., Li, M., Tian, L., Chen, J., Liu, R., & Ning, B. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/9494352 · Cited by 138
Leibinger, M., Zeitler, C., Gobrecht, P., Andreadaki, A., Gisselmann, G., & Fischer, D. (2019) · Nature Communications · doi:10.1038/s41467-020-20112-4 · Cited by 135
Optic nerve astrocyte reactivity protects function in experimental glaucoma and other nerve injuries
Sun, D., Moore, S., & Jakobs, T. C. (2017) · Journal of Experimental Medicine · doi:10.1084/jem.20160412 · Cited by 130
Extracellular matrix and traumatic brain injury
George, N., & Geller, H. M. (2018) · Journal of Neuroscience Research · doi:10.1002/jnr.24151 · Cited by 135
Molecular and metabolic heterogeneity of astrocytes and microglia
Hasel, P., Aisenberg, W. H., Bennett, F. C., & Liddelow, S. A. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.03.006 · Cited by 135
Strategies and prospects of effective neural circuits reconstruction after spinal cord injury
Yang, B., Zhang, F., Cheng, F., Ying, L., Wang, C., Shi, K., Wang, J., Xia, K., Gong, Z., Huang, X., et al. (2020) · Cell Death & Disease · doi:10.1038/s41419-020-2620-z · Cited by 128
A neuroprotective astrocyte state is induced by neuronal signal EphB1 but fails in ALS models
Tyzack, G. E., Hall, C. E., Sibley, C. R., Cymes, T., Forostyak, S., Carlino, G., Meyer, I. F., Schiavo, G., Zhang, S.-C., Gibbons, G. M., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-01283-z · Cited by 128
Cross‐talk between monocyte invasion and astrocyte proliferation regulates scarring in brain injury
Frik, J., Merl‐Pham, J., Plesnila, N., Mattugini, N., Kjell, J., Kraska, J., Gomez, R. M., Hauck, S. M., Sirko, S., & Götz, M. (2018) · EMBO Reports · doi:10.15252/embr.201745294 · Cited by 126
Shandra, O. O., Winemiller, A. R., Heithoff, B. P., Muñoz‐Ballester, C., George, K. K., Benko, M. J., Zuidhoek, I. A., Besser, M. N., Curley, D. E., Edwards, G. F., et al. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1067-18.2018 · Cited by 132
Prolonged inflammation leads to ongoing damage after spinal cord injury
Kwiecień, J. M., Dąbrowski, W., Dąbrowska‐Bouta, B., Sułkowski, G., Oakden, W., Kwiecien-Delaney, C. J., Yaron, J. R., Zhang, L., Schutz, L. N., Marzec‐Kotarska, B., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0226584 · Cited by 130
Diversity of astroglial responses across human neurodegenerative disorders and brain aging
Ferrer, I. (2017) · Brain Pathology · doi:10.1111/bpa.12538 · Cited by 135
Clark, D. P. Q., Perreau, V. M., Shultz, S. R., Brady, R. D., Lei, E., Dixit, S., Taylor, J. M., Beart, P. M., & Boon, W. C. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02721-8 · Cited by 132
Pang, Q.-M., Chen, S., Xu, Q.-J., Fu, S.-P., Yang, Y.-C., Zou, W.-H., Zhang, M., Liu, J., Wan, W.-H., Peng, J., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.751021 · Cited by 130
Glial scars are permeable to the neurotoxic environment of chronic stroke infarcts
Zbesko, J. C., Nguyen, T. V., Yang, T., Frye, J. B., Hussain, O. M., Hayes, M. I., Chung, A. G., Day, W. A., Stepanovic, K., Krumberger, M., et al. (2018) · Neurobiology of Disease · doi:10.1016/j.nbd.2018.01.007 · Cited by 128
Perelroizen, R., Philosof, B., Budick-Harmelin, N., Chernobylsky, T., Ron, A., Katzir, R., Shimon, D., Tessler, A., Adir, O., Gaoni-Yogev, A., et al. (2022) · Brain · doi:10.1093/brain/awac222 · Cited by 131
Natural and targeted circuit reorganization after spinal cord injury
Anderson, M. A., Squair, J. W., Gautier, M., Hutson, T. H., Kathe, C., Barraud, Q., Bloch, J., & Courtine, G. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01196-1 · Cited by 126
Self-citationPathophysiology of Spinal Cord Injury
Hachem, L. D., & Fehlings, M. G. (2021) · Neurosurgery Clinics of North America · doi:10.1016/j.nec.2021.03.002 · Cited by 123
Functional immune cell–astrocyte interactions
Sanmarco, L. M., Polonio, C. M., Wheeler, M. A., & Quintana, F. J. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20202715 · Cited by 134
Reactive Astrocytes in Brain Metastasis
Wasilewski, D., Priego, N., Torre, C. F., & Valiente, M. (2017) · Frontiers in Oncology · doi:10.3389/fonc.2017.00298 · Cited by 121
Single-cell and spatial atlases of spinal cord injury in the Tabulae Paralytica
Skinnider, M. A., Gautier, M., Teo, A. Y. Y., Kathe, C., Hutson, T. H., Laskaratos, A., de Coucy, A., Regazzi, N., Aureli, V., James, N. D., et al. (2024) · Nature · doi:10.1038/s41586-024-07504-y · Cited by 137
Self-citationAdvances in Biomaterial‐Based Spinal Cord Injury Repair
Shen, H., Fan, C., You, Z., Xiao, Z., Zhao, Y., & Dai, J. (2021) · Advanced Functional Materials · doi:10.1002/adfm.202110628 · Cited by 120
Puls, B., Ding, Y. P., Zhang, F., Pan, M., Lei, Z., Pei, Z., Jiang, M. H., Bai, Y., Forsyth, C., Metzger, M., et al. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.591883 · Cited by 124
Winston, C. N., Goetzl, E. J., Schwartz, J. B., Elahi, F. M., & Rissman, R. A. (2018) · Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring · doi:10.1016/j.dadm.2018.11.002 · Cited by 120
Nelson, D. W., & Gilbert, R. J. (2021) · Advanced Healthcare Materials · doi:10.1002/adhm.202101329 · Cited by 118
O’Shea, T. M., Ao, Y., Wang, S., Ren, Y., Cheng, A. L., Kawaguchi, R., Shi, Z., Swarup, V., & Sofroniew, M. V. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01684-6 · Cited by 129
Self-citation
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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