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Origin of New Glial Cells in Intact and Injured Adult Spinal Cord
Open accessAbstract
Several distinct cell types in the adult central nervous system have been suggested to act as stem or progenitor cells generating new cells under physiological or pathological conditions. We have assessed the origin of new cells in the adult mouse spinal cord by genetic fate mapping. Oligodendrocyte progenitors self-renew, give rise to new mature oligodendrocytes, and constitute the dominating proliferating cell population in the intact adult spinal cord. In contrast, astrocytes and ependymal cells, which are restricted to limited self-duplication in the intact spinal cord, generate the largest number of cells after spinal cord injury. Only ependymal cells generate progeny of multiple fates, and neural stem cell activity in the intact and injured adult spinal cord is confined to this cell population. We provide an integrated view of how several distinct cell types contribute in complementary ways to cell maintenance and the reaction to injury.
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In the citing paper
“TAM has been exploited experimentally to induce permanent reporter expression in, for example, newly-born neurons in the olfactory bulb and dentate gyrus [8], in physiologically-active neurons throughout the brain [9], and in progeny of ependymal cells of the intact and injured murine spinal cord [39].”
From Tamoxifen induces cellular stress in the nervous system by inhibiting cholesterol synthesis (2015) · cites this paper as [39]
In the citing paper
“Here, five daily treatments of TAM (80 mg/kg) were used to induce recombination in ependymal cells in FoxJ1-CreER mice in order to determine whether ependymal cells are multipotential in vitro, and in vivo following a spinal cord injury.”
From Tamoxifen induces cellular stress in the nervous system by inhibiting cholesterol synthesis (2015) · cites this paper as [39]
In the citing paper
“In vivo, reporter-expressing ependyma self-renewed and produced astrocytes and oligodendrocyte-lineage cells 5 days following the last TAM dose.”
From Tamoxifen induces cellular stress in the nervous system by inhibiting cholesterol synthesis (2015) · cites this paper as [39]
In the citing paper
“The in vitro studies showed that 3 days after cessation of TAM treatment, recombined ependyma could indeed give rise to neurospheres with cells expressing markers for neurons, astrocytes and oligodendrocyte-lineage cells.”
From Tamoxifen induces cellular stress in the nervous system by inhibiting cholesterol synthesis (2015) · cites this paper as [39]
Citations
Cites
Generalized lacZ expression with the ROSA26 Cre reporter strain
Soriano, P. (1999) · Nature Genetics · doi:10.1038/5007 · Cited by 5,237
Regeneration beyond the glial scar
Silver, J., & Miller, J. H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1326 · Cited by 3,151
Cahoy, J. D., Emery, B., Kaushal, A., Foo, L. C., Zamanian, J. L., Christopherson, K. S., Xing, Y., Lubischer, J. L., Krieg, P. A., Krupenko, S. A., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4178-07.2008 · Cited by 3,129
Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus
Srinivas, S., Watanabe, T., Lin, C.-S., William, C. M., Tanabe, Y., Jessell, T. M., & Costantini, F. (2001) · BMC Developmental Biology · doi:10.1186/1471-213x-1-4 · Cited by 3,121
Mechanisms and Functional Implications of Adult Neurogenesis
Zhao, C., Deng, W., & Gage, F. H. (2008) · Cell · doi:10.1016/j.cell.2008.01.033 · Cited by 3,007
Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation
Dor, Y., Brown, J., Martinez, O. I., & Melton, D. A. (2004) · Nature · doi:10.1038/nature02520 · Cited by 2,219
Identification of a Neural Stem Cell in the Adult Mammalian Central Nervous System
Johansson, C. B., Momma, S., Clarke, D. L., Risling, M., Lendahl, U., & Frisén, J. (1999) · Cell · doi:10.1016/s0092-8674(00)80956-3 · Cited by 1,875
Self-citationReactive Astrocytes Protect Tissue and Preserve Function after Spinal Cord Injury
Faulkner, J. R., Herrmann, J. E., Woo, M. J., Tansey, K. E., Doan, N., & Sofroniew, M. V. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3547-03.2004 · Cited by 1,652
Remyelination in the CNS: from biology to therapy
Franklin, R. J. M., & ffrench-Constant, C. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2480 · Cited by 1,544
Ito, M., Liu, Y., Yang, Z., Nguyen, J., Liang, F., Morris, R. J., & Cotsarelis, G. (2005) · Nature Medicine · doi:10.1038/nm1328 · Cited by 1,317
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Ming, G.-L., & Song, H. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.001 · Cited by 2,651
Ahuja, 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
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 1,509
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Khakh, B. S., & Sofroniew, M. V. (2015) · Nature Neuroscience · doi:10.1038/nn.4043 · Cited by 1,239
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Assinck, P., Duncan, G. J., Hilton, B. J., Plemel, J. R., & Tetzlaff, W. (2017) · Nature Neuroscience · doi:10.1038/nn.4541 · Cited by 960
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 903
A Pericyte Origin of Spinal Cord Scar Tissue
Göritz, C., Dias, D. O., Tomilin, N., Barbacid, M., Shupliakov, O., & Frisén, J. (2011) · Science · doi:10.1126/science.1203165 · Cited by 858
Self-citationSpinal 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 840
Sofroniew, M. V. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020420 · Cited by 695
Functional regeneration beyond the glial scar
Cregg, J. M., DePaul, M. A., Filous, A. R., Lang, B. T., Tran, A. P., & Silver, J. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2013.12.024 · Cited by 688
Oligodendrocytes in development, myelin generation and beyond
Kuhn, S., Gritti, L., Crooks, D., & Dombrowski, Y. (2019) · Cells · doi:10.3390/cells8111424 · Cited by 625
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Bergles, D. E., & Richardson, W. D. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020453 · Cited by 604
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Yeung, M. S. Y., Zdunek, S., Bergmann, O., Bernard, S., Salehpour, M., Alkass, K., Perl, S., Tisdale, J., Possnert, G., Brundin, L., et al. (2014) · Cell · doi:10.1016/j.cell.2014.10.011 · Cited by 541
Self-citationMicroenvironment 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 535
The stem cell potential of glia: lessons from reactive gliosis
Robel, S., Berninger, B., & Götz, M. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn2978 · Cited by 536
NADPH oxidase in brain injury and neurodegenerative disorders
Ma, M. W., Wang, J., Zhang, Q., Wang, R., Dhandapani, K. M., Vadlamudi, R. K., & Brann, D. W. (2017) · Molecular Neurodegeneration · doi:10.1186/s13024-017-0150-7 · Cited by 432
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Kjell, J., & Olson, L. (2016) · Disease Models & Mechanisms · doi:10.1242/dmm.025833 · Cited by 418
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 406
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Sirko, S., Behrendt, G., Johansson, P. A., Tripathi, P., Costa, M. R., Bek, S., Heinrich, C., Tiedt, S., Colak, D., Dichgans, M., et al. (2013) · Cell stem cell · doi:10.1016/j.stem.2013.01.019 · Cited by 399
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Sun, W., Cornwell, A., Li, J., Peng, S., Osorio, M. J., Aalling, N., Wang, S., Benraiss, A., Lou, N., Goldman, S. A., et al. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.3199-16.2017 · Cited by 357
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Stenudd, M., Sabelström, H., & Frisén, J. (2014) · JAMA Neurology · doi:10.1001/jamaneurol.2014.2927 · Cited by 336
Self-citationReactive Astrogliosis after Spinal Cord Injury—Beneficial and Detrimental Effects
Karimi-Abdolrezaee, S., & Billakanti, R. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8287-4 · Cited by 331
Simon, C., Götz, M., & Dimou, L. (2011) · Glia · doi:10.1002/glia.21156 · Cited by 313
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Sabelström, H., Stenudd, M., Réu, P., Dias, D. O., Elfineh, M., Zdunek, S., Damberg, P., Göritz, C., & Frisén, J. (2013) · Science · doi:10.1126/science.1242576 · Cited by 314
Self-citationNG2-glia as multipotent neural stem cells: fact or fantasy?
Richardson, W. D., Young, K. M., Tripathi, R. B., & McKenzie, I. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.013 · Cited by 300
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 289
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Birbrair, A., Zhang, T., Files, D. C., Mannava, S., Smith, T. L., Wang, Z., Messi, M. L., Mintz, A., & Delbono, O. (2014) · Stem Cell Research & Therapy · doi:10.1186/scrt512 · Cited by 291
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 280
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Fan, B., Wei, Z., & Feng, S. (2022) · Bone Research · doi:10.1038/s41413-022-00199-9 · Cited by 251
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Zhou, B., Zhu, Z., Ransom, B. R., & Tong, X. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-00930-0 · Cited by 245
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Cai, W., Yang, T., Liu, H., Han, L., Zhang, K., Hu, X., Zhang, X., Yin, K., Gao, Y., Bennett, M. V. L., et al. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2017.10.002 · Cited by 240
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Götz, M., Sirko, S., Beckers, J., & Irmler, M. (2015) · Glia · doi:10.1002/glia.22850 · Cited by 237
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Bhalala, O. G., Pan, L., Sahni, V., McGuire, T. L., Gruner, K., Tourtellotte, W. G., & Kessler, J. A. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3860-12.2012 · Cited by 220
Yang, Z., Zhang, A., Duan, H., Zhang, S., Hao, P., Ye, K., Sun, Y. E., & Li, X. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510194112 · Cited by 221
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Dias, D. O., Kalkitsas, J., Kelahmetoglu, Y., Estrada, C. P., Tatarishvili, J., Holl, D., Jansson, L., Banitalebi, S., Amiry-Moghaddam, M. R., Ernst, A., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25585-5 · Cited by 214
Self-citationThe glial scar in spinal cord injury and repair
Yuan, Y., & He, C. (2013) · Neuroscience Bulletin · doi:10.1007/s12264-013-1358-3 · Cited by 215
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Almad, A., Sahinkaya, F. R., & McTigue, D. M. (2011) · Neurotherapeutics · doi:10.1007/s13311-011-0033-5 · Cited by 218
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Katoh, H., Yokota, K., & Fehlings, M. G. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00248 · Cited by 204
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Plemel, J. R., Keough, M. B., Duncan, G. J., Sparling, J. S., Yong, V. W., Stys, P. K., & Tetzlaff, W. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2014.02.006 · Cited by 206
Shimada, I. S., LeComte, M. D., Granger, J. C., Quinlan, N. J., & Spees, J. L. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4303-11.2012 · Cited by 192
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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
Tai, W., Wu, W., Wang, L.-L., Ni, H., Chen, C., Yang, J., Zang, T., Zou, Y., Xu, X., & Zhang, C. (2021) · Cell stem cell · doi:10.1016/j.stem.2021.02.009 · Cited by 165
Astrocyte activation is suppressed in both normal and injured brain by FGF signaling
Kang, W., Balordi, F., Su, N. Y., Chen, L., Fishell, G., & Hébert, J. M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1320401111 · Cited by 163
Yang, Y., Fan, Y., Zhang, H., Zhang, Q., Zhao, Y., Xiao, Z., Liu, W., Chen, B., Gao, L., Sun, Z., et al. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2020.120479 · Cited by 159
El-Kheir, W. A., Gabr, H. M., Awad, M. R., Ghannam, O. E., Barakat, Y. A. G., Farghali, H. A. M. A., Maadawi, Z. M. E., Ewes, I., & Sabaawy, H. E. (2013) · Cell Transplantation · doi:10.3727/096368913x664540 · Cited by 156
Endogenous neural stem cell responses to stroke and spinal cord injury
Grégoire, C., Goldenstein, B., Floriddia, E. M., Barnabé‐Heider, F., & Fernandes, K. J. L. (2015) · Glia · doi:10.1002/glia.22851 · Cited by 156
Self-citationRen, 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
Myelinogenic Plasticity of Oligodendrocyte Precursor Cells following Spinal Cord Contusion Injury
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Ruff, C. A., Wilcox, J. T., & Fehlings, M. G. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.02.010 · Cited by 149
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Filous, A. R., & Silver, J. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.03.009 · Cited by 151
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Stephanopoulos, N., Freeman, R., North, H. A., Sur, S., Jeong, S. J., Tantakitti, F., Kessler, J. A., & Stupp, S. I. (2015) · Nano Letters · doi:10.1021/nl504079q · Cited by 138
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Ahuja, C. S., Mothe, A. J., Khazaei, M., Badhiwala, J. H., Gilbert, E. A. B., van der Kooy, D., Morshead, C. M., Tator, C. H., & Fehlings, M. G. (2020) · Stem Cells Translational Medicine · doi:10.1002/sctm.19-0135 · Cited by 148
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Kang, W., & Hébert, J. M. (2011) · Molecular Neurobiology · doi:10.1007/s12035-011-8163-7 · Cited by 148
Tien, A., Tsai, H., Molofsky, A. V., McMahon, M., Foo, L. C., Kaul, A., Dougherty, J. D., Heintz, N., Gutmann, D. H., Barres, B. A., et al. (2012) · Development · doi:10.1242/dev.077214 · Cited by 142
Li, X., Zhao, Y., Cheng, S., Han, S., Shu, M., Chen, B., Chen, X., Tang, F., Wang, N., Tu, Y., et al. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2017.05.027 · Cited by 138
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Gao, Z., Zhu, Q., Zhang, Y., Zhao, Y., Cai, L., Shields, C. B., & Cai, J. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8460-4 · Cited by 148
Zhu, R., Zhu, X., Zhu, Y., Wang, Z., He, X., Wu, Z., Xue, L., Fan, W., Huang, R., Xu, Z. Q., et al. (2021) · ACS Nano · doi:10.1021/acsnano.0c08727 · Cited by 133
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Götz, M., Nakafuku, M., & Petřík, D. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a018853 · Cited by 131
Hosseini, S. M., Borys, B., & Karimi‐Abdolrezaee, S. (2023) · Brain · doi:10.1093/brain/awad392 · Cited by 135
Zhu, Y., Lyapichev, K. A., Lee, D. H., Motti, D., Ferraro, N. M., Zhang, Y., Yahn, S. L., Soderblom, C., Zha, J., Bethea, J. R., et al. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.2751-16.2017 · Cited by 130
Karimi‐Abdolrezaee, S., Schut, D., Wang, J., & Fehlings, M. G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037589 · Cited by 129
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Lukovic, D., Stojković, M., Moreno‐Manzano, V., Jendelová, P., Syková, E., Bhattacharya, S. S., & Erceg, S. (2015) · Stem Cells · doi:10.1002/stem.1959 · Cited by 123
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Gazdic, M., Volarević, V., Harrell, C. R., Fellabaum, C., Jovicic, N. U., Arsenijević, N., & Stojković, M. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19041039 · Cited by 122
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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
Li, X., Liu, D., Xiao, Z., Zhao, Y., Han, S., Chen, B., & Dai, J. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2019.01.012 · Cited by 118
The fate and function of oligodendrocyte progenitor cells after traumatic spinal cord injury
Duncan, G. J., Manesh, S. B., Hilton, B. J., Assinck, P., Plemel, J. R., & Tetzlaff, W. (2019) · Glia · doi:10.1002/glia.23706 · Cited by 119
Decimo, I., Bifari, F., Rodríguez, F. J., Malpeli, G., Dolci, S., Lavarini, V., Pretto, S., Vásquez, S., Sciancalepore, M., Montalbano, A., et al. (2011) · Stem Cells · doi:10.1002/stem.766 · Cited by 119
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Metadata
- Authors
- Barnabé-Heider, F., Göritz, C., Sabelström, H., Takebayashi, H., Pfrieger, F. W., Meletis, K., & Frisén, J.
- Affiliations
- Karolinska Institutet (SE)
- Kumamoto University (JP)
- Centre National de la Recherche Scientifique (FR)
- Corresponding author
- Frisén, Jonas
- ORCID
- Venue
- Cell Stem Cell
- Publisher
- Elsevier BV
- Published
- 2010-10
- Volume
- 7
- Issue
- 4
- Pages
- 470-482
- ISSN
- 1875-9777 (ISSN-L)
- 1934-5909
- OpenAlex
- W2128475302
- Cited by
- 628
- References
- 58
- Citations by year
- 2026: 28 · 2025: 33 · 2024: 34 · 2023: 44 · 2022: 40 · 2021: 64 · 2020: 35 · 2019: 37 · 2018: 46 · 2017: 48 · 2016: 42 · 2015: 44 · 2014: 48 · 2013: 33 · 2012: 24
- FWCI
- 8.51
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell stem cell (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Funders
- Canadian Institutes of Health Research
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Clinical Neurology › Spinal Cord Injury Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- adult spinal cord, glial cell origin, spinal cord injury, oligodendrocyte progenitors, astrocytes, ependymal cells, neural stem cells, cell proliferation, self-renewal, genetic fate mapping
- MeSH terms
- Animals, Immunohistochemistry, Mice, Transgenic, Neuroglia, Spinal Cord Injuries, Stem Cells, Mice, Spinal Cord Regeneration
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