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Endogenous Progenitors Remyelinate Demyelinated Axons in the Adult CNS
Open accessAbstract
Remyelination occurs in demyelinated CNS regions in diseases such as multiple sclerosis. Identification of the cell type(s) responsible for this remyelination, however, has been elusive. Here, we examine one potential source of remyelinating oligodendrocytes-immature, cycling cells endogenous to adult white matter-and demonstrate that this population responds to demyelination by differentiating into myelinating oligodendrocytes. Dividing cells in subcortical white matter of adult rats were labeled by stereotactic injection of a replication-deficient lacZ-encoding retrovirus (BAG). Following a focal demyelination induced with lysolecithin, many of the BAG-labeled cells differentiated into myelinating oligodendrocytes engaging in repair of the lesion. Identification of endogenous cells capable of remyelination provides a target for the study of CNS repair processes in demyelinating diseases.
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“Importantly, however, a multitude of experimental evidence has shown that remyelination is associated with proliferation and differentiation of oligodendrocyte precursor cells into mature oligodendrocytes”
From BCAS1-positive oligodendrocytes enable efficient cortical remyelination in multiple sclerosis (2025) · cites this paper as [23]
Citations
Cites
Localization of the glial fibrillary acidic protein in astrocytes by immunofluorescence
Bignami, A., Eng, L. F., Dahl, D. R., & Uyeda, C. T. (1972) · Brain Research · doi:10.1016/0006-8993(72)90398-8 · Cited by 1,456
Use of a recombinant retrovirus to study post‐implantation cell lineage in mouse embryos.
Sanes, J. R., Rubenstein, J. L. R., & Nicolas, J. F. (1986) · The EMBO Journal · doi:10.1002/j.1460-2075.1986.tb04620.x · Cited by 1,116
Deibler, G. E., Martenson, R. E., & Kies, M. W. (1972) · Preparative Biochemistry · doi:10.1080/00327487208061467 · Cited by 939
Lineage analysis in the vertebrate nervous system by retrovirus-mediated gene transfer.
Price, J., Turner, D., & Cepko, C. L. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.1.156 · Cited by 870
Multiple sclerosis: Remyelination of nascent lesions: Remyelination of nascent lesions
Prineas, J. W., Barnard, R. O., Kwon, E. E., Sharer, L. R., & Cho, E. ‐. (1993) · Annals of Neurology · doi:10.1002/ana.410330203 · Cited by 574
Proliferation and differentiation of rat neuroepithelial precursor cells in vivo
Frederiksen, K., & McKay, R. D. G. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-04-01144.1988 · Cited by 551
Identification of an adult-specific glial progenitor cell
Wolswijk, G., & Noble, M. (1989) · Development · doi:10.1242/dev.105.2.387 · Cited by 487
Proliferating bipotential glial progenitor cells in adult rat optic nerve
ffrench‐Constant, C., & RAFF, M. C. (1986) · Nature · doi:10.1038/319499a0 · Cited by 385
Multiple Sclerosis: Remyelination in Acute Lesions
Raine, C. S., & WU, E. (1993) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/00005072-199305000-00003 · Cited by 285
Hall, S. M. (1972) · Journal of Cell Science · doi:10.1242/jcs.10.2.535 · Cited by 271
Research works printed but not linked: 7
- Allen, I.V., and Kirk, J. (1992). Demyelinating diseases. In Greenfield's Neuropathology, J.H. Adams and L.W. Duchen, eds. (New York: Oxford University Press), pp. 447–520.
- Prineas, 1989, Multiple sclerosis, Lab. Invest, 61, 489
- Raine, C.S. (1991). Demyelinating diseases. In Textbook of Neuropathology, R.L. Davis and D.M. Robertson, eds. (Baltimore: Williams and Wilkins), pp. 535–620.
- Raine, 1981, Multiple sclerosis, Lab. Invest, 45, 534
- Ramon y Cajal, S. (1995). Pathways from the temporal olfactory cortex. In Histology of the Nervous System of Man and Vertebrates, Volume II (New York: Oxford University Press), pp. 589–602.
- Szuchet, S. (1995). The morphology and ultrastructure of oligodendrocytes and their functional implications. In Neuroglia, H. Kettenmann and B.R. Ransom, eds. (New York: Oxford University Press), pp. 23–43.
- Wu, 1992, Multiple sclerosis, Lab. Invest, 67, 88
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Chari, D. M., & Blakemore, W. F. (2002) · Glia · doi:10.1002/glia.10038 · Cited by 163
Notch-1 activation by familial Alzheimer's disease (FAD)-linked mutant forms of presenilin-1
Nakajima, M., Shimizu, T., & Shirasawa, T. (2000) · Journal of Neuroscience Research · doi:10.1002/1097-4547(20001015)62:2 · Cited by 27
Murtie, J. C., Zhou, Y.-X., Le, T. Q., Vana, A. C., & Armstrong, R. C. (2005) · Neurobiology of Disease · doi:10.1016/j.nbd.2004.12.006 · Cited by 157
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Jung, C., Kim, H., Miron, V. E., Cook, S. P., Kennedy, T. E., Foster, C. A., Antel, J. P., & Soliven, B. C. (2007) · Glia · doi:10.1002/glia.20576 · Cited by 158
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Franklin, R. J. M., & Gallo, V. (2014) · Glia · doi:10.1002/glia.22622 · Cited by 162
Han, L., Cai, W., Mao, L., Liu, J., Li, P., Leak, R. K., Xu, Y., Hu, X., & Chen, J. (2015) · Stroke · doi:10.1161/strokeaha.115.010091 · Cited by 155
Selvaraju, R., Bernasconi, L., Losberger, C., Graber, P., Kadi, L., Avellana-Adalid, V., Picard-Riera, N., Van Evercooren, A. B., Cirillo, R., Kosco-Vilbois, M., et al. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2003.12.014 · Cited by 156
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Li, Q., Brus-Ramer, M., Martin, J. H., & McDonald, J. W. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.05.043 · Cited by 150
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de Castro, F., & Bribián, A. (2005) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.12.034 · Cited by 154
Franco, P. G., Silvestroff, L., Soto, E. F., & Pasquini, J. M. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2008.04.039 · Cited by 147
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Flygt, J., Djupsjö, A., Lenne, F., & Marklund, N. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12179 · Cited by 153
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Faulkner, J. R., & Keirstead, H. S. (2005) · Transplant Immunology · doi:10.1016/j.trim.2005.09.007 · Cited by 140
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Bigio, M. R. D., & Zhang, Y. W. (1998) · Experimental Neurology · doi:10.1006/exnr.1998.6922 · Cited by 135
Diers‐Fenger, M., Kirchhoff, F., Kettenmann, H., Levine, J. M., & Trotter, J. (2001) · Glia · doi:10.1002/glia.1055 · Cited by 135
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Lasiene, J., Shupe, L., Perlmutter, S., & Horner, P. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4756-07.2008 · Cited by 133
Neuronal activity in vivo enhances functional myelin repair
Ortíz, F. C., Habermacher, C., Graciarena, M., Houry, P.-Y., Nishiyama, A., Nait‐Oumesmar, B., & Angulo, M. C. (2019) · JCI Insight · doi:10.1172/jci.insight.123434 · Cited by 140
Cheng, X., Wang, Y., He, Q., Qiu, M. S., Whittemore, S. R., & Cao, Q. (2007) · Stem Cells · doi:10.1634/stemcells.2007-0284 · Cited by 136
Defining the NG2-expressing cell of the adult CNS
Horner, P. J., Thallmair, M., & Gage, F. H. (2002) · Journal of Neurocytology · doi:10.1023/a:1025739630398 · Cited by 133
A role for the NG2 proteoglycan in glioma progression
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Canoll, P., & Goldman, J. E. (2008) · Acta Neuropathologica · doi:10.1007/s00401-008-0432-9 · Cited by 128
Self-citationDulamea, A. O. (2017) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-319-47861-6_7 · Cited by 128
Goudarzvand, M., Javan, M., Mirnajafi‐Zadeh, J., Mozafari, S., & Tiraihi, T. (2009) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-009-9451-x · Cited by 128
Glezer, I., Lapointe, A., & Rivest, S. (2006) · The FASEB Journal · doi:10.1096/fj.05-5234fje · Cited by 131
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Sherafat, A., Pfeiffer, F., Reiss, A., Wood, W. M., & Nishiyama, A. (2021) · Nature Communications · doi:10.1038/s41467-021-22532-2 · Cited by 127
Veer, A. V., Du, Y., Fischer, T. Z., Boetig, D. R., Wood, M. R., & Dreyfus, C. F. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21841 · Cited by 121
Wilson, H., Scolding, N. J., & Raine, C. S. (2006) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2006.04.014 · Cited by 122
Bambakidis, N. C., & Miller, R. H. (2004) · The Spine Journal · doi:10.1016/j.spinee.2003.07.004 · Cited by 122
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Nishiyama, A., Boshans, L. L., Gonçalves, C. M., Wegrzyn, J., & Patel, K. D. (2015) · Brain Research · doi:10.1016/j.brainres.2015.08.013 · Cited by 128
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Sözmen, E. G., Rosenzweig, S., Llorente, I. L., DiTullio, D. J., Machnicki, M., Vinters, H. V., Havton, L. A., Giger, R. J., Hinman, J. D., & Carmichael, S. T. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1615322113 · Cited by 114
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Fernández-Castañeda, A., & Gaultier, A. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.01.005 · Cited by 117
Ruffini, F., Furlan, R., Poliani, P. L., Brambilla, E., Marconi, P., Bergami, A., Desina, G., Glorioso, J., Comı, G., & Martino, G. (2001) · Gene Therapy · doi:10.1038/sj.gt.3301523 · Cited by 112
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Hibbits, N., Pannu, R., Wu, T. J., & Armstrong, R. C. (2009) · ASN Neuro · doi:10.1042/an20090032 · Cited by 111
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Englander, E. W., Greeley, G. H., Wang, G., Perez-Polo, J. R., & Lee, H.-M. (1999) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19991015)58:2 · Cited by 51
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Paintlia, A. S., Paintlia, M. K., Khan, M., Vollmer, T. L., Singh, A. K., & Singh, I. (2005) · The FASEB Journal · doi:10.1096/fj.05-3861com · Cited by 107
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Canoll, P., Kraemer, R. T., Teng, K. K., Marchionni, M. A., & Salzer, J. L. (1999) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1998.0733 · Cited by 106
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Fakhoury, M. (2015) · Reviews in the Neurosciences · doi:10.1515/revneuro-2015-0001 · Cited by 105
Quraishe, S., Forbes, L. H., & Andrews, M. R. (2018) · Neural Plasticity · doi:10.1155/2018/2952386 · Cited by 108
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Zhang, L., Chopp, M., Zhang, R. L., Wang, L., Zhang, J., Wang, Y., Toh, Y., Santra, M., Lü, M., & Zhang, Z. G. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011016 · Cited by 108
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Miyamoto, N., Pham, L. D., Seo, J. H., Kim, K., Lo, E. H., & Arai, K. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1488-9 · Cited by 105
Fouad, K., Dietz, V., & Schwab, M. E. (2001) · Brain Research Reviews · doi:10.1016/s0165-0173(01)00096-0 · Cited by 103
Age-Related Decline in Oligodendrogenesis Retards White Matter Repair in Mice
Miyamoto, N., Pham, L. D., Hayakawa, K., Matsuzaki, T., Seo, J. H., Magnain, C. V., Ayata, C., Kim, K., Boas, D. A., Lo, E. H., et al. (2013) · Stroke · doi:10.1161/strokeaha.113.001530 · Cited by 104
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Terai, K., Soga, T., Takahashi, M. P., Kamohara, M., Ohno, K., Yatsugi, S., Okada, M., & Yamaguchi, T. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00791-1 · Cited by 102
NG2‐positive cells generate A2B5‐positive oligodendrocyte precursor cells
Baracskay, K. L., Kidd, G. J., Miller, R. H., & Trapp, B. D. (2007) · Glia · doi:10.1002/glia.20519 · Cited by 100
The NG2 proteoglycan promotes oligodendrocyte progenitor proliferation and developmental myelination
Kuchárová, K., & Stallcup, W. B. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.12.014 · Cited by 107
Heterogeneity of cycling glial progenitors in the adult mammalian cortex and white matter
Gensert, J. M., & Goldman, J. E. (2001) · Journal of Neurobiology · doi:10.1002/neu.1043 · Cited by 100
Self-citationMason, J. L., & Goldman, J. E. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1114 · Cited by 98
Self-citationNegative Impact of Statins on Oligodendrocytes and Myelin Formation In Vitro and In Vivo
Klopfleisch, S., Merkler, D., Schmitz, M., Klöppner, S., Schedensack, M., Jeserich, G., Althaus, H. H., & Brück, W. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2765-08.2008 · Cited by 97
Gregersen, R., Christensen, T., Lehrmann, E., Diemer, N. H., & Finsen, B. R. (2001) · Experimental Brain Research · doi:10.1007/s002210100715 · Cited by 97
Sullivan, G. M., Mierzwa, A. J., Kijpaisalratana, N., Tang, H., Wang, Y., Song, S., Selwyn, R. G., & Armstrong, R. C. (2013) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0000000000000009 · Cited by 99
Kay, J. N., & Blum, M. (2000) · Developmental Neuroscience · doi:10.1159/000017427 · Cited by 95
Cyclical and Dose-Dependent Responses of Adult Human Mature Oligodendrocytes to Fingolimod
Miron, V. E., Hall, J. A., Kennedy, T. E., Soliven, B. C., & Antel, J. P. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.080478 · Cited by 96
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Suo, N., Guo, Y., He, B., Gu, H., & Xie, X. (2019) · Glia · doi:10.1002/glia.23606 · Cited by 96
Björklund, A., & Lindvall, O. (2000) · Nature · doi:10.1038/35016175 · Cited by 94
Jin, J., Peng, Q., Hou, Z., Jiang, M., Wang, X., Langseth, A. J., Tao, M., Barker, P. B., Mori, S., Bergles, D. E., et al. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddv016 · Cited by 96
Boulanger, J. J., & Messier, C. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.03.063 · Cited by 93
Brousse, B., Magalon, K., Durbec, P., & Cayre, M. (2015) · Biology Open · doi:10.1242/bio.012773 · Cited by 91
Ness, J. P. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1149 · Cited by 91
Simvastatin regulates oligodendroglial process dynamics and survival
Miron, V. E., Rajasekharan, S., Jarjour, A. A., Zamvil, S. S., Kennedy, T. E., & Antel, J. P. (2006) · Glia · doi:10.1002/glia.20441 · Cited by 92
Wilson, H. C., Onischke, C., & Raine, C. S. (2003) · Glia · doi:10.1002/glia.10280 · Cited by 92
Jiang, T., Zhang, L., Pan, X., Zheng, H., Chen, X., Li, L., Luo, J., & Hu, X. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00404 · Cited by 91
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Mojaverrostami, S., Bojnordi, M. N., Ghasemi‐Kasman, M., Ebrahimzadeh, M. A., & Hamidabadi, H. G. (2018) · Advanced Pharmaceutical Bulletin · doi:10.15171/apb.2018.066 · Cited by 90
RESTORING FUNCTION AFTER SPINAL CORD INJURY
Becker, D., Sadowsky, C. L., & McDonald, J. W. (2003) · The Neurologist · doi:10.1097/01.nrl.0000038587.58012.05 · Cited by 88
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Alizadeh, A., & Karimi‐Abdolrezaee, S. (2016) · The Journal of Physiology · doi:10.1113/jp270895 · Cited by 93
Miyamoto, N., Tanaka, R., Shimura, H., Watanabe, T., Mori, H., Onodera, M., Mochizuki, H., Hattori, N., & Urabe, T. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2009.210 · Cited by 86
Lachapelle, F. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1124 · Cited by 85
Oligodendrocyte Progenitor Cell Susceptibility to Injury in Multiple Sclerosis
Cui, Q., Kuhlmann, T., Miron, V. E., Leong, S. Y., Fang, J. Q., Gris, P., Kennedy, T. E., Almazán, G., & Antel, J. P. (2013) · American Journal Of Pathology · doi:10.1016/j.ajpath.2013.04.016 · Cited by 86
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Egashira, Y., Zhao, H., Hua, Y., Keep, R. F., & Xi, G. (2015) · Stroke · doi:10.1161/strokeaha.115.010351 · Cited by 85
Farhadi, H. F., Lepage, P., Forghani, R., Friedman, H. C., Orfali, W., Jasmin, L., Miller, W., Hudson, T. J., & Peterson, A. C. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-32-10214.2003 · Cited by 83
Promoting Remyelination in Multiple Sclerosis—Recent Advances
Muenzel, E. J., & Williams, A. (2013) · Drugs · doi:10.1007/s40265-013-0146-8 · Cited by 89
Bansal, R., Miyake, H., Nakamura, I., Eto, H., Gotoh, A., Fujisawa, M., Okada, H., Arakawa, S., Kamidono, S., & Hara, I. (2002) · Developmental Neuroscience · doi:10.1159/000064944 · Cited by 82
Isolation and Characterization of Immature Oligodendrocyte Lineage Cells
Armstrong, R. C. (1998) · Methods · doi:10.1006/meth.1998.0685 · Cited by 83
Neural Stem and Progenitor Cells: A Strategy for Gene Therapy and Brain Repair
Pincus, D. W., Goodman, R. R., Fraser, R. A. R., Nedergaard, M., & Goldman, S. A. (1998) · Neurosurgery · doi:10.1097/00006123-199804000-00103 · Cited by 81
Talbott, J. F., Cao, Q., Enzmann, G. U., Benton, R. L., Achim, V., Cheng, X. X., Mills, M. D., Rao, M. S., & Whittemore, S. R. (2006) · Glia · doi:10.1002/glia.20369 · Cited by 79
Tanaka, K., Nogawa, S., Ito, D., Suzuki, S., Dembo, T., Kosakai, A., & Fukuuchi, Y. (2001) · Neuroreport · doi:10.1097/00001756-200107200-00025 · Cited by 80
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Mitome, M. (2001) · Brain · doi:10.1093/brain/124.11.2147 · Cited by 80
Muenzel, E. J., Schaefer, K., Obirei, B., Kremmer, E., Burton, E. A., Kuscha, V., Becker, C. G., Brösamle, C., Williams, A., & Becker, T. (2011) · Glia · doi:10.1002/glia.21260 · Cited by 77
Peng, H., Whitney, N. P., Wu, Y., Tian, C., Dou, H., Zhou, Y., & Zheng, J. (2008) · Glia · doi:10.1002/glia.20665 · Cited by 78
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Zhang, J., Zhang, Z. G., Morris, D. C., Li, Y., Roberts, C., Elias, S. B., & Chopp, M. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.09.054 · Cited by 78
Metadata
- Authors
- Gensert, J. M., & Goldman, J. E.
- Affiliations
- Columbia University Irving Medical Center (US)
- Columbia University (US)
- Corresponding author
- Gensert, JoAnn M
- ORCID
- Goldman, James E
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 1997-07
- Volume
- 19
- Issue
- 1
- Pages
- 197-203
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2005578607
- Cited by
- 544
- References
- 40
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 9 · 2023: 7 · 2022: 11 · 2021: 16 · 2020: 12 · 2019: 12 · 2018: 23 · 2017: 15 · 2016: 17 · 2015: 25 · 2014: 23 · 2013: 29 · 2012: 21
- FWCI
- 5.25
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Neuron (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (NS17125, R01NS017125)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
- Keywords
- remyelination, demyelination, oligodendrocyte precursor cells, myelinating oligodendrocytes, white matter, retroviral labeling, subcortical white matter, multiple sclerosis, CNS repair, adult neurogenesis
- MeSH terms
- Animals, Axons, Central Nervous System, Demyelinating Diseases, Female, Lysophosphatidylcholines, Stem Cells, Rats, Sprague-Dawley, Rats
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