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Progeny of Olig2-Expressing Progenitors in the Gray and White Matter of the Adult Mouse Cerebral Cortex
Open accessAbstract
Despite their abundance, still little is known about the rather frequent, constantly proliferating progenitors spread throughout the adult mouse brain parenchyma. The majority of these progenitors express the basic-helix-loop-helix transcription factor Olig2, and their number further increases after injury. Here, we examine the progeny of this progenitor population by genetic fate mapping using tamoxifen-inducible Cre-recombination in the Olig2 locus to turn on permanent reporter gene expression in the adult brain. Consistent with Olig2 expression in proliferating NG2(+) progenitors, most reporter(+) cells seen shortly after initiating recombination at adult stages incorporated BrdU and contained the proteoglycan NG2 in both the gray (GM) and the white matter (WM) of the cerebral cortex. However, at longer time points after induction, we observed profound differences in the identity of reporter(+) cells in the WM and GM. Whereas most of the Olig2(+) progenitors had generated mature, myelinating oligodendrocytes in the WM, hardly any reporter(+) cells showing mature oligodendrocyte characteristics were detectable even up to 6 months after recombination in the GM. In the GM, most reporter(+) cells remained NG2(+), even after injury, but stopped proliferating rather soon after recombination. Thus, our results demonstrate the continuous generation of mature, myelinating oligodendrocytes in the WM, whereas cells in the GM generated mostly postmitotic NG2(+) glia.
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“Oligodendrocyte precursors (OPs) continue to proliferate and generate myelinating oligodendrocytes (OLs) well into adulthood.”
From Oligodendrocyte Dynamics in the Healthy Adult CNS: Evidence for Myelin Remodeling (2013) · cites this paper as Dimou et al., 2008
Experimental — accuracy not yet measuredIn the citing paper
“The dataset-specific component of factor 28 showed that subject MD5828 had high expression of immediate early genes within polydendrocytes (Figure 4D), consistent with an acute injury (Dimou et al., 2008).”
From Single-Cell Multi-omic Integration Compares and Contrasts Features of Brain Cell Identity (2019) · cites this paper as Dimou et al., 2008
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Citations
Cites
Generalized lacZ expression with the ROSA26 Cre reporter strain
Soriano, P. (1999) · Nature Genetics · doi:10.1038/5007 · Cited by 5,237
White matter in learning, cognition, and psychiatric disorders
Fields, R. D. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.04.001 · Cited by 1,337
Origin of oligodendrocytes in the subventricular zone of the adult brain
Menn, B., Garcia-Verdugo, J. M., Yaschine, C., Gonzalez-Perez, O., Rowitch, D., & Alvarez-Buylla, A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1299-06.2006 · Cited by 972
NG2 cells generate both oligodendrocytes and gray matter astrocytes
Zhu, X., Bergles, D. E., & Nishiyama, A. (2007) · Development · doi:10.1242/dev.004895 · Cited by 699
The oligodendrocyte precursor cell in health and disease
Levine, J. M., Reynolds, R., & Fawcett, J. W. (2001) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01691-x · Cited by 673
Widespread recombinase expression using FLPeR (Flipper) mice
Farley, F. W., Soriano, P. M., Steffen, L. S., & Dymecki, S. M. (2000) · genesis · doi:10.1002/1526-968x(200011/12)28:3/4 · Cited by 602
Endogenous progenitors remyelinate demyelinated axons in the adult CNS
Gensert, J. M., & Goldman, J. E. (1997) · Neuron · doi:10.1016/s0896-6273(00)80359-1 · Cited by 544
Dynamic Contribution of Nestin-Expressing Stem Cells to Adult Neurogenesis
Lagace, D. C., Whitman, M. C., Noonan, M. A., Ables, J. L., DeCarolis, N. A., Arguello, A. A., Donovan, M. H., Fischer, S. J., Farnbauch, L. A., Beech, R. D., et al. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.3812-07.2007 · Cited by 502
Takebayashi, H., Nabeshima, Y., Yoshida, S., Chisaka, O., Ikenaka, K., & Nabeshima, Y. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00926-0 · Cited by 500
Shen, S., Sandoval, J., Swiss, V. A., Li, J., Dupree, J. L., Franklin, R. J. M., & Casaccia‐Bonnefil, P. (2008) · Nature Neuroscience · doi:10.1038/nn.2172 · Cited by 499
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Cullen, C., Pepper, R. E., Clutterbuck, M. T., Pitman, K. A., Oorschot, V., Auderset, L., Tang, A., Ramm, G., Emery, B., Rodger, J., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2020.108641 · Cited by 86
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Young, K. M., Mitsumori, T., Pringle, N. P., Grist, M., Kessaris, N., & Richardson, W. D. (2010) · Glia · doi:10.1002/glia.20976 · Cited by 98
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Viganò, F., Schneider, S. E., Cimino, M., Bonfanti, E., Gelosa, P., Sironi, L., Abbracchio, M. P., & Dimou, L. (2015) · Glia · doi:10.1002/glia.22929 · Cited by 91
Woerman, A. L., Oehler, A., Kazmi, S. A., Lee, J., Halliday, G. M., Middleton, L. T., Gentleman, S., Mordes, D. A., Spina, S., Grinberg, L. T., et al. (2019) · Acta Neuropathologica · doi:10.1007/s00401-019-01959-4 · Cited by 89
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Simon, C., Lickert, H., Götz, M., & Dimou, L. (2011) · genesis · doi:10.1002/dvg.22003 · Cited by 92
Pepper, R., Pitman, K. A., Cullen, C. L., & Young, K. M. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00399 · Cited by 86
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Levine, J. M. (2015) · Brain Research · doi:10.1016/j.brainres.2015.07.026 · Cited by 81
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Dimou, L., & Simons, M. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.09.015 · Cited by 86
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Prolo, L. M., Vogel, H. S., & Reimer, R. J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3005-09.2009 · Cited by 76
Regeneration of the central nervous system-principles from brain regeneration in adult zebrafish
Zambusi, A., & Ninkovic, J. (2019) · World Journal of Stem Cells · doi:10.4252/wjsc.v12.i1.8 · Cited by 72
Oligodendrocyte degeneration and recovery after focal cerebral ischemia
McIver, S. R., Muccigrosso, M. M., Gonzales, E. R., Lee, J., Roberts, M. S., Sands, M. S., & Goldberg, M. P. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.04.070 · Cited by 73
Injury-induced neurogenesis in the mammalian forebrain
Ohira, K. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0552-y · Cited by 73
The heterogeneous nature of NG2-glia
Viganò, F., & Dimou, L. (2015) · Brain Research · doi:10.1016/j.brainres.2015.09.012 · Cited by 72
Mitochondria in Myelinating Oligodendrocytes: Slow and Out of Breath?
Meyer, N., & Rinholm, J. E. (2021) · Metabolites · doi:10.3390/metabo11060359 · Cited by 78
Al-Mayhani, M. T. F., Grenfell, R. D., Narita, M., Piccirillo, S. G. M., Kenney-Herbert, E., Fawcett, J. W., Collins, V. P., Ichimura, K., & Watts, C. (2011) · Neuro-Oncology · doi:10.1093/neuonc/nor088 · Cited by 74
Properties of human astrocytes and NG2 glia
Bedner, P., Jabs, R., & Steinhäuser, C. (2020) · Glia · doi:10.1002/glia.23725 · Cited by 71
Bribián, A., Fontana, X., Llorens, F., Gavín, R., Reina, M., García-Verdugo, J. M., Torres, J. M., de Castro, F., & Río, J. A. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033872 · Cited by 70
Astrocyte development in the cerebral cortex: Complexity of their origin, genesis, and maturation
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Quan, L., Uyeda, A., & Muramatsu, R. (2022) · Inflammation and Regeneration · doi:10.1186/s41232-022-00193-y · Cited by 75
Dimovasili, C., Fair, A. E., Garza, I., Batterman, K. V., Mortazavi, F., Moore, T. L., & Rosene, D. L. (2022) · GeroScience · doi:10.1007/s11357-022-00621-4 · Cited by 74
Fate determination of adult human glial progenitor cells
Sim, F. J., Windrem, M. S., & Goldman, S. A. (2009) · Neuron Glia Biology · doi:10.1017/s1740925x09990317 · Cited by 68
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Matsumoto, Y., Tsunekawa, Y., Nomura, T., Suto, F., Matsumata, M., Tsuchiya, S., & Osumi, N. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027628 · Cited by 66
Pitter, K. L., Tamagno, I., Feng, X., Ghosal, K., Amankulor, N., Holland, E. C., & Hambardzumyan, D. (2014) · Glia · doi:10.1002/glia.22702 · Cited by 65
Albumin is taken up by hippocampal NG2 cells and astrocytes and decreases gap junction coupling
Braganza, O., Bedner, P., Hüttmann, K., von Staden, E., Friedman, A., Seifert, G., & Steinhäuser, C. (2012) · Epilepsia · doi:10.1111/j.1528-1167.2012.03665.x · Cited by 64
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Bove, R. M., & Green, A. (2017) · Neurotherapeutics · doi:10.1007/s13311-017-0577-0 · Cited by 66
Ghoumari, A. M., Abi‐Ghanem, C., Asbelaoui, N., Schumacher, M., & Hussain, R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21093163 · Cited by 68
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Auderset, L., Cullen, C. L., & Young, K. M. (2016) · PLOS ONE · doi:10.1371/journal.pone.0155878 · Cited by 62
Ferrer, I. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.07.004 · Cited by 65
Schneider, S. E., Gruart, A., Grade, S., Zhang, Y., Kröger, S., Kirchhoff, F., Gregor Eichele, C., García, J. M. D., & Dimou, L. (2016) · Glia · doi:10.1002/glia.23055 · Cited by 66
Curzio, D. L. D., Buist, R. J., & Bigio, M. R. D. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.06.004 · Cited by 61
Newville, J., Valenzuela, C. F., Li, L., Jantzie, L. L., & Cunningham, L. A. (2017) · Glia · doi:10.1002/glia.23164 · Cited by 70
Lentferink, D. H., Jongsma, J. M., Werkman, I. L., & Baron, W. (2018) · Scientific Reports · doi:10.1038/s41598-018-19934-6 · Cited by 63
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Hua, K., Schindler, M. K., McQuail, J. A., Forbes, M. E., & Riddle, D. R. (2012) · PLoS ONE · doi:10.1371/journal.pone.0052728 · Cited by 60
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Yazdankhah, M., Shang, P., Ghosh, S., Hose, S., Liu, H., Weiss, J., Fitting, C. S., Bhutto, I. A., Zigler, J. S., Qian, J. X., et al. (2020) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2020.100886 · Cited by 57
Ehrman, L. A., Nardini, D., Ehrman, S. E., Rizvi, T. A., Gulick, J. M., Krenz, M., Dasgupta, B., Robbins, J. M., Ratner, N., Nakafuku, M., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3515-13.2014 · Cited by 56
Kronenberg, G., Gertz, K. R., Cheung, G. T. Y., Buffo, A., Kettenmann, H., Götz, M., & Endres, M. (2010) · Stroke · doi:10.1161/strokeaha.110.583039 · Cited by 56
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Medina-Rodriguez, E. M., Bribián, A., Boyd, A. L., Palomo, V., Pastor, J., Lagares, A., Gil, C., Martı́nez, A., Williams, A., & de Castro, F. (2017) · Scientific Reports · doi:10.1038/srep43545 · Cited by 55
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SomethiNG 2 talk about—Transcriptional regulation in embryonic and adult oligodendrocyte precursors
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Schnieder, J., Mamazhakypov, A., Birnhuber, A., Wilhelm, J., Kwapiszewska, G., Ruppert, C., Markart, P., Wujak, L. A., Rubio, K., Barreto, G., et al. (2019) · Matrix Biology · doi:10.1016/j.matbio.2019.12.001 · Cited by 58
Winters, J. J., Ferguson, C., Lenk, G. M., Giger-Mateeva, V. I., Shrager, P. G., Meisler, M. H., & Giger, R. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1482-11.2011 · Cited by 54
Chacon-De-La-Rocha, I., Fryatt, G., Rivera, A. D., Verkhratsky, A., Raineteau, O., Gomez-Nicola, D., & Butt, A. M. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.575082 · Cited by 52
Méndez‐Gómez, H. R., Vergaño‐Vera, E., Abad, J. L., Bulfone, A., Moratalla, R., de Pablo, F., & Vicario‐Abejón, C. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.08.011 · Cited by 49
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März, M., Viales, R. R., Rastegar, S., & Strähle, U. (2010) · Developmental Dynamics · doi:10.1002/dvdy.22455 · Cited by 52
Rivera, A. D., Vanzulli, I., Rodriguez, J. J., & Butt, A. M. (2016) · Current Alzheimer Research · doi:10.2174/1567205013666151116125518 · Cited by 50
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Blum, R., Heinrich, C., Sánchez, R., Lepier, A., Gundelfinger, E. D., Berninger, B., & Götz, M. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq107 · Cited by 54
Auderset, L., Landowski, L. M., Foa, L. C., & Young, K. M. (2016) · Stem Cells International · doi:10.1155/2016/2108495 · Cited by 51
Wachter, B., Schürger, S., Rolinger, J., von Ameln-Mayerhofer, A., Berg, D., Wagner, H.-J., & Küppers, E. (2010) · Cell and Tissue Research · doi:10.1007/s00441-010-1061-x · Cited by 54
Caillava, C., Vandenbosch, R., Jablonska, B., Deboux, C., Spigoni, G., Gallo, V., Malgrange, B., & Evercooren, A. B. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201004146 · Cited by 55
Balia, M., Benamer, N., & Angulo, M. C. (2017) · Glia · doi:10.1002/glia.23197 · Cited by 50
Resident cell lineages are preserved in pulmonary vascular remodeling
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Zimmer, T. S., Broekaart, D. W. M., Gruber, V.-E., van Vliet, E. A., Mühlebner, A., & Aronica, E. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.01028 · Cited by 48
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Passlick, S., Grauer, M., Schafer, C., Jabs, R., Seifert, G., & Steinhäuser, C. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5562-12.2013 · Cited by 50
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Metadata
- Authors
- Dimou, L., Simon, C., Kirchhoff, F., Takebayashi, H., & Götz, M.
- Affiliations
- Physiologisches Institut (DE)
- Helmholtz Munich (DE)
- Max Planck Society (DE)
- National Institute for Physiological Sciences (JP)
- Center for Integrated Protein Science Munich (DE)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2008-10-08
- Volume
- 28
- Issue
- 41
- Pages
- 10434-10442
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6671038
- OpenAlex
- W2095490681
- Cited by
- 551
- References
- 51
- Citations by year
- 2026: 19 · 2025: 19 · 2024: 22 · 2023: 30 · 2022: 26 · 2021: 38 · 2020: 45 · 2019: 35 · 2018: 32 · 2017: 35 · 2016: 33 · 2015: 40 · 2014: 42 · 2013: 36 · 2012: 23
- FWCI
- 7.73
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Max Planck Institute for Plasma Physics (submittedVersion)
- Site cant be reached (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- European Commission
- Deutsche Forschungsgemeinschaft
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Oncology › Glioma Diagnosis and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Keywords
- Olig2, cerebral cortex, gray matter, white matter, NG2 glia, oligodendrocyte differentiation, myelination, fate mapping, Cre recombination, BrdU labeling, brain injury, progenitor cell proliferation
- MeSH terms
- Oligodendrocyte Transcription Factor 2, Chondroitin Sulfate Proteoglycan 4, Animals, Antigens, Cell Differentiation, Cerebral Cortex, Mice, Inbred C57BL, Mitosis, Myelin Sheath, Nerve Tissue Proteins, Neuroglia, Oligodendroglia, Periaqueductal Gray, Proteoglycans, Stem Cells, Tamoxifen, Wounds, Stab, Gene Expression, Genes, Reporter, Integrases, Animals, Genetically Modified, Cell Proliferation, Mice, Basic Helix-Loop-Helix Proteins
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