Progenitors in the adult cerebral cortex: cell cycle properties and regulation by physiological stimuli and injury
Abstract
The adult brain parenchyma contains a widespread population of progenitors generating different cells of the oligodendrocyte lineage such as NG2+ cells and some mature oligodendrocytes. However, it is still largely unknown how proliferation and lineage decisions of these progenitors are regulated. Here, we first characterized the cell cycle length, proliferative fraction, and progeny of dividing cells in the adult cerebral cortex and then compared these proliferation characteristics after two distinct stimuli, invasive acute brain injury and increased physiological activity by voluntary physical exercise. Our data show that adult parenchymal progenitors have a very long cell cycle due to an extended G1 phase, many of them can divide at least twice and only a limited proportion of the progeny differentiates into mature oligodendrocytes. After stab wound injury, however, many of these progenitors re-enter the cell cycle very fast, suggesting that the normally long G1 phase is subject to regulation and can be abruptly shortened. In striking contrast, voluntary physical exercise shows the opposite effect with increased exit of the cell cycle followed by an enhanced and fast differentiation into mature oligodendrocytes. Taken together, our data demonstrate that the endogenous population of adult brain parenchymal progenitors is subject to profound modulation by environmental stimuli in both directions, either faster proliferation or faster differentiation.
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The recalculated TC in cortical gray matter of P60 mice is approximately 36 days, in close agreement with a recent estimate of approximately 37 days in 2- to 3-month-old mice.
“For example, we now recalculate TC in the cortical gray matter of P60 mice to be ∼36 days, in close agreement with a recent estimate of ∼37 days in 2- to 3-month-old mice (Simon et al., 2011).”
From Oligodendrocyte Dynamics in the Healthy Adult CNS: Evidence for Myelin Remodeling (2013) · cites this paper as Simon et al., 2011
Cites
Running increases cell proliferation and neurogenesis in the adult mouse dentate gyrus
van Praag, H., Kempermann, G., & Gage, F. H. (1999) · Nature Neuroscience · doi:10.1038/6368 · Cited by 3,880 · see citing works
Brain Structures Differ between Musicians and Non-Musicians
Christian Gaser, B., & Gottfried Schlaug, A. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-27-09240.2003 · Cited by 1,626 · see citing works
Adult neurogenesis produces a large pool of new granule cells in the dentate gyrus
Cameron, H. A., & Mckay, R. D. G. (2001) · Journal of Comparative Neurology · doi:10.1002/cne.1040 · Cited by 1,585 · see citing works
Extensive piano practicing has regionally specific effects on white matter development
Bengtsson, S. L., Nagy, Z., Skare, S., Forsman, L., Forssberg, H., & Ullén, F. (2005) · Nature Neuroscience · doi:10.1038/nn1516 · Cited by 1,193 · see citing works
Glutamatergic synapses on oligodendrocyte precursor cells in the hippocampus
Bergles, D. E., Roberts, J. D. B., Somogyi, P., & Jahr, C. E. (2000) · Nature · doi:10.1038/35012083 · Cited by 1,062 · see citing works
PDGFRA/NG2 glia generate myelinating oligodendrocytes and piriform projection neurons in adult mice
Rivers, L. E., Young, K. M., Rizzi, M., Jamen, F., Psachoulia, K., Wade, A., Kessaris, N., & Richardson, W. D. (2008) · Nature Neuroscience · doi:10.1038/nn.2220 · Cited by 961 · see citing works
Dawson, M. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00210-0 · Cited by 927 · see citing works
Polydendrocytes (NG2 cells): multifunctional cells with lineage plasticity
Nishiyama, A., Komitova, M., Suzuki, R., & Zhu, X. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2495 · Cited by 865 · see citing works
The oligodendrocyte and its many cellular processes
Pfeiffer, S. E., Warrington, A. E., & Bansal, R. (1993) · Trends in Cell Biology · doi:10.1016/0962-8924(93)90213-k · Cited by 852 · see citing works
Kang, S., Fukaya, M., Yang, J. K., Rothstein, J., & Bergles, D. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.009 · Cited by 778 · see citing works
Proliferation and Differentiation of Progenitor Cells Throughout the Intact Adult Rat Spinal Cord
Horner, P. J., Power, A. E., Kempermann, G., Kuhn, H. G., Palmer, T. D., Winkler, J., Thal, L. J., & Gage, F. H. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-06-02218.2000 · Cited by 777 · see citing works
Origin and progeny of reactive gliosis: A source of multipotent cells in the injured brain
Buffo, A., Rite, I., Tripathi, P., Lepier, A., Colak, D., Horn, A.-P., Mori, T., & Götz, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709002105 · Cited by 766 · see citing works
Self-citationNowakowski, R. S., Lewin, S. B., & Miller, M. W. (1989) · Journal of Neurocytology · doi:10.1007/bf01190834 · Cited by 755 · see citing works
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 678 · see citing works
Nunes, M. C., Roy, N. S., Keyoung, H. M., Goodman, R. R., McKhann, G. M., Jiang, L., Kang, J., Nedergaard, M., & Goldman, S. A. (2003) · Nature Medicine · doi:10.1038/nm837 · Cited by 659 · see citing works
Zawadzka, M., Rivers, L. E., Fancy, S. P. J., Zhao, C., Tripathi, R., Jamen, F., Young, K., Goncharevich, A., Pohl, H., Rizzi, M., et al. (2010) · Cell stem cell · doi:10.1016/j.stem.2010.04.002 · Cited by 650 · see citing works
Taupin, P. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2006.08.002 · Cited by 645 · see citing works
Origin of New Glial Cells in Intact and Injured Adult Spinal Cord
Barnabé-Heider, F., Göritz, C., Sabelström, H., Takebayashi, H., Pfrieger, F. W., Meletis, K., & Frisén, J. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.07.014 · Cited by 628 · see citing works
Dimou, L., Simon, C., Kirchhoff, F., Takebayashi, H., & Götz, M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2831-08.2008 · Cited by 551 · see citing works
Stevens (2002) · doi:10.1016/s0896-6273(02)01067-x · Cited by 543 · see citing works
Belachew, S. M., Chittajallu, R., Aguirre, A. A., Yuan, X. Q., Kirby, M., Anderson, S. M., & Gallo, V. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200210110 · Cited by 489 · see citing works
Identification of an adult-specific glial progenitor cell
Wolswijk, G., & Noble, M. A. (1989) · Development · doi:10.1242/dev.105.2.387 · Cited by 485 · see citing works
Nagelhus, E. A., Horio, Y., Inanobe, A., Fujita, A., Haug, F. Š., Nielsen, S., Kurachi, Y., & Ottersen, O. P. (1999) · Glia · doi:10.1002/(sici)1098-1136(199903)26:1 · Cited by 472 · see citing works
The life, death, and replacement of oligodendrocytes in the adult CNS
McTigue, D. M., & Tripathi, R. B. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05570.x · Cited by 455 · see citing works
Lin, S.-C., & Bergles, D. (2004) · Nature Neuroscience · doi:10.1038/nn1162 · Cited by 449 · see citing works
McTigue, D. M., Wei, P., & Stokes, B. T. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-10-03392.2001 · Cited by 423 · see citing works
Buffo, A., Vosko, M., Ertürk, D., Hamann, G., Jucker, M., Rowitch, D., & Götz, M. (2005) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0506535102 · Cited by 402 · see citing works
Self-citationIncreased expression of the NG2 chondroitin-sulfate proteoglycan after brain injury
Levine, J. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-08-04716.1994 · Cited by 395 · see citing works
Control of oligodendrocyte number in the developing rat optic nerve
Barres, B. A., & RAFF, M. C. (1994) · Neuron · doi:10.1016/0896-6273(94)90305-0 · Cited by 385 · see citing works
Spiking and nonspiking classes of oligodendrocyte precursor glia in CNS white matter
Káradóttir, R. T., Hamilton, N. B., Bakiri, Y., & Attwell, D. (2008) · Nature Neuroscience · doi:10.1038/nn2060 · Cited by 370 · see citing works
Ehninger, D. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.8.845 · Cited by 314 · see citing works
Levine, J. M., & Reynolds, R. (1999) · Experimental Neurology · doi:10.1006/exnr.1999.7224 · Cited by 282 · see citing works
Development and differentiation of glial precursor cells in the rat cerebellum
Levine, J. M., Stincone, F., & Lee, Y. (1993) · Glia · doi:10.1002/glia.440070406 · Cited by 279 · see citing works
Myelination: An Overlooked Mechanism of Synaptic Plasticity?
Fields, R. D. (2005) · The Neuroscientist · doi:10.1177/1073858405282304 · Cited by 271 · see citing works
NG2 cells: Properties, progeny and origin
Trotter, J., Karram, K., & Nishiyama, A. (2010) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.12.006 · Cited by 264 · see citing works
Differentiation of proliferated NG2-positive glial progenitor cells in a remyelinating lesion
Watanabe, M., Toyama, Y., & Nishiyama, A. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10338 · Cited by 261 · see citing works
Cell cycle dynamics of NG2 cells in the postnatal and ageing brain
Psachoulia, K., Jamen, F., Young, K. M., & Richardson, W. D. (2009) · Neuron Glia Biology · doi:10.1017/s1740925x09990354 · Cited by 257 · see citing works
Adult hippocampal neurogenesis and voluntary running activity: Circadian and dose‐dependent effects
Holmes, M. M., Galea, L. A. M., Mistlberger, R. E., & Kempermann, G. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20039 · Cited by 233 · see citing works
Aguirre, A. A., & Gallo, V. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3572-04.2004 · Cited by 224 · see citing works
Yuan, X. Q., Eisen, A. M., McBain, C. J., & Gallo, V. (1998) · Development · doi:10.1242/dev.125.15.2901 · Cited by 221 · see citing works
Purification and Characterization of Adult Oligodendrocyte Precursor Cells from the Rat Optic Nerve
Shi, J., Marinovich, A. M., & Barres, B. A. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-12-04627.1998 · Cited by 219 · see citing works
Amankulor, N. M., Hambardzumyan, D., Pyonteck, S. M., Becher, O. J., Joyce, J. A., & Holland, E. C. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2500-09.2009 · Cited by 200 · see citing works
Long-Term Impact of Radiation on the Stem Cell and Oligodendrocyte Precursors in the Brain
Panagiotakos, G., Al-Shamy, G., Chan, B., Abrams, R. M. C., Greenberg, E. D., Saxena, A., Bradbury, M. S., Edgar, M. A., Gutin, P. H., & Tabar, V. S. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000588 · Cited by 184 · see citing works
Adult-born SVZ progenitors receive transient synapses during remyelination in corpus callosum
Etxeberría, A., Mangin, J., Aguirre, A. A., & Gallo, V. (2010) · Nature Neuroscience · doi:10.1038/nn.2500 · Cited by 181 · see citing works
Alonso, G. (2004) · Glia · doi:10.1002/glia.20121 · Cited by 178 · see citing works
Mason, J. L., Xuan, S., Dragatsis, I., Efstratiadis, A., & Goldman, J. E. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-20-07710.2003 · Cited by 177 · see citing works
Hampton, D. W., Rhodes, K. E., Zhao, C., Franklin, R. J. M., & Fawcett, J. W. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.05.028 · Cited by 157 · see citing works
Fortin, D. A., Rom, E., Sun, H. D., Yayon, A., & Bansal, R. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2120-05.2005 · Cited by 156 · see citing works
Alterations in the Thickness of Motor Cortical Subregions After Motor-Skill Learning and ExercisePreprint
Anderson, B. J., Eckburg, P. B., & Relucio, K. I. (2002) · Learning & Memory · doi:10.1101/lm.43402 · Cited by 142 · see citing works
NG2+/Olig2+ Cells are the Major Cycle‐Related Cell Population of the Adult Human Normal Brain
Geha, S., Pallud, J., Junier, M., Devaux, B. C., Léonard, N., Chassoux, F., Chneiweiss, H., Daumas‐Duport, C., & Varlet, P. (2009) · Brain Pathology · doi:10.1111/j.1750-3639.2009.00295.x · Cited by 138 · see citing works
NG2: a component of the glial scar that inhibits axon growth
Tan, A. M., Zhang, W., & Levine, J. M. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00452.x · Cited by 129 · see citing works
Rhodes, K. E., Raivich, G., & Fawcett, J. W. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.01.055 · Cited by 128 · see citing works
NG2‐expressing cells in the nervous system revealed by the NG2‐EYFP‐knockin mouse
Karram, K., Goebbels, S., Schwab, M. H., Jennissen, K., Seifert, G., Steinhäuser, C., Nave, K., & Trotter, J. (2008) · genesis · doi:10.1002/dvg.20440 · Cited by 126 · see citing works
Attenuation of proliferation in oligodendrocyte precursor cells by activated microglia
Taylor, D. L., Pirianov, G., Holland, S., McGinnity, C. J., Norman, A. L., Reali, C., Diemel, L. T., Gveric, D. O., Yeung, D., & Mehmet, H. (2010) · Journal of Neuroscience Research · doi:10.1002/jnr.22335 · Cited by 111 · see citing works
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 · see citing works
Mason, J. L., & Goldman, J. E. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1114 · Cited by 98 · see citing works
Inhibition of CXCR2 signaling promotes recovery in models of multiple sclerosis
Kerstetter, A. E., Padovani-Claudio, D. A., Bai, L., & Miller, R. H. (2009) · Experimental Neurology · doi:10.1016/j.expneurol.2009.07.010 · Cited by 95 · see citing works
Endl, E., & Gerdes, J. (2000) · Journal of Cellular Physiology · doi:10.1002/(sici)1097-4652(200003)182:3 · Cited by 89 · see citing works
Inhibition of Axon Growth by Oligodendrocyte Precursor Cells
Chen, Z. J., Ughrin, Y., & Levine, J. M. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1102 · Cited by 86 · see citing works
Rhodes, K. E., Moon, L. D. F., & Fawcett, J. W. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00285-9 · Cited by 85 · see citing works
Müller, J., Reyes‐Haro, D., Pivneva, T. A., et al. (2009) · The Journal of General Physiology · doi:10.1085/jgp.200910194 · Cited by 79 · see citing works
Bednarczyk, M. R., Aumont, A., Décary, S., Bergeron, R., & Fernandes, K. J. L. (2009) · Hippocampus · doi:10.1002/hipo.20621 · Cited by 79 · see citing works
Tripathi, R. B., & McTigue, D. M. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21787 · Cited by 67 · see citing works
Voluntary Exercise Increases Oligodendrogenesis in Spinal Cord
Krityakiarana, W., Monteros, A. E. D. L., Ghiani, C. A., Zhao, P. M., Topaldjikian, N., Gómez‐Pinilla, F., Yamaguchi, M., Kotchabhakdi, N., & de Vellis, J. (2010) · International Journal of Neuroscience · doi:10.3109/00207450903222741 · Cited by 65 · see citing works
Winkler, M. K., & Benveniste, E. N. (1998) · Glia · doi:10.1002/(sici)1098-1136(199802)22:2 · Cited by 50 · see citing works
A novel family of ancient vertebrate odorant receptors
Berghard, A., & Dryer, L. (1998) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(19981115)37:3 · Cited by 50 · see citing works
Irvine, K., & Blakemore, W. F. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05313.x · Cited by 45 · see citing works
Hancock, A. M., Priester, C., Kidder, E., et al. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.11.050 · Cited by 33 · see citing works
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McKenzie, I. A., Ohayon, D., Li, H., Paes de Faria, J., Emery, B., Tohyama, K., & Richardson, W. D. (2014) · Science · doi:10.1126/science.1254960 · Cited by 1,177 · see citing works
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Young, K. M., Psachoulia, K., Tripathi, R. B., Dunn, S.-J., Cossell, L., Attwell, D., Tohyama, K., & Richardson, W. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.006 · Cited by 872 · see citing works
“However, others reported a higher growth fraction; Simon et al. (2011) reported that 80% of neocortical gray matter OPs incorporated BrdU during a 37 day labeling period, and Kang et al. (2010) reported that all OPs incorporated BrdU during 30 days.”
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Xin, W., & Chan, J. R. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-00379-8 · Cited by 329 · see citing works
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Richardson, W. D., Young, K. M., Tripathi, R. B., & McKenzie, I. (2011) · Neuron · doi:10.1016/j.neuron.2011.05.013 · Cited by 300 · see citing works
Ortega, F., Gascón, S., Masserdotti, G., Deshpande, A., Simon, C., Fischer, J., Dimou, L., Chichung Lie, D., Schroeder, T., & Berninger, B. (2013) · Nature Cell Biology · doi:10.1038/ncb2736 · Cited by 247 · see citing works
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Kang, Z., Wang, C., Zepp, J., Wu, L., Sun, K., Zhao, J., Chandrasekharan, U., DiCorleto, P. E., Trapp, B. D., Ransohoff, R. M., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3505 · Cited by 218 · see citing works
Behrendt, G., Baer, K., Buffo, A., Curtis, M. A., Faull, R. L., Rees, M. I., Götz, M., & Dimou, L. (2013) · Glia · doi:10.1002/glia.22432 · Cited by 219 · see citing works
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Sirko, S., Irmler, M., Gascón, S., Bek, S., Schneider, S., Dimou, L., Obermann, J., De Souza Paiva, D., Poirier, F., Beckers, J., et al. (2015) · Glia · doi:10.1002/glia.22898 · Cited by 126 · see citing works
Self-citationDziedzic, A., Miller, E., Saluk-Bijak, J., & Bijak, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21051852 · Cited by 38 · see citing works
- Authors
- Simon, C., Götz, M., & Dimou, L.
- Affiliations
- Helmholtz Munich (DE)
- Corresponding author
- Götz, Magdalena
- Dimou, Leda
- Venue
- Glia
- Publisher
- Wiley
- Published
- 2011-03-28
- Volume
- 59
- Issue
- 6
- Pages
- 869-881
- ISSN
- 0894-1491 (ISSN-L)
- 1098-1136
- OpenAlex
- W1967017576
- Cited by
- 313
- References
- 68
- Citations by year
- 2026: 4 · 2025: 9 · 2024: 13 · 2023: 16 · 2022: 12 · 2021: 22 · 2020: 26 · 2019: 31 · 2018: 30 · 2017: 36 · 2016: 10 · 2015: 23 · 2014: 28 · 2013: 32 · 2012: 13
- FWCI
- 8.49
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Glia (publishedVersion)
- PubMed (publishedVersion)
- Site cant be reached (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Neonatal and fetal brain pathology
- Health Sciences › Medicine › Genetics › Glioma Diagnosis and Treatment
- Keywords
- cerebral cortex, cell cycle, G1 phase, oligodendrocyte lineage, oligodendrocyte precursor cells, stab wounds, progenitor cell proliferation, progenitor cell differentiation
- MeSH terms
- Animals, Cell Differentiation, Cerebral Cortex, Disease Models, Animal, Oligodendroglia, Stem Cells, Cell Lineage, Cell Proliferation, Mice
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