Disruption of oligodendrogenesis impairs memory consolidation in adult mice
Open accessAbstract
The generation of myelin-forming oligodendrocytes persists throughout life and is regulated by neural activity. Here we tested whether experience-driven changes in oligodendrogenesis are important for memory consolidation. We found that water maze learning promotes oligodendrogenesis and de novo myelination in the cortex and associated white matter tracts. Preventing these learning-induced increases in oligodendrogenesis without affecting existing oligodendrocytes impaired memory consolidation of water maze, as well as contextual fear, memories. These results suggest that de novo myelination tunes activated circuits, promoting coordinated activity that is important for memory consolidation. Consistent with this, contextual fear learning increased the coupling of hippocampal sharp wave ripples and cortical spindles, and these learning-induced increases in ripple-spindle coupling were blocked when oligodendrogenesis was suppressed. Our results identify a non-neuronal form of plasticity that remodels hippocampal-cortical networks following learning and is required for memory consolidation.
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Even small changes in myelination can exert profound effects on neural circuit dynamics and consequently on cognitive function.
“even small changes in myelination can exert profound effects on neural circuit dynamics and consequently on cognitive function (Steadman et al., 2020; Noori et al., 2020; Pajevic et al., 2014).”
From Mild respiratory COVID can cause multi-lineage neural cell and myelin dysregulation (2022) · cites this paper as Steadman et al., 2020
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Cites
Diekelmann, S., & Born, J. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2762 · Cited by 3,760 · see citing works
Regional Development of the Brain in Early Life
(1968) · Archives of Disease in Childhood · doi:10.1136/adc.43.229.388 · Cited by 2,107 · see citing works
(1967) · Medical Entomology and Zoology · Cited by 1,713 · see citing works
Plasticity in gray and white: neuroimaging changes in brain structure during learning
Zatorre, R. J., Fields, R. D., & Johansen-Berg, H. (2012) · Nature Neuroscience · doi:10.1038/nn.3045 · Cited by 1,685 · see citing works
Training induces changes in white-matter architecture
Scholz, J., Klein, M. C., Behrens, T. E. J., & Johansen-Berg, H. (2009) · Nature Neuroscience · doi:10.1038/nn.2412 · Cited by 1,508 · see citing works
Neuronal activity promotes oligodendrogenesis and adaptive myelination in the mammalian brain
Gibson, E. M., Purger, D., Mount, C. W., Goldstein, A. K., Lin, G. L., Wood, L. S., Inema, I., Miller, S. E., Bieri, G., Zuchero, J. B., et al. (2014) · Science · doi:10.1126/science.1252304 · Cited by 1,472 · see citing works
Self-citationBrain-state- and cell-type-specific firing of hippocampal interneurons in vivo
Klausberger, T., Magill, P. J., Márton, L. F., Roberts, J. D. B., Cobden, P. M., Buzsáki, G., & Somogyi, P. (2003) · Nature · doi:10.1038/nature01374 · Cited by 1,345 · see citing works
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 · see citing works
Motor skill learning requires active central myelination
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
Engrams and circuits crucial for systems consolidation of a memory
Kitamura, T., Ogawa, S. K., Roy, D. S., Okuyama, T., Morrissey, M. D., Smith, L. M., Redondo, R. L., & Tonegawa, S. (2017) · Science · doi:10.1126/science.aam6808 · Cited by 1,104 · see citing works
Coordinated interactions between hippocampal Ripples and Cortical Spindles during Slow-Wave Sleep
Siapas, A. G., & Wilson, M. A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80629-7 · Cited by 1,052 · 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
Hippocampal replay in the awake state: a potential substrate for memory consolidation and retrieval
Carr, M. F., Jadhav, S. P., & Frank, L. M. (2011) · Nature Neuroscience · doi:10.1038/nn.2732 · Cited by 958 · see citing works
The Hippocampo-Neocortical Dialogue
Buzsáki, G. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.2.81 · Cited by 938 · see citing works
Hughes, E. G., Kang, S. H., Fukaya, M., & Bergles, D. E. (2013) · Nature Neuroscience · doi:10.1038/nn.3390 · Cited by 808 · see citing works
A new mechanism of nervous system plasticity: activity-dependent myelination
Fields, R. D. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn4023 · Cited by 794 · 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
Replay of rule-learning related neural patterns in the prefrontal cortex during sleep
Peyrache, A., Khamassi, M., Benchenane, K., Wiener, S. I., & Battaglia, F. P. (2009) · Nature Neuroscience · doi:10.1038/nn.2337 · Cited by 767 · see citing works
Causal evidence for the role of REM sleep theta rhythm in contextual memory consolidation
Boyce, R., Glasgow, S. D., Williams, S., & Adamantidis, A. (2016) · Science · doi:10.1126/science.aad5252 · Cited by 696 · see citing works
Josselyn, S. A., Köhler, S., & Frankland, P. W. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn4000 · Cited by 687 · see citing works
Self-citationInduction of myelination in the central nervous system by electrical activity
Demerens, C., Stankoff, B., Logak, M., Anglade, P., Allinquant, B., Couraud, F., Zalc, B., & Lubetzki, C. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.18.9887 · Cited by 678 · see citing works
Proliferation of oligodendrocyte precursor cells depends on electrical activity in axons
Barres, B. A., & Raff, M. C. (1993) · Nature · doi:10.1038/361258a0 · Cited by 673 · see citing works
Hippocampo-cortical coupling mediates memory consolidation during sleep
Maingret, N., Girardeau, G., Todorova, R., Goutierre, M., & Zugaro, M. (2016) · Nature Neuroscience · doi:10.1038/nn.4304 · Cited by 667 · see citing works
The synaptic plasticity and memory hypothesis: encoding, storage and persistence
Takeuchi, T., Duszkiewicz, A. J., & Morris, R. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0288 · Cited by 664 · see citing works
Control of local protein synthesis and initial events in myelination by action potentials
Wake, H., Lee, P. R., & Fields, R. D. (2011) · Science · doi:10.1126/science.1206998 · Cited by 636 · see citing works
A Neural Circuit for Memory Specificity and Generalization
Xu, W., & Südhof, T. C. (2013) · Science · doi:10.1126/science.1229534 · Cited by 634 · see citing works
Distinct Profiles of Myelin Distribution Along Single Axons of Pyramidal Neurons in the Neocortex
Tomassy, G. S., Berger, D. R., Chen, H.-H., Kasthuri, N., Hayworth, K. J., Vercelli, A., Seung, H. S., Lichtman, J. W., & Arlotta, P. (2014) · Science · doi:10.1126/science.1249766 · Cited by 600 · see citing works
Myelin gene regulatory factor is a critical transcriptional regulator required for CNS myelination
Emery, B., Agalliu, D., Cahoy, J. D., Watkins, T. A., Dugas, J. C., Mulinyawe, S. B., Ibrahim, A., Ligon, K. L., Rowitch, D. H., & Barres, B. A. (2009) · Cell · doi:10.1016/j.cell.2009.04.031 · Cited by 559 · see citing works
Dynamics of Oligodendrocyte Generation and Myelination in the Human Brain
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 · see citing works
Myelin remodeling through experience-dependent oligodendrogenesis in the adult somatosensory cortex
Hughes, E. G., Orthmann-Murphy, J. L., Langseth, A. J., & Bergles, D. E. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0121-5 · Cited by 540 · see citing works
Rapid production of new oligodendrocytes is required in the earliest stages of motor-skill learning
Xiao, L., Ohayon, D., McKenzie, I. A., Sinclair-Wilson, A., Wright, J. L., Fudge, A. D., Emery, B., Li, H., & Richardson, W. D. (2016) · Nature Neuroscience · doi:10.1038/nn.4351 · Cited by 507 · cited 6× · see citing works
“Such myelin remodeling likely contributes to memory encoding (Geraghty et al., 2019; McKenzie et al., 2014; Xiao et al., 2016).”
BackgroundResultInfluentialLifelong cortical myelin plasticity and age-related degeneration in the live mammalian brain
Hill, R. A., Li, A. M., & Grutzendler, J. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0120-6 · Cited by 467 · see citing works
The role of engram cells in the systems consolidation of memory
Tonegawa, S., Morrissey, M. D., & 北村, 貴. (2018) · Nature reviews. Neuroscience · doi:10.1038/s41583-018-0031-2 · Cited by 454 · see citing works
Neuronal activity biases axon selection for myelination in vivo
Hines, J. H., Ravanelli, A. M., Schwindt, R. K., Scott, E. K., & Appel, B. (2015) · Nature Neuroscience · doi:10.1038/nn.3992 · Cited by 453 · see citing works
White Matter Plasticity in the Adult Brain
Sampaio‐Baptista, C., & Johansen‐Berg, H. (2017) · Neuron · doi:10.1016/j.neuron.2017.11.026 · Cited by 414 · see citing works
Synaptic vesicle release regulates myelin sheath number of individual oligodendrocytes in vivo
Mensch, S., Baraban, M., Almeida, R., Czopka, T., Ausborn, J., El Manira, A., & Lyons, D. A. (2015) · Nature Neuroscience · doi:10.1038/nn.3991 · Cited by 398 · see citing works
Early Tagging of Cortical Networks Is Required for the Formation of Enduring Associative Memory
Lesburguères, E., Gobbo, O. L., Alaux‐Cantin, S., Hambücken, A., Trifilieff, P., & Bontempi, B. (2011) · Science · doi:10.1126/science.1196164 · Cited by 390 · see citing works
Role of myelin plasticity in oscillations and synchrony of neuronal activity
Pajevic, S., Basser, P. J., & Fields, R. D. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2013.11.007 · Cited by 378 · see citing works
Pharmacogenetic stimulation of neuronal activity increases myelination in an axon-specific manner
Mitew, S., Gobius, I., Fenlon, L. R., McDougall, S. J., Hawkes, D. J., Xing, Y. L., Bujalka, H., Gundlach, A. L., Richards, L. J., Kilpatrick, T. J., et al. (2018) · Nature Communications · doi:10.1038/s41467-017-02719-2 · Cited by 345 · see citing works
Individual Oligodendrocytes Have Only a Few Hours in which to Generate New Myelin Sheaths In Vivo
Czopka, T., ffrench‐Constant, C., & Lyons, D. A. (2013) · Developmental Cell · doi:10.1016/j.devcel.2013.05.013 · Cited by 332 · see citing works
Chemogenetic Interrogation of a Brain-wide Fear Memory Network in Mice
Vetere, G., Kenney, J. W., Tran, L. M., Xia, F., Steadman, P. E., Parkinson, J., Josselyn, S. A., & Frankland, P. W. (2017) · Neuron · doi:10.1016/j.neuron.2017.03.037 · Cited by 293 · see citing works
Self-citationLoss of adaptive myelination contributes to methotrexate chemotherapy-related cognitive impairment
Geraghty, A. C., Gibson, E. M., Ghanem, R. A., Greene, J. J., Ocampo, A., Goldstein, A. K., Ni, L., Yang, T., Marton, R. M., Paşca, S. P., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.04.032 · Cited by 288 · see citing works
Self-citationDiffusion MRI of Structural Brain Plasticity Induced by a Learning and Memory Task
Blumenfeld‐Katzir, T., Pasternak, O., Dagan, M., & Assaf, Y. (2011) · PLoS ONE · doi:10.1371/journal.pone.0020678 · Cited by 285 · see citing works
Involvement of the Anterior Cingulate Cortex in the Expression of Remote Spatial Memory
Teixeira, C. M., Pomedli, S., Maei, H. R., Kee, N., & Frankland, P. W. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1068-06.2006 · Cited by 282 · see citing works
Self-citationA large fraction of neocortical myelin ensheathes axons of local inhibitory neurons
Micheva, K. D., Wolman, D. N., Mensh, B. D., Pax, E., Buchanan, J., Smith, S. J., & Bock, D. D. (2016) · eLife · doi:10.7554/elife.15784 · Cited by 271 · see citing works
Elevated Sleep Spindle Density after Learning or after Retrieval in Rats
Eschenko, O., Mölle, M., Jan Born, A., & Sara, S. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3175-06.2006 · Cited by 257 · see citing works
Inhibition recruitment in prefrontal cortex during sleep spindles and gating of hippocampal inputs
Peyrache, A., Battaglia, F. P., & Destexhe, A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1103612108 · Cited by 254 · see citing works
Wrapped to Adapt: Experience-Dependent Myelination
Mount, C., & Monje, M. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.009 · Cited by 251 · see citing works
Self-citationOgnjanovski, N., Schaeffer, S. M., Wu, J., Mofakham, S., Maruyama, D., Żochowski, M., & Aton, S. J. (2017) · Nature Communications · doi:10.1038/ncomms15039 · Cited by 221 · see citing works
Xia, F., Richards, B. A., Tran, M. M., Josselyn, S. A., Takehara‐Nishiuchi, K., & Frankland, P. W. (2017) · eLife · doi:10.7554/elife.27868 · Cited by 202 · see citing works
Self-citationVetere, G., Restivo, L., Cole, C. J., Ross, P. J., Ammassari‐Teule, M., Josselyn, S. A., & Frankland, P. W. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016275108 · Cited by 183 · see citing works
Self-citationAdhikari, A., Sigurdsson, T., Topiwala, M. A., & Gordon, J. A. (2010) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2010.06.019 · Cited by 111 · see citing works
Entorhinal cortex and consolidated memory
Takehara‐Nishiuchi, K. (2014) · Neuroscience Research · doi:10.1016/j.neures.2014.02.012 · Cited by 105 · see citing works
Stedehouder, J., Brizee, D., Shpak, G., & Kushner, S. A. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0074-18.2018 · Cited by 105 · see citing works
Bad wrap: Myelin and myelin plasticity in health and disease
Gibson, E. M., Geraghty, A. C., & Monje, M. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22541 · Cited by 87 · see citing works
Self-citationHippocampal Network Oscillations Rescue Memory Consolidation Deficits Caused by Sleep Loss
Ognjanovski, N., Broussard, C., Żochowski, M., & Aton, S. J. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy174 · Cited by 74 · see citing works
Effect of mediodorsal thalamic nucleus lesion on contextual fear conditioning in rats
Li, X. B., Inoue, T., Nakagawa, S., & Koyama, T. (2004) · Brain Research · doi:10.1016/j.brainres.2004.02.038 · Cited by 71 · see citing works
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- Authors
- Steadman, P. E., Xia, F., Ahmed, M., Mocle, A. J., Penning, A. R. A., Geraghty, A. C., Steenland, H. W., Monje, M., Josselyn, S. A., & Frankland, P. W.
- Affiliations
- University of Toronto (CA)
- Hospital for Sick Children (CA)
- Stanford University (US)
- Canadian Institute for Advanced Research (CA)
- Corresponding author
- Frankland, Paul W.
- ORCID
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2020-01
- Volume
- 105
- Issue
- 1
- Pages
- 150-164.e6
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC7579726
- OpenAlex
- W2983638220
- Cited by
- 426
- References
- 57
- Citations by year
- 2026: 52 · 2025: 61 · 2024: 67 · 2023: 60 · 2022: 66 · 2021: 73 · 2020: 44 · 2019: 2
- FWCI
- 17.41
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion)
- Funders
- Canadian Institutes of Health Research (FDN143227, PJT156164, MOP74650)
- CIHR (Vanier graduate scholarship, Arnie Aberman fellowship, McLaughlin MD/PhD studentship)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- oligodendrogenesis, memory consolidation, water maze learning, contextual fear memory, sharp-wave ripples, white matter
- MeSH terms
- Memory Consolidation, Animals, Cell Differentiation, Cerebral Cortex, Conditioning, Psychological, Electric Stimulation, Fear, Female, Hippocampus, Male, Mice, Transgenic, Myelin Sheath, Neural Pathways, Oligodendroglia, Transcription Factors, Maze Learning, Mice
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