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PKM-ζ is not required for hippocampal synaptic plasticity, learning and memory
Open accessAbstract
Long-term potentiation (LTP), a well-characterized form of synaptic plasticity, has long been postulated as a cellular correlate of learning and memory. Although LTP can persist for long periods of time, the mechanisms underlying LTP maintenance, in the midst of ongoing protein turnover and synaptic activity, remain elusive. Sustained activation of the brain-specific protein kinase C (PKC) isoform protein kinase M-ζ (PKM-ζ) has been reported to be necessary for both LTP maintenance and long-term memory. Inhibiting PKM-ζ activity using a synthetic zeta inhibitory peptide (ZIP) based on the PKC-ζ pseudosubstrate sequence reverses established LTP in vitro and in vivo. More notably, infusion of ZIP eliminates memories for a growing list of experience-dependent behaviours, including active place avoidance, conditioned taste aversion, fear conditioning and spatial learning. However, most of the evidence supporting a role for PKM-ζ in LTP and memory relies heavily on pharmacological inhibition of PKM-ζ by ZIP. To further investigate the involvement of PKM-ζ in the maintenance of LTP and memory, we generated transgenic mice lacking PKC-ζ and PKM-ζ. We find that both conventional and conditional PKC-ζ/PKM-ζ knockout mice show normal synaptic transmission and LTP at Schaffer collateral-CA1 synapses, and have no deficits in several hippocampal-dependent learning and memory tasks. Notably, ZIP still reverses LTP in PKC-ζ/PKM-ζ knockout mice, indicating that the effects of ZIP are independent of PKM-ζ.
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“Positive feedback loops that maintain key kinases and other molecules in persistently active states at strengthened synapses may also contribute to such long-term memory storage75–79.”
From The right time to learn: Mechanisms and optimization of spaced learning (2016) · cites this paper as [78]
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Rodríguez, C. I., Buchholz, F., Galloway, J. L., Sequerra, R., Kasper, J. S., Ayala, R., Stewart, A. F., & Dymecki, S. M. (2000) · Nature Genetics · doi:10.1038/75973 · Cited by 1,162
Storage of spatial information by the maintenance mechanism of LTP
Pastalkova, E., Serrano, P., Pinkhasova, D., Wallace, E., Fenton, A. A., & Sacktor, T. C. (2006) · Science · doi:10.1126/science.1128657 · Cited by 848
Huang, Y.-Y., & Kandel, E. R. (1994) · Learning & Memory · doi:10.1101/lm.1.1.74 · Cited by 477
Protein kinase Mζ is necessary and sufficient for LTP maintenance
Ling, D. S. F., Benardo, L. S., Serrano, P. A., Blace, N., Kelly, M. T., Crary, J. F., & Sacktor, T. C. (2002) · Nature Neuroscience · doi:10.1038/nn829 · Cited by 419
Rapid Erasure of Long-Term Memory Associations in the Cortex by an Inhibitor of PKMζ
Shema, R., Sacktor, T. C., & Dudai, Y. (2007) · Science · doi:10.1126/science.1144334 · Cited by 353
Abraham, W. C., Logan, B. J., Greenwood, J. M., & Dragunow, M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-21-09626.2002 · Cited by 338
PKMζ Maintains Spatial, Instrumental, and Classically Conditioned Long-Term Memories
Serrano, P. A., Friedman, E., Kenney, J., Taubenfeld, S. M., Zimmerman, J., Hanna, J., Alberini, C. M., Kelley, A. E., Maren, S., Rudy, J. W., et al. (2008) · PLoS Biology · doi:10.1371/journal.pbio.0060318 · Cited by 267
Hernandez, A. I., Blace, N., Crary, J. F., Serrano, P. A., Leitges, M., Libien, J. M., Weinstein, G., Tcherapanov, A., & Sacktor, T. C. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m307065200 · Cited by 264
Persistent Phosphorylation by Protein Kinase Mζ Maintains Late-Phase Long-Term Potentiation
Serrano, P. A., Yao, Y., & Sacktor, T. C. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.5132-04.2005 · Cited by 226
Chapter 2 PKMζ, LTP maintenance, and the dynamic molecular biology of memory storage
Sacktor, T. C. (2008) · Progress in Brain Research · doi:10.1016/s0079-6123(07)00002-7 · Cited by 208
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Zhang, G., Zhao, H., Choi, E. M., Svestka, M., Wang, X., Nagayach, A., Singh, A., Cook, R. G., & Geller, A. I. (2019) · Hippocampus · doi:10.1002/hipo.23068 · Cited by 8
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Metadata
- Authors
- Volk, L. J., Bachman, J. L., Johnson, R., Yu, Y., & Huganir, R. L.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Huganir, Richard L.
- Venue
- Nature
- Published
- 2013-01-02
- Volume
- 493
- Issue
- 7432
- Pages
- 420-423
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3830948
- OpenAlex
- W2063017515
- Cited by
- 310
- References
- 28
- Citations by year
- 2026: 7 · 2025: 6 · 2024: 15 · 2023: 7 · 2022: 10 · 2021: 17 · 2020: 10 · 2019: 24 · 2018: 22 · 2017: 33 · 2016: 33 · 2015: 37 · 2014: 37 · 2013: 50
- FWCI
- 25.67
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health
- National Institute of Mental Health (T32MH15330, T32MH015330)
- National Eye Institute (T32EY017203)
- National Institute of Neurological Disorders and Stroke (NS36715, P30NS050274, R01NS036715, R37NS036715)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- PKM, protein kinase M, long-term potentiation, synaptic plasticity, learning and memory, protein kinase C, LTP maintenance, memory maintenance, hippocampus, memory formation, fear conditioning, spatial learning, conditioned taste aversion, place avoidance, PKCδ, protein kinase C epsilon
- MeSH terms
- Protein Kinase C zeta, Animals, Avoidance Learning, Behavior, Animal, Conditioning, Classical, Fear, Female, Hippocampus, Isoenzymes, Male, Synaptic Transmission, Neuronal Plasticity, Protein Kinase C, Synapses, Long-Term Potentiation, Mice, Knockout, Mice, Lipopeptides, Memory, Long-Term, Cell-Penetrating Peptides
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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