The DOI matches its Crossref record; 62 of the 62 references it cites were found in a registry or an index.
CaMKII "Autonomy" Is Required for Initiating But Not for Maintaining Neuronal Long-Term Information Storage
Open accessAbstract
Ca(2+)/calmodulin (CaM)-dependent protein kinase II (CaMKII) "autonomy" (T286-autophosphorylation-induced Ca(2+)-independent activity) is required for long-term potentiation (LTP) and for learning and memory, as demonstrated by CaMKII T286A mutant mice. The >20-year-old hypothesis that CaMKII stimulation is required for LTP induction, while CaMKII autonomy is required for LTP maintenance was recently supported using the cell-penetrating fusion-peptide inhibitor antCN27. However, we demonstrate here that ant/penetratin fusion to CN27 compromised CaMKII-selectivity, by enhancing a previously unnoticed direct binding of CaM to ant/penetratin. In contrast to antCN27, the improved cell-penetrating inhibitor tatCN21 (5 mum) showed neither CaM binding nor inhibition of basal synaptic transmission. In vitro, tatCN21 inhibited stimulated and autonomous CaMKII activity with equal potency. In rat hippocampal slices, tatCN21 inhibited LTP induction, but not LTP maintenance. Correspondingly, tatCN21 also inhibited learning, but not memory storage or retrieval in a mouse in vivo model. Thus, CaMKII autonomy provides a short-term molecular memory that is important in the signal computation leading to memory formation, but is not required as long-term memory store.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Numerous studies using peptide inhibitors have confirmed the block of LTP (200–203).”
From Synaptic memory and CaMKII (2023) · cites this paper as [202]
The cited source says what the claim attributes to it.
In the citing paper
“In addition, pharmacological inhibition of CaMKII activity has generally been reported not to affect synaptic responses (198, 200–203, 357, 358).”
From Synaptic memory and CaMKII (2023) · cites this paper as [202]
The cited source says what the claim attributes to it.
In the citing paper
“However, numerous previous studies have failed to reverse established LTP (Refs. 198, 200–203, but see Ref. 357).”
From Synaptic memory and CaMKII (2023) · cites this paper as [202]
The cited source says what the claim attributes to it.
In the citing paper
“Third, as discussed in sect. 8, concentrations of CaMKII inhibitors that block the induction of LTP failed to affect maintenance (Refs. 198, 200–203, but see Ref. 357).”
From Synaptic memory and CaMKII (2023) · cites this paper as [202]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968
Long-Term Potentiation--A Decade of Progress?
Malenka, R. C., & Nicoll, A. R. A. (1999) · Science · doi:10.1126/science.285.5435.1870 · Cited by 2,729
In Vivo Protein Transduction: Delivery of a Biologically Active Protein into the Mouse
Schwarze, S. R., Ho, A. L., Vocero-Akbani, A. M., & Dowdy, S. F. (1999) · Science · doi:10.1126/science.285.5433.1569 · Cited by 2,418
The molecular basis of CaMKII function in synaptic and behavioural memory
Lisman, J., Schulman, H., & Cline, H. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn753 · Cited by 1,860
Hayashi, Y., Shi, S.-H., Esteban, J. A., Piccini, A., Poncer, J.-C., & Malinow, R. (2000) · Science · doi:10.1126/science.287.5461.2262 · Cited by 1,524
Deficient Hippocampal Long-Term Potentiation in α-Calcium-Calmodulin Kinase II Mutant Mice
Silva, A. J., Stevens, C. F., Tonegawa, S., & Wang, Y. (1992) · Science · doi:10.1126/science.1378648 · Cited by 1,472
Self-citationImpaired Spatial Learning in α-Calcium-Calmodulin Kinase II Mutant Mice
Silva, A. J., Paylor, R. E., Wehner, J. M., & Tonegawa, S. (1992) · Science · doi:10.1126/science.1321493 · Cited by 1,366
Self-citationInhibition of Postsynaptic PKC or CaMKII Blocks Induction But Not Expression of LTP
Malinow, R., Schulman, H., & Tsien, R. W. (1989) · Science · doi:10.1126/science.2549638 · Cited by 1,325
Sensitivity of CaM Kinase II to the Frequency of Ca 2+ Oscillations
De Koninck, P., & Schulman, H. (1998) · Science · doi:10.1126/science.279.5348.227 · Cited by 1,269
Cited by
Sorted by citations
Mechanisms of CaMKII action in long-term potentiation
Lisman, J., Yasuda, R., & Raghavachari, S. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3192 · Cited by 1,134
The Cell Biology of Synaptic Plasticity
Ho, V. M., Lee, J.-A., & Martin, K. C. (2011) · Science · doi:10.1126/science.1209236 · Cited by 573
CaMKII: a central molecular organizer of synaptic plasticity, learning and memory
Yasuda, R., Hayashi, Y., & Hell, J. W. (2022) · Nature Reviews Neuroscience · doi:10.1038/s41583-022-00624-2 · Cited by 431
CaMKII: Claiming Center Stage in Postsynaptic Function and Organization
Hell, J. W. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.024 · Cited by 364
Long-term potentiation and long-term depression: a clinical perspective
Bliss, T. V. P., & Cooke, S. F. (2011) · Clinics · doi:10.1590/s1807-59322011001300002 · Cited by 333
CaM Kinase: Still Inspiring at 40
Bayer, K. U., & Schulman, H. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.033 · Cited by 314
Self-citationCaMKII regulation in information processing and storage
Coultrap, S. J., & Bayer, K. U. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.05.003 · Cited by 323
Self-citationRole of the CaMKII/NMDA Receptor Complex in the Maintenance of Synaptic Strength
Sanhueza, M., Fernandez-Villalobos, G., Stein, I. S., Kasumova, G., Zhang, P., Bayer, K. U., Otmakhov, N., Hell, J. W., & Lisman, J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1250-11.2011 · Cited by 248
Self-citationCaMKII binding to GluN2B is critical during memory consolidation
Halt, A. R., Dallapiazza, R. F., Zhou, Y., Stein, I. S., Qian, H., Juntti, S., Wojcik, S., Brose, N., Silva, A. J., & Hell, J. W. (2012) · The EMBO Journal · doi:10.1038/emboj.2011.482 · Cited by 243
Self-citationCaMKII inhibitors: from research tools to therapeutic agents
Pellicena, P., & Schulman, H. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00021 · Cited by 235
The roles of protein kinases in learning and memoryPreprint
Giese, K.-P., & Mizuno, K. (2013) · Learning & Memory · doi:10.1101/lm.028449.112 · Cited by 238
Dysregulation of neuronal calcium homeostasis in Alzheimer's disease – A therapeutic opportunity?
Александровна, П. Е., Pchitskaya, E. I., & Борисович, Б. И. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.09.053 · Cited by 218
Plasticity of Spine Structure: Local Signaling, Translation and Cytoskeletal Reorganization
Nakahata, Y., & Yasuda, R. (2018) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2018.00029 · Cited by 209
Coultrap, S. J., Freund, R. K., O’Leary, H., Sanderson, J. L., Roche, K. W., Dell’Acqua, M. L., & Bayer, K. U. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.01.005 · Cited by 207
Self-citationDistribution of CaMKIIα expression in the brain in vivo, studied by CaMKIIα-GFP mice
Wang, X., Zhang, C., Szabó, G., & Sun, Q. (2013) · Brain Research · doi:10.1016/j.brainres.2013.04.042 · Cited by 206
The role of metaplasticity mechanisms in regulating memory destabilization and reconsolidation
Finnie, P. S. B., & Nader, K. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.03.008 · Cited by 189
CaMKII Isoforms in Learning and Memory: Localization and Function
Zalcman, G., Federman, N., & Romano, A. G. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00445 · Cited by 185
Cai, X., Kallarackal, A. J., Kvarta, M. D., Goluskin, S., Gaylor, K., Bailey, A. M., Lee, H.-K., Huganir, R. L., & Thompson, S. M. (2013) · Nature Neuroscience · doi:10.1038/nn.3355 · Cited by 180
Chang, J.-Y., Parra-Bueno, P., Laviv, T., Szatmari, E. M., Lee, S.-J. R., & Yasuda, R. (2017) · Neuron · doi:10.1016/j.neuron.2017.04.041 · Cited by 161
Coultrap, S. J., Vest, R. S., Ashpole, N. M., Hudmon, A., & Bayer, K. U. (2011) · Acta Pharmacologica Sinica · doi:10.1038/aps.2011.68 · Cited by 148
Self-citationMurakoshi, H., Shin, M. E., Parra-Bueno, P., Szatmari, E. M., Shibata, A. C. E., & Yasuda, R. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.036 · Cited by 140
Mechanisms of CaMKII Activation in the Heart
Erickson, J. R. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00059 · Cited by 146
Graupner, M. (2010) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2010.00136 · Cited by 132
Cognitive neuroepigenetics: A role for epigenetic mechanisms in learning and memory
Day, J. J., & Sweatt, J. D. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.12.008 · Cited by 137
CaMKII as a Therapeutic Target in Cardiovascular Disease
Gaido, O. E. R., Nkashama, L. J., Schole, K. L., Wang, Q., Umapathi, P., Mesubi, O. O., Konstantinidis, K., Luczak, E. D., & Anderson, M. E. (2022) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-051421-111814 · Cited by 129
Analysis of CaM-kinase signaling in cells
Wayman, G. A., Tokumitsu, H., Davare, M. A., & Soderling, T. R. (2011) · Cell Calcium · doi:10.1016/j.ceca.2011.02.007 · Cited by 128
Nicoll, R. A., & Schulman, H. (2023) · Physiological Reviews · doi:10.1152/physrev.00034.2022 · Cited by 126
Coordination of Protein Phosphorylation and Dephosphorylation in Synaptic Plasticity
Woolfrey, K. M., & Dell’Acqua, M. L. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.r115.657262 · Cited by 125
Self-citationLTP induction by structural rather than enzymatic functions of CaMKII
Tullis, J. E., Larsen, M. E., Rumian, N. L., Freund, R. K., Boxer, E. E., Brown, C. N., Coultrap, S. J., Schulman, H., Aoto, J., Dell’Acqua, M. L., et al. (2023) · Nature · doi:10.1038/s41586-023-06465-y · Cited by 112
Self-citationBazzari, A. H., & Parri, H. R. (2019) · Brain Sciences · doi:10.3390/brainsci9110300 · Cited by 107
Fujii, H., Inoue, M., Okuno, H., Sano, Y., Takemoto‐Kimura, S., Kitamura, K., Kano, M., & Bito, H. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.03.033 · Cited by 94
Novel insights into CaMKII function and regulation during memory formation
Lucchesi, W., Mizuno, K., & Giese, K.-P. (2010) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2010.10.009 · Cited by 106
Memory Erasure Experiments Indicate a Critical Role of CaMKII in Memory Storage
Rossetti, T., Banerjee, S., Kim, C., Leubner, M., Lamar, C., Gupta, P., Lee, B., Neve, R., & Lisman, J. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.010 · Cited by 94
Ferrari, L. F., Bogen, O., Chu, C. E., & Levine, J. D. (2013) · Journal of Pain · doi:10.1016/j.jpain.2013.01.779 · Cited by 86
Ferrari, L. F., Bogen, O., & Levine, J. D. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1785-13.2013 · Cited by 84
Coultrap, S. J., & Bayer, K. U. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.558254 · Cited by 83
Self-citationO’Leary, H., Liu, W. H., Rorabaugh, J. M., Coultrap, S. J., & Bayer, K. U. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.233668 · Cited by 77
Self-citationMyo1c binding to submembrane actin mediates insulin-induced tethering of GLUT4 vesicles
Boguslavsky, S., Chiu, T. T., Foley, K. P., Osorio‐Fuentealba, C., Antonescu, C. N., Bayer, K. U., Bilan, P. J., & Klip, A. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-04-0263 · Cited by 74
Self-citationAdaikkan, C., Taha, E., Barrera, I., David, O., & Rosenblum, K. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.11.028 · Cited by 79
CaMKII holoenzyme mechanisms that govern the LTP versus LTD decision
Cook, S. G., Buonarati, O. R., Coultrap, S. J., & Bayer, K. U. (2021) · Science Advances · doi:10.1126/sciadv.abe2300 · Cited by 74
Self-citationInitial memory consolidation and the synaptic tagging and capture hypothesis
Okuda, K., Højgaard, K., Privitera, L., Bayraktar, G., & Takeuchi, T. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14902 · Cited by 74
Signalling pathways underlying structural plasticity of dendritic spines
Patterson, M., & Yasuda, R. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01328.x · Cited by 76
Synaptic memory requires CaMKII
Tao, W., Lee, J., Chen, X., Díaz-Alonso, J., Zhou, J., Pleasure, S., & Nicoll, R. A. (2021) · eLife · doi:10.7554/elife.60360 · Cited by 72
Bell, K. F. S., Bent, R. J., Meese‐Tamuri, S., Ali, A., Forder, J. P., & Aarts, M. M. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12176 · Cited by 63
Excitotoxic glutamate insults block autophagic flux in hippocampal neurons
Kulbe, J. R., Levy, J. M. M., Coultrap, S. J., Thorburn, A. M., & Bayer, K. U. (2013) · Brain Research · doi:10.1016/j.brainres.2013.10.032 · Cited by 62
Self-citationDeng, G., Orfila, J. E., Dietz, R. M., Moreno‐Garcia, M., Rodgers, K. M., Coultrap, S. J., Quillinan, N., Traystman, R. J., Bayer, K. U., & Herson, P. S. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.01.011 · Cited by 61
Self-citationCook, S. G., Bourke, A. M., O’Leary, H., Zaegel, V., Lasda, E. L., Mize-Berge, J., Quillinan, N., Tucker, C. L., Coultrap, S. J., Herson, P. S., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-23779-4 · Cited by 54
Self-citationInterplay of enzymatic and structural functions of Ca MKII in long‐term potentiation
Kim, K., Saneyoshi, T., Hosokawa, T., Okamoto, K., & Hayashi, Y. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13672 · Cited by 53
Autonomous CaMKII requires further stimulation by Ca 2+ /calmodulin for enhancing synaptic strength
Barcomb, K., Buard, I., Coultrap, S. J., Kulbe, J. R., O'Leary, H., Benke, T. A., & Bayer, K. U. (2014) · The FASEB Journal · doi:10.1096/fj.14-250407 · Cited by 52
Self-citationMohanan, A. G., Gunasekaran, S., Jacob, R. S., & Omkumar, R. V. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.855752 · Cited by 55
Klug, J. R., Mathur, B. N., Kash, T. L., Wang, H.-D., Matthews, R. T., Robison, A. J., Anderson, M. E., Deutch, A. Y., Lovinger, D. M., Colbran, R. J., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045323 · Cited by 49
The intersections of NMDAR-dependent synaptic plasticity and cell survival
Bartlett, T. E., & Wang, Y. T. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.01.012 · Cited by 50
AMPAR-Independent Effect of Striatal αCaMKII Promotes the Sensitization of Cocaine Reward
Kourrich, S., Klug, J. R., Mayford, M. R., & Thomas, M. J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6391-11.2012 · Cited by 49
Long-term memory consolidation: The role of RNA-binding proteins with prion-like domains
Sudhakaran, I. P., & Ramaswami, M. (2016) · RNA Biology · doi:10.1080/15476286.2016.1244588 · Cited by 48
Improving a Natural CaMKII Inhibitor by Random and Rational Design
Coultrap, S. J., & Bayer, K. U. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025245 · Cited by 43
Self-citationQuantitative estimates of the cytoplasmic, PSD, and NMDAR-bound pools of CaMKII in dendritic spines
Feng, B., Raghavachari, S., & Lisman, J. (2011) · Brain Research · doi:10.1016/j.brainres.2011.08.051 · Cited by 46
Temporal and Region-Specific Requirements of αCaMKII in Spatial and Contextual Learning
Achterberg, K. G., Buitendijk, G. H. S., Kool, M. J., Goorden, S. M. I., Post, L., Slump, D. E., Silva, A. J., van Woerden, G. M., Kushner, S. A., & Elgersma, Y. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.0640-14.2014 · Cited by 44
Self-citationA revised view of the role of CaMKII in learning and memory
Bayer, K. U., & Giese, K.-P. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01809-x · Cited by 51
Self-citationPersistent Reversal of Enhanced Amphetamine Intake by Transient CaMKII Inhibition
Loweth, J. A., Li, D., Cortright, J. J., Wilke, G. A., Jeyifous, O., Neve, R. L., Bayer, K. U., & Vezina, P. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4386-13.2013 · Cited by 42
Self-citationZhang, Y., Wu, K., Su, W., Zhang, D., Wang, P., Qiao, X., Yao, Q., Yuan, Z., Yao, Y., Liu, G., et al. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0681-17.2017 · Cited by 43
What does LTP tell us about the roles of CaMKII and PKMζ in memory?
Sacktor, T. C., & Fenton, A. A. (2018) · Molecular Brain · doi:10.1186/s13041-018-0420-5 · Cited by 43
Studying CaMKII: Tools and standards
Brown, C. N., & Bayer, K. U. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113982 · Cited by 39
Self-citationPrevention of long-term memory loss after retrieval by an endogenous CaMKII inhibitor
Vigil, F. A., Mizuno, K., Lucchesi, W., Valls-Comamala, V., & Giese, K.-P. (2017) · Scientific Reports · doi:10.1038/s41598-017-04355-8 · Cited by 38
Second Messengers Mediating the Expression of Neuroplasticity in a Model of Chronic Pain in the Rat
Ferrari, L. F., Bogen, O., & Levine, J. D. (2014) · Journal of Pain · doi:10.1016/j.jpain.2013.12.005 · Cited by 37
CaMKII Mediates Recruitment and Activation of the Deubiquitinase CYLD at the Postsynaptic Density
Thein, S. H., Tao-Cheng, J.-H., Li, Y., Bayer, K. U., Reese, T. S., & Döṣemeci, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0091312 · Cited by 37
Self-citationBustos, F. J., Jury, N., Martínez, P., Ampuero, E., Campos, M., Abarzúa, S., Jaramillo, K., Ibing, S., Mardones, M. D., Haensgen, H., et al. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.25843 · Cited by 35
Phosphorylation Hypothesis of Sleep
Ode, K. L., & Ueda, H. R. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.575328 · Cited by 38
CaMKII autophosphorylation is the only enzymatic event required for synaptic memory
Chen, X., Cai, Q., Zhou, J., Pleasure, S. J., Schulman, H., Zhang, M., & Nicoll, R. A. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2402783121 · Cited by 41
Yang, Y., Tao-Cheng, J.-H., Bayer, K. U., Reese, T. S., & Dosemeci, A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071795 · Cited by 35
Self-citationA molecular mechanism underlying gustatory memory trace for an association in the insular cortex
Adaikkan, C., & Rosenblum, K. (2015) · eLife · doi:10.7554/elife.07582 · Cited by 34
Role of amyloid-β CSF levels in cognitive deficit in MS
Gentile, A., Mori, F., Bernardini, S., & Centonze, D. (2015) · Clinica Chimica Acta · doi:10.1016/j.cca.2015.01.035 · Cited by 32
Coultrap, S. J., Barcomb, K., & Bayer, K. U. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037176 · Cited by 33
Self-citationBeneficial Effects of a CaMKIIα Inhibitor TatCN21 Peptide in Global Cerebral Ischemia
Ahmed, M. E., Dong, Y., Lu, Y., Tucker, D., Wang, R., & Zhang, Q. (2016) · Journal of Molecular Neuroscience · doi:10.1007/s12031-016-0830-8 · Cited by 31
Ghosh, S., Reuveni, I., Lamprecht, R., & Barkai, E. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2123-14.2015 · Cited by 34
Liu, X., Liu, Y. U., Zhong, P., Wilkinson, B., Qi, J., Olsen, C. M., Bayer, K. U., & Liu, Q.-S. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.299 · Cited by 33
Self-citationCalcium/calmodulin‐dependent kinase II and memory destabilization: a new role in memory maintenance
Vigil, F. A., & Giese, K.-P. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14454 · Cited by 32
KIBRA anchoring the action of PKMζ maintains the persistence of memory
Tsokas, P., Hsieh, C., Flores‐Obando, R. E., Bernabo, M., Tcherepanov, A., Hernandez, A. I., Thomas, C., Bergold, P. J., Cottrell, J. E., Kremerskothen, J., et al. (2024) · Science Advances · doi:10.1126/sciadv.adl0030 · Cited by 29
Tao-Cheng, J.-H., Yang, Y., Bayer, K. U., Reese, T. S., & Döṣemeci, A. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.03.063 · Cited by 28
Self-citationThe Delicate Bistability of CaMKII
Michalski, P. J. (2013) · Biophysical Journal · doi:10.1016/j.bpj.2013.06.038 · Cited by 24
PTENα Modulates CaMKII Signaling and Controls Contextual Fear Memory and Spatial Learning
Wang, P., Mei, F., Hu, J., Zhu, M., Qi, H., Chen, X., Li, R., McNutt, M. A., & Yin, Y. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.05.088 · Cited by 26
Tang, Q., Ke, H. Q., Wu, C., Zeng, J., Li, Z., Liu, Y., Feng, S., Xue, Q., & Xu, X. (2019) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2019.111925 · Cited by 26
Furini, C. R. G., Nachtigall, E. G., Behling, J. A. K., Brasil, E. S. D. A., Saenger, B. F., Narvaes, R. F., Myskiw, J. D. C., & Izquierdo, I. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.03.047 · Cited by 28
Characterization of a selective CaMKII peptide inhibitor
Gomez-Monterrey, I. M., Sala, M., Rusciano, M. R., Monaco, S., Maione, A. S., Iaccarino, G., Tortorella, P., D’Ursi, A. M., Scrima, M., Carotenuto, A., et al. (2013) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2012.12.053 · Cited by 25
Bernard, P. B., Castano, A. M., Bayer, K. U., & Benke, T. A. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.04.011 · Cited by 25
Self-citationCaMKII Inhibition is a Novel Therapeutic Strategy to Prevent Diabetic Cardiomyopathy
Veitch, C. R., Power, A., & Erickson, J. R. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.695401 · Cited by 23
Ca2+/Calmodulin-Dependent Protein Kinase II (CaMKII)
Coultrap, S. J., & Bayer, K. U. (2012) · Neuromethods · doi:10.1007/978-1-61779-824-5_4 · Cited by 22
Self-citationBarcomb, K., Coultrap, S. J., & Bayer, K. U. (2013) · Molecular Pharmacology · doi:10.1124/mol.113.089045 · Cited by 22
Self-citationGhosh, S., Reuveni, I., Barkai, E., & Lamprecht, R. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13505 · Cited by 22
Freund, R. K., Graw, S. L., Choo, K. S., Stevens, K. E., Leonard, S. S., & Dell’Acqua, M. L. (2016) · Neuroscience Letters · doi:10.1016/j.neulet.2016.05.043 · Cited by 21
Self-citationCaMKII inhibitor 1 (CaMK2N1) mRNA is upregulated following LTP induction in hippocampal slices
Astudillo, D., Karmelic, D., Casas, B. S., Otmakhov, N., Palma, V., & Sanhueza, M. (2020) · Synapse · doi:10.1002/syn.22158 · Cited by 18
Th e Role of Protein Phosphorylation in the Gustatory Cortex and Amygdala During Taste Learning
Adaikkan, C., & Rosenblum, K. (2012) · Experimental Neurobiology · doi:10.5607/en.2012.21.2.37 · Cited by 22
Rosenberg, T., Elkobi, A., Dieterich, D. C., & Rosenblum, K. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.01.002 · Cited by 21
LTP expression mediated by autonomous activity of GluN2B-bound CaMKII
Rumian, N. L., Barker, C. M., Larsen, M. E., Tullis, J. E., Freund, R. K., Taslimi, A., Coultrap, S. J., Tucker, C. L., Dell’Acqua, M. L., & Bayer, K. U. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114866 · Cited by 20
Self-citationShetty, M., & Sajikumar, S. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.07.020 · Cited by 16
CaMKII isoforms differ in their specific requirements for regulation by nitric oxide
Coultrap, S. J., Zaegel, V., & Bayer, K. U. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.10.039 · Cited by 19
Self-citationSelective kinase inhibitors as tools for neuroscience research
Martin, K. J., & Arthur, J. S. C. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.07.024 · Cited by 19
Sahara, Y., Matsuzawa, D., Ishii, D., Fuchida, T., Goto, T., Sutoh, C., & Shimizu, E. (2018) · Developmental Psychobiology · doi:10.1002/dev.21801 · Cited by 18
Reduced exploratory behavior in neuronal nucleoredoxin knockout mice
Tran, B. N., Valek, L., Wilken‐Schmitz, A., Fuhrmann, D. C., Namgaladze, D., Wittig, I., & Tegeder, I. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102054 · Cited by 17
In memoriam: John Lisman – commentaries on CaMKII as a memory molecule
Bear, M. F., Cooke, S. F., Giese, K.-P., Kaang, B., Kennedy, M. B., Kim, J., Morris, R., & Park, P. (2018) · Molecular Brain · doi:10.1186/s13041-018-0419-y · Cited by 17
CaMKII Binding to GluN2B Is Differentially Affected by Macromolecular Crowding Reagents
Goodell, D. J., Eliseeva, T. A., Coultrap, S. J., & Bayer, K. U. (2014) · PLoS ONE · doi:10.1371/journal.pone.0096522 · Cited by 16
Self-citation
Metadata
- Authors
- Buard, I., Coultrap, S. J., Freund, R. K., Lee, Y.-S., Dell'Acqua, M. L., Silva, A. J., & Bayer, K. U.
- Affiliations
- University of Colorado Anschutz (US)
- University of California, Los Angeles (US)
- Venue
- Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2010-06-16
- Volume
- 30
- Issue
- 24
- Pages
- 8214-8220
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC2891520
- OpenAlex
- W2028360365
- Cited by
- 160
- References
- 61
- Citations by year
- 2025: 10 · 2024: 10 · 2023: 9 · 2022: 9 · 2021: 8 · 2020: 6 · 2019: 7 · 2018: 10 · 2017: 10 · 2016: 10 · 2015: 9 · 2014: 15 · 2013: 18 · 2012: 17
- FWCI
- 6.21
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- Funders
- National Institutes of Health
- University of Colorado Denver
- National Institute on Aging (R37AG013622)
- National Cancer Institute (P30CA046934)
- National Institute of Neurological Disorders and Stroke (P30NS048154, R01NS040701, R01NS052644)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- long-term potentiation, LTP maintenance, learning and memory, calmodulin binding, hippocampus, synaptic transmission
- MeSH terms
- Benzenesulfonamides, Animals, Behavior, Animal, Benzylamines, Carrier Proteins, Conditioning, Classical, Dose-Response Relationship, Drug, Electric Stimulation, Hippocampus, Male, Memory, Neural Inhibition, Neurons, Peptide Fragments, Phosphorylation, Recombinant Fusion Proteins, Sulfonamides, Viral Fusion Proteins, Rats, Sprague-Dawley, Long-Term Potentiation, Patch-Clamp Techniques, Protein Kinase Inhibitors, Mice, Rats, Calcium-Calmodulin-Dependent Protein Kinase Type 2, Cell-Penetrating Peptides, In Vitro Techniques
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 ›
Are you an author, or do you see a problem with this page? Request a review