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Expression of c-Fos and Arc in hippocampal region CA1 marks neurons that exhibit learning-related activity changes

https://doi.org/10.1101/644526
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cne.21003openalex-snapshot
Spatial exploration induces ARC , a plasticity‐related immediate‐early gene, only in calcium/calmodulin‐dependent protein kinase II‐positive principal excitatory and inhibitory neurons of the rat forebrain
inferredcites →https://doi.org/10.1016/0165-0270(89)90150-7openalex-snapshot
The use of c-fos as a metabolic marker in neuronal pathway tracing
inferredcites →https://doi.org/10.1016/0896-6273(95)90299-6openalex-snapshot
Arc, a growth factor and activity-regulated gene, encodes a novel cytoskeleton-associated protein that is enriched in neuronal dendrites
inferredcites →https://doi.org/10.1016/j.cell.2012.02.062openalex-snapshot
Inverse Synaptic Tagging of Inactive Synapses via Dynamic Interaction of Arc/Arg3.1 with CaMKIIβ
inferredcites →https://doi.org/10.1016/j.neures.2010.12.007openalex-snapshot
Regulation and function of immediate-early genes in the brain: Beyond neuronal activity markers
inferredcites →https://doi.org/10.1016/j.neuron.2006.08.024openalex-snapshot
Arc/Arg3.1 Is Essential for the Consolidation of Synaptic Plasticity and Memories
inferredcites →https://doi.org/10.1016/j.neuron.2009.08.009openalex-snapshot
Automated Analysis of Cellular Signals from Large-Scale Calcium Imaging Data
inferredcites →https://doi.org/10.1016/j.neuron.2010.11.029openalex-snapshot
An Embedded Subnetwork of Highly Active Neurons in the Neocortex
inferredcites →https://doi.org/10.1016/j.neuron.2013.07.020openalex-snapshot
Experience-Induced Arc/Arg3.1 Primes CA1 Pyramidal Neurons for Metabotropic Glutamate Receptor-Dependent Long-Term Synaptic Depression
inferredcites →https://doi.org/10.1016/j.neuron.2014.05.018openalex-snapshot
Hippocampal Memory Traces Are Differentially Modulated by Experience, Time, and Adult Neurogenesis
inferredcites →https://doi.org/10.1016/j.neuron.2014.09.037openalex-snapshot
Cortical Representations Are Reinstated by the Hippocampus during Memory Retrieval
inferredcites →https://doi.org/10.1016/j.neuron.2018.05.012openalex-snapshot
The Temporal Dynamics of Arc Expression Regulate Cognitive Flexibility
inferredcites →https://doi.org/10.1016/s0959-4388(00)00076-3openalex-snapshot
Natural patterns of activity and long-term synaptic plasticity
inferredcites →https://doi.org/10.1038/19978openalex-snapshot
Dendritic spine changes associated with hippocampal long-term synaptic plasticity
inferredcites →https://doi.org/10.1038/340474a0openalex-snapshot
Rapid increase of an immediate early gene messenger RNA in hippocampal neurons by synaptic NMDA receptor activation
inferredcites →https://doi.org/10.1038/nature11028openalex-snapshot
Optogenetic stimulation of a hippocampal engram activates fear memory recall
inferredcites →https://doi.org/10.1038/nn.3329openalex-snapshot
Long-term dynamics of CA1 hippocampal place codes
inferredcites →https://doi.org/10.1038/nn.4385openalex-snapshot
Experience-dependent spatial expectations in mouse visual cortex
inferredcites →https://doi.org/10.1073/pnas.1006546107openalex-snapshot
Arc regulates spine morphology and maintains network stability in vivo
inferredcites →https://doi.org/10.1073/pnas.92.12.5734openalex-snapshot
Somatodendritic expression of an immediate early gene is regulated by synaptic activity.
inferredcites →https://doi.org/10.1113/jphysiol.1973.sp010274openalex-snapshot
Long‐lasting potentiation of synaptic transmission in the dentate area of the unanaesthetized rabbit following stimulation of the perforant path
inferredcites →https://doi.org/10.1126/science.1214985openalex-snapshot
Generation of a Synthetic Memory Trace
inferredcites →https://doi.org/10.1126/science.1239073openalex-snapshot
Creating a False Memory in the Hippocampus
inferredcites →https://doi.org/10.1126/science.283.5409.1923openalex-snapshot
Rapid Dendritic Morphogenesis in CA1 Hippocampal Dendrites Induced by Synaptic Activity
inferredcites →https://doi.org/10.1126/science.aaa5542openalex-snapshot
Engram cells retain memory under retrograde amnesia
inferredcites →https://doi.org/10.1126/science.aat5397openalex-snapshot
The hippocampal engram maps experience but not place
inferredcites →https://doi.org/10.1146/annurev.biochem.67.1.509openalex-snapshot
THE GREEN FLUORESCENT PROTEIN
inferredcites →https://doi.org/10.1152/jn.00319.2011openalex-snapshot
Modulation of LTP at rat hippocampal CA3-CA1 synapses by direct current stimulation
inferredcites →https://doi.org/10.1523/jneurosci.13-11-04776.1993openalex-snapshot
Thresholds for synaptic activation of transcription factors in hippocampus: correlation with long-term enhancement
inferredcites →https://doi.org/10.1523/jneurosci.18-24-10464.1998openalex-snapshot
Synaptic Modifications in Cultured Hippocampal Neurons: Dependence on Spike Timing, Synaptic Strength, and Postsynaptic Cell Type
inferredcites →https://doi.org/10.1523/jneurosci.20-01-00266.2000openalex-snapshot
Critical Dependence of cAMP Response Element-Binding Protein Phosphorylation on L-Type Calcium Channels Supports a Selective Response to EPSPs in Preference to Action Potentials
inferredcites →https://doi.org/10.1523/jneurosci.20-07-02711.2000openalex-snapshot
Fos Imaging Reveals Differential Patterns of Hippocampal and Parahippocampal Subfield Activation in Rats in Response to Different Spatial Memory Tests
inferredcites →https://doi.org/10.1523/jneurosci.20-11-03993.2000openalex-snapshot
Inhibition of Activity-Dependent Arc Protein Expression in the Rat Hippocampus Impairs the Maintenance of Long-Term Potentiation and the Consolidation of Long-Term Memory
inferredcites →https://doi.org/10.1523/jneurosci.21-14-05089.2001openalex-snapshot
Experience-Dependent Gene Expression in the Rat Hippocampus after Spatial Learning: A Comparison of the Immediate-Early Genes Arc , c- fos , and zif268
inferredcites →https://doi.org/10.1523/jneurosci.23-27-09116.2003openalex-snapshot
Impaired Long-Term Memory and NR2A-Type NMDA Receptor-Dependent Synaptic Plasticity in Mice Lacking c-Fos in the CNS
inferredcites →https://doi.org/10.1523/jneurosci.3762-09.2010openalex-snapshot
Vibrissa-Based Object Localization in Head-Fixed Mice
inferredcites →https://doi.org/10.1523/jneurosci.4737-03.2004openalex-snapshot
Alteration of Neuronal Firing Properties afterIn VivoExperience in a FosGFP Transgenic Mouse
inferredcites →https://doi.org/10.3389/fnmol.2015.00078openalex-snapshot
Role of Immediate-Early Genes in Synaptic Plasticity and Neuronal Ensembles Underlying the Memory Trace
inferredcites →https://doi.org/10.3389/fnmol.2017.00435openalex-snapshot
Delayed Degradation and Impaired Dendritic Delivery of Intron-Lacking EGFP-Arc/Arg3.1 mRNA in EGFP-Arc Transgenic Mice
inferredcites →https://doi.org/10.3791/50885openalex-snapshot
Two-photon Calcium Imaging in Mice Navigating a Virtual Reality Environment
inferredcites →https://doi.org/10.7554/elife.12727openalex-snapshot
Sensitive red protein calcium indicators for imaging neural activity

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/hipo.70011openalex-snapshot
Brain Networks Differ According to Levels of Interference in Spatiotemporal Processing
inferred← citeshttps://doi.org/10.1002/hipo.70030openalex-snapshot
Combinative Protein Expression of Immediate Early Genes c‐Fos, Arc, and Npas4 Along Aversive and Appetitive Experience‐Related Neural Networks
inferred← citeshttps://doi.org/10.1007/978-3-031-88907-3_11openalex-snapshot
Gene Expression in the Hippocampus
inferred← citeshttps://doi.org/10.1016/j.conb.2019.11.011openalex-snapshot
Parenting — a paradigm for investigating the neural circuit basis of behavior
inferred← citeshttps://doi.org/10.1016/j.matpr.2022.10.234openalex-snapshot
Expression analysis of synaptic plasticity genes in curcumin-treated amnesic mice model
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2024.01.007openalex-snapshot
Hippocampal Trauma Memory Processing Conveying Susceptibility to Traumatic Stress
inferred← citeshttps://doi.org/10.1016/j.nlm.2024.107952openalex-snapshot
Neural correlates of learning and memory are altered by early-life stress
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.05.033openalex-snapshot
The essence of the engram: Cellular or synaptic?
inferred← citeshttps://doi.org/10.1038/s41467-022-33947-wopenalex-snapshot
ΔFosB accumulation in hippocampal granule cells drives cFos pattern separation during spatial learning
inferred← citeshttps://doi.org/10.1038/s41587-022-01524-7openalex-snapshot
Time-tagged ticker tapes for intracellular recordings
inferred← citeshttps://doi.org/10.1038/s41593-020-0652-4openalex-snapshot
Memory trace interference impairs recall in a mouse model of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1101/2020.02.05.935759openalex-snapshot
Transcriptome analysis of hippocampal subfields identifies gene expression profiles associated with long-term active place avoidance memory
inferred← citeshttps://doi.org/10.1101/2020.08.29.273391openalex-snapshot
cFos ensembles in the dentate gyrus rapidly segregate over time and do not form a stable map of space
inferred← citeshttps://doi.org/10.1101/2020.12.07.415109openalex-snapshot
Selective increase of functional network connectivity in Arc-positive neuronal engrams after long-term potentiation
inferred← citeshttps://doi.org/10.1101/2023.09.04.556168openalex-snapshot
Neuronal FOS reports synchronized activity of presynaptic neurons
inferred← citeshttps://doi.org/10.1101/2025.04.21.649441openalex-snapshot
Combinative protein expression of immediate early genes c-Fos, Arc, and Npas4 along aversive- and reward-related neural networks
inferred← citeshttps://doi.org/10.1523/eneuro.0540-20.2021openalex-snapshot
Selective Increase of Correlated Activity in Arc-Positive Neurons after Chemically Induced Long-Term Potentiation in Cultured Hippocampal Neurons
inferred← citeshttps://doi.org/10.24072/pcjournal.156openalex-snapshot
Functional correlates of immediate early gene expression in mouse visual cortex
inferred← citeshttps://doi.org/10.3389/fncel.2023.1310724openalex-snapshot
Approaches and considerations of studying neuronal ensembles: a brief review
inferred← citeshttps://doi.org/10.3390/cells14020143openalex-snapshot
Brain Plasticity and Cell Competition: Immediate Early Genes Are the Focus
inferred← citeshttps://doi.org/10.4103/1673-5374.393102openalex-snapshot
Neuroprotective effects of G9a inhibition through modulation of peroxisome-proliferator activator receptor gamma-dependent pathways by miR-128
inferred← citeshttps://doi.org/10.70675/af05b2d4zc031z48d7z9ebaz859f489a8450openalex-snapshot
On the developmental origin of CA1 pyramidal neuron diversity in the adult mouse hippocampus
inferred← citeshttps://doi.org/10.7554/elife.111896openalex-snapshot
Electroconvulsive stimulation drives cortical spreading depression dependent immediate early gene expression in mice
inferred← citeshttps://doi.org/10.7554/elife.111896.1openalex-snapshot
Electroconvulsive stimulation drives cortical spreading depression dependent immediate early gene expression in mice
inferred← citeshttps://doi.org/10.7554/elife.111896.2openalex-snapshot
Electroconvulsive stimulation drives cortical spreading depression dependent immediate early gene expression in mice
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