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Dynamic embedding of salience coding in hippocampal spatial maps

https://doi.org/10.1101/266767
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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/(sici)1098-1063(1996)6:6<749::aid-hipo16>3.0.co;2-0openalex-snapshot
Neuronal computations underlying the firing of place cells and their role in navigation
inferredcites →https://doi.org/10.1002/hipo.20203openalex-snapshot
Hippocampal place cells: Parallel input streams, subregional processing, and implications for episodic memory
inferredcites →https://doi.org/10.1002/hipo.450010207openalex-snapshot
Experience‐dependent modifications of hippocampal place cell firing
inferredcites →https://doi.org/10.1002/hipo.450040404openalex-snapshot
Spatial information content and reliability of hippocampal CA1 neurons: Effects of visual input
inferredcites →https://doi.org/10.1007/bf00239813openalex-snapshot
Hippocampal place units in the freely moving rat: Why they fire where they fire
inferredcites →https://doi.org/10.1016/0014-4886(78)90058-4openalex-snapshot
First occurrence of hippocampal spatial firing in a new environment
inferredcites →https://doi.org/10.1016/j.cub.2013.01.036openalex-snapshot
Traces of Experience in the Lateral Entorhinal Cortex
inferredcites →https://doi.org/10.1016/j.neuron.2005.09.007openalex-snapshot
Progressive Transformation of Hippocampal Neuronal Representations in “Morphed” Environments
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.2009.11.016openalex-snapshot
Rewarded Outcomes Enhance Reactivation of Experience in the Hippocampus
inferredcites →https://doi.org/10.1016/j.neuron.2014.03.034openalex-snapshot
Parvalbumin-Positive Basket Cells Differentiate among Hippocampal Pyramidal Cells
inferredcites →https://doi.org/10.1016/j.neuron.2014.07.032openalex-snapshot
Can We Reconcile the Declarative Memory and Spatial Navigation Views on Hippocampal Function?
inferredcites →https://doi.org/10.1016/j.neuron.2015.05.006openalex-snapshot
A Top-Down Cortical Circuit for Accurate Sensory Perception
inferredcites →https://doi.org/10.1016/j.neuron.2015.11.037openalex-snapshot
Simultaneous Denoising, Deconvolution, and Demixing of Calcium Imaging Data
inferredcites →https://doi.org/10.1016/j.neuron.2016.06.020openalex-snapshot
Sublayer-Specific Coding Dynamics during Spatial Navigation and Learning in Hippocampal Area CA1
inferredcites →https://doi.org/10.1016/j.nlm.2016.07.006openalex-snapshot
In vivo two-photon imaging of striatal neuronal circuits in mice
inferredcites →https://doi.org/10.1016/s0896-6273(00)00084-2openalex-snapshot
Imaging Neuronal Subsets in Transgenic Mice Expressing Multiple Spectral Variants of GFP
inferredcites →https://doi.org/10.1016/s0896-6273(04)00192-8openalex-snapshot
Increased Attention to Spatial Context Increases Both Place Field Stability and Spatial Memory
inferredcites →https://doi.org/10.1037/0735-7044.111.1.20openalex-snapshot
Hippocampal place fields are altered by the removal of single visual cues in a distance-dependent manner.
inferredcites →https://doi.org/10.1038/416090aopenalex-snapshot
Long-term plasticity in hippocampal place-cell representation of environmental geometry
inferredcites →https://doi.org/10.1038/nature13871openalex-snapshot
Calcium transient prevalence across the dendritic arbour predicts place field properties
inferredcites →https://doi.org/10.1038/ncomms14531openalex-snapshot
Place cells are more strongly tied to landmarks in deep than in superficial CA1
inferredcites →https://doi.org/10.1038/nn.2599openalex-snapshot
The reorganization and reactivation of hippocampal maps predict spatial memory performance
inferredcites →https://doi.org/10.1038/nn.2648openalex-snapshot
Functional imaging of hippocampal place cells at cellular resolution during virtual navigation
inferredcites →https://doi.org/10.1038/nn.2894openalex-snapshot
Hippocampal CA1 pyramidal cells form functionally distinct sublayers
inferredcites →https://doi.org/10.1038/nn.3329openalex-snapshot
Long-term dynamics of CA1 hippocampal place codes
inferredcites →https://doi.org/10.1038/nn.3614openalex-snapshot
Cell type–specific genetic and optogenetic tools reveal hippocampal CA2 circuits
inferredcites →https://doi.org/10.1038/nn.3843openalex-snapshot
Dopaminergic neurons promote hippocampal reactivation and spatial memory persistence
inferredcites →https://doi.org/10.1038/nn.4062openalex-snapshot
Conjunctive input processing drives feature selectivity in hippocampal CA1 neurons
inferredcites →https://doi.org/10.1038/nn.4074openalex-snapshot
Determinants of different deep and superficial CA1 pyramidal cell dynamics during sharp-wave ripples
inferredcites →https://doi.org/10.1073/pnas.1108261109openalex-snapshot
Experience-dependent regulation of CaMKII activity within single visual cortex synapses in vivo
inferredcites →https://doi.org/10.1073/pnas.1215834110openalex-snapshot
How vision and movement combine in the hippocampal place code
inferredcites →https://doi.org/10.1073/pnas.94.16.8918openalex-snapshot
Experience-dependent, asymmetric expansion of hippocampal place fields
inferredcites →https://doi.org/10.1101/207043openalex-snapshot
Context-Invariant Encoding of Reward Location in a Distinct Hippocampal Population
inferredcites →https://doi.org/10.1101/215145openalex-snapshot
Automatic sorting system for large calcium imaging data
inferredcites →https://doi.org/10.1101/lm.023523.111openalex-snapshot
Visual landmarks facilitate rodent spatial navigation in virtual reality environments
inferredcites →https://doi.org/10.1117/1.nph.2.2.021014openalex-snapshot
Comparison of genetically encoded calcium indicators for monitoring action potentials in mammalian brain by two-photon excitation fluorescence microscopy
inferredcites →https://doi.org/10.1126/science.1114037openalex-snapshot
Independent Codes for Spatial and Episodic Memory in Hippocampal Neuronal Ensembles
inferredcites →https://doi.org/10.1126/science.1232655openalex-snapshot
Multisensory Control of Hippocampal Spatiotemporal Selectivity
inferredcites →https://doi.org/10.1126/science.8351520openalex-snapshot
Dynamics of the Hippocampal Ensemble Code for Space
inferredcites →https://doi.org/10.1126/science.aaa5694openalex-snapshot
Gating of hippocampal activity, plasticity, and memory by entorhinal cortex long-range inhibition
inferredcites →https://doi.org/10.1152/jn.00214.2009openalex-snapshot
Neural Correlates of Novel Object and Novel Location Recognition Behavior in the Mouse Anterior Cingulate Cortex
inferredcites →https://doi.org/10.1152/jn.00758.2014openalex-snapshot
Offline reactivation of experience-dependent neuronal firing patterns in the rat ventral tegmental area
inferredcites →https://doi.org/10.1152/jn.01073.2009openalex-snapshot
Fast Nonnegative Deconvolution for Spike Train Inference From Population Calcium Imaging
inferredcites →https://doi.org/10.1152/jn.1998.79.2.1017openalex-snapshot
Interpreting Neuronal Population Activity by Reconstruction: Unified Framework With Application to Hippocampal Place Cells
inferredcites →https://doi.org/10.1371/journal.pone.0051286openalex-snapshot
Genetically Encoded Green Fluorescent Ca2+ Indicators with Improved Detectability for Neuronal Ca2+ Signals
inferredcites →https://doi.org/10.1371/journal.pone.0125354openalex-snapshot
Generation and Imaging of Transgenic Mice that Express G-CaMP7 under a Tetracycline Response Element
inferredcites →https://doi.org/10.1523/eneuro.0369-16.2017openalex-snapshot
Hippocampus-Dependent Goal Localization by Head-Fixed Mice in Virtual Reality
inferredcites →https://doi.org/10.1523/jneurosci.07-07-01951.1987openalex-snapshot
The effects of changes in the environment on the spatial firing of hippocampal complex-spike cells
inferredcites →https://doi.org/10.1523/jneurosci.09-08-02737.1989openalex-snapshot
Spatial and behavioral correlates of hippocampal neuronal activity
inferredcites →https://doi.org/10.1523/jneurosci.1378-09.2009openalex-snapshot
Robust Conjunctive Item–Place Coding by Hippocampal Neurons Parallels Learning What Happens Where
inferredcites →https://doi.org/10.1523/jneurosci.16-02-00823.1996openalex-snapshot
Binding of hippocampal CA1 neural activity to multiple reference frames in a landmark-based navigation task
inferredcites →https://doi.org/10.1523/jneurosci.1958-04.2004openalex-snapshot
Hippocampal Plasticity across Multiple Days of Exposure to Novel Environments
inferredcites →https://doi.org/10.1523/jneurosci.21-05-01635.2001openalex-snapshot
Accumulation of Hippocampal Place Fields at the Goal Location in an Annular Watermaze Task
inferredcites →https://doi.org/10.1523/jneurosci.2451-08.2008openalex-snapshot
Distinctive Features of Adult Ocular Dominance Plasticity
inferredcites →https://doi.org/10.3389/fnbeh.2011.00069openalex-snapshot
Representation of Non-Spatial and Spatial Information in the Lateral Entorhinal Cortex
inferredcites →https://doi.org/10.7554/elife.05360openalex-snapshot
VTA neurons coordinate with the hippocampal reactivation of spatial experience

What points at this work

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

inferred← citeshttps://doi.org/10.1016/j.cell.2020.09.024openalex-snapshot
The Statistical Structure of the Hippocampal Code for Space as a Function of Time, Context, and Value
inferred← citeshttps://doi.org/10.1016/j.neuron.2018.06.008openalex-snapshot
A Dedicated Population for Reward Coding in the Hippocampus
inferred← citeshttps://doi.org/10.1038/s41467-019-10683-2openalex-snapshot
Orchestrated ensemble activities constitute a hippocampal memory engram
inferred← citeshttps://doi.org/10.1038/s41467-025-58860-wopenalex-snapshot
Parallel processing of past and future memories through reactivation and synaptic plasticity mechanisms during sleep
inferred← citeshttps://doi.org/10.1101/2021.11.16.468862openalex-snapshot
Population dynamics underlying associative learning in the dorsal and ventral hippocampus
inferred← citeshttps://doi.org/10.1101/207043openalex-snapshot
Context-Invariant Encoding of Reward Location in a Distinct Hippocampal Population
inferred← citeshttps://doi.org/10.1186/s13041-020-0547-zopenalex-snapshot
Pcdhβ deficiency affects hippocampal CA1 ensemble activity and contextual fear discrimination
inferred← citeshttps://doi.org/10.1242/bio.059666openalex-snapshot
Sevoflurane-induced amnesia is associated with inhibition of hippocampal cell ensemble activity after learning
inferred← citeshttps://doi.org/10.70675/6fbbdcbaz764ez4136z96f1z5e7b485b0942openalex-snapshot
Electrophysiologie de l’hippocampe in vivo pendant le comportement : étude de l'impact de la locomotion sur le potentiel de membrane des cellules pyramidales de CA1 de l'hippocampe chez la souris naviguant dans un environnement virtuel
inferred← citeshttps://doi.org/10.70675/e5b36e93za976z4c91zbe75z1fa58bfb6985openalex-snapshot
Spatial resolution of the cognitive map : investigation on the influence of proximal visual cues on spatial coding resolution in area CA1 of the dorsal hippocampus using virtual reality
inferred← citeshttps://doi.org/10.7554/elife.44487openalex-snapshot
Dynamic control of hippocampal spatial coding resolution by local visual cues
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