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Manipulation of hippocampal CA3 firing via luminopsins modulates spatial and episodic short-term memory, especially working memory, but not long-term memory

https://doi.org/10.1016/j.nlm.2018.09.009

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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/hipo.450020209openalex-snapshot

Computational constraints suggest the need for two distinct input systems to the hippocampal CA3 network

inferredcites →https://doi.org/10.1002/jnr.24152openalex-snapshot

Novel luciferase–opsin combinations for improved luminopsins

inferredcites →https://doi.org/10.1007/bf00177557openalex-snapshot

Delay-dependent short-term memory deficits in aged rats

inferredcites →https://doi.org/10.1016/0166-2236(87)90011-7openalex-snapshot

Hippocampal synaptic enhancement and information storage within a distributed memory system

inferredcites →https://doi.org/10.1016/j.celrep.2015.04.017openalex-snapshot

Chronic Optogenetic Activation Augments Aβ Pathology in a Mouse Model of Alzheimer Disease

inferredcites →https://doi.org/10.1016/j.neubiorev.2014.11.009openalex-snapshot

A computational theory of hippocampal function, and tests of the theory: New developments

inferredcites →https://doi.org/10.1016/j.neuron.2012.12.032openalex-snapshot

NMDA Receptors Subserve Persistent Neuronal Firing during Working Memory in Dorsolateral Prefrontal Cortex

inferredcites →https://doi.org/10.1016/j.neuron.2015.09.024openalex-snapshot

Disinhibition, a Circuit Mechanism for Associative Learning and Memory

inferredcites →https://doi.org/10.1016/j.nlm.2016.02.001openalex-snapshot

Pattern separation and pattern completion in the hippocampal system. Introduction to the Special Issue

inferredcites →https://doi.org/10.1016/j.pneurobio.2006.04.005openalex-snapshot

A computational theory of hippocampal function, and empirical tests of the theory

inferredcites →https://doi.org/10.1016/s0079-6123(08)61237-6openalex-snapshot

Chapter 1 Chapter Neurons, numbers and the hippocampal network

inferredcites →https://doi.org/10.1016/s0169-328x(01)00344-8openalex-snapshot

Age-related changes in the protein expression of subunits of the NMDA receptor

inferredcites →https://doi.org/10.1016/s0896-6273(03)00165-xopenalex-snapshot

Hippocampal CA3 NMDA Receptors Are Crucial for Memory Acquisition of One-Time Experience

inferredcites →https://doi.org/10.1016/s0896-6273(04)00266-1openalex-snapshot

Excitation-Neurogenesis Coupling in Adult Neural Stem/Progenitor Cells

inferredcites →https://doi.org/10.1037/0735-7044.117.5.1044openalex-snapshot

Differential roles of dorsal hippocampal subregions in spatial working memory with short versus intermediate delay.

inferredcites →https://doi.org/10.1038/nature10360openalex-snapshot

Neocortical excitation/inhibition balance in information processing and social dysfunction

inferredcites →https://doi.org/10.1038/nature17172openalex-snapshot

Memory retrieval by activating engram cells in mouse models of early Alzheimer’s disease

inferredcites →https://doi.org/10.1038/nrn.2017.10openalex-snapshot

Operation and plasticity of hippocampal CA3 circuits: implications for memory encoding

inferredcites →https://doi.org/10.1038/nrn2335openalex-snapshot

The hippocampus and memory: insights from spatial processing

inferredcites →https://doi.org/10.1038/nrn3677openalex-snapshot

Hippocampal synaptic plasticity, spatial memory and anxiety

inferredcites →https://doi.org/10.1038/srep14366openalex-snapshot

Inhibitory luminopsins: genetically-encoded bioluminescent opsins for versatile, scalable and hardware-independent optogenetic inhibition

inferredcites →https://doi.org/10.1073/pnas.0335786100openalex-snapshot

Developmental loss of miniature N -methyl- d -aspartate receptor currents in NR2A knockout mice

inferredcites →https://doi.org/10.1073/pnas.0605238103openalex-snapshot

NMDA receptor surface mobility depends on NR2A-2B subunits

inferredcites →https://doi.org/10.1073/pnas.1405648111openalex-snapshot

Left–right dissociation of hippocampal memory processes in mice

inferredcites →https://doi.org/10.1073/pnas.1510899113openalex-snapshot

Luminopsins integrate opto- and chemogenetics by using physical and biological light sources for opsin activation

inferredcites →https://doi.org/10.1084/jem.20081588openalex-snapshot

Valproic acid inhibits Aβ production, neuritic plaque formation, and behavioral deficits in Alzheimer's disease mouse models

inferredcites →https://doi.org/10.1098/rstb.2016.0049openalex-snapshot

Complementary learning systems within the hippocampus: a neural network modelling approach to reconciling episodic memory with statistical learning

inferredcites →https://doi.org/10.1101/lm.631207openalex-snapshot

An attractor network in the hippocampus: Theory and neurophysiology

inferredcites →https://doi.org/10.1101/lm.703907openalex-snapshot

Pattern separation, pattern completion, and new neuronal codes within a continuous CA3 map

inferredcites →https://doi.org/10.1111/ejn.12617openalex-snapshot

Saccade deficits in amnestic mild cognitive impairment resemble mild Alzheimer's disease

inferredcites →https://doi.org/10.1111/j.1460-9568.2006.04992.xopenalex-snapshot

Hippocampal CA3 pyramidal cells selectively innervate aspiny interneurons

inferredcites →https://doi.org/10.1111/j.1460-9568.2007.05431.xopenalex-snapshot

Maintenance of superior learning and memory function in NR2B transgenic mice during ageing

inferredcites →https://doi.org/10.1126/science.1082609openalex-snapshot

Asymmetrical Allocation of NMDA Receptor ε2 Subunits in Hippocampal Circuitry

inferredcites →https://doi.org/10.1126/science.1096615openalex-snapshot

Role of NMDA Receptor Subtypes in Governing the Direction of Hippocampal Synaptic Plasticity

inferredcites →https://doi.org/10.1126/science.1151120openalex-snapshot

Transgenic Inhibition of Synaptic Transmission Reveals Role of CA3 Output in Hippocampal Learning

inferredcites →https://doi.org/10.1146/annurev-neuro-061010-113817openalex-snapshot

The Development and Application of Optogenetics

inferredcites →https://doi.org/10.1146/annurev.neuro.25.112701.142758openalex-snapshot

AMPA Receptor Trafficking and Synaptic Plasticity

inferredcites →https://doi.org/10.1146/annurev.psych.53.100901.135114openalex-snapshot

Episodic Memory: From Mind to Brain

inferredcites →https://doi.org/10.1155/2015/748212openalex-snapshot

Working Memory and Executive Function Decline across Normal Aging, Mild Cognitive Impairment, and Alzheimer’s Disease

inferredcites →https://doi.org/10.1371/journal.pone.0059759openalex-snapshot

Light-Emitting Channelrhodopsins for Combined Optogenetic and Chemical-Genetic Control of Neurons

inferredcites →https://doi.org/10.1523/jneurosci.1678-15.2016openalex-snapshot

Reactivation of Rate Remapping in CA3

inferredcites →https://doi.org/10.1523/jneurosci.1697-04.2004openalex-snapshot

Differential Roles of NR2A and NR2B-Containing NMDA Receptors in Cortical Long-Term Potentiation and Long-Term Depression

inferredcites →https://doi.org/10.1523/jneurosci.2332-16.2016openalex-snapshot

NR2A-Containing NMDARs in the Prefrontal Cortex Are Required for Working Memory and Associated with Age-Related Cognitive Decline

inferredcites →https://doi.org/10.1523/jneurosci.4257-13.2014openalex-snapshot

Amygdala Inputs to the Ventral Hippocampus Bidirectionally Modulate Social Behavior

inferredcites →https://doi.org/10.3389/fncel.2013.00098openalex-snapshot

A quantitative theory of the functions of the hippocampal CA3 network in memory

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/glia.24185openalex-snapshot

Abnormal innate and learned behavior induced by neuron–microglia miscommunication is related to CA3 reconfiguration

inferred← citeshttps://doi.org/10.1007/978-3-032-18121-3_12openalex-snapshot

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Bioluminescence Driving Opsins

inferred← citeshttps://doi.org/10.1016/j.cbpa.2020.07.006openalex-snapshot

Imaging voltage and brain chemistry with genetically encoded sensors and modulators

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Selective postnatal excitation of neocortical pyramidal neurons results in distinctive behavioral and circuit deficits in adulthood

inferred← citeshttps://doi.org/10.1016/j.pneurobio.2021.102209openalex-snapshot

Optogenetic stimulation of CA3 pyramidal neurons restores synaptic deficits to improve spatial short-term memory in APP/PS1 mice

inferred← citeshttps://doi.org/10.1101/2023.06.26.545546openalex-snapshot

A New Highly Efficient Molecule for Both Optogenetic and Chemogenetic Control Driven by FRET Amplification of BioLuminescence

inferred← citeshttps://doi.org/10.1117/1.nph.11.2.021005openalex-snapshot

Efficient opto- and chemogenetic control in a single molecule driven by FRET-modified bioluminescence

inferred← citeshttps://doi.org/10.1117/1.nph.11.2.024208openalex-snapshot

Engineering luminopsins with improved coupling efficiencies

inferred← citeshttps://doi.org/10.1117/1.nph.9.s1.013001openalex-snapshot

Neurophotonic tools for microscopic measurements and manipulation: status report

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Neuropathic Pain Causes a Decrease in the Dendritic Tree Complexity of Hippocampal CA3 Pyramidal Neurons

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Prenatal cyanuric acid exposure induced spatial learning impairments associated with alteration of acetylcholine-mediated neural information flow at the hippocampal CA3-CA1 synapses of male rats

inferred← citeshttps://doi.org/10.1364/brain.2020.bw4c.1openalex-snapshot

Trans-synaptic Neuronal Communication via Bioluminescent Optogenetics

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The Anti-Depression-Like Effects of Zhengtian Capsule via Induction of Neurogenesis and the Neurotrophic Signaling Pathway

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A Potential Mechanism Underlying the Therapeutic Effects of Progesterone and Allopregnanolone on Ketamine-Induced Cognitive Deficits

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Coelenterazine-Type Bioluminescence-Induced Optical Probes for Sensing and Controlling Biological Processes

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