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Astrocyte subdomains respond independently in vivo

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What this work says

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

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Ca2+transients in astrocyte fine processes occur via Ca2+influx in the adult mouse hippocampus

inferredcites →https://doi.org/10.1016/0361-9230(92)90056-4openalex-snapshot

The evidence for astrocytes as a target for central noradrenergic activity: Expression of adrenergic receptors

inferredcites →https://doi.org/10.1016/j.bbrc.2018.10.027openalex-snapshot

Astrocytes in the mouse visual cortex reliably respond to visual stimulation

inferredcites →https://doi.org/10.1016/j.ceca.2013.08.003openalex-snapshot

Subcellular location of astrocytic calcium stores favors extrasynaptic neuron–astrocyte communication

inferredcites →https://doi.org/10.1016/j.ceca.2013.09.001openalex-snapshot

α1-Adrenergic receptors mediate coordinated Ca2+ signaling of cortical astrocytes in awake, behaving mice

inferredcites →https://doi.org/10.1016/j.ceca.2013.12.006openalex-snapshot

Spatiotemporal calcium dynamics in single astrocytes and its modulation by neuronal activity

inferredcites →https://doi.org/10.1016/j.cell.2011.07.022openalex-snapshot

Astrocytes Are Endogenous Regulators of Basal Transmission at Central Synapses

inferredcites →https://doi.org/10.1016/j.nbd.2015.03.025openalex-snapshot

Astrogliopathology in neurological, neurodevelopmental and psychiatric disorders

inferredcites →https://doi.org/10.1016/j.neuron.2004.08.011openalex-snapshot

Neuronal Synchrony Mediated by Astrocytic Glutamate through Activation of Extrasynaptic NMDA Receptors

inferredcites →https://doi.org/10.1016/j.neuron.2008.10.013openalex-snapshot

The Mystery and Magic of Glia: A Perspective on Their Roles in Health and Disease

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.2012.08.019openalex-snapshot

Synaptic Energy Use and Supply

inferredcites →https://doi.org/10.1016/j.neuron.2014.02.006openalex-snapshot

State Dependence of Noise Correlations in Macaque Primary Visual Cortex

inferredcites →https://doi.org/10.1016/j.neuron.2014.04.038openalex-snapshot

Norepinephrine Controls Astroglial Responsiveness to Local Circuit Activity

inferredcites →https://doi.org/10.1016/j.neuron.2015.06.035openalex-snapshot

The Nature of Shared Cortical Variability

inferredcites →https://doi.org/10.1016/j.neuron.2016.12.034openalex-snapshot

Transient Opening of the Mitochondrial Permeability Transition Pore Induces Microdomain Calcium Transients in Astrocyte Processes

inferredcites →https://doi.org/10.1016/j.neuron.2017.02.035openalex-snapshot

GABAergic Neurons in Ferret Visual Cortex Participate in Functionally Specific Networks

inferredcites →https://doi.org/10.1016/j.neuron.2017.04.021openalex-snapshot

Septal Cholinergic Neuromodulation Tunes the Astrocyte-Dependent Gating of Hippocampal NMDA Receptors to Wakefulness

inferredcites →https://doi.org/10.1016/j.tcb.2016.01.003openalex-snapshot

Probing the Complexities of Astrocyte Calcium Signaling

inferredcites →https://doi.org/10.1016/j.tins.2015.07.006openalex-snapshot

Do stars govern our actions? Astrocyte involvement in rodent behavior

inferredcites →https://doi.org/10.1038/76609openalex-snapshot

From form to function: calcium compartmentalization in dendritic spines

inferredcites →https://doi.org/10.1038/nature17965openalex-snapshot

Neural correlates of single-vessel haemodynamic responses in vivo

inferredcites →https://doi.org/10.1038/ncomms11450openalex-snapshot

Imaging large-scale cellular activity in spinal cord of freely behaving mice

inferredcites →https://doi.org/10.1038/ncomms12270openalex-snapshot

Spatial clustering of tuning in mouse primary visual cortex

inferredcites →https://doi.org/10.1038/nn.2929openalex-snapshot

Local Ca2+ detection and modulation of synaptic release by astrocytes

inferredcites →https://doi.org/10.1038/nn.3711openalex-snapshot

Partitioning neuronal variability

inferredcites →https://doi.org/10.1038/nn.3906openalex-snapshot

Calcium dynamics in astrocyte processes during neurovascular coupling

inferredcites →https://doi.org/10.1038/nn.4001openalex-snapshot

Ca2+ signaling in astrocytes from Ip3r2−/− mice in brain slices and during startle responses in vivo

inferredcites →https://doi.org/10.1038/nn.4142openalex-snapshot

Do glia drive synaptic and cognitive impairment in disease?

inferredcites →https://doi.org/10.1038/nn.4201openalex-snapshot

Astrocyte calcium signaling: the third wave

inferredcites →https://doi.org/10.1038/nn.4323openalex-snapshot

Orientation selectivity and the functional clustering of synaptic inputs in primary visual cortex

inferredcites →https://doi.org/10.1038/nn.4647openalex-snapshot

Astrocytes control synaptic strength by two distinct v-SNARE-dependent release pathways

inferredcites →https://doi.org/10.1038/nn1703openalex-snapshot

Astrocytic Ca2+ signaling evoked by sensory stimulation in vivo

inferredcites →https://doi.org/10.1038/nrn3725openalex-snapshot

Astrocyte Ca2+ signalling: an unexpected complexity

inferredcites →https://doi.org/10.1038/nrn3878openalex-snapshot

Disentangling calcium-driven astrocyte physiology

inferredcites →https://doi.org/10.1073/pnas.1206557109openalex-snapshot

Nucleus basalis-enabled stimulus-specific plasticity in the visual cortex is mediated by astrocytes

inferredcites →https://doi.org/10.1073/pnas.1209448109openalex-snapshot

General anesthesia selectively disrupts astrocyte calcium signaling in the awake mouse cortex

inferredcites →https://doi.org/10.1073/pnas.1310065110openalex-snapshot

Rapid stimulus-evoked astrocyte Ca 2+ elevations and hemodynamic responses in mouse somatosensory cortex in vivo

inferredcites →https://doi.org/10.1073/pnas.1520759113openalex-snapshot

Astrocytes regulate cortical state switching in vivo

inferredcites →https://doi.org/10.1073/pnas.1617782114openalex-snapshot

Astrocytes locally translate transcripts in their peripheral processes

inferredcites →https://doi.org/10.1085/jgp.201210949openalex-snapshot

Imaging calcium microdomains within entire astrocyte territories and endfeet with GCaMPs expressed using adeno-associated viruses

inferredcites →https://doi.org/10.1093/cercor/bhw078openalex-snapshot

Homer1 Scaffold Proteins Govern Ca2+ Dynamics in Normal and Reactive Astrocytes

inferredcites →https://doi.org/10.1093/cercor/bhw366openalex-snapshot

Long-term In Vivo Calcium Imaging of Astrocytes Reveals Distinct Cellular Compartment Responses to Sensory Stimulation

inferredcites →https://doi.org/10.1101/381434openalex-snapshot

Astrocytes integrate local sensory and brain-wide neuromodulatory signals

inferredcites →https://doi.org/10.1101/cshperspect.a020404openalex-snapshot

Astrocyte Calcium Signaling: From Observations to Functions and the Challenges Therein

inferredcites →https://doi.org/10.1126/science.1144640openalex-snapshot

Astrocytes Potentiate Transmitter Release at Single Hippocampal Synapses

inferredcites →https://doi.org/10.1126/science.1156120openalex-snapshot

Tuned Responses of Astrocytes and Their Influence on Hemodynamic Signals in the Visual Cortex

inferredcites →https://doi.org/10.1126/science.1967852openalex-snapshot

Glutamate Induces Calcium Waves in Cultured Astrocytes: Long-Range Glial Signaling

inferredcites →https://doi.org/10.1126/science.aai8185openalex-snapshot

Three-dimensional Ca 2+ imaging advances understanding of astrocyte biology

inferredcites →https://doi.org/10.1146/annurev-physiol-021113-170400openalex-snapshot

Plasticity of Dendritic Spines: Subcompartmentalization of Signaling

inferredcites →https://doi.org/10.1152/jn.00268.2001openalex-snapshot

Hippocampal Astrocytes In Situ Exhibit Calcium Oscillations That Occur Independent of Neuronal Activity

inferredcites →https://doi.org/10.1163/156856897x00357openalex-snapshot

The Psychophysics Toolbox

inferredcites →https://doi.org/10.1371/journal.pone.0049998openalex-snapshot

Nicotine Uses Neuron-Glia Communication to Enhance Hippocampal Synaptic Transmission and Long-term Memory

inferredcites →https://doi.org/10.1523/jneurosci.16-16-05073.1996openalex-snapshot

Hippocampal AstrocytesIn SituRespond to Glutamate Released from Synaptic Terminals

inferredcites →https://doi.org/10.1523/jneurosci.2761-16.2017openalex-snapshot

Astrocyte-Mediated Neuronal Synchronization Properties Revealed by False Gliotransmitter Release

inferredcites →https://doi.org/10.1523/jneurosci.5289-11.2011openalex-snapshot

Astrocyte Calcium Signaling Transforms Cholinergic Modulation to Cortical Plasticity In Vivo

inferredcites →https://doi.org/10.17615/s4kv-rg05openalex-snapshot

Hippocampal Astrocytes In Situ Respond to Glutamate Released from Synaptic Terminals

What points at this work

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

inferred← citeshttps://doi.org/10.1073/pnas.2219150120openalex-snapshot

Building transformers from neurons and astrocytes

inferred← citeshttps://doi.org/10.3389/fncel.2022.972827openalex-snapshot

From nociception to pain perception, possible implications of astrocytes

inferred← citeshttps://doi.org/10.3390/cells9020439openalex-snapshot

Astroglial Isopotentiality and Calcium-Associated Biomagnetic Field Effects on Cortical Neuronal Coupling

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