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Spontaneous astrocytic Ca2+ oscillations in situ drive NMDAR-mediated neuronal excitation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Intercellular calcium signaling and gap junctional communication in astrocytes
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Axonal guidance during development of the great cerebral commissures: Descriptive and experimental studies, in vivo, on the role of preformed glial pathways
inferredcites →https://doi.org/10.1002/cne.903350103openalex-snapshot
The early development of thalamocortical and corticothalarnic projections
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Distribution of four types of synapse on physiologically identified relay neurons in the ventral posterior thalamic nucleus of the cat
inferredcites →https://doi.org/10.1002/glia.440130204openalex-snapshot
GFAP‐positive hippocampal astrocytes in situ respond to glutamatergic neuroligands with increases in [Ca2+]i
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Evidence for glutamate‐mediated activation of hippocampal neurons by glial calcium waves
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Distribution of AMPA selective glutamate receptors in the thalamus of adult rats and during postnatal development. A light and ultrastructural immunocytochemical study
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Development of firing patterns and electrical properties in neurons of the rat ventrobasal thalamus
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Memories of NMDA receptors and LTP
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Intercellular signaling in glial cells: Calcium waves and oscillations in response to mechanical stimulation and glutamate
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Neuronal activity triggers calcium waves in hippocampal astrocyte networks
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The role of Ca2+ entry via synaptically activated NMDA receptors in the induction of long-term potentiation
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Developmental and regional expression in the rat brain and functional properties of four NMDA receptors
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Neuronal domains in developing neocortex: Mechanisms of coactivation
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Recognition, adhesion, transmembrane signaling and cell motility in guided neuronal migration
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Developmental mechanisms that generate precise patterns of neuronal connectivity
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Tripartite synapses: glia, the unacknowledged partner
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Reciprocal communication systems between astrocytes and neurones
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Neuronal Calcium Signaling
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Calcium Stores in Hippocampal Synaptic Boutons Mediate Short-Term Plasticity, Store-Operated Ca2+ Entry, and Spontaneous Transmitter Release
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Prostaglandins stimulate calcium-dependent glutamate release in astrocytes
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Astrocyte-mediated potentiation of inhibitory synaptic transmission
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Glutamate-mediated astrocyte–neuron signalling
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Distinct aspects of neuronal differentiation encoded by frequency of spontaneous Ca2+ transients
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Glutamate-dependent astrocyte modulation of synaptic transmission between cultured hippocampal neurons
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Developmental and Regional Expression of NMDA Receptor Subtypes Containing the NR2D Subunit in Rat Brain
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Immunocytochemical demonstration of vimentin in astrocytes and ependymal cells of developing and adult mouse nervous system
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Single‐channel activations and concentration jumps: comparison of recombinant NR1a/NR2A and NR1a/NR2D NMDA receptors
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Slow deactivation kinetics of NMDA receptors containing NR1 and NR2D subunits in rat cerebellar Purkinje cells
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Sensory input and burst firing output of rat and cat thalamocortical cells: the role of NMDA and non‐NMDA receptors.
inferredcites →https://doi.org/10.1126/science.1496379openalex-snapshot
Neuronal Domains in Developing Neocortex
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.271.5251.978openalex-snapshot
Chain Migration of Neuronal Precursors
inferredcites →https://doi.org/10.1126/science.274.5290.1133openalex-snapshot
Synaptic Activity and the Construction of Cortical Circuits
inferredcites →https://doi.org/10.1126/science.281.5376.559openalex-snapshot
Activity-Dependent Cortical Target Selection by Thalamic Axons
inferredcites →https://doi.org/10.1126/science.8134839openalex-snapshot
Direct Signaling from Astrocytes to Neurons in Cultures of Mammalian Brain Cells
inferredcites →https://doi.org/10.1152/jn.1998.80.1.143openalex-snapshot
Progression of Change in NMDA, non-NMDA, and Metabotropic Glutamate Receptor Function at the Developing Corticothalamic Synapse
inferredcites →https://doi.org/10.1159/000112107openalex-snapshot
Glia-Neuron Intercellular Calcium Signaling
inferredcites →https://doi.org/10.1523/jneurosci.17-20-07817.1997openalex-snapshot
Intracellular Calcium Oscillations in Astrocytes: A Highly Plastic, Bidirectional Form of Communication between Neurons and AstrocytesIn Situ
inferredcites →https://doi.org/10.1523/jneurosci.18-03-00854.1998openalex-snapshot
Sodium Current in Rat and Cat Thalamocortical Neurons: Role of a Non-Inactivating Component in Tonic and Burst Firing
inferredcites →https://doi.org/10.1523/jneurosci.18-11-04022.1998openalex-snapshot
Modulation of Neuronal Activity by Glial Cells in the Retina
inferredcites →https://doi.org/10.1523/jneurosci.18-17-06822.1998openalex-snapshot
Calcium Elevation in Astrocytes Causes an NMDA Receptor-Dependent Increase in the Frequency of Miniature Synaptic Currents in Cultured Hippocampal Neurons
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Glutamate Receptor Activity Is Required for Normal Development of Tectal Cell Dendrites In Vivo
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ATP Released from Astrocytes Mediates Glial Calcium Waves
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SNARE Protein-Dependent Glutamate Release from Astrocytes
inferredcites →https://doi.org/10.1523/jneurosci.20-05-01800.2000openalex-snapshot
Imaging Extracellular Waves of Glutamate during Calcium Signaling in Cultured Astrocytes
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Postnatal Development of Mouse “Whisker” Thalamus: Ventroposterior Medial Nucleus (VPM), Barreloids, and Their Thalamocortical Relay Neurons
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Astrocyte control of the cerebrovasculature
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Spontaneous NA+ transients in individual mitochondria of intact astrocytes.
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Differential NMDA‐dependent activation of glial cells in mouse hippocampus
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Olfactory ensheathing cell membrane properties are shaped by connectivity
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Optogenetic manipulation of astrocytes from synapses to neuronal networks: A potential therapeutic strategy for neurodegenerative diseases
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Astrocyte calcium signals at Schaffer collateral to CA1 pyramidal cell synapses correlate with the number of activated synapses but not with synaptic strength
inferred← citeshttps://doi.org/10.1002/j.2040-4603.1984.tb01020.xopenalex-snapshot
The Cerebral Microcirculation
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Astrocyte‐induced synapse formation and ischemic stroke
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Attenuation of inhibitory synaptic transmission by glial dysfunction in rat thalamus
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Monitoring Intracellular Ca2+ in Brain Slices with Fluorescent Indicators
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Glutamate release from astrocytes: impact on neuronal function
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Synaptic Information Processing by Astrocytes
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Mechanisms of transmitter release from astrocytes
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Astrocyte control of blood flow
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Calcium signaling in glia
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Astrocyte gap junctions and glutamate-induced neurotoxicity
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Glutamate-mediated bi-directional signaling between neurons and astrocytes
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The regulated release of transmitters from astrocytes
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Astrocytic Gap Junctions Contribute to Aberrant Neuronal Synchronization in a Mouse Model of MeCP2 Duplication Syndrome
inferred← citeshttps://doi.org/10.1007/s12559-011-9115-2openalex-snapshot
Qualitative Information Processing in Tripartite Synapses: A Hypothetical Model
inferred← citeshttps://doi.org/10.1007/s40675-014-0005-5openalex-snapshot
Astrocytic Regulation of Sleep Processes
inferred← citeshttps://doi.org/10.1007/springerreference_124444openalex-snapshot
Thalamic Neurotransmitters and Neuromodulators
inferred← citeshttps://doi.org/10.1016/b978-0-12-374530-9.00013-9openalex-snapshot
The Cerebral Microcirculation
inferred← citeshttps://doi.org/10.1016/b978-0-12-415804-7.00012-5openalex-snapshot
Astrocytic Regulation of Synapses, Neuronal Networks, and Behavior
inferred← citeshttps://doi.org/10.1016/b978-0-12-415901-3.00004-9openalex-snapshot
Astroglial Calcium Signaling and Calcium Waves
inferred← citeshttps://doi.org/10.1016/b978-0-12-415901-3.00013-xopenalex-snapshot
Gap Junctions Regulate Seizure Activity – But in Unexpected Ways
inferred← citeshttps://doi.org/10.1016/b978-0-12-802401-0.00006-5openalex-snapshot
Astrocyte Calcium Signaling
inferred← citeshttps://doi.org/10.1016/b978-0-444-53839-0.00010-7openalex-snapshot
Infraslow (<0.1Hz) oscillations in thalamic relay nuclei
inferred← citeshttps://doi.org/10.1016/b978-012369437-9/50022-0openalex-snapshot
Exocytic Release of Glutamate from Astrocytes: Comparison to Neurons
inferred← citeshttps://doi.org/10.1016/b978-012373961-2.00353-2openalex-snapshot
IMAGING | Optical Monitoring of Circuitry Activity In vitro
inferred← citeshttps://doi.org/10.1016/j.abb.2025.110494openalex-snapshot
Effect of metformin on spontaneous calcium signaling in cultured astrocytes during normoxic and hypoxic conditions
inferred← citeshttps://doi.org/10.1016/j.addicn.2022.100022openalex-snapshot
Regulation of glutamate homeostasis in the nucleus accumbens by astrocytic CB1 receptors and its role in cocaine-motivated behaviors
inferred← citeshttps://doi.org/10.1016/j.addr.2006.07.001openalex-snapshot
Imaging of cortical astrocytes using 2-photon laser scanning microscopy in the intact mouse brain
inferred← citeshttps://doi.org/10.1016/j.apm.2017.11.002openalex-snapshot
Contribution of calcium fluxes to astrocyte spontaneous calcium oscillations in deterministic and stochastic models
inferred← citeshttps://doi.org/10.1016/j.arr.2014.07.004openalex-snapshot
When astrocytes become harmful: Functional and inflammatory responses that contribute to Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2010.11.006openalex-snapshot
Ca2+ sources for the exocytotic release of glutamate from astrocytes
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2012.12.017openalex-snapshot
In vivo functional calcium imaging of induced or spontaneous activity in the fly brain using a GFP-apoaequorin-based bioluminescent approach
inferred← citeshttps://doi.org/10.1016/j.bbrc.2007.11.090openalex-snapshot
Identification of new functions of Ca2+ release from intracellular stores in central nervous system
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.01.064openalex-snapshot
Cell–cell communication induces random spikes of spontaneous calcium oscillations in multi-BV-2 microglial cells
inferred← citeshttps://doi.org/10.1016/j.bcp.2021.114457openalex-snapshot
Chemogenetic manipulation of astrocytic activity: Is it possible to reveal the roles of astrocytes?
inferred← citeshttps://doi.org/10.1016/j.biochi.2021.04.006openalex-snapshot
Aquaporins implicated in the cell proliferation and the signaling pathways of cell stemness
inferred← citeshttps://doi.org/10.1016/j.biolcel.2003.10.007openalex-snapshot
Calcium signal communication in the central nervous system
inferred← citeshttps://doi.org/10.1016/j.bpj.2009.08.030openalex-snapshot
Simulation of Spontaneous Ca2+ Oscillations in Astrocytes Mediated by Voltage-Gated Calcium Channels
inferred← citeshttps://doi.org/10.1016/j.brainres.2023.148444openalex-snapshot
Pilocarpine-induced acute seizure causes rapid area-specific astrogliosis and alters purinergic signaling in rat hippocampus
inferred← citeshttps://doi.org/10.1016/j.brainresrev.2009.10.005openalex-snapshot
GLIA modulates synaptic transmission
inferred← citeshttps://doi.org/10.1016/j.brainresrev.2009.10.006openalex-snapshot
Ion changes and signalling in perisynaptic glia
inferred← citeshttps://doi.org/10.1016/j.brainresrev.2009.11.008openalex-snapshot
Gliotransmission: Exocytotic release from astrocytes
inferred← citeshttps://doi.org/10.1016/j.ceca.2005.06.015openalex-snapshot
Glial calcium signaling and neuron–glia communication
inferred← citeshttps://doi.org/10.1016/j.ceca.2005.09.009openalex-snapshot
Hypoxia stimulates Ca2+ release from intracellular stores in astrocytes via cyclic ADP ribose-mediated activation of ryanodine receptors
inferred← citeshttps://doi.org/10.1016/j.ceca.2005.11.008openalex-snapshot
ATP autocrine/paracrine signaling induces calcium oscillations and NFAT activation in human mesenchymal stem cells
inferred← citeshttps://doi.org/10.1016/j.ceca.2007.06.002openalex-snapshot
Temperature and nitric oxide control spontaneous calcium transients in astrocytes
inferred← citeshttps://doi.org/10.1016/j.ceca.2011.02.009openalex-snapshot
Long-term facilitation of spontaneous calcium oscillations in astrocytes with endogenous adenosine in hippocampal slice cultures
inferred← citeshttps://doi.org/10.1016/j.ceca.2013.08.002openalex-snapshot
Mechanisms for L-channel-mediated increase in [Ca2+] and its reduction by anti-bipolar drugs in cultured astrocytes combined with its mRNA expression in freshly isolated cells support the importance of astrocytic L-channels
inferred← citeshttps://doi.org/10.1016/j.ceca.2013.09.001openalex-snapshot
α1-Adrenergic receptors mediate coordinated Ca2+ signaling of cortical astrocytes in awake, behaving mice
inferred← citeshttps://doi.org/10.1016/j.ceca.2013.10.004openalex-snapshot
Astrocyte calcium microdomains are inhibited by Bafilomycin A1 and cannot be replicated by low-level Schaffer collateral stimulation in situ
inferred← citeshttps://doi.org/10.1016/j.celrep.2012.03.007openalex-snapshot
Backpropagating Action Potentials Enable Detection of Extrasynaptic Glutamate by NMDA Receptors
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115726openalex-snapshot
Machine-guided cell-fate engineering
inferred← citeshttps://doi.org/10.1016/j.chaos.2016.08.009openalex-snapshot
Dynamic transition on the seizure-like neuronal activity by astrocytic calcium channel block
inferred← citeshttps://doi.org/10.1016/j.chaos.2022.112135openalex-snapshot
Switching behavior of the gamma power in the neuronal network modulated by the astrocytes
inferred← citeshttps://doi.org/10.1016/j.chaos.2022.112969openalex-snapshot
Resonance effects in neuronal-astrocyte model with ion channel blockage
inferred← citeshttps://doi.org/10.1016/j.clinph.2008.07.222openalex-snapshot
Ictal intracranial infraslow EEG activity
inferred← citeshttps://doi.org/10.1016/j.clinph.2013.10.014openalex-snapshot
Interictal infraslow activity in patients with epilepsy
inferred← citeshttps://doi.org/10.1016/j.clinph.2014.05.028openalex-snapshot
Intracranially recorded ictal direct current shifts may precede high frequency oscillations in human epilepsy
inferred← citeshttps://doi.org/10.1016/j.clinph.2015.03.020openalex-snapshot
Ictal infraslow activity in stereoelectroencephalography: Beyond the “DC shift”
inferred← citeshttps://doi.org/10.1016/j.clinph.2017.10.014openalex-snapshot
Frontal infraslow activity marks the motor spasms of anti-LGI1 encephalitis
inferred← citeshttps://doi.org/10.1016/j.cogsys.2018.03.001openalex-snapshot
Interactions between astrocytes and the reward-attention circuit: A model for attention focusing in the presence of nicotine
inferred← citeshttps://doi.org/10.1016/j.conb.2012.03.009openalex-snapshot
Astrocytes conspire with neurons during progression of neurological disease
inferred← citeshttps://doi.org/10.1016/j.conb.2013.11.001openalex-snapshot
Cortical maps: a role for astrocytes?
inferred← citeshttps://doi.org/10.1016/j.ddmod.2008.07.002openalex-snapshot
Models of astrocytic Ca2+ dynamics and epilepsy
inferred← citeshttps://doi.org/10.1016/j.dyepig.2021.109451openalex-snapshot
Recent progress in the development of sensing systems for in vivo detection of biological hydrogen sulfide
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106828openalex-snapshot
The developmental profile of visual cortex astrocytes
inferred← citeshttps://doi.org/10.1016/j.isci.2025.113640openalex-snapshot
Photoactivated adenylyl cyclase in cortical astrocytes promotes synaptic potentiation and reveals alterations in Huntington’s disease
inferred← citeshttps://doi.org/10.1016/j.jfca.2024.106022openalex-snapshot
A symmetric pyrylium based near-infrared probe with large Stokes shift for detection of H2S in water, food, and living cells
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2004.05.013openalex-snapshot
Ballistic labeling and dynamic imaging of astrocytes in organotypic hippocampal slice cultures
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2007.11.022openalex-snapshot
Developmental profile and properties of sulforhodamine 101—Labeled glial cells in acute brain slices of rat hippocampus
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2010.05.004openalex-snapshot
CXCR4-mediated glutamate exocytosis from astrocytes
inferred← citeshttps://doi.org/10.1016/j.jphysparis.2005.12.003openalex-snapshot
Synaptic information processing by astrocytes
inferred← citeshttps://doi.org/10.1016/j.jtbi.2006.01.002openalex-snapshot
Modeling of ATP-mediated signal transduction and wave propagation in astrocytic cellular networks
inferred← citeshttps://doi.org/10.1016/j.jtbi.2007.12.011openalex-snapshot
A mathematical model of spontaneous calcium(II) oscillations in astrocytes
inferred← citeshttps://doi.org/10.1016/j.jtbi.2022.111164openalex-snapshot
A new real-time analog circuit of Ca2+ Li-Rinzel astrocyte model based on analytical method
inferred← citeshttps://doi.org/10.1016/j.mce.2006.04.017openalex-snapshot
Quantitative proteomics identifies a change in glial glutamate metabolism at the time of female puberty
inferred← citeshttps://doi.org/10.1016/j.mce.2011.08.039openalex-snapshot
Calcium signalling in astroglia
inferred← citeshttps://doi.org/10.1016/j.neuint.2003.07.004openalex-snapshot
Neurons set the tone of gap junctional communication in astrocytic networks
inferred← citeshttps://doi.org/10.1016/j.neuint.2007.03.003openalex-snapshot
Evidence that α7 nicotinic receptor modulates glutamate release from mouse neocortical gliosomes
inferred← citeshttps://doi.org/10.1016/j.neuint.2008.12.018openalex-snapshot
The trinity of Ca2+ sources for the exocytotic glutamate release from astrocytes
inferred← citeshttps://doi.org/10.1016/j.neuint.2010.02.007openalex-snapshot
Regulated exocytosis in astrocytic signal integration
inferred← citeshttps://doi.org/10.1016/j.neuint.2011.12.001openalex-snapshot
The astrocyte excitability brief: From receptors to gliotransmission
inferred← citeshttps://doi.org/10.1016/j.neuint.2013.01.017openalex-snapshot
Glial cell changes in epilepsy: Overview of the clinical problem and therapeutic opportunities
inferred← citeshttps://doi.org/10.1016/j.neuint.2018.02.005openalex-snapshot
Alterations of L-type voltage dependent calcium channel alpha 1 subunit in the hippocampal CA3 region during and after pilocarpine-induced epilepsy
inferred← citeshttps://doi.org/10.1016/j.neuint.2020.104942openalex-snapshot
Astroglial adrenoreceptors modulate synaptic transmission and contextual fear memory formation in dentate gyrus
inferred← citeshttps://doi.org/10.1016/j.neulet.2014.06.047openalex-snapshot
Glutamate release from satellite glial cells of the murine trigeminal ganglion
inferred← citeshttps://doi.org/10.1016/j.neures.2003.11.002openalex-snapshot
Localization of SNARE proteins and secretory organelle proteins in astrocytes in vitro and in situ
inferred← citeshttps://doi.org/10.1016/j.neures.2013.01.014openalex-snapshot
The astrocytic contribution to neurovascular coupling – Still more questions than answers?
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2012.02.060openalex-snapshot
Infra-slow fluctuations in electrophysiological recordings, blood-oxygenation-level-dependent signals, and psychophysical time series
inferred← citeshttps://doi.org/10.1016/j.neuron.2004.08.011openalex-snapshot
Neuronal Synchrony Mediated by Astrocytic Glutamate through Activation of Extrasynaptic NMDA Receptors
inferred← citeshttps://doi.org/10.1016/j.neuron.2007.04.032openalex-snapshot
Selective Stimulation of Astrocyte Calcium In Situ Does Not Affect Neuronal Excitatory Synaptic Activity
inferred← citeshttps://doi.org/10.1016/j.neuron.2007.05.008openalex-snapshot
Defining the Role of Astrocytes in Neuromodulation
inferred← citeshttps://doi.org/10.1016/j.neuron.2008.01.029openalex-snapshot
Endocannabinoids Mediate Neuron-Astrocyte Communication
inferred← citeshttps://doi.org/10.1016/j.neuron.2008.04.002openalex-snapshot
Astrocytes in the Epileptic Brain
inferred← citeshttps://doi.org/10.1016/j.neuron.2008.09.004openalex-snapshot
What Is the Role of Astrocyte Calcium in Neurophysiology?
inferred← citeshttps://doi.org/10.1016/j.neuron.2010.08.043openalex-snapshot
Endocannabinoids Potentiate Synaptic Transmission through Stimulation of Astrocytes
inferred← citeshttps://doi.org/10.1016/j.neuron.2012.03.027openalex-snapshot
Relevance of Exocytotic Glutamate Release from Retinal Glia
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