Astrocyte Ca2+ signalling: an unexpected complexity

Ultrasensitive fluorescent proteins for imaging neuronal activity

Chen, T.-W., Wardill, T. J., Sun, Y., Pulver, S. R., Renninger, S. L., Baohan, A., Schreiter, E. R., Kerr, R. A., Orger, M. B., Jayaraman, V., et al. (2013) · Nature · doi:10.1038/nature12354 · Cited by 6,474

Calcium signalling: dynamics, homeostasis and remodelling

Berridge, M. J., Bootman, M. D., & Roderick, H. L. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1155 · Cited by 5,719

Fluorescent indicators for Ca2+based on green fluorescent proteins and calmodulin

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Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators

Tian, L., Hires, S. A., Mao, T., Huber, D., Chiappe, M. E., Chalasani, S. H., Petreanu, L., Akerboom, J., McKinney, S. A., Schreiter, E. R., et al. (2009) · Nature Methods · doi:10.1038/nmeth.1398 · Cited by 1,967

Calcium oscillations increase the efficiency and specificity of gene expression

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Astrocytes, from brain glue to communication elements: the revolution continues

Volterra, A., & Meldolesi, J. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1722 · Cited by 1,837

Tripartite synapses: astrocytes process and control synaptic information

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Glutamate-mediated astrocyte–neuron signalling

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Protoplasmic Astrocytes in CA1 Stratum Radiatum Occupy Separate Anatomical Domains

Bushong, E. A., Martone, M. E., Jones, Y. Z., & Ellisman, M. H. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-01-00183.2002 · Cited by 1,578

Imaging Calcium in Neurons

Grienberger, C., & Konnerth, A. (2012) · Neuron · doi:10.1016/j.neuron.2012.02.011 · Cited by 1,459

Activity Dependent Changes to Astrocyte Resting Calcium

Mehina, E. M. F. (2016) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/24694

Altered synaptic signaling due to $$\beta $$ -amyloid interference in astrocytes: A modeling study

Havela, R., Manninen, T., & Linne, M. (2017) · World Congress on Medical Physics and Biomedical Engineering, September 7 - 12, 2009, Munich, Germany · doi:10.1007/978-981-10-5122-7_170

Investigating adrenoceptor regulation of the astroglial glycogen reserve

Jiang, X. (2017) · Figshare

Dinámica del calcio reticular en astrocitos corticales

Rodríguez-Prados, M. (2017) · doi:10.35376/10324/28634

Whole cell patch clamp analysis of non-synaptic and synaptic signaling in rodent and human supragranular neocortex

Rózsa, M. (2018) · SZTE Repository of Dissertations (University of Szeged) · doi:10.14232/phd.9755

Contribution of Piezo1 mechanosensitive channels to astrocyte calcium signaling

Ko, R. W. Y. (2018) · cIRcle (University of British Columbia) · doi:10.14288/1.0368787

Up to Date on Astrocytes

Kim, J. W. (2018) · International Neurourology Journal · doi:10.5213/inj.1820edi.008

Sarcoplasmic reticulum Ca2+ dynamics in aging Drosophila and correlation with sarcopenia

Delrio-Lorenzo, A. (2020) · UVaDOC UVaDOC University of Valladolid Documentary Repository (University of Valladolid) · doi:10.35376/10324/43643

Faculty Opinions recommendation of Exosome reporter mice reveal the involvement of exosomes in mediating neuron to astroglia communication in the CNS.

Wu, L., & Bosco, D. B. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.736600651.793568650

Faculty Opinions recommendation of Hyperactivity with Disrupted Attention by Activation of an Astrocyte Synaptogenic Cue.

Goda, Y., & Chater, T. E. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735606871.793560276

Faculty Opinions recommendation of An Optical Neuron-Astrocyte Proximity Assay at Synaptic Distance Scales.

Deneen, B. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732983977.793545232

Mecanismos de protección frente a rotenona por PDGF-BB en un modelo astrocitario

Pérez, R. J. C. (2020) · doi:10.11144/javeriana.10554.38509

Stimulation Paradigms and Transduction Patterns for Optogenetic Intervention of Astrocytes

Balachandar, L. (2021) · FIU - Digital Commons (Florida International University) · doi:10.25148/etd.fidc010179

Astroglial Cells as Gonadal Hormone Targets: Mediators of Sex Differences in Development and Adulthood

Rurak, G. M. (2023) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2023-15750

Arachidonic acid metabolites and cortical depression: From local to spatial model

Verisokin, A. Y., Вячеславовна, В. Д., & Brazhe, A. (2024) · Izvestiya of Saratov University Physics · doi:10.18500/1817-3020-2024-24-3-250-261

Activation of Bradykinin B2 Receptors in Astrocytes Stimulates the Release of Leukemia Inhibitory Factor for Autocrine and Paracrine Signaling

Lu, Y., Gu, Y., Chan, A. S. L., Yung, L. Y., & Wong, Y. H. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms252313079

Reviewer #2 (Public review): A spatial threshold for astrocyte calcium surge

(2024) · eLife · doi:10.7554/elife.90046.3.sa1

Analysis of Epilepsy Treatment Strategies Based on an Astrocyte–Neuron-Coupled Network Model

Lan, J., & Wang, R. (2025) · Brain Sciences · doi:10.3390/brainsci15050465

Genetic-Designed Tools to Unveil the Role of Astrocytes in Neuronal Circuits and Animal Behavior

Ashouri, F., Sánchez-Ruiz, A., Alberquilla, S., & Perea, G. (2025) · Springer eBooks · doi:10.1007/978-3-031-94215-0_5

The Neuroplastic Narrative of Antidepressant Ketamine Involves Early and Sustained Effects that Counteract Mechanisms Underlying Stress, Inflammation, and Neurodegeneration

Lullau, A. P. M., & Haga, E. M. W. (2025) · Neuromethods · doi:10.1007/978-1-0716-4603-8_3

Endocannabinoid in nonneuronal cells of the CNS

Araque, A., & Noriega‐Prieto, J. A. (2025) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-443-13908-6.00002-5

Cortical astrocytes flexibly encode reward contingencies and shape conditioned behaviorPreprint

Paniccia, J. E., Grant, R. I., Westphal, A. M., Clarke, R. E., Doncheck, E. M., Pagoota, B. E., Carroll-Deaton, J., Bordieanu, B., Buchmaier, S., Klumb, L. G., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.08.693010

Brain Synapses: Neurons, Astrocytes, and Extracellular Vesicles in Health and Diseases

Meldolesi, J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms27010159

Complex dynamics of glutamate-induced calcium responses in astrocytes from the nucleus of the solitary tract of mice

de Souza, M. M., Zacharias, L. R., & Leão, R. M. (2026) · Brazilian Journal of Medical and Biological Research · doi:10.1590/1414-431x2025e15017

Astrocytes as central integrators of neural circuit function: Mechanisms and dysregulation in neuropsychiatric disorders

Liu, X., Zhou, X., Meng, R., Chen, Y., Chen, Y., Highet, B., Curtis, M. A., Hirt, B., Yu, S., Zhou, J., et al. (2026) · Clinical and Translational Discovery · doi:10.1002/ctd2.70128

Astrocyte-induced dynamics of a pyramidal cell with a dendrite-connected astrocyte

Přibylová, L., Ševčík, J., Egorova, A., Husa, Š., Kajanová, L., Kopřivová, E., Mega, L. A., & Eclerová, V. (2026) · Journal of Computational Neuroscience · doi:10.1007/s10827-026-00924-x

Neurophysiological bases of memory formation and consolidation : contents and dynamics of hippocampal cell assembly sequences in rats

Drieu, C. (2017) · theses.fr (ABES) · doi:10.70675/494fc3ecz7079z4410z8adfz9d0a3e21cc17

Circuits neuronaux sous-tendant la régulation émotionnelle par le système ocytocinergique

Goyon, S. (2018) · theses.fr (ABES) · doi:10.70675/c8c9bec0z7b79z4826z862az93b128e1ada6

Study of the Neuron-Astrocyte Relationship in a Rodent Model of Tauopathy

de Gérando, A. M. (2019) · theses.fr (ABES) · doi:10.70675/04658671zaca3z4fefza24dz2f5a011bebfe

Roles of astroglial cannabinoid type 1 receptors (CB1) in memory and synaptic plasticity

Robin, L. M. (2018) · theses.fr (ABES) · doi:10.70675/1fd1dda8z3f4bz404azbdf6z5b648e4c4053

Evaluation du canal calcique TRPA1 comme cible thérapeutique potentielle dans la pathogénèse de la maladie d’Alzheimer

Paumier, A. (2020) · theses.fr (ABES) · doi:10.70675/46cbb4bazf458z47a7z9fefzcdb3585ce4e9

Role of astrocytic calcium signaling in synaptic transmission, plasticity and memory : implications for neurodegenerative diseases

Moukarzel, E. (2021) · theses.fr (ABES) · doi:10.70675/27d6c756z50c6z470azbb76z72a4a03ad5b0

Modeling of neuron-astrocyte interaction : application to signal and image processing

Lorenzo, J. (2022) · theses.fr (ABES) · doi:10.70675/9e7d026ezff73z4f89z8b1azef7f2e29fb41

Rôle des astrocytes dans la période critique de la plasticité visuelle

Breton, R. (2023) · theses.fr (ABES) · doi:10.70675/9140a00az6c88z4fb6zaabfz9eb16e7593ca

Excitatory neurons and astrocytes‐specific dysregulation and aberrant interactions are vulnerable to FCDI as suggested by single‐cell spatial transcriptomics

Zhang, Y. M., Zou, Q., Liu, Y., Li, Y., Fang, Y., Huang, T., Yu, J., Sui, L., Cao, D., & Zhou, L. (2026) · Clinical and Translational Medicine · doi:10.1002/ctm2.70673

(2R,6R)-Hydroxynorketamine elicits rapid antidepressant effects by promoting astrocytic µ-δ opioid receptor heterodimerizationPreprint

Liang, Y., Wang, L., Li, Y., Li, X., Sun, Y., Yang, M., Guo, X., Mu, J., Xu, C., Thapa, R., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.31.729044

Microfluidic System for On-Demand Imaging of Organotypic SlicesPreprint

Petr, J. B., Ferrari, E., Hagelüken, L., Cassano, M., Hierlemann, A. R., & Modena, M. M. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.18.733098

Spatiotemporally distinctive astrocytic and neuronal responses to repetitive intracortical microstimulation

Grundfest, D., Kim, K., Wang, Q., Yonza, A. K. I., Podsiadlo, J. T., Tao, L., zhang, X., Kucharz, K., Zhang, Y., Han, A., et al. (2026) · Journal of Neural Engineering · doi:10.1088/1741-2552/ae829c

Astrocytic Calcium and Default Mode Network Dysfunction in Early Stage AD

Larrivee, D. (2026) · IntechOpen eBooks · doi:10.5772/intechopen.1016224

The emerging role of astrocytes in spatial cognition, action and Alzheimer’s disease

Gaborit, M., Arabi, A., & Mariotti, L. (2026) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2026.1811370

Neuroprotective effect of curcumin against reserpine-induced oxidative damage in the cerebellum of mice in an acute model of Parkinson's disease: Combined in vivo study, molecular docking and molecular dynamicsPreprint

Oukhrib, M., Tamegart, L., Hejji, L., Ghachi, H. E., Khedraoui, M., Draoui, A., Haida, M., Hammoudan, I., Chtita, S., Gamrani, H., et al. (2026) · Research Square · doi:10.21203/rs.3.rs-10974731/v1

Wakefulness enhances somatic Ca²⁺ activity of microglia and astrocytes in the auditory cortex via distinct neuronal dependencies

Ding, F., Xu, M., Chen, Y., Sun, J., Cheng, X., Li, C., & 杨思思 (2026) · Cell Calcium · doi:10.1016/j.ceca.2026.103204

Making sense of astrocytic calcium signals — from acquisition to interpretation

Semyanov, A., Henneberger, C., & Agarwal, A. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-0361-8 · Cited by 269

Disentangling calcium-driven astrocyte physiology

Rusakov, D. A. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn3878 · Cited by 181

Astrocyte as Spatiotemporal Integrating Detector of Neuronal Activity

Gordleeva, S. Y., Ermolaeva, A. V., Kastalskiy, I. A., & Kazantsev, V. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00294 · Cited by 58

Synaptic information processing by astrocytes

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Astrocytes process synaptic information

Araque, A. (2008) · Neuron Glia Biology · doi:10.1017/s1740925x09000064 · Cited by 117