The DOI matches its Crossref record; 134 of the 134 references it cites were found in a registry or an index.
Gliotransmitters Travel in Time and Space
Open accessAbstract
The identification of the presence of active signaling between astrocytes and neurons in a process termed gliotransmission has caused a paradigm shift in our thinking about brain function. However, we are still in the early days of the conceptualization of how astrocytes influence synapses, neurons, networks, and ultimately behavior. In this Perspective, our goal is to identify emerging principles governing gliotransmission and consider the specific properties of this process that endow the astrocyte with unique functions in brain signal integration. We develop and present hypotheses aimed at reconciling confounding reports and define open questions to provide a conceptual framework for future studies. We propose that astrocytes mainly signal through high-affinity slowly desensitizing receptors to modulate neurons and perform integration in spatiotemporal domains complementary to those of neurons.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“astrocyte interactions with synaptic circuits are multimodal and multiscale, occur under physiological conditions 2-5 and contribute to behavior 6-8 .”
From Astrocyte function from information processing to cognition and cognitive impairment (2019) · cites this paper as [2]
In the citing paper
“Astrocytes contribute to synaptic plasticity by releasing fast mediators that directly modify synaptic function 2, 4 .”
From Astrocyte function from information processing to cognition and cognitive impairment (2019) · cites this paper as [2]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Glutamate receptor ion channels
Mayer, M. L. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.05.004 · Cited by 3,655
Glutamate Receptor Ion Channels: Structure, Regulation, and Function
Traynelis, S. F., Wollmuth, L. P., McBain, C. J., Menniti, F. S., Vance, K. M., Ogden, K. K., Hansen, K. B., Yuan, H., Myers, S. J., & Dingledine, R. (2010) · Pharmacological Reviews · doi:10.1124/pr.109.002451 · Cited by 3,568
The Glutamate Receptor Ion Channels
Dingledine, R., Borges, K., Bowie, D., & Traynelis, S. F. (1999) · Pharmacological Reviews · doi:10.1016/s0031-6997(24)01394-2 · Cited by 3,554
Pellerin, L., & Magistretti, P. J. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.22.10625 · Cited by 2,927
Tripartite synapses: glia, the unacknowledged partner
Araque, A., Parpura, V., Sanzgiri, R. P., & Haydon, P. G. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01349-6 · Cited by 2,529
Self-citationGlial and neuronal control of brain blood flow
Attwell, D., Buchan, A. M., Charpak, S., Lauritzen, M., MacVicar, B. A., & Newman, E. A. (2010) · Nature · doi:10.1038/nature09613 · Cited by 2,511
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
Self-citationTripartite synapses: astrocytes process and control synaptic information
Perea, G., Navarrete, M., & Araque, A. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.05.001 · Cited by 1,820
Self-citationGlutamate-mediated astrocyte–neuron signalling
Parpura, V., Basarsky, T. A., Liu, F., Jeftinija, K., Jeftinija, S., & Haydon, P. G. (1994) · Nature · doi:10.1038/369744a0 · Cited by 1,768
Self-citationSynaptic scaling mediated by glial TNF-α
Stellwagen, D., & Malenka, R. C. (2006) · Nature · doi:10.1038/nature04671 · Cited by 1,715
Flagged first, then by citations
Cited by
Sorted by citations
Items 401–500 of 999
Neuroglia: Realising their true potential
Butt, A. M., & Verkhratsky, A. (2018) · Brain and Neuroscience Advances · doi:10.1177/2398212818817495 · Cited by 52
Foll, C. L. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.01036 · Cited by 46
Functional and transcriptional characterization of complex neuronal co-cultures
Enright, H. A., Lam, D., Sebastian, A., Sales, A. P., Cadena, J., Hum, N. R., Osburn, J. J., Peters, S. K. G., Petkus, B., Soscia, D. A., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-67691-2 · Cited by 46
Terminal Schwann Cell Aging: Implications for Age-Associated Neuromuscular Dysfunction
Fuertes-Álvarez, S., & Izeta, A. (2021) · Aging and Disease · doi:10.14336/ad.2020.0708 · Cited by 46
On the role of the extracellular space on the holistic behavior of the brain
Marcoli, M., Agnati, L. F., Benedetti, F., Genedani, S., Guidolin, D., Ferraro, L., Maura, G., & Fuxé, K. (2015) · Reviews in the Neurosciences · doi:10.1515/revneuro-2015-0007 · Cited by 45
Makovkin, S., Александрович, К. Е., Ivanchenko, M., & Gordleeva, S. (2022) · Scientific Reports · doi:10.1038/s41598-022-10649-3 · Cited by 44
The stress of losing sleep: Sex-specific neurobiological outcomes
Wright, C. J., Milosavljevic, S., & Pocivavsek, A. (2023) · Neurobiology of Stress · doi:10.1016/j.ynstr.2023.100543 · Cited by 47
Neuron–Glial Interactions: Implications for Plasticity, Behavior, and Cognition
Rangel‐Gomez, M., Alberini, C. M., Deneen, B., Drummond, G. T., Manninen, T., Sur, M., & Vicentic, A. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1231-24.2024 · Cited by 49
Roles of Glial Cells in Sculpting Inhibitory Synapses and Neural Circuits
Um, J. W. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00381 · Cited by 45
Modeling of Astrocyte Networks: Toward Realistic Topology and Dynamics
Вячеславовна, В. Д., Verisokin, A. Y., Postnov, D. E., & Brazhe, A. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.645068 · Cited by 44
“Tripartite Synapses” in Taste Buds: A Role for Type I Glial-like Taste Cells
Rodriguez, Y. A., Roebber, J. K., Dvoryanchikov, G., Makhoul, V., Roper, S. D., & Chaudhari, N. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1444-21.2021 · Cited by 42
Plasticity of the Melanocortin System: Determinants and Possible Consequences on Food Intake
Nuzzaci, D., Laderrière, A., Lemoine, A., Nédélec, E., Pénicaud, L., Rigault, C., & Bénani, A. (2015) · Frontiers in Endocrinology · doi:10.3389/fendo.2015.00143 · Cited by 44
Scalable Networks-on-Chip Interconnected Architecture for Astrocyte-Neuron Networks
Liu, J., Harkin, J., Maguire, L., Mcdaid, L. J., Wade, J. J., & Martin, G. (2016) · IEEE Transactions on Circuits and Systems I Regular Papers · doi:10.1109/tcsi.2016.2615051 · Cited by 42
Gap junction channels as potential targets for the treatment of major depressive disorder
Ren, Q., Wang, Z., Chu, S., Xia, C., & Chen, N. (2017) · Psychopharmacology · doi:10.1007/s00213-017-4782-7 · Cited by 41
Wellmann, M., Álvarez‐Ferradas, C., Maturana, C. J., Sáez, J. C., & Bonansco, C. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00446 · Cited by 42
Regulation of Synaptosomal GLT-1 and GLAST during Epileptogenesis
Peterson, A. R., & Binder, D. K. (2019) · Neuroscience · doi:10.1016/j.neuroscience.2019.05.048 · Cited by 42
Yu, X., Moye, S. L., & Khakh, B. S. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0085-21.2021 · Cited by 47
Fairless, R., Bading, H., & Diem, R. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.741280 · Cited by 45
Taste Bud Connectome: Implications for Taste Information Processing
Wilson, C., Lasher, R. S., Yang, R., Dzowo, Y. K., Kinnamon, J. C., & Finger, T. E. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0838-21.2021 · Cited by 42
Emerging role of astrocytes in oxytocin-mediated control of neural circuits and brain functions
Baudon, A., Creusot, E. C., Althammer, F., Schaaf, C. P., & Charlet, A. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102328 · Cited by 44
Active Dendrites and Local Field Potentials: Biophysical Mechanisms and Computational Explorations
Sinha, M., & Narayanan, R. (2021) · Neuroscience · doi:10.1016/j.neuroscience.2021.08.035 · Cited by 44
Astrocytes functionally integrate multiple synapses via specialized leaflet domains
Benoit, L., Hristovska, I., Liaudet, N., Jouneau, P., Fertin, A., Ceglia, R. D., Litvin, D. G., Castro, M. A. D., Jevtic, M., Zalachoras, I., et al. (2025) · Cell · doi:10.1016/j.cell.2025.08.036 · Cited by 48
Self-citationGlutamate receptors in the kidney
Dryer, S. E. (2015) · Nephrology Dialysis Transplantation · doi:10.1093/ndt/gfv028 · Cited by 44
Spinal dorsal horn astrocytes release GABA in response to synaptic activation
Christensen, R. K., Delgado‐Lezama, R., Russo, R. E., Lind, B. L., Loeza‐Alcocer, E., Rath, M. F., Fabbiani, G., Schmitt, N., Lauritzen, M., Petersen, A. V., et al. (2018) · The Journal of Physiology · doi:10.1113/jp276562 · Cited by 39
Astrocyte-induced intermittent synchronization of neurons in a minimal network
Makovkin, S., Shkerin, I. V., Gordleeva, S., & Ivanchenko, M. (2020) · Chaos Solitons & Fractals · doi:10.1016/j.chaos.2020.109951 · Cited by 41
Inflammation: A Major Target for Compounds to Control Alzheimer’s Disease
Maccioni, R. B., Navarrete, L. P., González, A., González-Canacer, A., Guzmán‐Martínez, L., & Cortés, N. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-191014 · Cited by 42
MECP2 and the biology of MECP2 duplication syndrome
D’Mello, S. R. (2021) · Journal of Neurochemistry · doi:10.1111/jnc.15331 · Cited by 42
Astrocytes mediate analogous memory in a multi-layer neuron–astrocyte network
Tsybina, Y., Kastalskiy, I. A., Krivonosov, M., Zaikin, A. A., Kazantsev, V., Gorban, A. N., & Gordleeva, S. (2022) · Neural Computing and Applications · doi:10.1007/s00521-022-06936-9 · Cited by 41
Sowa, J. E., & Tokarski, K. (2021) · Pharmacological Reports · doi:10.1007/s43440-021-00323-2 · Cited by 41
Bouvier, D. S., Fixemer, S., Heurtaux, T., Jeannelle, F., Frauenknecht, K. B. M., & Mittelbronn, M. G. A. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.814889 · Cited by 43
Chen, Y., Lin, S., Jin, S., & Gao, T. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2024.04.013 · Cited by 42
Nuclear pore complex remodeling by p75NTR cleavage controls TGF-β signaling and astrocyte functions
Schachtrup, C., Ryu, J. K., Mammadzada, K., Khan, A. S., Carlton, P. M., Perez, A. J., Frank, C., Moan, N. L., Vagena, E., Baeza-Raja, B., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4054 · Cited by 40
Human astrocytes are distinct contributors to the complexity of synaptic function
Krencik, R., van Asperen, J. V., & Ullian, E. M. (2016) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2016.08.012 · Cited by 43
Assessment of astrocytes as a mediator of memory and learning in rodents
Akther, S., & Hirase, H. (2021) · Glia · doi:10.1002/glia.24099 · Cited by 38
Ca 2+ activity maps of astrocytes tagged by axoastrocytic AAV transfer
Georgiou, L., Echeverría, A., Georgiou, A., & Kühn, B. (2022) · Science Advances · doi:10.1126/sciadv.abe5371 · Cited by 38
Astrocyte Calcium SignalingPreprint
Ahrens, M. B., Khakh, B. S., & Poskanzer, K. E. (2024) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041353 · Cited by 44
Suthard, R. L., Senne, R. A., Buzharsky, M. D., Pyo, A. Y., Dorst, K. E., Diep, A. H., Cole, R. H., & Ramirez, S. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1775-22.2023 · Cited by 39
Essential Role of Astrocytes in Learning and Memory
Escalada, P., Ezkurdia, A., Ramírez, M. J., & Solas, M. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25031899 · Cited by 46
Functional MRI in Mice Lacking IP 3 -Dependent Calcium Signaling in Astrocytes
Jego, P., Pacheco‐Torres, J., Araque, A., & Canals, S. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2014.144 · Cited by 41
Self-citationAstrocytes and lysosomal storage diseases
Rao, K. V. R., & Kielian, T. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.05.061 · Cited by 42
Astrocytic cell adhesion genes linked to schizophrenia correlate with synaptic programs in neurons
Pietiläinen, O. P. H., Trehan, A., Meyer, D., Mitchell, J. M., Tegtmeyer, M., Valakh, V., Gebre, H., Chen, T., Vartiainen, E., Farhi, S. L., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2022.111988 · Cited by 36
Neuronal and astrocyte determinants of critical periods of plasticity
Andrade‐Talavera, Y., Pérez-Rodríguez, M., Prius-Mengual, J., & Moreno, A. R. (2023) · Trends in Neurosciences · doi:10.1016/j.tins.2023.04.005 · Cited by 39
Bukharaeva, E. A., Shakirzyanova, A., Khuzakhmetova, V. F., Ситдикова, Г. Ф., & Giniatullin, R. A. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00391 · Cited by 38
Gómez‐Gonzalo, M., Zehnder, T., Requie, L. M., Bezzi, P., & Carmignoto, G. (2018) · Glia · doi:10.1002/glia.23473 · Cited by 41
Self-citationDarabid, H., St-Pierre-See, A., & Robitaille, R. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.075 · Cited by 39
Self-citationAstrocytes in the Ventrolateral Preoptic Area Promote Sleep
Kim, J., Choi, I., Jeong, J.-Y., Jang, I., Lee, M., & Suk, K. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1486-20.2020 · Cited by 38
Sensing and Regulating Synaptic Activity by Astrocytes at Tripartite Synapse
Noriega‐Prieto, J. A., & Araque, A. (2021) · Neurochemical Research · doi:10.1007/s11064-021-03317-x · Cited by 45
Self-citationMitochondria: new players in homeostatic regulation of firing rate set points
Ruggiero, A., Katsenelson, M., & Slutsky, I. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.03.002 · Cited by 37
Oligodendroglial GABAergic Signaling: More Than Inhibition!
Bai, X., Kirchhoff, F., & Scheller, A. (2021) · Neuroscience Bulletin · doi:10.1007/s12264-021-00693-w · Cited by 40
Extracellular Calcium Influx Pathways in Astrocyte Calcium Microdomain Physiology
Ahmadpour, N., Kantroo, M., & Stobart, J. L. (2021) · Biomolecules · doi:10.3390/biom11101467 · Cited by 43
Astrocyte Gliotransmission in the Regulation of Systemic Metabolism
Murat, C. D. B., & García‐Cáceres, C. (2021) · Metabolites · doi:10.3390/metabo11110732 · Cited by 38
Liao, Z., Tao, Y., Guo, X.-M., Cheng, D., Wang, F., Liu, X., & Ma, L. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00396 · Cited by 39
Borbor, M., Yin, D., Brockmeier, U., Wang, C., Doeckel, M., Pillath‐Eilers, M., Kaltwasser, B., Hermann, D. M., & Dzyubenko, E. (2023) · Glia · doi:10.1002/glia.24357 · Cited by 39
Astroglial calcium signaling displays short-term plasticity and adjusts synaptic efficacy
Sibille, J., Zapata, J., Teillon, J., & Rouach, N. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00189 · Cited by 37
GABA B receptor-mediated activation of astrocytes by gamma-hydroxybutyric acid
Gould, T. M., Chen, L., Emri, Z., Pirttimäki, T., Errington, A. C., Crunelli, V., & Parri, H. R. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0607 · Cited by 37
Mukunda, C. L., & Narayanan, R. (2016) · The Journal of Physiology · doi:10.1113/jp273482 · Cited by 39
Ryczko, D., Hanini‐Daoud, M., Condamine, S., Bréant, B. J. B., Fougère, M., Araya, R., & Kolta, A. (2020) · The Journal of Physiology · doi:10.1113/jp280501 · Cited by 32
Glial amplification of synaptic signals
Beppu, K., Kubo, N., & Matsui, K. (2021) · The Journal of Physiology · doi:10.1113/jp280857 · Cited by 37
Glial-neuronal ensembles: partners in drug addiction-associated synaptic plasticity
Cadet, J. L., & Bisagno, V. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00204 · Cited by 40
Artificial Neuron–Glia Networks Learning Approach Based on Cooperative Coevolution
Mesejo, P., Ibáñez, O. C., Fernández-Blanco, E., Cedrón, F., Pazos, A., & Porto-Pazos, A. B. (2015) · International Journal of Neural Systems · doi:10.1142/s0129065715500124 · Cited by 37
Neuroglia and their roles in central respiratory control; an overview
Funk, G. D., Rajani, V., Alvares, T., Revill, A. L., Zhang, Y., Chu, N. Y., Biancardi, V., Taxini, C. L., Katzell, A., & Reklow, R. (2015) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2015.01.010 · Cited by 37
Mapelli, J., Gandolfi, D., Vilella, A., Zoli, M., & Bigiani, A. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1601194113 · Cited by 45
Functional remodeling of subtype-specific markers surrounding implanted neuroprostheses
Salatino, J. W., Winter, B. M., Drazin, M. H., & Purcell, E. K. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00162.2017 · Cited by 32
Ephaptic Coupling of Cortical Neurons: Possible Contribution of Astroglial Magnetic Fields?
Martı́nez, M. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.07.072 · Cited by 34
Pham, C., Hérault, K., Oheim, M., Maldera, S., Vialou, V., Cauli, B., & Li, D. (2021) · Acta Neuropathologica Communications · doi:10.1186/s40478-021-01146-1 · Cited by 36
Choi, I., Kim, J., Jeong, J., Lee, M., Suk, K., & Jang, I. (2022) · Glia · doi:10.1002/glia.24225 · Cited by 36
Iqbal, Z., Lei, Z., Ramkrishnan, A. S., Liu, S., Hasan, M., Akter, M., Lam, Y. Y., & Li, Y. (2023) · Communications Biology · doi:10.1038/s42003-022-04405-6 · Cited by 33
Bull, C., Syed, W. A., Minter, S. C., & Bowers, M. S. (2015) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.12683 · Cited by 37
EphB3 signaling propagates synaptic dysfunction in the traumatic injured brain
Perez, E. J., Cepero, M. L., Perez, S. U., Coyle, J. T., Sick, T. J., & Liebl, D. J. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.06.007 · Cited by 35
Sobrinho, C. R., Gonçalves, C. M., Takakura, A. C. T., Mulkey, D. K., & Moreira, T. S. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00032.2017 · Cited by 36
Konstantinidis, E., Portal, B., Mothes, T., Beretta, C., Lindskog, M., & Erlandsson, A. (2023) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02687-5 · Cited by 35
Genetic control of astrocyte function in neural circuits
Jahn, H. M., Scheller, A., & Kirchhoff, F. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00310 · Cited by 35
New Tools to Study Astrocyte Ca2+ Signal Dynamics in Brain Networks In Vivo
Losi, G., Mariotti, L., Sessolo, M., & Carmignoto, G. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00134 · Cited by 35
Self-citationSaito, K., Shigetomi, E., Yasuda, R., Sato, R., Nakano, M., Tashiro, K., Tanaka, K. F., Ikenaka, K., Mikoshiba, K., Mizuta, I., et al. (2018) · Glia · doi:10.1002/glia.23300 · Cited by 37
Diversity of Astroglial Effects on Aging- and Experience-Related Cortical Metaplasticity
Lalo, U., Bogdanov, A., & Pankratov, Y. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00239 · Cited by 37
Imaging tripartite synapses using super-resolution microscopy
Heller, J. P., Odii, T., Zheng, K., & Rusakov, D. A. (2019) · Methods · doi:10.1016/j.ymeth.2019.05.024 · Cited by 36
Neuro-Immune Cross-Talk in the Striatum: From Basal Ganglia Physiology to Circuit Dysfunction
Mancini, A., Ghiglieri, V., Parnetti, L., Calabresi, P., & Filippo, M. D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.644294 · Cited by 38
Liu, Y., Liu, T., Zhou, Y., Li, W., Wang, M., Song, N., Zhang, W., Jiang, J., Yuan, S., Ding, J., et al. (2022) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2022.07.021 · Cited by 36
Stargazing: Monitoring subcellular dynamics of brain astrocytes
Kacerovsky, J. B., & Murai, K. K. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.07.007 · Cited by 35
Engram reactivation mimics cellular signatures of fear
Suthard, R. L., Senne, R. A., Buzharsky, M. D., Diep, A. H., Pyo, A. Y., & Ramirez, S. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113850 · Cited by 33
Purinergic neurone-glia signalling in cognitive-related pathologies
Illés, P., & Verkhratsky, A. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.08.005 · Cited by 34
Age- and Experience-Related Plasticity of ATP-Mediated Signaling in the Neocortex
Lalo, U., Bogdanov, A., & Pankratov, Y. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00242 · Cited by 34
MacDonald, A. J., & Ellacott, K. L. J. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.112982 · Cited by 35
Presenilin-2 and Calcium Handling: Molecules, Organelles, Cells and Brain Networks
Pizzo, P., Basso, E., Filadi, R., Greotti, E., Leparulo, A., Pendin, D., Redolfi, N., Rossini, M., Vajente, N., Pozzan, T., et al. (2020) · Cells · doi:10.3390/cells9102166 · Cited by 36
Tendilla‐Beltrán, H., Sanchez-Islas, N. D. C., Marina-Ramos, M., Leza, J. C., & Flores, G. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101967 · Cited by 36
Cervelli, M., Averna, M., Vergani, L., Pedrazzi, M., Amato, S., Fiorucci, C., Rossi, M. N., Maura, G., Mariottini, P., Cervetto, C., et al. (2022) · Biomedicines · doi:10.3390/biomedicines10071756 · Cited by 34
Parkhurst, S., Adhikari, P., Navarrete, J. S., Legendre, A., Manansala, M., & Wolf, F. W. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.01.049 · Cited by 34
The glutamatergic synapse: a complex machinery for information processing
Maio, V. D. (2021) · Cognitive Neurodynamics · doi:10.1007/s11571-021-09679-w · Cited by 38
D-Amino acids from foods and gut microbiota and their effects in health and disease
Roskjær, A. B., Roager, H. M., & Dragsted, L. O. (2024) · Food Reviews International · doi:10.1080/87559129.2024.2347472 · Cited by 35
Shigetomi, E., Suzuki, H., Hirayama, Y. J., Sano, F., Nagai, Y., Yoshihara, K., Koga, K., Tateoka, T., Yoshioka, H., Shinozaki, Y., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-50190-7 · Cited by 33
Pierozan, P., Biasibetti, H., Schmitz, F., Ávila, H., Parisi, M. M., Barbé-Tuana, F., Wyse, A., & Pessoa-Pureur, R. (2016) · Biochimica et Biophysica Acta · doi:10.1016/j.bbamcr.2016.09.014 · Cited by 30
Nakamoto, K., Aizawa, F., Kinoshita, M., Kōyama, Y., & Tokuyama, S. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00401 · Cited by 33
Modeling Neuron–Glia Interactions with the Brian 2 Simulator
Stimberg, M., Goodman, D. F. M., Brette, R., & Pittà, M. D. (2019) · Springer series in computational neuroscience · doi:10.1007/978-3-030-00817-8_18 · Cited by 32
Dobrachinski, F., Gerbatin, R. R., Sartori, G., Golombieski, R. M., Antoniazzi, A. Q., Nogueira, C. W., Royes, L. F. F., Fighera, M. R., Porciúncula, L. O., Cunha, R. A., et al. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1296-1 · Cited by 33
Parallel astrocyte calcium signaling modulates olfactory bulb responses
Ung, K., Tepe, B., Pekarek, B. T., Arenkiel, B. R., & Deneen, B. (2020) · Journal of Neuroscience Research · doi:10.1002/jnr.24634 · Cited by 35
How astrocytic ATP shapes neuronal activity and brain circuits
Lezmy, J. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102685 · Cited by 35
Verkhratsky, A., & Butt, A. M. (2023) · Elsevier eBooks · doi:10.1016/b978-0-12-821565-4.00008-0 · Cited by 31
Dang, R., Liu, A., Zhou, Y., Li, X., Wu, M., Cao, K., Meng, Y., Zhang, H., Gan, G., Xie, W., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-52974-3 · Cited by 33
A neurotransmitter atlas of C. elegans males and hermaphrodites
Wang, C., Vidal, B., Sural, S., Loer, C. M., Aguilar, G. R., Merritt, D. M., Toker, I. A., Vogt, M. C., Cros, C., & Hobert, O. (2024) · eLife · doi:10.7554/elife.95402.3 · Cited by 35
Brain energy metabolism and multiple sclerosis: progress and prospects
Park, S. J., & Choi, J. W. (2020) · Archives of Pharmacal Research · doi:10.1007/s12272-020-01278-3 · Cited by 32
Metadata
- Authors
- Araque, A., Carmignoto, G., Haydon, P. G., Oliet, S. H. R., Robitaille, R., & Volterra, A.
- Affiliations
- University of Minnesota (US)
- University of Padua (IT)
- Tufts University (US)
- Université de Bordeaux (FR)
- Université de Montréal (CA)
- University of Lausanne (CH)
- Corresponding author
- Carmignoto, Giorgio
- ORCID
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2014-02
- Volume
- 81
- Issue
- 4
- Pages
- 728-739
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC4107238
- OpenAlex
- W2042681276
- Cited by
- 1,308
- References
- 134
- Citations by year
- 2026: 73 · 2025: 101 · 2024: 115 · 2023: 125 · 2022: 116 · 2021: 153 · 2020: 116 · 2019: 95 · 2018: 105 · 2017: 84 · 2016: 86 · 2015: 105 · 2014: 32
- FWCI
- 11.69
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- SERVAL (Université de Lausanne) (acceptedVersion, other-oa)
- IRIS (submittedVersion)
- HAL (submittedVersion)
- Funders
- National Science Foundation
- Sbarro Health Research Organization
- European Commission (202167, 340368)
- Institut National de la Santé et de la Recherche Médicale
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (140999, 31003A, 203729)
- LabEx BRAIN
- National Institutes of Health
- Canadian Institutes of Health Research (MOP‐14137, MOP‐111070)
- National Institute on Alcohol Abuse and Alcoholism (R01AA020183)
- National Institute of Mental Health (R01MH095385)
- National Institute on Drug Abuse (R01DA025967)
- National Institute of Neurological Disorders and Stroke (R01NS037585)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- gliotransmission, astrocytes, astrocyte-neuron communication, high-affinity receptor, spatiotemporal signaling, astrocyte function
- MeSH terms
- Animals, Astrocytes, Cell Communication, Humans, Synaptic Transmission, Neuronal Plasticity, Neurons, Synapses
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
