Long-term potentiation depends on release of d-serine from astrocytes
Open accessAbstract
Long-term potentiation (LTP) of synaptic transmission provides an experimental model for studying mechanisms of memory. The classical form of LTP relies on N-methyl-D-aspartate receptors (NMDARs), and it has been shown that astroglia can regulate their activation through Ca(2+)-dependent release of the NMDAR co-agonist D-serine. Release of D-serine from glia enables LTP in cultures and explains a correlation between glial coverage of synapses and LTP in the supraoptic nucleus. However, increases in Ca(2+) concentration in astroglia can also release other signalling molecules, most prominently glutamate, ATP and tumour necrosis factor-alpha, whereas neurons themselves can synthesize and supply D-serine. Furthermore, loading an astrocyte with exogenous Ca(2+) buffers does not suppress LTP in hippocampal area CA1 (refs 14-16), and the physiological relevance of experiments in cultures or strong exogenous stimuli applied to astrocytes has been questioned. The involvement of glia in LTP induction therefore remains controversial. Here we show that clamping internal Ca(2+) in individual CA1 astrocytes blocks LTP induction at nearby excitatory synapses by decreasing the occupancy of the NMDAR co-agonist sites. This LTP blockade can be reversed by exogenous D-serine or glycine, whereas depletion of D-serine or disruption of exocytosis in an individual astrocyte blocks local LTP. We therefore demonstrate that Ca(2+)-dependent release of D-serine from an astrocyte controls NMDAR-dependent plasticity in many thousands of excitatory synapses nearby.
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
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?
The intermediate behavior of astrocytes is consistent with the view that astrocytes are not simply support cells but play an active role in computational processing.
“The intermediate behavior of astrocytes is therefore consistent with the emerging view that they are not simply support cells, but they play an active role in computational processing (Henneberger et al., 2010).”
From Molecular Architecture of the Mouse Nervous System (2018) · cites this paper as Henneberger et al., 2010
Classical NMDAR-dependent LTP at hippocampal CA1 synapses requires transient D-serine release from astrocytes.
“classical NMDAR-dependent LTP at hippocampal CA1 synapses requires transient D-serine release from the astrocytes 18, 29, 30 .”
From Astrocyte function from information processing to cognition and cognitive impairment (2019) · cites this paper as [29]
At the microscale, an entire astrocyte activates and may exert coordinated influence on synaptic ensembles in its territory.
“second, a microscale, on the order of a single astrocyte, at which the entire cell activates and may exert a coordinated influence on synaptic ensembles residing in its territory 29, 129”
From Astrocyte function from information processing to cognition and cognitive impairment (2019) · cites this paper as [29]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
A synaptic model of memory: long-term potentiation in the hippocampus
Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566 · see citing works
Astrocytes, from brain glue to communication elements: the revolution continues
Volterra, A., & Meldolesi, J. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1722 · Cited by 1,763 · see citing works
Synaptic scaling mediated by glial TNF-α
Stellwagen, D., & Malenka, R. C. (2006) · Nature · doi:10.1038/nature04671 · Cited by 1,715 · see citing works
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 · see citing works
Astrocytic Purinergic Signaling Coordinates Synaptic Networks
Pascual, O., Casper, K. B., Kubera, C., Zhang, J., Revilla-Sanchez, R., Sul, J.-Y., Takano, H., Moss, S. J., McCarthy, K., & Haydon, P. G. (2005) · Science · doi:10.1126/science.1116916 · Cited by 1,280 · see citing works
D-serine is an endogenous ligand for the glycine site of the N-methyl-D-aspartate receptor.
Mothet, J., Parent, A., Wolosker, H., Brady, R., Linden, D. J., Ferris, C., Rogawski, M., & Snyder, S. (2000) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.97.9.4926 · Cited by 1,164 · see citing works
Prostaglandins stimulate calcium-dependent glutamate release in astrocytes
Bezzi, P., Carmignoto, G., Pasti, L., Vesce, S., Rossi, D., Rizzini, B. L., Pozzan, T., & Volterra, A. (1998) · Nature · doi:10.1038/34651 · Cited by 1,143 · see citing works
Fellin, T., Pascual, O., Gobbo, S., Pozzan, T., Haydon, P. G., & Carmignoto, G. (2004) · Neuron · doi:10.1016/j.neuron.2004.08.011 · Cited by 970 · see citing works
Bezzi, P., Domercq, M., Brambilla, L., Galli, R., Schols, D., De Clercq, E., Vescovi, A., Bagetta, G., Kollias, G., Meldolesi, J., et al. (2001) · Nature Neuroscience · doi:10.1038/89490 · Cited by 964 · see citing works
Glia-Derived d-Serine Controls NMDA Receptor Activity and Synaptic Memory
Panatier, A., Theodosis, D. T., Mothet, J.-P., Touquet, B., Pollegioni, L., Poulain, D. A., & Oliet, S. H. R. (2006) · Cell · doi:10.1016/j.cell.2006.02.051 · Cited by 934 · see citing works
Self-citationAstroglial Metabolic Networks Sustain Hippocampal Synaptic Transmission
Rouach, N., Koulakoff, A., Abudara, V., Willecke, K., & Giaume, C. (2008) · Science · doi:10.1126/science.1164022 · Cited by 861 · see citing works
Schell, M. J., Molliver, M. E., & Snyder, S. H. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.9.3948 · Cited by 832 · see citing works
Astrocytes Potentiate Transmitter Release at Single Hippocampal Synapses
Perea, G., & Araque, A. (2007) · Science · doi:10.1126/science.1144640 · Cited by 727 · see citing works
Hippocampal AstrocytesIn SituRespond to Glutamate Released from Synaptic Terminals
Porter, J. T., & McCarthy, K. D. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05073.1996 · Cited by 672 · see citing works
What Is the Role of Astrocyte Calcium in Neurophysiology?
Agulhon, C., Petravicz, J., McMullen, A. B., Sweger, E. J., Minton, S. K., Taves, S., Casper, K. B., Fiacco, T. A., & McCarthy, K. D. (2008) · Neuron · doi:10.1016/j.neuron.2008.09.004 · Cited by 567 · see citing works
Hippocampal Astrocytes In Situ Respond to Glutamate Released from Synaptic Terminals
Porter, J. T., & McCarthy, K. D. (2021) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/s4kv-rg05 · Cited by 561 · see citing works
Yang, Y., Ge, W., Chen, Y., Zhang, Z., Shen, W., Wu, C., Poo, M., & Duan, S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2431073100 · Cited by 533 · see citing works
Ca2+ signaling requirements for long-term depression in the hippocampus.
Cummings, J. A., Mulkey, R., Nicoll, R., & Malenka, R. (1996) · Neuron · doi:10.1016/s0896-6273(00)80102-6 · Cited by 471 · see citing works
Mothet, J., Pollegioni, L., Ouanounou, G., Martineau, M., Fossier, P., & Baux, G. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408483102 · Cited by 461 · see citing works
Rusakov, D. A., & Kullmann, D. M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-09-03158.1998 · Cited by 438 · see citing works
Self-citationMultiple kinetic components of exocytosis distinguished by neurotoxin sensitivity
Xu, T., Binz, T., Niemann, H., & Neher, E. (1998) · Nature Neuroscience · doi:10.1038/642 · Cited by 333 · see citing works
Facilitation at single synapses probed with optical quantal analysis
Oertner, T. G., Sabatini, B. L., Nimchinsky, E. A., & Svoboda, K. (2002) · Nature Neuroscience · doi:10.1038/nn867 · Cited by 324 · see citing works
Fiacco, T. A., Agulhon, C., Taves, S., Petravicz, J., Casper, K. B., Dong, X., Chen, J., & McCarthy, K. D. (2007) · Neuron · doi:10.1016/j.neuron.2007.04.032 · Cited by 316 · see citing works
Bergles, D. E., & Jahr, C. E. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-19-07709.1998 · Cited by 298 · see citing works
Neuron-derived D-Serine Release Provides a Novel Means to Activate N-Methyl-D-aspartate Receptors
Kartvelishvily, E., Shleper, M., Balan, L., Dumin, E., & Wolosker, H. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m512927200 · Cited by 277 · see citing works
Serine racemase is predominantly localized in neurons in mouse brain
Miya, K., Inoue, R., Takata, Y., Abe, M., Natsume, R., Sakimura, K., Hongou, K., Miyawaki, T., & Mori, H. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21822 · Cited by 243 · see citing works
Fellin, T., Halassa, M. M., Terunuma, M., Succol, F., Takano, H., Frank, M., Moss, S. J., & Haydon, P. G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906419106 · Cited by 227 · see citing works
Rusakov, D. A., & Fine, A. (2003) · Neuron · doi:10.1016/s0896-6273(03)00025-4 · Cited by 200 · see citing works
Self-citationDuffy, S., Labrie, V., & Roder, J. C. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301486 · Cited by 173 · see citing works
Glutamate Release Monitored with Astrocyte Transporter Currents during LTP
Diamond, J. S., Bergles, D. E., & Jahr, C. E. (1998) · Neuron · doi:10.1016/s0896-6273(00)80551-6 · Cited by 143 · see citing works
Monitoring Glutamate Release during LTP with Glial Transporter Currents
Lüscher, C., Malenka, R. C., & Nicoll, R. A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80552-8 · Cited by 123 · see citing works
Střı́šovský, K., Jirásková, J., Mikulová, A., Rulı́šek, L., & Konvalinka, J. (2005) · Biochemistry · doi:10.1021/bi051201o · Cited by 117 · see citing works
Confocal imaging and tracking of the exocytotic routes for D ‐serine‐mediated gliotransmission
Martineau, M., Galli, T., Baux, G., & Mothet, J. (2008) · Glia · doi:10.1002/glia.20696 · Cited by 109 · see citing works
Analog Modulation of Mossy Fiber Transmission Is Uncoupled from Changes in Presynaptic Ca2+
Scott, R. S., Ruiz, A. J., Henneberger, C., Kullmann, D. M., & Rusakov, D. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1296-08.2008 · Cited by 63 · see citing works
Self-citationSzerb, J. C., & Issekutz, B., Jr. (1987) · Brain Research · doi:10.1016/s0006-8993(87)80030-6 · Cited by 63 · see citing works
Glycine Site of NMDA Receptor Serves as a Spatiotemporal Detector of Synaptic Activity Patterns
Li, Y., Krupa, B., Kang, J., Bolshakov, V. Y., & Liu, G. (2009) · Journal of Neurophysiology · doi:10.1152/jn.91342.2008 · Cited by 47 · see citing works
Ge, W., & Duan, S. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00146.2006 · Cited by 36 · see citing works
Calcium clamp of the intracellular environment
Baker, P. F., KNIGHT, D. E., & Umbach, J. A. (1985) · Cell Calcium · doi:10.1016/0143-4160(85)90030-2 · Cited by 32 · see citing works
Linden, H. R. (1995) · The Electricity Journal · doi:10.1016/1040-6190(95)90142-6 · Cited by 31 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Molecular Architecture of the Mouse Nervous System
Zeisel, A., Hochgerner, H., Lönnerberg, P., Johnsson, A., Memic, F., van der Zwan, J., Häring, M., Braun, E., Borm, L. E., La Manno, G., et al. (2018) · Cell · doi:10.1016/j.cell.2018.06.021 · Cited by 2,995 · see citing works
Astrocyte-Neuron Lactate Transport Is Required for Long-Term Memory Formation
Suzuki, A., Stern, S. A., Bozdagi, O., Huntley, G. W., Walker, R. H., Magistretti, P. J., & Alberini, C. M. (2011) · Cell · doi:10.1016/j.cell.2011.02.018 · Cited by 1,711 · see citing works
Verkhratsky, A., & Nedergaard, M. (2018) · Physiological Reviews · doi:10.1152/physrev.00042.2016 · Cited by 1,678 · see citing works
Immune modulation of learning, memory, neural plasticity and neurogenesis
Yirmiya, R., & Goshen, I. (2011) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2010.10.015 · Cited by 1,483 · see citing works
Reactive Gliosis and the Multicellular Response to CNS Damage and Disease
Burda, J. E., & Sofroniew, M. V. (2014) · Neuron · doi:10.1016/j.neuron.2013.12.034 · Cited by 1,431 · see citing works
Gliotransmitters Travel in Time and Space
Araque, A., Carmignoto, G., Haydon, P. G., Oliet, S. H. R., Robitaille, R., & Volterra, A. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.007 · Cited by 1,308 · see citing works
Self-citationKetamine and Ketamine Metabolite Pharmacology: Insights into Therapeutic Mechanisms
Zanos, P., Moaddel, R., Morris, P. J., Riggs, L. M., Highland, J. N., Georgiou, P., Pereira, E. F. R., Albuquerque, E. X., Thomas, C. J., Zarate, C. A., et al. (2018) · Pharmacological Reviews · doi:10.1124/pr.117.015198 · Cited by 1,260 · see citing works
Diversity of astrocyte functions and phenotypes in neural circuits
Khakh, B. S., & Sofroniew, M. V. (2015) · Nature Neuroscience · doi:10.1038/nn.4043 · Cited by 1,239 · see citing works
The Role of Microglia in the Healthy Brain: Figure 1.
Tremblay, M.-È., Stevens, B., Sierra, A., Wake, H., Bessis, A., & Nimmerjahn, A. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4158-11.2011 · Cited by 992 · see citing works
Astrocyte calcium signaling: the third wave
Bazargani, N., & Attwell, D. (2016) · Nature Neuroscience · doi:10.1038/nn.4201 · Cited by 949 · see citing works
Hol, E. M., & Pekny, M. (2015) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2015.02.004 · Cited by 917 · see citing works
Blood–brain barrier breakdown as a therapeutic target in traumatic brain injury
Shlosberg, D., Benifla, M., Kaufer, D., & Friedman, A. (2010) · Nature Reviews Neurology · doi:10.1038/nrneurol.2010.74 · Cited by 897 · see citing works
Glia and epilepsy: excitability and inflammation
Devinsky, O., Vezzani, A., Najjar, S., de Lanerolle, N. C., & Rogawski, M. A. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2012.11.008 · Cited by 868 · see citing works
Astrocytes Control Breathing Through pH-Dependent Release of ATP
Gourine, A. V., Kasymov, V., Marina, N., Tang, F., Figueiredo, M. F., Lane, S., Teschemacher, A. G., Spyer, K. M., Deisseroth, K. A., & Kasparov, S. (2010) · Science · doi:10.1126/science.1190721 · Cited by 856 · see citing works
GABA from reactive astrocytes impairs memory in mouse models of Alzheimer's disease
Jo, S., Yarishkin, O., Hwang, Y. J., Chun, Y. E., Park, M., Woo, D. H., Bae, J. Y., Kim, T., Lee, J., Chun, H., et al. (2014) · Nature Medicine · doi:10.1038/nm.3639 · Cited by 783 · see citing works
Astrocytes: a central element in neurological diseases
Pekny, M., Pekna, M., Messing, A., Steinhäuser, C., Lee, J., Parpura, V., Hol, E. M., Sofroniew, M. V., & Verkhratsky, A. (2015) · Acta Neuropathologica · doi:10.1007/s00401-015-1513-1 · Cited by 755 · see citing works
Synaptic and Extrasynaptic NMDA Receptors Are Gated by Different Endogenous Coagonists
Papouin, T., Ladépêche, L., Ruel, J., Sacchi, S., Labasque, M., Hanini, M., Groc, L., Pollegioni, L., Mothet, J., & Oliet, S. H. R. (2012) · Cell · doi:10.1016/j.cell.2012.06.029 · Cited by 752 · see citing works
Self-citationAstrocyte function from information processing to cognition and cognitive impairment
Santello, M., Toni, N., & Volterra, A. (2019) · Nature Neuroscience · doi:10.1038/s41593-018-0325-8 · Cited by 737 · see citing works
Chronic Glutamate Toxicity in Neurodegenerative Diseases—What is the Evidence?
Lewerenz, J., & Maher, P. A. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00469 · Cited by 721 · see citing works
Sofroniew, M. V. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a020420 · Cited by 695 · see citing works
Microglia activation triggers astrocyte-mediated modulation of excitatory neurotransmission
Pascual, O., Ben Achour, S., Rostaing, P., Triller, A., & Bessis, A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1111098109 · Cited by 693 · see citing works
Do astrocytes really exocytose neurotransmitters?
Hamilton, N. B., & Attwell, D. (2010) · Nature reviews. Neuroscience · doi:10.1038/nrn2803 · Cited by 674 · see citing works
Astrocytes Are Endogenous Regulators of Basal Transmission at Central Synapses
Panatier, A., Vallée, J., Haber, M., Murai, K. K., Lacaille, J.-C., & Robitaille, R. (2011) · Cell · doi:10.1016/j.cell.2011.07.022 · Cited by 650 · see citing works
Heterogeneity of astrocytic form and function.
Oberheim, N. A., Goldman, S. A., & Nedergaard, M. (2012) · Methods in Molecular Biology · doi:10.1007/978-1-61779-452-0_3 · Cited by 638 · see citing works
Astrocytic Activation Generates De Novo Neuronal Potentiation and Memory Enhancement
Adamsky, A., Kol, A., Kreisel, T., Doron, A., Ozeri-Engelhard, N., Melcer, T., Refaeli, R., Horn, H., Regev, L., Groysman, M., et al. (2018) · Cell · doi:10.1016/j.cell.2018.05.002 · Cited by 631 · see citing works
The immune system and developmental programming of brain and behavior
Bilbo, S. D., & Schwarz, J. M. (2012) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2012.08.006 · Cited by 579 · see citing works
The Cell Biology of Synaptic Plasticity
Ho, V. M., Lee, J.-A., & Martin, K. C. (2011) · Science · doi:10.1126/science.1209236 · Cited by 573 · see citing works
Glial cells in (patho)physiology
Parpura, V., Heneka, M. T., Montana, V., Oliet, S. H. R., Schousboe, A., Haydon, P. G., Stout, R. F., Spray, D. C., Reichenbach, A., Pannicke, T., et al. (2012) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2012.07664.x · Cited by 561 · see citing works
Self-citationLocal Ca2+ detection and modulation of synaptic release by astrocytes
Di Castro, M. A., Chuquet, J., Liaudet, N., Bhaukaurally, K., Santello, M., Bouvier, D., Tiret, P., & Volterra, A. (2011) · Nature Neuroscience · doi:10.1038/nn.2929 · Cited by 529 · see citing works
Nilius, B., & SZALLASI, A. (2014) · Pharmacological Reviews · doi:10.1124/pr.113.008268 · Cited by 504 · see citing works
Lactate Produced by Glycogenolysis in Astrocytes Regulates Memory Processing
Newman, L. A., Korol, D. L., & Gold, P. E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028427 · Cited by 473 · see citing works
TRPA1 channels regulate astrocyte resting calcium and inhibitory synapse efficacy through GAT-3
Shigetomi, E., Tong, X., Kwan, K. Y., Corey, D. P., & Khakh, B. S. (2011) · Nature Neuroscience · doi:10.1038/nn.3000 · Cited by 472 · see citing works
The contribution of neuroinflammation to amyloid toxicity in Alzheimer's disease
Minter, M. R., Taylor, J. M., & Crack, P. J. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13411 · Cited by 451 · see citing works
Astrocyte Ca2+ signalling: an unexpected complexity
Volterra, A., Liaudet, N., & Savtchouk, I. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3725 · Cited by 446 · see citing works
Neurobiological after-effects of non-invasive brain stimulation
Cirillo, G., Di Pino, G., Capone, F., Ranieri, F., Florio, L., Todisco, V., Tedeschi, G., Funke, K., & Di Lazzaro, V. (2017) · Brain Stimulation · doi:10.1016/j.brs.2016.11.009 · Cited by 446 · see citing works
Astrocytes Control Circadian Timekeeping in the Suprachiasmatic Nucleus via Glutamatergic Signaling
Brancaccio, M., Patton, A. P., Chesham, J. E., Maywood, E. S., & Hastings, M. H. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.030 · Cited by 437 · see citing works
Inflammatory process in Alzheimer's Disease
Meraz-Ríos, M. A., Toral-Rios, D., Franco-Bocanegra, D., Villeda-Hernández, J., & Campos-Peña, V. (2013) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2013.00059 · Cited by 427 · see citing works
Monai, H., Ohkura, M., Tanaka, M., Oe, Y., Konno, A., Hirai, H., Mikoshiba, K., Itohara, S., Nakai, J., Iwai, Y., et al. (2016) · Nature Communications · doi:10.1038/ncomms11100 · Cited by 410 · see citing works
Functions of Astrocytes and their Potential As Therapeutic Targets
Kimelberg, H. K., & Nedergaard, M. (2010) · Neurotherapeutics · doi:10.1016/j.nurt.2010.07.006 · Cited by 409 · see citing works
Astrocytes as secretory cells of the central nervous system: idiosyncrasies of vesicular secretion
Verkhratsky, A., Matteoli, M., Parpura, V., Mothet, J., & Zorec, R. (2016) · The EMBO Journal · doi:10.15252/embj.201592705 · Cited by 397 · see citing works
Astrocytes Mediate In Vivo Cholinergic-Induced Synaptic Plasticity
Navarrete, M., Perea, G., de Sevilla, D. F., Gómez-Gonzalo, M., Núñez, A., Martín, E. D., & Araque, A. (2012) · PLoS Biology · doi:10.1371/journal.pbio.1001259 · Cited by 387 · see citing works
Do glia drive synaptic and cognitive impairment in disease?
Chung, W.-S., Welsh, C. A., Barres, B. A., & Stevens, B. (2015) · Nature Neuroscience · doi:10.1038/nn.4142 · Cited by 385 · see citing works
Astrocyte Calcium Signaling Transforms Cholinergic Modulation to Cortical Plasticity <i>In Vivo</i>
Takata, N., Mishima, T., Hisatsune, C., Nagai, T., Ebisui, E., Mikoshiba, K., & Hirase, H. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5289-11.2011 · Cited by 382 · see citing works
Bernardinelli, Y., Randall, J., Janett, E., Nikonenko, I., König, S., Jones, E. V., Flores, C. E., Murai, K. K., Bochet, C. G., Holtmaat, A., et al. (2014) · Current Biology · doi:10.1016/j.cub.2014.06.025 · Cited by 369 · see citing works
Reactive Astrocytes As Therapeutic Targets for CNS Disorders
Hamby, M. E., & Sofroniew, M. V. (2010) · Neurotherapeutics · doi:10.1016/j.nurt.2010.07.003 · Cited by 367 · see citing works
TNFα Controls Glutamatergic Gliotransmission in the Hippocampal Dentate Gyrus
Santello, M., Bezzi, P., & Volterra, A. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.003 · Cited by 362 · see citing works
Astrocyte signaling controls spike timing–dependent depression at neocortical synapses
Min, R., & Nevian, T. (2012) · Nature Neuroscience · doi:10.1038/nn.3075 · Cited by 361 · see citing works
Synapse-specific astrocyte gating of amygdala-related behavior
Martin-Fernandez, M., Jamison, S., Robin, L. M., Zhao, Z., Martin, E. D., Aguilar, J., Benneyworth, M. A., Marsicano, G., & Araque, A. (2017) · Nature Neuroscience · doi:10.1038/nn.4649 · Cited by 345 · see citing works
Astrocyte regulation of synaptic behavior
Allen, N. J. (2014) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-100913-013053 · Cited by 343 · see citing works
Three-dimensional Ca <sup>2+</sup> imaging advances understanding of astrocyte biology
Bindocci, E., Savtchouk, I., Liaudet, N., Becker, D., Carriero, G., & Volterra, A. (2017) · Science · doi:10.1126/science.aai8185 · Cited by 342 · see citing works
Lactate-mediated glia-neuronal signalling in the mammalian brain
Tang, F., Lane, S., KORSAK, A. S., Paton, J. F. R., Gourine, A. V., Kasparov, S., & Teschemacher, A. G. (2014) · Nature Communications · doi:10.1038/ncomms4284 · Cited by 340 · see citing works
Multiple Roles for Astrocytes as Effectors of Cytokines and Inflammatory Mediators
Sofroniew, M. V. (2014) · The Neuroscientist · doi:10.1177/1073858413504466 · Cited by 333 · see citing works
Dopamine-Evoked Synaptic Regulation in the Nucleus Accumbens Requires Astrocyte Activity
Corkrum, M., Covelo, A., Lines, J., Bellocchio, L., Pisansky, M., Loke, K., Quintana, R., Rothwell, P. E., Lujan, R., Marsicano, G., et al. (2020) · Neuron · doi:10.1016/j.neuron.2019.12.026 · Cited by 327 · see citing works
Douce, J. L., Maugard, M., Veran, J., Matos, M., Jégo, P., Vigneron, P.-A., Faivre, É., Toussay, X., Vandenberghe, M. E., Balbastre, Y., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2020.02.004 · Cited by 326 · see citing works
Self-citationGliotransmission: Beyond Black-and-White
Savtchouk, I., & Volterra, A. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.0017-17.2017 · Cited by 325 · see citing works
Zhang, K., Förster, R., He, W., Liao, X., Li, J., Yang, C., Qin, H., Wang, M., Ding, R., Li, R., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00949-8 · Cited by 325 · see citing works
Going the Extra (Synaptic) Mile: Excitotoxicity as the Road Toward Neurodegenerative Diseases
Armada‐Moreira, A., Gomes, J. I., Pina, C. C., Savchak, O. K., Gonçalves‐Ribeiro, J., Rei, N., Pinto, S., Morais, T. P., Martins, R. S., Ribeiro, F. F., et al. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00090 · Cited by 323 · see citing works
Shigetomi, E., Jackson‐Weaver, O., Huckstepp, R. T. R., O’Dell, T. J., & Khakh, B. S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5779-12.2013 · Cited by 322 · see citing works
Hyperactivity with Disrupted Attention by Activation of an Astrocyte Synaptogenic Cue
Nagai, J., Rajbhandari, A. K., Gangwani, M. R., Hachisuka, A., Coppola, G., Masmanidis, S. C., Fanselow, M. S., & Khakh, B. S. (2019) · Cell · doi:10.1016/j.cell.2019.03.019 · Cited by 322 · see citing works
Neuroplastic changes in depression: A role for the immune system
Eyre, H., & Baune, B. T. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.03.019 · Cited by 319 · see citing works
Astrogliosis: An integral player in the pathogenesis of Alzheimer's disease
Osborn, L. M., Kamphuis, W., Wadman, W. J., & Hol, E. M. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2016.01.001 · Cited by 312 · see citing works
Astrocyte glycogen and lactate: New insights into learning and memory mechanisms
Alberini, C. M., Cruz, E., Descalzi, G., Bessières, B., & Gao, V. (2017) · Glia · doi:10.1002/glia.23250 · Cited by 286 · see citing works
Specialized astrocytes mediate glutamatergic gliotransmission in the CNS
Ceglia, R. D., Ledonne, A., Litvin, D. G., Lind, B. L., Carriero, G., Latagliata, E. C., Bindocci, E., Castro, M. A. D., Savtchouk, I., Vitali, I., et al. (2023) · Nature · doi:10.1038/s41586-023-06502-w · Cited by 285 · see citing works
Synaptic Integration of Adult-Born Hippocampal Neurons Is Locally Controlled by Astrocytes
Sultan, S., Li, L., Moss, J., Petrelli, F., Cassé, F., Gebara, E., Lopatar, J., Pfrieger, F. W., Bezzi, P., Bischofberger, J., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.10.037 · Cited by 284 · see citing works
Dysfunction of NMDA receptors in Alzheimer’s disease
Zhang, Y., Li, P., Feng, J., & Wu, M. (2016) · Neurological Sciences · doi:10.1007/s10072-016-2546-5 · Cited by 282 · see citing works
“The increased influx of calcium transform into chemical signals which in turn, leading to the establishment of LTP, a process believed to underlie learning and memory [18].”
BackgroundDeciphering the astrocyte reaction in Alzheimer's disease
Perez-Nievas, B. G., & Serrano-Pozo, A. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00114 · Cited by 282 · see citing works
Neuronal activity determines distinct gliotransmitter release from a single astrocyte
Covelo, A., & Araque, A. (2018) · eLife · doi:10.7554/elife.32237 · Cited by 276 · see citing works
Astrocytes in the initiation and progression of epilepsy
Vezzani, A., Ravizza, T., Bedner, P., Aronica, E., Steinhäuser, C., & Boison, D. (2022) · Nature Reviews Neurology · doi:10.1038/s41582-022-00727-5 · Cited by 272 · see citing works
Exocytosis of ATP From Astrocytes Modulates Phasic and Tonic Inhibition in the Neocortex
Lalo, U., Palygin, O., Rasooli-Nejad, S., Andrew, J., Haydon, P. G., & Pankratov, Y. (2014) · PLoS Biology · doi:10.1371/journal.pbio.1001747 · Cited by 270 · see citing works
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 · see citing works
Self-citationAstroglial Excitability and Gliotransmission: An Appraisal of Ca 2+ as a Signalling Route
Zorec, R., Araque, A., Carmignoto, G., Haydon, P. G., Verkhratsky, A., & Parpura, V. (2012) · ASN NEURO · doi:10.1042/an20110061 · Cited by 268 · see citing works
LTP Induction Boosts Glutamate Spillover by Driving Withdrawal of Perisynaptic Astroglia
Henneberger, C., Bard, L., Panatier, A., Reynolds, J. R., Kopach, O., Medvedev, N. I., Minge, D., Herde, M. K., Anders, S., Kraev, I., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.030 · Cited by 268 · see citing works
Self-citationMolecular signals of plasticity at the tetrapartite synapse
Dityatev, A., & Rusakov, D. A. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2010.12.006 · Cited by 267 · see citing works
Self-citationMultifunctional role of astrocytes as gatekeepers of neuronal energy supply
Stobart, J. L., & Anderson, C. M. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00038 · Cited by 266 · see citing works
Astrocytes: Orchestrating synaptic plasticity?
Pittà, M. D., Brunel, N., & Volterra, A. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.04.001 · Cited by 263 · see citing works
Astroglial CB1 Receptors Determine Synaptic D-Serine Availability to Enable Recognition Memory
Robin, L. M., Oliveira da Cruz, J. F., Langlais, V. C., Martin-Fernandez, M., Metna-Laurent, M., Busquets-Garcia, A., Bellocchio, L., Soria-Gomez, E., Papouin, T., Varilh, M., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.04.034 · Cited by 262 · see citing works
Self-citationAstrocytes contribute to gamma oscillations and recognition memory
Lee, H. S., Ghetti, A., Pinto‐Duarte, A., Wang, X., Dziewczapolski, G., Galimi, F., Huitrón‐Reséndiz, S., Piña-Crespo, J., Roberts, A. J., Verma, I. M., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1410893111 · Cited by 259 · see citing works
Astrocytes as Active Participants in Memory
Asher, S. M., & Goshen, I. (2025) · Journal of Neurochemistry · doi:10.1111/jnc.70258 · Cited by 258 · see citing works
TRPV1 channels are critical brain inflammation detectors and neuropathic pain biomarkers in mice
Marrone, M. C., Morabito, A., Giustizieri, M., Chiurchiù, V., Leuti, A., Mattioli, M., Marinelli, S., Riganti, L., Lombardi, M., Murana, E., et al. (2017) · Nature Communications · doi:10.1038/ncomms15292 · Cited by 247 · see citing works
Neuromodulation of Spike-Timing-Dependent Plasticity: Past, Present, and Future
Brzosko, Z., Mierau, S. B., & Paulsen, O. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.041 · Cited by 247 · see citing works
Harada, K., Kamiya, T., & Tsuboi, T. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00499 · Cited by 246 · see citing works
Papouin, T., Dunphy, J. M., Tolman, M., Dineley, K. T., & Haydon, P. G. (2017) · Neuron · doi:10.1016/j.neuron.2017.04.021 · Cited by 243 · see citing works
Self-citationAstrocyte-Synapse Structural Plasticity
Bernardinelli, Y., Müller, D., & Nikonenko, I. (2014) · Neural Plasticity · doi:10.1155/2014/232105 · Cited by 243 · see citing works
Role of Astrocytes in EpilepsyPreprint
Coulter, D. A., & Steinhäuser, C. (2015) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a022434 · Cited by 243 · see citing works
The NMDA receptor as a target for cognitive enhancement
Collingridge, G. L., Volianskis, A., Bannister, N. J., France, G., Hanna, L., Mercier, M., Tidball, P., Fang, G., Irvine, M. W., Costa, B. M., et al. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.06.051 · Cited by 239 · see citing works
Stehberg, J., Moraga‐Amaro, R., Salazar, C. M., Becerra, Á., Echeverría, C., Orellana, J. A., Bultynck, G., Ponsaerts, R., Leybaert, L., Simón, F., et al. (2012) · The FASEB Journal · doi:10.1096/fj.11-198416 · Cited by 238 · see citing works
Diniz, L. P., Almeida, J. C., Tortelli, V., Lopes, C. V., Setti-Perdigão, P., Stipursky, J., Kahn, S. A., Romão, L. F., Miranda, J. D., Alves‐Leon, S. V., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.380824 · Cited by 237 · see citing works
Optogenetic astrocyte activation modulates response selectivity of visual cortex neurons in vivo
Perea, G., Yang, A., Boyden, E. S., & Sur, M. (2014) · Nature Communications · doi:10.1038/ncomms4262 · Cited by 236 · see citing works
Astrocytes: Conductors of the Alzheimer disease neuroinflammatory symphony
Medeiros, R., & LaFerla, F. M. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.10.007 · Cited by 236 · see citing works
The Role of Astrocytes in the Regulation of Synaptic Plasticity and Memory Formation
Ota, Y., Zanetti, A. T., & Hallock, R. M. (2013) · Neural Plasticity · doi:10.1155/2013/185463 · Cited by 233 · see citing works
Glia: The many ways to modulate synaptic plasticity
Achour, S. B., & Pascual, O. (2010) · Neurochemistry International · doi:10.1016/j.neuint.2010.02.013 · Cited by 232 · see citing works
Astrocytic control of synaptic function
Papouin, T., Dunphy, J. M., Tolman, M., Foley, J., & Haydon, P. G. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0154 · Cited by 229 · see citing works
Self-citationRosenberg, D., Artoul, S., Segal, A. C., Kolodney, G., Radzishevsky, I. S., Dikopoltsev, E., Foltyn, V. N., Inoue, R., Mori, H., Billard, J., et al. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3836-12.2013 · Cited by 228 · see citing works
Kimura, T., Hamase, K., Miyoshi, Y., Yamamoto, R., Yasuda, K., Mita, M., Rakugi, H., Hayashi, T., & Isaka, Y. (2016) · Scientific Reports · doi:10.1038/srep26137 · Cited by 225 · see citing works
Chirality Effects on Peptide Self-Assembly Unraveled from Molecules to Materials
Garcia, A. M., Iglesias, D., Parisi, E., Styan, K. E., Waddington, L. J., Deganutti, C., Zorzi, R. D., Grassi, M., Melchionna, M., Vargiu, A. V., et al. (2018) · Chem · doi:10.1016/j.chempr.2018.05.016 · Cited by 225 · see citing works
Neuron-glia networks: integral gear of brain function
Perea, G., Sur, M., & Araque, A. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00378 · Cited by 224 · see citing works
Calcium signalling in astroglia
Verkhratsky, A., Rodriguez, J. J., & Parpura, V. (2011) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2011.08.039 · Cited by 224 · see citing works
Astroglial Glutamate Signaling and Uptake in the Hippocampus
Rose, C. R., Felix, L., Zeug, A., Dietrich, D., Reiner, A., & Henneberger, C. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00451 · Cited by 224 · see citing works
Self-citationAn astroglial basis of major depressive disorder? An overview
Wang, Q., Jie, W., Liu, J., Yang, J., & Gao, T. (2017) · Glia · doi:10.1002/glia.23143 · Cited by 222 · see citing works
An Excitatory Loop with Astrocytes Contributes to Drive Neurons to Seizure Threshold
Gómez‐Gonzalo, M., Losi, G., Chiavegato, A., Zonta, M., Cammarota, M., Brondi, M., Vetri, F., Uva, L., Pozzan, T., de Curtis, M., et al. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000352 · Cited by 222 · see citing works
- Authors
- Henneberger, C., Papouin, T., Oliet, S. H. R., & Rusakov, D. A.
- Affiliations
- UCL Queen Square Institute of Neurology (GB)
- Université de Bordeaux (FR)
- Corresponding author
- Oliet, Stéphane H. R.
- Rusakov, Dmitri A.
- Venue
- Nature
- Published
- 2010-01-14
- Volume
- 463
- Issue
- 7278
- Pages
- 232-236
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC2807667
- OpenAlex
- W2109909801
- Cited by
- 1,389
- References
- 39
- Citations by year
- 2026: 52 · 2025: 71 · 2024: 63 · 2023: 73 · 2022: 80 · 2021: 122 · 2020: 73 · 2019: 78 · 2018: 91 · 2017: 81 · 2016: 94 · 2015: 78 · 2014: 99 · 2013: 82 · 2012: 103
- FWCI
- 42.88
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- HAL (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Wellcome Trust (084311, 91064)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- long-term potentiation, astrocytes, D-serine, NMDA receptor co-agonist, synaptic plasticity, hippocampal CA1, excitatory synapses, glycine, astrocyte-neuron interaction, memory mechanisms, calcium buffering, glutamate release
- MeSH terms
- Animals, Astrocytes, Calcium, Exocytosis, Glycine, Hippocampus, Male, Memory, Serine, Synapses, Receptors, N-Methyl-D-Aspartate, Rats, Sprague-Dawley, Rats, Wistar, Long-Term Potentiation, Rats
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