Ectopic Release of Synaptic Vesicles

Glutamatergic synapses on oligodendrocyte precursor cells in the hippocampus

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Postnatal development of the cerebellar cortex in the rat. II. Phases in the maturation of Purkinje cells and of the molecular layer

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Local and diffuse synaptic actions of GABA in the hippocampus

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Two components of transmitter release at a central synapse.

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Determinants of the Time Course of Facilitation at the Granule Cell to Purkinje Cell Synapse

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Desensitization of AMPA receptors upon multiquantal neurotransmitter release

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Transport, capture and exocytosis of single synaptic vesicles at active zones

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Benzothiadiazides inhibit rapid glutamate receptor desensitization and enhance glutamatergic synaptic currents

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Calcium-Permeable AMPA-Kainate Receptors in Fusiform Cerebellar Glial Cells

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Glia-Synapse Interaction Through Ca2+-Permeable AMPA Receptors in Bergmann Glia

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Multivesicular Release at Climbing Fiber-Purkinje Cell Synapses

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Calcium Dependence of Exocytosis and Endocytosis at the Cochlear Inner Hair Cell Afferent Synapse

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GYKI 52466, a 2,3-benzodiazepine, is a highly selective, noncompetitive antagonist of AMPA/kainate receptor responses

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The kinetics of transmitter release at the frog neuromuscular junction

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Calmodulin mediates rapid recruitment of fast-releasing synaptic vesicles at a calyx-type synapse.

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Three-Dimensional Comparison of Ultrastructural Characteristics at Depressing and Facilitating Synapses onto Cerebellar Purkinje Cells

Xu‐Friedman, M. A., Harris, K. M., & Regehr, W. G. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-17-06666.2001 · Cited by 313 · see citing works

Asynchronous release of synaptic vesicles determines the time course of the AMPA receptor-mediated EPSC

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Calcium Secretion Coupling at Calyx of Held Governed by Nonuniform Channel–Vesicle Topography

Meinrenken, C., Borst, J. G., & Sakmann, B. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-05-01648.2002 · Cited by 290 · see citing works

Locus of frequency‐dependent depression identified with multiple‐probability fluctuation analysis at rat climbing fibre‐Purkinje cell synapses

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Ontogenesis of olivocerebellar relationships. I. Studies by intracellular recordings of the multiple innervation of Purkinje cells by climbing fibers in the developing rat cerebellum

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Neuronal Glutamate Transporters Limit Activation of NMDA Receptors by Neurotransmitter Spillover on CA1 Pyramidal Cells

Diamond, J. S. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-21-08328.2001 · Cited by 255 · see citing works

Delayed Release of Neurotransmitter from Cerebellar Granule Cells

Atluri, P. P., & Regehr, W. G. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-20-08214.1998 · Cited by 250 · see citing works

Functional Differentiation of Multiple Climbing Fiber Inputs during Synapse Elimination in the Developing Cerebellum

Hashimoto, K., & Kano, M. (2003) · Neuron · doi:10.1016/s0896-6273(03)00298-8 · Cited by 245 · see citing works

Fast Kinetics of Exocytosis Revealed by Simultaneous Measurements of Presynaptic Capacitance and Postsynaptic Currents at a Central Synapse

Sun, J., & Wu, L. (2001) · Neuron · doi:10.1016/s0896-6273(01)00271-9 · Cited by 231 · see citing works

Spillover of Glutamate onto Synaptic AMPA Receptors Enhances Fast Transmission at a Cerebellar Synapse

DiGregorio, D. A., Nusser, Z., & Silver, R. A. (2002) · Neuron · doi:10.1016/s0896-6273(02)00787-0 · Cited by 231 · see citing works

Glutamate transporter currents in Bergmann glial cells follow the time course of extrasynaptic glutamate

Bergles, D. E., Dzubay, J. A., & Jahr, C. E. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.26.14821 · Cited by 228 · see citing works

Independent Sources of Quantal Variability at Single Glutamatergic Synapses

Franks, K. M., Stevens, C. F., & Sejnowski, T. J. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-08-03186.2003 · Cited by 224 · see citing works

Effects of reduced vesicular filling on synaptic transmission in rat hippocampal neurones

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The concentration of synaptically released glutamate outside of the climbing fiber-Purkinje cell synaptic cleft

Dzubay, J. A., & Jahr, C. E. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-13-05265.1999 · Cited by 213 · see citing works

Counting quanta: Direct measurements of transmitter release at a central synapse

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Imaging Calcium Entry Sites and Ribbon Structures in Two Presynaptic Cells

Zenisek, D., Davila, V., Wan, L., & Almers, W. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-07-02538.2003 · Cited by 196 · see citing works

Three-dimensional analysis of dendritic spines

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A benzodiazepine recognition site associated with the non-NMDA glutamate receptor

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Depolarization Redistributes Synaptic Membrane and Creates a Gradient of Vesicles on the Synaptic Body at a Ribbon Synapse

Lenzi, D., Crum, J. K., Ellisman, M. H., & Roberts, W. M. (2002) · Neuron · doi:10.1016/s0896-6273(02)01025-5 · Cited by 184 · see citing works

An Evaluation of Synapse Independence

Barbour, B. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-20-07969.2001 · Cited by 175 · see citing works

Bergmann glial cells form distinct morphological structures to interact with cerebellar neurons

Grosche, J., Kettenmann, H., & Reichenbach, A. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10197 · Cited by 171 · see citing works

Blocking effect of 1-naphthyl acetyl spermine on Ca2+-permeable AMPA receptors in cultured rat hippocampal neurons

Koike‐Tani, M., Iino, M., & Ozawa, S. (1997) · Neuroscience Research · doi:10.1016/s0168-0102(97)00067-9 · Cited by 165 · see citing works

A Novel Presynaptic Inhibitory Mechanism Underlies Paired Pulse Depression at a Fast Central Synapse

Bellingham, M. C., & Walmsley, B. D. (1999) · Neuron · doi:10.1016/s0896-6273(00)80762-x · Cited by 157 · see citing works

Ultrastructural Contributions to Desensitization at Cerebellar Mossy Fiber to Granule Cell Synapses

Xu‐Friedman, M. A., & Regehr, W. G. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-06-02182.2003 · Cited by 142 · see citing works

Phasic secretion of acetylcholine at a mammalian neuromuscular junction.

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Probing Fundamental Aspects of Synaptic Transmission with Strontium

Xu-Friedman, M. A., & Regehr, W. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-12-04414.2000 · Cited by 134 · see citing works

Role of intercellular interactions in heterosynaptic long-term depression

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Interaction of Postsynaptic Receptor Saturation with Presynaptic Mechanisms Produces a Reliable Synapse

Foster, K. A., Kreitzer, A. C., & Regehr, W. G. (2002) · Neuron · doi:10.1016/s0896-6273(02)01106-6 · Cited by 117 · see citing works

Dendritic release of glutamate suppresses synaptic inhibition of pyramidal neurons in rat neocortex

Zilberter, Y. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00489.x · Cited by 114 · see citing works

Estimating the timing of quantal releases during end‐plate currents at the frog neuromuscular junction.

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Mechanisms underlying presynaptic facilitatory effect of cyclothiazide at the calyx of Held of juvenile rats

Ishikawa, T., & Takahashi, T. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.0423a.x · Cited by 79 · see citing works

Receptor Occupancy Limits Synaptic Depression at Climbing Fiber Synapses

Harrison, J., & Jahr, C. E. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-02-00377.2003 · Cited by 71 · see citing works

Pardaxin induces exocytosis in bovine adrenal medullary chromaffin cells independent of calcium.

Lazarovici, P., & Lelkes, P. I. (1992) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)10473-4 · Cited by 35 · see citing works

Characterization With Barium of Potassium Currents in Turtle Retinal Müller Cells

Solessio, E. C., Linn, D. M., Perlman, I., & Lasater, E. M. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.1.418 · Cited by 18 · see citing works

Untitled work

(2000) · doi:10.1002/(sici)1096-9861(20000228)418:1

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

Glutamate exocytosis from astrocytes controls synaptic strength

Jourdain, P., Bergersen, L. H., Bhaukaurally, K., Bezzi, P., Santello, M., Domercq, M., Matute, C., Tonello, F., Gundersen, V., & Volterra, A. (2007) · Nature Neuroscience · doi:10.1038/nn1849 · Cited by 806 · see citing works

Astrocytes contain a vesicular compartment that is competent for regulated exocytosis of glutamate

Bezzi, P., Gundersen, V., Galbete, J. L., Seifert, G., Steinhäuser, C., Pilati, E., & Volterra, A. (2004) · Nature Neuroscience · doi:10.1038/nn1246 · Cited by 737 · see citing works

Astrocytic Ca2+ signaling evoked by sensory stimulation in vivo

Wang, X., Lou, N., Xu, Q., Tian, G.-F., Peng, W. G., Han, X., Kang, J., Takano, T., & Nedergaard, M. (2006) · Nature Neuroscience · doi:10.1038/nn1703 · Cited by 685 · 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

<i>In vivo</i> diffusion analysis with quantum dots and dextrans predicts the width of brain extracellular space

Thorne, R. G., & Nicholson, C. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509425103 · Cited by 641 · see citing works

Local 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

Nanodomain coupling between Ca2+ channels and sensors of exocytosis at fast mammalian synapses

Eggermann, E., Bucurenciu, I., Goswami, S. P., & Jonas, P. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3125 · Cited by 500 · see citing works

The astrocyte odyssey

Wang, D. D., & Bordey, A. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2008.09.015 · Cited by 517 · see citing works

Vesicular glutamate release from axons in white matter

Kukley, M., Capetillo‐Zarate, E., & Dietrich, D. (2007) · Nature Neuroscience · doi:10.1038/nn1850 · Cited by 460 · see citing works

Regulation of Ca2+-permeable AMPA receptors: synaptic plasticity and beyond.

Cull-Candy, S., Kelly, L., & Farrant, M. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.05.012 · Cited by 479 · see citing works

Vesicular Dopamine Release Elicits an Inhibitory Postsynaptic Current in Midbrain Dopamine Neurons

Beckstead, M. J., Grandy, D. K., Wickman, K. D., & Williams, J. T. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.019 · Cited by 368 · see citing works

Signaling between glia and neurons: focus on synaptic plasticity

Allen, N. J., & Barres, B. A. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.08.006 · Cited by 321 · see citing works

Expression of the vesicular glutamate transporters during development indicates the widespread corelease of multiple neurotransmitters

Boulland, J., Qureshi, T., Seal, R. P., Rafiki, A., Gundersen, V., Bergersen, L. H., Fremeau, R. T., Edwards, R. H., Storm‐Mathisen, J., & Chaudhry, F. A. (2004) · Journal of Comparative Neurology · doi:10.1002/cne.20354 · Cited by 280 · see citing works

Glutamate transporters bring competition to the synapse

Huang, Y. H., & Bergles, D. E. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.05.007 · Cited by 269 · see citing works

Ultrafast endocytosis at Caenorhabditis elegans neuromuscular junctions

Watanabe, S., Liu, Q., Davis, M. W., Hollopeter, G., Thomas, N., Jorgensen, N. B., & Jorgensen, E. M. (2013) · eLife · doi:10.7554/elife.00723 · Cited by 248 · see citing works

Multiple climbing fibers signal to molecular layer interneurons exclusively via glutamate spillover

Szapiro, G., & Barbour, B. (2007) · Nature Neuroscience · doi:10.1038/nn1907 · Cited by 247 · see citing works

Coordinated multivesicular release at a mammalian ribbon synapse

Singer, J. H., Lassová, L., Vardi, N., & Diamond, J. S. (2004) · Nature Neuroscience · doi:10.1038/nn1280 · Cited by 220 · see citing works

Modulation of Glutamate Mobility Reveals the Mechanism Underlying Slow-Rising AMPAR EPSCs and the Diffusion Coefficient in the Synaptic Cleft

Nielsen, T. A., DiGregorio, D. A., & Silver, R. A. (2004) · Neuron · doi:10.1016/j.neuron.2004.04.003 · Cited by 207 · see citing works

Open Syntaxin Docks Synaptic Vesicles

Hammarlund, M., Palfreyman, M. T., Watanabe, S., Olsen, S. R., & Jørgensen, E. M. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050198 · Cited by 201 · see citing works

Spontaneous and evoked glutamate release activate two populations of NMDA receptors with limited overlap

Atasoy, D., Ertunç, M., Moulder, K., Blackwell, J., Chung, C.-Y., Su, J.-Z., & Kavalali, E. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2432-08.2008 · Cited by 201 · see citing works

Optogenetic Countering of Glial Acidosis Suppresses Glial Glutamate Release and Ischemic Brain Damage

Beppu, K., Sasaki, T., Tanaka, K. F., Yamanaka, A., Fukazawa, Y., Shigemoto, R., & Matsui, K. (2014) · Neuron · doi:10.1016/j.neuron.2013.11.011 · Cited by 195 · see citing works

Climbing fiber innervation of NG2-expressing glia in the mammalian cerebellum.

Lin, S.-C., Huck, J., Roberts, J. D., Macklin, W. B., Somogyi, P., & Bergles, D. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.025 · Cited by 201 · see citing works

Evidence for Ectopic Neurotransmission at a Neuronal Synapse

Coggan, J. S., Bartol, T. M., Esquenazi, E., Stiles, J. R., Lamont, S., Martone, M. E., Berg, D. K., Ellisman, M. H., & B, T. J. S. A. (2005) · Science · doi:10.1126/science.1108239 · Cited by 184 · see citing works

Sorting Out Astrocyte Physiology from Pharmacology

Fiacco, T. A., Agulhon, C., & McCarthy, K. D. (2008) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.011008.145602 · Cited by 185 · see citing works

Astrocyte physiopathology: At the crossroads of intercellular networking, inflammation and cell death

Rossi, D. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.04.003 · Cited by 178 · see citing works

Parallel Processing in Two Transmitter Microenvironments at the Cone Photoreceptor Synapse

DeVries, S. H., Li, W., & Saszik, S. M. (2006) · Neuron · doi:10.1016/j.neuron.2006.04.034 · Cited by 175 · see citing works

Origin, lineage and function of cerebellar glia

Buffo, A., & Rossi, F. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.08.001 · Cited by 170 · see citing works

Deriving the Glutamate Clearance Time Course from Transporter Currents in CA1 Hippocampal Astrocytes: Transmitter Uptake Gets Faster during Development

Diamond, J. S. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.5125-04.2005 · Cited by 164 · see citing works

Application of an optogenetic byway for perturbing neuronal activity via glial photostimulation

Sasaki, T., Beppu, K., Tanaka, K. F., Fukazawa, Y., Shigemoto, R., & Matsui, K. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1213458109 · Cited by 156 · see citing works

Imaging extrasynaptic glutamate dynamics in the brain

Okubo, Y., Sekiya, H., Namiki, S., Sakamoto, H., Iinuma, S., Yamasaki, M., Watanabe, M., Hirose, K., & Iino, M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913154107 · Cited by 153 · see citing works

High-Concentration Rapid Transients of Glutamate Mediate Neural-Glial Communication via Ectopic Release

Matsui, K., Jahr, C. E., & Rubio, M. E. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1927-05.2005 · Cited by 143 · see citing works

Synaptic signaling between neurons and glia

Lin, S., & Bergles, D. E. (2004) · Glia · doi:10.1002/glia.20060 · Cited by 141 · see citing works

Interactions between Purkinje neurones and Bergmann glia

Bellamy, T. C. (2006) · The Cerebellum · doi:10.1080/14734220600724569 · Cited by 135 · see citing works

Involvement of extrasynaptic glutamate in physiological and pathophysiological changes of neuronal excitability

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Postnatal Switch from Synaptic to Extrasynaptic Transmission between Interneurons and NG2 Cells

Vélez‐Fort, M., Maldonado, P. P., Butt, A. M., Audinat, É., & Angulo, M. C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0238-10.2010 · Cited by 118 · see citing works

Ionotropic receptors in neuronal–astroglial signalling: What is the role of “excitable” molecules in non-excitable cells

Lalo, U., Pankratov, Y., Parpura, V., & Verkhratsky, A. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2010.09.007 · Cited by 116 · see citing works

Selective regulation of long-form calcium-permeable AMPA receptors by an atypical TARP, γ-5

Soto, D., Coombs, I. D., Renzi, M., Zonouzi, M., Farrant, M., & Cull-Candy, S. G. (2009) · Nature Neuroscience · doi:10.1038/nn.2266 · Cited by 107 · see citing works

Input-Specific GABAergic Signaling to Newborn Neurons in Adult Dentate Gyrus

Markwardt, S. J., Wadiche, J. I., & Overstreet‐Wadiche, L. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2727-09.2009 · Cited by 99 · see citing works

Synaptic communication between neurons and NG2+ cells

Paukert, M., & Bergles, D. E. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.08.009 · Cited by 97 · see citing works

Synapses on NG2‐expressing progenitors in the brain: multiple functions?

Gallo, V., Mangin, J., Kukley, M., & Dietrich, D. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.158436 · Cited by 97 · see citing works

Differential Control of Synaptic and Ectopic Vesicular Release of Glutamate

Matsui, K., & Jahr, C. E. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2650-04.2004 · Cited by 92 · see citing works

Axonal Motility and Its Modulation by Activity Are Branch-Type Specific in the Intact Adult Cerebellum

Nishiyama, H., Fukaya, M., Watanabe, M., & Linden, D. J. (2007) · Neuron · doi:10.1016/j.neuron.2007.09.010 · Cited by 86 · see citing works

Glutamatergic and Purinergic Receptor-Mediated Calcium Transients in Bergmann Glial Cells

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Synapse Geometry and Receptor Dynamics Modulate Synaptic Strength

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Glutamate, a neurotransmitter—And so much more

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Astrocytic Calcium Signaling: Mechanism and Implications for Functional Brain Imaging

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Spontaneous Neurotransmission: An Independent Pathway for Neuronal Signaling?

Kavalali, E. T., Chung, C., Khvotchev, M., Leitz, J., Nosyreva, E., Raingo, J., & Ramirez, D. M. O. (2011) · Physiology · doi:10.1152/physiol.00040.2010 · Cited by 104 · see citing works

Detecting Activity in Olfactory Bulb Glomeruli with Astrocyte Recording

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Diffusion of Flexible Random-Coil Dextran Polymers Measured in Anisotropic Brain Extracellular Space by Integrative Optical Imaging

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Dynamical Organization of Syntaxin-1A at the Presynaptic Active Zone

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Transmembrane AMPA receptor regulatory proteins and AMPA receptor function in the cerebellum

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The Activation of Excitatory Glutamate Receptors Evokes a Long-Lasting Increase in the Release of GABA from Cerebellar Stellate Cells

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