Ectopic Release of Synaptic Vesicles

Glutamatergic synapses on oligodendrocyte precursor cells in the hippocampus

Bergles, D. E., Roberts, J. D. B., Somogyi, P., & Jahr, C. E. (2000) · Nature · doi:10.1038/35012083 · Cited by 1,062

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

Altman, J. (1972) · Journal of Comparative Neurology · doi:10.1002/cne.901450402 · Cited by 996

Local and diffuse synaptic actions of GABA in the hippocampus

Isaacson, J. S., Solis, J. M., & Nicoll, R. A. (1993) · Neuron · doi:10.1016/0896-6273(93)90308-e · Cited by 688

Two components of transmitter release at a central synapse.

Goda, Y., & Stevens, C. F. (1994) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.91.26.12942 · Cited by 529

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

Atluri, P. P., & Regehr, W. G. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-18-05661.1996 · Cited by 513

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

Zenisek, D., Steyer, J. A., & Almers, W. (2000) · Nature · doi:10.1038/35022500 · Cited by 463

Desensitization of AMPA receptors upon multiquantal neurotransmitter release

Trussell, L. O., Zhang, S., & Ramant, I. M. (1993) · Neuron · doi:10.1016/0896-6273(93)90066-z · Cited by 460

Benzothiadiazides inhibit rapid glutamate receptor desensitization and enhance glutamatergic synaptic currents

Yamada, K., & Tang, C. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-09-03904.1993 · Cited by 440

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

Burnashev, N., Khodorova, A. B., Jónás, P., Helm, P. J., Wisden, W., Monyer, H., Seeburg, P. H., & Sakmann, B. J. (1992) · Science · doi:10.1126/science.1317970 · Cited by 430

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

Iino, M., Goto, K., Kakegawa, W., Okado, H., Sudo, M., Ishiuchi, S., Miwa, A., Takayasu, Y., Saito, I., Tsuzuki, K., et al. (2001) · Science · doi:10.1126/science.1058827 · Cited by 392

Multivesicular Release at Climbing Fiber-Purkinje Cell Synapses

Wadiche, J. I., & Jahr, C. E. (2001) · Neuron · doi:10.1016/s0896-6273(01)00488-3 · Cited by 374

Calmodulin Mediates Rapid Recruitment of Fast-Releasing Synaptic Vesicles at a Calyx-Type Synapse

Sakaba, T., & Neher, E. (2001) · Neuron · doi:10.1016/s0896-6273(01)00543-8 · Cited by 363

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

Donevan, S. D., & Rogawski, M. A. (1993) · Neuron · doi:10.1016/0896-6273(93)90241-i · Cited by 359

The kinetics of transmitter release at the frog neuromuscular junction

Barrett, E. F., & Stevens, C. F. (1972) · The Journal of Physiology · doi:10.1113/jphysiol.1972.sp010054 · Cited by 356

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

Beutner, D., Voets, T., Neher, E., & Moser, T. (2001) · Neuron · doi:10.1016/s0896-6273(01)00243-4 · Cited by 352

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

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

Diamond, J. S., & Jahr, C. E. (1995) · Neuron · doi:10.1016/0896-6273(95)90098-5 · Cited by 301

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

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

Silver, R., Momiyama, A., & Cull-Candy, S. (1998) · Journal of Physiology · doi:10.1111/j.1469-7793.1998.881bj.x · Cited by 279

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

Mariani, J., & Changeux, J. (1981) · Journal of Neuroscience · doi:10.1523/jneurosci.01-07-00696.1981 · Cited by 269

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 258

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 252

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

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

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

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 230

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

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

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

Zhou, Q., Petersen, C. C. H., & Nicoll, R. A. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.t01-1-00195.x · Cited by 212

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

Isaacson, J. S., & Walmsley, B. D. (1995) · Neuron · doi:10.1016/0896-6273(95)90178-7 · Cited by 201

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

Three-dimensional analysis of dendritic spines

Špaček, J. (1985) · Anatomy and Embryology · doi:10.1007/bf00341419 · Cited by 193

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

Zorumski, C. F., Yamada, K. A., Price, M. T., & Olney, J. W. (1993) · Neuron · doi:10.1016/0896-6273(93)90242-j · Cited by 186

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

An Evaluation of Synapse Independence

Barbour, B. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-20-07969.2001 · Cited by 173

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

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

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

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

Phasic secretion of acetylcholine at a mammalian neuromuscular junction.

Datyner, N. B., & Gage, P. W. (1980) · The Journal of Physiology · doi:10.1113/jphysiol.1980.sp013286 · Cited by 139

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

Role of intercellular interactions in heterosynaptic long-term depression

Scanziani, M., Malenka, R. C., & Nicoll, R. A. (1996) · Nature · doi:10.1038/380446a0 · Cited by 119

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

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

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

der Kloot, W. V. (1988) · The Journal of Physiology · doi:10.1113/jphysiol.1988.sp017224 · Cited by 94

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

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

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

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

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 1,837

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

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 671

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

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

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

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

Distribution of vesicle pools in cerebellar parallel fibre terminals after depression of ectopic transmission

Dobson, K. L., Smith, Z. H., & Bellamy, T. C. (2018) · PLoS ONE · doi:10.1371/journal.pone.0200937 · Cited by 1

Ectopic release sites lack fast vesicle recycling mechanisms, causing long‐term depression of neuron‐glial transmission in rat cerebellum

Balakrishnan, S., Jackson, C. L. M., Russell, N. A., & Bellamy, T. C. (2010) · Glia · doi:10.1002/glia.21078 · Cited by 12

Multivesicular Release at Climbing Fiber-Purkinje Cell Synapses

Wadiche, J. I., & Jahr, C. E. (2001) · Neuron · doi:10.1016/s0896-6273(01)00488-3 · Cited by 374