CoChat
Sign Up
Cited by 52

The DOI matches its Crossref record; 20 of the 20 references it cites were found in a registry or an index.

The Cerebellar Mossy Fiber Synapse as a Model for High-Frequency Transmission in the Mammalian CNS

Delvendahl, Igor, Hallermann, Stefan·2016·Trends in Neurosciences
DOI 10.1016/j.tins.2016.09.006
Open this paper in CoChat — free account

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.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.tins.2016.09.006

Cites

20 of 20 references verified0 citation errors · 0 not checkable

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.

A few free checks a day · papers already verified open instantly · results are public

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?

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

Research works printed but not linked: 130

  1. Bale, 2015, Microsecond-scale timing precision in rodent trigeminal primary afferents, J. Neurosci., 35, 5935, 10.1523/JNEUROSCI.3876-14.2015 · DOI
  2. Wagner, 2005, Microsecond precision of phase delay in the auditory system of the barn owl, J. Neurophysiol., 94, 1655, 10.1152/jn.01226.2004 · DOI
  3. Kumar, 2010, Spiking activity propagation in neuronal networks: reconciling different perspectives on neural coding, Nat. Rev. Neurosci., 11, 615, 10.1038/nrn2886 · DOI
  4. Wolfe, 2010, Sparse and powerful cortical spikes, Curr. Opin. Neurobiol., 20, 306, 10.1016/j.conb.2010.03.006 · DOI
  5. Tchumatchenko, 2011, Ultrafast population encoding by cortical neurons, J. Neurosci., 31, 12171, 10.1523/JNEUROSCI.2182-11.2011 · DOI
  6. Alle, 2009, Energy-efficient action potentials in hippocampal mossy fibers, Science, 325, 1405, 10.1126/science.1174331 · DOI · Paper page
  7. Carter, 2011, Incomplete inactivation and rapid recovery of voltage-dependent sodium channels during high-frequency firing in cerebellar Purkinje neurons, J. Neurophysiol., 105, 860, 10.1152/jn.01056.2010 · DOI
  8. Hallermann, 2012, State and location dependence of action potential metabolic cost in cortical pyramidal neurons, Nat. Neurosci., 15, 1007, 10.1038/nn.3132 · DOI
  9. Ritzau-Jost, 2014, Ultrafast action potentials mediate kilohertz signaling at a central synapse, Neuron, 84, 152, 10.1016/j.neuron.2014.08.036 · DOI
  10. Attwell, 2005, Neuroenergetics and the kinetic design of excitatory synapses, Nat. Rev. Neurosci., 6, 841, 10.1038/nrn1784 · DOI
  11. Gray, 1996, Chattering cells: superficial pyramidal neurons contributing to the generation of synchronous oscillations in the visual cortex, Science, 274, 109, 10.1126/science.274.5284.109 · DOI
  12. Trussell, 1999, Synaptic mechanisms for coding timing in auditory neurons, Annu. Rev. Physiol., 61, 477, 10.1146/annurev.physiol.61.1.477 · DOI
  13. Kim, 2013, Dysmyelination of auditory afferent axons increases the jitter of action potential timing during high-frequency firing, J. Neurosci., 33, 9402, 10.1523/JNEUROSCI.3389-12.2013 · DOI
  14. Scott, 2007, Weak action potential backpropagation is associated with high-frequency axonal firing capability in principal neurons of the gerbil medial superior olive, J. Physiol., 583, 647, 10.1113/jphysiol.2007.136366 · DOI
  15. Oertel, 2000, Detection of synchrony in the activity of auditory nerve fibers by octopus cells of the mammalian cochlear nucleus, Proc. Natl. Acad. Sci. U.S.A., 97, 11773, 10.1073/pnas.97.22.11773 · DOI
  16. Rancz, 2007, High-fidelity transmission of sensory information by single cerebellar mossy fibre boutons, Nature, 450, 1245, 10.1038/nature05995 · DOI
  17. Garwicz, 1998, Cutaneous receptive fields and topography of mossy fibres and climbing fibres projecting to cat cerebellar C3 zone, J. Physiol., 512, 277, 10.1111/j.1469-7793.1998.277bf.x · DOI
  18. Sultan, 2012, Unravelling cerebellar pathways with high temporal precision targeting motor and extensive sensory and parietal networks, Nat. Commun., 3, 924, 10.1038/ncomms1912 · DOI
  19. Ritter, 2008, High-frequency (600Hz) population spikes in human EEG delineate thalamic and cortical fMRI activation sites, NeuroImage, 42, 483, 10.1016/j.neuroimage.2008.05.026 · DOI
  20. McCormick, 1997, Sleep and arousal: thalamocortical mechanisms, Annu. Rev. Neurosci., 20, 185, 10.1146/annurev.neuro.20.1.185 · DOI · Paper page
  21. Sauer, 2015, Impaired fast-spiking interneuron function in a genetic mouse model of depression, eLife, 4, e04979, 10.7554/eLife.04979 · DOI
  22. Albert, 2001, Arthropod touch reception: spider hair sensilla as rapid touch detectors, J. Comp. Physiol. A, 187, 303, 10.1007/s003590100202 · DOI
  23. Pugh, 2006, Potentiation of mossy fiber EPSCs in the cerebellar nuclei by NMDA receptor activation followed by postinhibitory rebound current, Neuron, 51, 113, 10.1016/j.neuron.2006.05.021 · DOI
  24. Kalinovsky, 2011, Development of axon-target specificity of ponto-cerebellar afferents, PLoS Biol., 9, e1001013, 10.1371/journal.pbio.1001013 · DOI
  25. Kim, 2013, Three-dimensional imaging of cerebellar mossy fiber rosettes by ion-abrasion scanning electron microscopy, Microsc. Microanal., 19, 172, 10.1017/S1431927613012609 · DOI
  26. Xu-Friedman, 2003, Ultrastructural contributions to desensitization at cerebellar mossy fiber to granule cell synapses, J. Neurosci., 23, 2182, 10.1523/JNEUROSCI.23-06-02182.2003 · DOI
  27. Silver, 1992, Rapid-time-course miniature and evoked excitatory currents at cerebellar synapses in situ, Nature, 355, 163, 10.1038/355163a0 · DOI
  28. Delvendahl, 2015, Dendritic patch-clamp recordings from cerebellar granule cells demonstrate electrotonic compactness, Front. Cell. Neurosci., 9, 93, 10.3389/fncel.2015.00093 · DOI
  29. Wichmann, 2015, Relating structure and function of inner hair cell ribbon synapses, Cell. Tissue Res., 361, 95, 10.1007/s00441-014-2102-7 · DOI
  30. Cathala, 2005, Changes in synaptic structure underlie the developmental speeding of AMPA receptor-mediated EPSCs, Nat. Neurosci., 8, 1310, 10.1038/nn1534 · DOI
  31. Billings, 2014, Network structure within the cerebellar input layer enables lossless sparse encoding, Neuron, 83, 960, 10.1016/j.neuron.2014.07.020 · DOI
  32. D’Angelo, 1990, Dual-component NMDA receptor currents at a single central synapse, Nature, 346, 467, 10.1038/346467a0 · DOI
  33. Maffei, 2002, Presynaptic current changes at the mossy fiber-granule cell synapse of cerebellum during LTP, J. Neurophysiol., 88, 627, 10.1152/jn.2002.88.2.627 · DOI
  34. Thomsen, 2010, Presynaptic calcium signalling in cerebellar mossy fibres, Front. Neural Circuits, 4, 1
  35. Delvendahl, 2016, Fast, temperature-sensitive and clathrin-independent endocytosis at central synapses, Neuron, 90, 492, 10.1016/j.neuron.2016.03.013 · DOI · Paper page
  36. Delvendahl, 2015, Reduced endogenous Ca2+ buffering speeds active zone Ca2+ signaling, Proc. Natl. Acad. Sci. U.S.A., 112, E3075, 10.1073/pnas.1508419112 · DOI
  37. Gao, 2016, Excitatory cerebellar nucleocortical circuit provides internal amplification during associative conditioning, Neuron, 89, 645, 10.1016/j.neuron.2016.01.008 · DOI
  38. Powell, 2015, Synaptic representation of locomotion in single cerebellar granule cells, eLife, 4, e07290, 10.7554/eLife.07290 · DOI
  39. Chadderton, 2004, Integration of quanta in cerebellar granule cells during sensory processing, Nature, 428, 856, 10.1038/nature02442 · DOI
  40. Kawaguchi, 2015, Control of inhibitory synaptic outputs by low excitability of axon terminals revealed by direct recording, Neuron, 85, 1273, 10.1016/j.neuron.2015.02.013 · DOI
  41. Begum, 2016, Action potential broadening in a presynaptic channelopathy, Nat. Commun., 7, 12102, 10.1038/ncomms12102 · DOI
  42. Hu, 2014, A supercritical density of Na+ channels ensures fast signaling in GABAergic interneuron axons, Nat. Neurosci., 17, 686, 10.1038/nn.3678 · DOI · Paper page
  43. Gittis, 2010, Mechanisms of sustained high firing rates in two classes of vestibular nucleus neurons: differential contributions of resurgent Na, Kv3, and BK currents, J. Neurophysiol., 104, 1625, 10.1152/jn.00378.2010 · DOI
  44. Carter, 2009, Sodium entry during action potentials of mammalian neurons: incomplete inactivation and reduced metabolic efficiency in fast-spiking neurons, Neuron, 64, 898, 10.1016/j.neuron.2009.12.011 · DOI
  45. Alle, 2011, Sparse but highly efficient Kv3 outpace BKCa channels in action potential repolarization at hippocampal mossy fiber boutons, J. Neurosci., 31, 8001, 10.1523/JNEUROSCI.0972-11.2011 · DOI
  46. Yang, 2014, Enhancing the fidelity of neurotransmission by activity-dependent facilitation of presynaptic potassium currents, Nat. Commun., 5, 4564, 10.1038/ncomms5564 · DOI
  47. Helmchen, 1997, Calcium dynamics associated with a single action potential in a CNS presynaptic terminal, Biophys. J., 72, 1458, 10.1016/S0006-3495(97)78792-7 · DOI
  48. Jackson, 2003, Calcium dynamics, buffering, and buffer saturation in the boutons of dentate granule-cell axons in the hilus, J. Neurosci., 23, 1612, 10.1523/JNEUROSCI.23-05-01612.2003 · DOI
  49. Koester, 2000, Calcium dynamics associated with action potentials in single nerve terminals of pyramidal cells in layer 2/3 of the young rat neocortex, J. Physiol., 529, 625, 10.1111/j.1469-7793.2000.00625.x · DOI · Paper page
  50. Stanley, 2016, The nanophysiology of fast transmitter release, Trends Neurosci., 39, 183, 10.1016/j.tins.2016.01.005 · DOI
  51. Sargent, 2005, Rapid vesicular release, quantal variability, and spillover contribute to the precision and reliability of transmission at a glomerular synapse, J. Neurosci., 25, 8173, 10.1523/JNEUROSCI.2051-05.2005 · DOI
  52. Wang, 2008, Synaptic vesicles in mature calyx of Held synapses sense higher nanodomain calcium concentrations during action potential-evoked glutamate release, J. Neurosci., 28, 14450, 10.1523/JNEUROSCI.4245-08.2008 · DOI
  53. Schmidt, 2013, Nanodomain coupling at an excitatory cortical synapse, Curr. Biol., 23, 244, 10.1016/j.cub.2012.12.007 · DOI
  54. Vyleta, 2014, Loose coupling between Ca2+ channels and release sensors at a plastic hippocampal synapse, Science, 343, 665, 10.1126/science.1244811 · DOI · Paper page
  55. Rozov, 2001, Transmitter release modulation by intracellular Ca2+ buffers in facilitating and depressing nerve terminals of pyramidal cells in layer 2/3 of the rat neocortex indicates a target cell-specific difference in presynaptic calcium dynamics, J. Physiol., 531, 807, 10.1111/j.1469-7793.2001.0807h.x · DOI
  56. Ohana, 1998, Transmitter release modulation in nerve terminals of rat neocortical pyramidal cells by intracellular calcium buffers, J. Physiol., 513, 135, 10.1111/j.1469-7793.1998.135by.x · DOI
  57. Saviane, 2006, Fast vesicle reloading and a large pool sustain high bandwidth transmission at a central synapse, Nature, 439, 983, 10.1038/nature04509 · DOI · Paper page
  58. Hallermann, 2013, Sustaining rapid vesicular release at active zones: potential roles for vesicle tethering, Trends Neurosci., 36, 185, 10.1016/j.tins.2012.10.001 · DOI
  59. Neher, 2008, Multiple roles of calcium ions in the regulation of neurotransmitter release, Neuron, 59, 861, 10.1016/j.neuron.2008.08.019 · DOI
  60. Sakaba, 2006, Roles of the fast-releasing and the slowly releasing vesicles in synaptic transmission at the calyx of Held, J. Neurosci., 26, 5863, 10.1523/JNEUROSCI.0182-06.2006 · DOI
  61. Rothman, 2016, Physical determinants of vesicle mobility and supply at a central synapse, eLife, 5, e15133, 10.7554/eLife.15133 · DOI
  62. Kononenko, 2015, Molecular mechanisms of presynaptic membrane retrieval and synaptic vesicle reformation, Neuron, 85, 484, 10.1016/j.neuron.2014.12.016 · DOI · Paper page
  63. Leitz, 2014, Fast retrieval and autonomous regulation of single spontaneously recycling synaptic vesicles, eLife, 3, e03658, 10.7554/eLife.03658 · DOI · Paper page
  64. Van Hook, 2012, Rapid synaptic vesicle endocytosis in cone photoreceptors of salamander retina, J. Neurosci., 32, 18112, 10.1523/JNEUROSCI.1764-12.2012 · DOI
  65. Sun, 2002, Single and multiple vesicle fusion induce different rates of endocytosis at a central synapse, Nature, 417, 555, 10.1038/417555a · DOI
  66. Yamashita, 2005, Vesicle endocytosis requires dynamin-dependent GTP hydrolysis at a fast CNS synapse, Science, 307, 124, 10.1126/science.1103631 · DOI
  67. Geiger, 1995, Relative abundance of subunit mRNAs determines gating and Ca2+ permeability of AMPA receptors in principal neurons and interneurons in rat CNS, Neuron, 15, 193, 10.1016/0896-6273(95)90076-4 · DOI · Paper page
  68. D’Angelo, 1995, Synaptic excitation of individual rat cerebellar granule cells in situ: evidence for the role of NMDA receptors, J. Physiol., 484, 397, 10.1113/jphysiol.1995.sp020673 · DOI
  69. Baade, 2016, NMDA receptors amplify mossy fiber synaptic inputs at frequencies up to at least 750Hz in cerebellar granule cells, Synapse, 70, 269, 10.1002/syn.21898 · DOI
  70. DiGregorio, 2007, Desensitization properties of AMPA receptors at the cerebellar mossy fiber granule cell synapse, J. Neurosci., 27, 8344, 10.1523/JNEUROSCI.2399-07.2007 · DOI
  71. DiGregorio, 2002, Spillover of glutamate onto synaptic AMPA receptors enhances fast transmission at a cerebellar synapse, Neuron, 35, 521, 10.1016/S0896-6273(02)00787-0 · DOI
  72. Hámori, 1983, Differentiation of cerebellar mossy fiber synapses in the rat: a quantitative electron microscope study, J. Comp. Neurol., 220, 365, 10.1002/cne.902200402 · DOI
  73. Taschenberger, 2002, Optimizing synaptic architecture and efficiency for high-frequency transmission, Neuron, 36, 1127, 10.1016/S0896-6273(02)01137-6 · DOI
  74. D’Angelo, 1993, Different proportions of N-methyl-D-aspartate and non-N-methyl-D-aspartate receptor currents at the mossy fibre-granule cell synapse of developing rat cerebellum, Neuroscience, 53, 121, 10.1016/0306-4522(93)90290-V · DOI
  75. Golding, 2012, Synaptic integration in dendrites: exceptional need for speed, J. Physiol., 590, 5563, 10.1113/jphysiol.2012.229328 · DOI
  76. van Kan, 1993, Movement-related inputs to intermediate cerebellum of the monkey, J. Neurophysiol., 69, 74, 10.1152/jn.1993.69.1.74 · DOI
  77. Prsa, 2009, Characteristics of responses of Golgi cells and mossy fibers to eye saccades and saccadic adaptation recorded from the posterior vermis of the cerebellum, J. Neurosci., 29, 250, 10.1523/JNEUROSCI.4791-08.2009 · DOI
  78. Arenz, 2008, The contribution of single synapses to sensory representation in vivo, Science, 321, 977, 10.1126/science.1158391 · DOI
  79. Marr, 1969, A theory of cerebellar cortex, J. Physiol., 202, 437, 10.1113/jphysiol.1969.sp008820 · DOI · Paper page
  80. D’Angelo, 2009, Timing and plasticity in the cerebellum: focus on the granular layer, Trends Neurosci., 32, 30, 10.1016/j.tins.2008.09.007 · DOI
  81. Jörntell, 2006, Properties of somatosensory synaptic integration in cerebellar granule cells in vivo, J. Neurosci., 26, 11786, 10.1523/JNEUROSCI.2939-06.2006 · DOI
  82. Dean, 2010, The cerebellar microcircuit as an adaptive filter: experimental and computational evidence, Nat. Rev. Neurosci., 11, 30, 10.1038/nrn2756 · DOI
  83. Kennedy, 2014, A temporal basis for predicting the sensory consequences of motor commands in an electric fish, Nat. Neurosci., 17, 416, 10.1038/nn.3650 · DOI
  84. Heck, 2001, Sequential stimulation of rat cerebellar granular layer in vivo: Further evidence of a ‘tidal-wave’ timing mechanism in the cerebellum, Neurocomputing, 38, 641, 10.1016/S0925-2312(01)00421-0 · DOI
  85. Medina, 2000, Timing mechanisms in the cerebellum: testing predictions of a large-scale computer simulation, J. Neurosci., 20, 5516, 10.1523/JNEUROSCI.20-14-05516.2000 · DOI
  86. Mauk, 2004, The neural basis of temporal processing, Annu. Rev. Neurosci., 27, 307, 10.1146/annurev.neuro.27.070203.144247 · DOI · Paper page
  87. Ehmann, 2014, Quantitative super-resolution imaging of Bruchpilot distinguishes active zone states, Nat. Commun., 5, 4650, 10.1038/ncomms5650 · DOI
  88. Nanguneri, 2012, Three-dimensional, tomographic super-resolution fluorescence imaging of serially sectioned thick samples, PLoS ONE, 7, e38098, 10.1371/journal.pone.0038098 · DOI
  89. Neher, 2015, Merits and limitations of vesicle pool models in view of heterogeneous populations of synaptic vesicles, Neuron, 87, 1131, 10.1016/j.neuron.2015.08.038 · DOI · Paper page
  90. Thanawala, 2013, Presynaptic calcium influx controls neurotransmitter release in part by regulating the effective size of the readily releasable pool, J. Neurosci., 33, 4625, 10.1523/JNEUROSCI.4031-12.2013 · DOI
  91. Pan, 2009, A general model of synaptic transmission and short-term plasticity, Neuron, 62, 539, 10.1016/j.neuron.2009.03.025 · DOI
  92. Kole, 2011, First node of Ranvier facilitates high-frequency burst encoding, Neuron, 71, 671, 10.1016/j.neuron.2011.06.024 · DOI
  93. de Kock, 2008, High frequency action potential bursts (>or= 100Hz) in L2/3 and L5B thick tufted neurons in anaesthetized and awake rat primary somatosensory cortex, J. Physiol., 586, 3353, 10.1113/jphysiol.2008.155580 · DOI
  94. Renden, 2007, Synaptic vesicle endocytosis at a CNS nerve terminal: faster kinetics at physiological temperatures and increased endocytotic capacity during maturation, J. Neurophysiol., 98, 3349, 10.1152/jn.00898.2007 · DOI
  95. Pernia-Andrade, 2014, Theta-gamma-modulated synaptic currents in hippocampal granule cells in vivo define a mechanism for network oscillations, Neuron, 81, 140, 10.1016/j.neuron.2013.09.046 · DOI
  96. Lisman, 1997, Bursts as a unit of neural information: making unreliable synapses reliable, Trends Neurosci., 20, 38, 10.1016/S0166-2236(96)10070-9 · DOI
  97. Forsythe, 1994, Direct patch recording from identified presynaptic terminals mediating glutamatergic EPSCs in the rat CNS, in vitro, J. Physiol., 479, 381, 10.1113/jphysiol.1994.sp020303 · DOI
  98. Geiger, 2000, Dynamic control of presynaptic Ca2+ inflow by fast-inactivating K+ channels in hippocampal mossy fiber boutons, Neuron, 28, 927, 10.1016/S0896-6273(00)00164-1 · DOI
  99. Jakab, 1988, Quantitative morphology and synaptology of cerebellar glomeruli in the rat, Anat. Embryol., 179, 81, 10.1007/BF00305102 · DOI
  100. Hoffpauir, 2006, Synaptogenesis of the calyx of Held: rapid onset of function and one-to-one morphological innervation, J. Neurosci., 26, 5511, 10.1523/JNEUROSCI.5525-05.2006 · DOI
  101. Koester, 2005, Target cell-dependent normalization of transmitter release at neocortical synapses, Science, 308, 863, 10.1126/science.1100815 · DOI
  102. Sätzler, 2002, Three-dimensional reconstruction of a calyx of Held and its postsynaptic principal neuron in the medial nucleus of the trapezoid body, J. Neurosci., 22, 10567, 10.1523/JNEUROSCI.22-24-10567.2002 · DOI
  103. Silver, 2003, High-probability uniquantal transmission at excitatory synapses in barrel cortex, Science, 302, 1981, 10.1126/science.1087160 · DOI
  104. Schikorski, 1997, Quantitative ultrastructural analysis of hippocampal excitatory synapses, J. Neurosci., 17, 5858, 10.1523/JNEUROSCI.17-15-05858.1997 · DOI · Paper page
  105. Taschenberger, 2000, Fine-tuning an auditory synapse for speed and fidelity: developmental changes in presynaptic waveform, EPSC kinetics, and synaptic plasticity, J. Neurosci., 20, 9162, 10.1523/JNEUROSCI.20-24-09162.2000 · DOI
  106. Kole, 2007, Axon initial segment Kv1 channels control axonal action potential waveform and synaptic efficacy, Neuron, 55, 633, 10.1016/j.neuron.2007.07.031 · DOI
  107. Leão, 2005, Presynaptic Na+ channels: locus, development, and recovery from inactivation at a high-fidelity synapse, J. Neurosci., 25, 3724, 10.1523/JNEUROSCI.3983-04.2005 · DOI
  108. Sola, 2004, Increased neurotransmitter release during long-term potentiation at mossy fibre-granule cell synapses in rat cerebellum, J. Physiol., 557, 843, 10.1113/jphysiol.2003.060285 · DOI
  109. Schneggenburger, 2000, Intracellular calcium dependence of transmitter release rates at a fast central synapse, Nature, 406, 889, 10.1038/35022702 · DOI
  110. Hosoi, 2007, Quantitative analysis of calcium-dependent vesicle recruitment and its functional role at the calyx of Held synapse, J. Neurosci., 27, 14286, 10.1523/JNEUROSCI.4122-07.2007 · DOI
  111. Rosenmund, 1993, Nonuniform probability of glutamate release at a hippocampal synapse, Science, 262, 754, 10.1126/science.7901909 · DOI
  112. Branco, 2008, Local dendritic activity sets release probability at hippocampal synapses, Neuron, 59, 475, 10.1016/j.neuron.2008.07.006 · DOI · Paper page
  113. Nadkarni, 2012, Short-term plasticity constrains spatial organization of a hippocampal presynaptic terminal, Proc. Natl. Acad. Sci. U.S.A., 109, 14657, 10.1073/pnas.1211971109 · DOI
  114. Schikorski, 2001, Morphological correlates of functionally defined synaptic vesicle populations, Nat. Neurosci., 4, 391, 10.1038/86042 · DOI · Paper page
  115. Kushmerick, 2006, Physiological temperatures reduce the rate of vesicle pool depletion and short-term depression via an acceleration of vesicle recruitment, J. Neurosci., 26, 1366, 10.1523/JNEUROSCI.3889-05.2006 · DOI
  116. Neher, 2010, What is rate-limiting during sustained synaptic activity: vesicle supply or the availability of release sites, Front. Synaptic Neurosci., 2, 144, 10.3389/fnsyn.2010.00144 · DOI
  117. Klyachko, 2006, Temperature-dependent shift of balance among the components of short-term plasticity in hippocampal synapses, J. Neurosci., 26, 6945, 10.1523/JNEUROSCI.1382-06.2006 · DOI
  118. Lin, 2011, Presynaptic Ca2+ influx and vesicle exocytosis at the mouse endbulb of Held: a comparison of two auditory nerve terminals, J. Physiol., 589, 4301, 10.1113/jphysiol.2011.209189 · DOI
  119. Han, 2015, RIM1 and RIM2 redundantly determine Ca2+ channel density and readily releasable pool size at a large hindbrain synapse, J. Neurophysiol., 113, 255, 10.1152/jn.00488.2014 · DOI
  120. Bischofberger, 2002, Timing and efficacy of Ca2+ channel activation in hippocampal mossy fiber boutons, J. Neurosci., 22, 10593, 10.1523/JNEUROSCI.22-24-10593.2002 · DOI
  121. Novak, 2013, Nanoscale-targeted patch-clamp recordings of functional presynaptic ion channels, Neuron, 79, 1067, 10.1016/j.neuron.2013.07.012 · DOI
  122. Müller, 2005, Endogenous Ca2+ buffer concentration and Ca2+ microdomains in hippocampal neurons, J. Neurosci., 25, 558, 10.1523/JNEUROSCI.3799-04.2005 · DOI
  123. Shu, 2006, Modulation of intracortical synaptic potentials by presynaptic somatic membrane potential, Nature, 441, 761, 10.1038/nature04720 · DOI
  124. Smith, 2004, Recordings from single neocortical nerve terminals reveal a nonselective cation channel activated by decreases in extracellular calcium, Neuron, 41, 243, 10.1016/S0896-6273(03)00837-7 · DOI
  125. Sasaki, 2011, Action-potential modulation during axonal conduction, Science, 331, 599, 10.1126/science.1197598 · DOI
  126. Chabrol, 2015, Synaptic diversity enables temporal coding of coincident multisensory inputs in single neurons, Nat. Neurosci., 18, 718, 10.1038/nn.3974 · DOI · Paper page
  127. Guzman, 2016, Synaptic mechanisms of pattern completion in the hippocampal CA3 network, Science, 353, 1117, 10.1126/science.aaf1836 · DOI
  128. Keller, 2015, An exclusion zone for Ca2+ channels around docked vesicles explains release control by multiple channels at a CNS synapse, PLoS Comput. Biol., 11, e1004253, 10.1371/journal.pcbi.1004253 · DOI
  129. Lee, 2012, Actin-dependent rapid recruitment of reluctant synaptic vesicles into a fast-releasing vesicle pool, Proc. Natl. Acad. Sci. U.S.A., 109, E765, 10.1073/pnas.1114072109 · DOI
  130. Yuji, 2016, Distinct modes of endocytotic presynaptic membrane and protein uptake at the calyx of Held terminal of rats and mice, eLife, 5, e14643, 10.7554/eLife.14643 · DOI

Cited by

Sorted by citations

See all 52

Metadata

Authors
Delvendahl, I., & Hallermann, S.
Venue
Trends in Neurosciences
Publisher
Elsevier BV
Published
2016-11
Volume
39
Issue
11
Pages
722-737
ISSN
0166-2236
DOI
10.1016/j.tins.2016.09.006
Cited by
52
References
20
Language
en
Licence
www.elsevier.com/tdm/userlicense/1.0/ (tdm)

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