The DOI matches its Crossref record; 79 of the 80 references it cites were found in a registry or an index.
Short-Term Plasticity at Hippocampal Mossy Fiber Synapses Is Induced by Natural Activity Patterns and Associated with Vesicle Pool Engram Formation
Open accessAbstract
Post-tetanic potentiation (PTP) is an attractive candidate mechanism for hippocampus-dependent short-term memory. Although PTP has a uniquely large magnitude at hippocampal mossy fiber-CA3 pyramidal neuron synapses, it is unclear whether it can be induced by natural activity and whether its lifetime is sufficient to support short-term memory. We combined in vivo recordings from granule cells (GCs), in vitro paired recordings from mossy fiber terminals and postsynaptic CA3 neurons, and "flash and freeze" electron microscopy. PTP was induced at single synapses and showed a low induction threshold adapted to sparse GC activity in vivo. PTP was mainly generated by enlargement of the readily releasable pool of synaptic vesicles, allowing multiplicative interaction with other plasticity forms. PTP was associated with an increase in the docked vesicle pool, suggesting formation of structural "pool engrams." Absence of presynaptic activity extended the lifetime of the potentiation, enabling prolonged information storage in the hippocampal network.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“For example, high-frequency stimulation (HFS) induces several cyclic adenosine monophosphate (cAMP)-dependent forms of presynaptic plasticity [21,28–33].”
From Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons (2024) · cites this paper as [21]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Thus, both short- and long-term mechanisms may involve the formation of vesicle pool engrams [21].”
From Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons (2024) · cites this paper as [21]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“Previous work showed that facilitation and PTP may lead to conditional detonation or plasticity-dependent detonation at this synapse [21,51].”
From Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons (2024) · cites this paper as [21]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Thus, chemical potentiation primarily involved an increase in pool size but also an increase in Pr, reminiscent of hippocampal mossy fiber PTP [21].”
From Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons (2024) · cites this paper as [21]
The cited source says what the claim attributes to it.
In the citing paper
“Second, it has a unique extent of presynaptic plasticity, including facilitation, post-tetanic potentiation (PTP) [21], and long-term potentiation (LTP) [27].”
From Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons (2024) · cites this paper as [21]
The cited source says what the claim attributes to it.
In the citing paper
“This is consistent with a decrease in strength of synaptic transmission after H-89 application [21].”
From Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons (2024) · cites this paper as [21]
The cited source says what the claim attributes to it.
In the citing paper
“Moreover, our results revealed that baseline activity of cAMP-PKA signaling pathway is important for coupling distance, basal synaptic transmission, and the induction of presynaptic potentiation, as the application of PKA antagonists led to “uncoupling” of Munc13-1 and CaV2.1 (Figs 5 and S9) and a decrease in synaptic strength [21].”
From Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons (2024) · cites this paper as [21]
The cited source says what the claim attributes to it.
In the citing paper
“Changes in both RRP and Pr have been also reported during PTP [21].”
From Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons (2024) · cites this paper as [21]
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
An Introduction to the Bootstrap
Efron, B., & Tibshirani, R. (1995) · Journal of the Royal Statistical Society Series A (Statistics in Society) · doi:10.2307/2983304 · Cited by 22,453
Short-Term Synaptic Plasticity
Zucker, R. S., & Regehr, W. G. (2002) · Annual Review of Physiology · doi:10.1146/annurev.physiol.64.092501.114547 · Cited by 5,068
An Energy Budget for Signaling in the Grey Matter of the Brain
Attwell, D., & Laughlin, S. B. (2001) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200110000-00001 · Cited by 3,543
The Medial Temporal Lobe Memory System
Squire, L. R., & Zola-Morgan, S. (1991) · Science · doi:10.1126/science.1896849 · Cited by 3,282
Cellular basis of working memory
Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663
Abbott, L. F., & Regehr, W. G. (2004) · Nature · doi:10.1038/nature03010 · Cited by 1,684
Optogenetic stimulation of a hippocampal engram activates fear memory recall
Liu, X., Ramirez, S., Pang, P. T., Puryear, C. B., Govindarajan, A., Deisseroth, K. A., & Tonegawa, S. (2012) · Nature · doi:10.1038/nature11028 · Cited by 1,669
Brain-state- and cell-type-specific firing of hippocampal interneurons in vivo
Klausberger, T., Magill, P. J., Márton, L. F., Roberts, J. D. B., Cobden, P. M., Buzsáki, G., & Somogyi, P. (2003) · Nature · doi:10.1038/nature01374 · Cited by 1,345
Geiger, J. R. P., Melcher, T., Koh, D.-S., Sakmann, B., Seeburg, P. H., Jonas, P., & Monyer, H. (1995) · Neuron · doi:10.1016/0896-6273(95)90076-4 · Cited by 1,260
Synaptic theory of working memory
Mongillo, G., Barak, O., & Tsodyks, M. (2008) · Science · doi:10.1126/science.1150769 · Cited by 1,253
Memory engrams: Recalling the past and imagining the future
Josselyn, S. A., & Tonegawa, S. (2020) · Science · doi:10.1126/science.aaw4325 · Cited by 1,087
Actin in action: the interplay between the actin cytoskeleton and synaptic efficacy.
Cingolani, L. A., & Goda, Y. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2373 · Cited by 831
GABAergic Cells Are the Major Postsynaptic Targets of Mossy Fibers in the Rat Hippocampus
Acsády, L., Kamondi, A., Sı́k, A., Freund, T., & Buzsáki, G. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-09-03386.1998 · Cited by 741
Control of timing, rate and bursts of hippocampal place cells by dendritic and somatic inhibition
Royer, S., Zemelman, B. V., Losonczy, A., Kim, J., Chance, F., Magee, J. C., & Buzsáki, G. (2012) · Nature Neuroscience · doi:10.1038/nn.3077 · Cited by 728
Synaptic plasticity at hippocampal mossy fibre synapses
Nicoll, R. A., & Schmitz, D. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1786 · Cited by 653
Schneggenburger, R., Meyer, A. C., & Neher, E. (1999) · Neuron · doi:10.1016/s0896-6273(00)80789-8 · Cited by 627
Geiger, J. R. P., & Jónás, P. (2000) · Neuron · doi:10.1016/s0896-6273(00)00164-1 · Cited by 621
Mediation of Hippocampal Mossy Fiber Long-Term Potentiation by Cyclic AMP
Weisskopf, M. G., Castillo, P. E., Zalutsky, R. A., & Nicoll, R. A. (1994) · Science · doi:10.1126/science.7916482 · Cited by 618
Ultrafast endocytosis at mouse hippocampal synapses
Watanabe, S., Rost, B. R., Camacho-Pérez, M., Davis, M. W., Söhl-Kielczynski, B., Rosenmund, C., & Jorgensen, E. M. (2013) · Nature · doi:10.1038/nature12809 · Cited by 607
Conjunctive input processing drives feature selectivity in hippocampal CA1 neurons
Bittner, K. C., Grienberger, C., Vaidya, S. P., Milstein, A. D., Macklin, J. J., Suh, J., Tonegawa, S., & Magee, J. C. (2015) · Nature Neuroscience · doi:10.1038/nn.4062 · Cited by 540
Chapter 1 Chapter Neurons, numbers and the hippocampal network
Amaral, D. G., Ishizuka, N., & Claiborne, B. J. (1990) · Progress in brain research · doi:10.1016/s0079-6123(08)61237-6 · Cited by 523
The mechanisms and functions of synaptic facilitation.
Jackman, S. L., & Regehr, W. G. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.047 · Cited by 489
Silver, R. A. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2864 · Cited by 481 · cited 1×
“In combination, these changes enrich the repertoire of single-synapse computations (Abbott and Regehr, 2004; Silver, 2010; Henze et al., 2002; Vyleta et al., 2016; Chamberland et al., 2018).”
BackgroundSingle granule cells reliably discharge targets in the hippocampal CA3 network in vivo
Henze, D. A., Wittner, L., & Buzsáki, G. (2002) · Nature Neuroscience · doi:10.1038/nn887 · Cited by 480
Distinct short-term plasticity at two excitatory synapses in the hippocampus
Salin, P. A., Scanziani, M., Malenka, R. C., & Nicoll, R. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.23.13304 · Cited by 438
Structural Components of Synaptic Plasticity and Memory ConsolidationPreprint
Bailey, C. H., Kandel, E. R., & Harris, K. M. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021758 · Cited by 419
Chicurel, M. E., & Harris, K. M. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903250204 · Cited by 417
The Morphological and Molecular Nature of Synaptic Vesicle Priming at Presynaptic Active Zones
Imig, C., Min, S.-W., Krinner, S., Arancillo, M., Rosenmund, C., Südhof, T. C., Rhee, J., Brose, N., & Cooper, B. H. (2014) · Neuron · doi:10.1016/j.neuron.2014.10.009 · Cited by 389
Zenke, F., Agnes, E. J., & Wulfram Gerstner, B. (2015) · Nature Communications · doi:10.1038/ncomms7922 · Cited by 374
Patch-clamp recording from mossy fiber terminals in hippocampal slices
Bischofberger, J., Engel, D., Li, L., Geiger, J. R., & Jónás, P. (2006) · Nature Protocols · doi:10.1038/nprot.2006.312 · Cited by 311
High-fidelity transmission of sensory information by single cerebellar mossy fibre boutons
Rancz, E. A., Ishikawa, T., Duguid, I., Chadderton, P. T., Mahon, S., & Häusser, M. (2007) · Nature · doi:10.1038/nature05995 · Cited by 291
The role of presynaptic calcium in short-term enhancement at the hippocampal mossy fiber synapse
Regehr, W. G., Delaney, K., & Tank, D. W. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-02-00523.1994 · Cited by 269
Genes regulating lymphangiogenesis control venous valve formation and maintenance in mice
Bazigou, E., Lyons, O., Smith, A., Venn, G. E., Cope, C., Brown, N. A., & Mäkinen, T. (2011) · Journal of Clinical Investigation · doi:10.1172/jci58050 · Cited by 269
Differential Mechanisms of Transmission at Three Types of Mossy Fiber Synapse
Toth, K., Suares, G., Lawrence, J. J., Philips-Tansey, E., & McBain, C. J. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-22-08279.2000 · Cited by 262
Reversal of synaptic vesicle docking at central synapses
Murthy, V. N., & Stevens, C. F. (1999) · Nature Neuroscience · doi:10.1038/9149 · Cited by 254
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
Structural determinants of transmission at large hippocampal mossy fiber synapses
Rollenhagen, A., Sätzler, K., Rodríguez, E. P., Jonas, P., Frotscher, M., & Lübke, J. H. R. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1946-07.2007 · Cited by 246
Neher, E. (2015) · Neuron · doi:10.1016/j.neuron.2015.08.038 · Cited by 236
Hippocampal ensemble activity during spatial delayed-nonmatch-to-sample performance in rats
Deadwyler, S., Bunn, T., & Hampson, R. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-01-00354.1996 · Cited by 233
Pernía‐Andrade, A. J., & Jónás, P. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.046 · Cited by 227
Huang, Y.-Y., & Kandel, E. R. (1996) · Neuron · doi:10.1016/s0896-6273(00)80080-x · Cited by 199
Voltage-clamp analysis of mossy fiber synaptic input to hippocampal neurons
Brown, T. H., & Johnston, D. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.50.2.487 · Cited by 196
SNARE assembly and disassembly exhibit a pronounced hysteresis
Fasshauer, D., Antonin, W., Subramaniam, V., & Jahn, R. (2002) · Nature Structural Biology · doi:10.1038/nsb750 · Cited by 194
Loose Coupling Between Ca 2+ Channels and Release Sensors at a Plastic Hippocampal Synapse
Vyleta, N. P., & Jonas, P. (2014) · Science · doi:10.1126/science.1244811 · Cited by 189
The low synaptic release probability in vivo
Borst, J. G. G. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.03.003 · Cited by 177
Hippocampal granule cells opt for early retirement
Alme, C. B., Buzzetti, R. A., Marrone, D. F., Leutgeb, J. K., Chawla, M. K., Schaner, M. J., Bohanick, J. D., Khoboko, T., Leutgeb, S., Moser, E. I., et al. (2010) · Hippocampus · doi:10.1002/hipo.20810 · Cited by 175
Spatial Firing Correlates of Physiologically Distinct Cell Types of the Rat Dentate Gyrus
Neunuebel, J. P., & Knierim, J. J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6038-11.2012 · Cited by 167
Stimfit: quantifying electrophysiological data with Python
Guzman, S. J., Schlögl, A., & Schmidt‐Hieber, C. (2014) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2014.00016 · Cited by 161
PTP and LTP at a hippocampal mossy fiber-interneuron synapse
Alle, H., Jonas, P., & Geiger, J. R. P. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.251610898 · Cited by 158
Thanawala, M. S., & Regehr, W. G. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4031-12.2013 · Cited by 145
Involvement of Actin Polymerization in Vesicle Recruitment at the Calyx of Held Synapse
Sakaba, T., & Neher, E. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-03-00837.2003 · Cited by 134
Taschenberger, H., Woehler, A., & Neher, E. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1606383113 · Cited by 128
Synapsin IIa Controls the Reserve Pool of Glutamatergic Synaptic Vesicles
Gitler, D., Cheng, Q., Greengard, P., & Augustine, G. J. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0924-08.2008 · Cited by 121
Post‐tetanic potentiation in the rat calyx of Held synapse
Habets, R. L. P., & Borst, J. G. G. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2004.079160 · Cited by 111
Functional Imaging of Dentate Granule Cells in the Adult Mouse Hippocampus
Pilz, G.-A., Carta, S., Stäuble, A., Ayaz, A., Jessberger, S., & Helmchen, F. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3065-15.2016 · Cited by 100
Korogod, N., Lou, X., & Schneggenburger, R. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1295-05.2005 · Cited by 96
Kowalski, J., Gan, J., Jonas, P., & Pernía‐Andrade, A. J. (2016) · Hippocampus · doi:10.1002/hipo.22550 · Cited by 96
Superpriming of synaptic vesicles after their recruitment to the readily releasable pool
Lee, J. S., Ho, W., Neher, E., & Lee, S. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1314427110 · Cited by 95
Plasticity-dependent, full detonation at hippocampal mossy fiber-CA3 pyramidal neuron synapses
Vyleta, N. P., Borges-Merjane, C., & Jonas, P. (2016) · eLife · doi:10.7554/elife.17977 · Cited by 91
Self-citationDynamic Filtering of Recognition Memory Codes in the Hippocampus
Wiebe, S. P., & Staubli, U. V. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-23-10562.1999 · Cited by 88
Neuromodulator Signaling Bidirectionally Controls Vesicle Numbers in Human Synapses
Patzke, C., Brockmann, M. M., Dai, J., Gan, K. J., Grauel, M. K., Fenske, P., Liu, Y., Acuna, C., Rosenmund, C., & Südhof, T. C. (2019) · Cell · doi:10.1016/j.cell.2019.09.011 · Cited by 85
Pernía‐Andrade, A. J., Goswami, S. P., Stickler, Y., Fröbe, U., Schlögl, A., & Jónás, P. (2012) · Biophysical Journal · doi:10.1016/j.bpj.2012.08.039 · Cited by 83
Lee, J. S., Kim, M., Ho, W., & Lee, S. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.2165-08.2008 · Cited by 80
Optical detection of three modes of endocytosis at hippocampal synapses
Chanaday, N. L., & Kavalali, E. T. (2018) · eLife · doi:10.7554/elife.36097 · Cited by 78
Midorikawa, M., & Sakaba, T. (2017) · Neuron · doi:10.1016/j.neuron.2017.10.016 · Cited by 71
Measuring the Firing Rate of High-Resistance Neurons with Cell-Attached Recording
Alcamí, P., Franconville, R., Llano, I., & Marty, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5371-11.2012 · Cited by 69
Krause, J. (2016) · Apress eBooks · doi:10.1007/978-1-4842-2382-6_2 · Cited by 67
Lee, J. S., Ho, W., & Lee, S. (2010) · The Journal of General Physiology · doi:10.1085/jgp.201010437 · Cited by 61
Borges-Merjane, C., Kim, O., & Jonas, P. (2020) · Neuron · doi:10.1016/j.neuron.2019.12.022 · Cited by 60
Self-citationVoltage-clamp analysis of posttetanic potentiation of the mossy fiber to CA3 synapse in hippocampus
Griffith, W. H. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.63.3.491 · Cited by 59
Miki, T., Nakamura, Y., Malagon, G., Neher, E., & Marty, A. (2018) · Nature Communications · doi:10.1038/s41467-018-06336-5 · Cited by 53
Langdon, R. B., Johnson, J. W., & Barrionuevo, G. (1995) · Journal of Neurobiology · doi:10.1002/neu.480260309 · Cited by 52
Habets, R. L. P., & Borst, J. G. G. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2006.127365 · Cited by 50
Calcium-Dependent Isoforms of Protein Kinase C Mediate Posttetanic Potentiation at the Calyx of Held
Fioravante, D., Chu, Y., Myoga, M. H., Leitges, M., & Regehr, W. G. (2011) · Neuron · doi:10.1016/j.neuron.2011.04.019 · Cited by 49
Calcium-Dependent PKC Isoforms Have Specialized Roles in Short-Term Synaptic Plasticity
Chu, Y., Fioravante, D., Leitges, M., & Regehr, W. G. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.003 · Cited by 42
Chamberland, S., Timofeeva, Y., Evstratova, A., Volynski, K. E., & Tóth, K. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1720659115 · Cited by 40
Dentate gyrus granule cell firing patterns can induce mossy fiber long‐term potentiation in vitro
Mistry, R. B., Dennis, S. H., Frerking, M. E., & Mellor, J. R. (2010) · Hippocampus · doi:10.1002/hipo.20815 · Cited by 35
Targeted deletion of AKAP7 in dentate granule cells impairs spatial discrimination
Jones, B. W., Deem, J. D., Younts, T. J., Weisenhaus, M., Sanford, C. A., Slack, M., Chin, J., Nachmanson, D., McKennon, A., Castillo, P. E., et al. (2016) · eLife · doi:10.7554/elife.20695 · Cited by 35
Gundlfinger, A., Breustedt, J., Sullivan, D. W., & Schmitz, D. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009961 · Cited by 28
Flagged first, then by citations
1 of the 80 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Astrocytes phagocytose adult hippocampal synapses for circuit homeostasis
Lee, J.-H., Kim, J. S., Noh, S., Lee, H., Lee, S. Y., Mun, J. Y., Park, H., & Chung, W. (2020) · Nature · doi:10.1038/s41586-020-03060-3 · Cited by 407
Calcium-dependent docking of synaptic vesicles
Silva, M., Tran, V., & Marty, A. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.04.003 · Cited by 87
Synapsins and the Synaptic Vesicle Reserve Pool: Floats or Anchors?
Zhang, M., & Augustine, G. J. (2021) · Cells · doi:10.3390/cells10030658 · Cited by 66
Guzman, S. J., Schlögl, A., Espinoza, C., Zhang, X., Suter, B. A., & Jónás, P. (2021) · Nature Computational Science · doi:10.1038/s43588-021-00157-1 · Cited by 58
Self-citationCalcium dependence of neurotransmitter release at a high fidelity synapse
Eshra, A., Schmidt, H., Eilers, J., & Hallermann, S. (2021) · eLife · doi:10.7554/elife.70408 · Cited by 56
Metadata
- Authors
- Vandael, D., Borges-Merjane, C., Zhang, X., & Jonas, P.
- Affiliations
- Institute of Science and Technology Austria (AT)
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2020-08
- Volume
- 107
- Issue
- 3
- Pages
- 509-521.e7
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC7427323
- OpenAlex
- W3032084133
- Cited by
- 114
- References
- 80
- Citations by year
- 2026: 16 · 2025: 13 · 2024: 17 · 2023: 24 · 2022: 15 · 2021: 23 · 2020: 6
- FWCI
- 7.79
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Neuron (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- Horizon 2020 (692692)
- European Research Council
- Austrian Science Fund (V 739-B27, Z 312-B27)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- post-tetanic potentiation, short-term plasticity, mossy fiber synapses, hippocampus, CA3 pyramidal cells, granule cells, synaptic vesicle pools, readily releasable pool, docked vesicles, short-term memory, synaptic plasticity, presynaptic activity
- MeSH terms
- Action Potentials, Animals, Memory, Short-Term, Microscopy, Electron, Neuronal Plasticity, Synapses, Synaptic Vesicles, Pyramidal Cells, Patch-Clamp Techniques, Dentate Gyrus, Mossy Fibers, Hippocampal, Mice, Rats, Synaptic Potentials, CA3 Region, Hippocampal
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