The DOI matches its Crossref record; 67 of the 67 references it cites were found in a registry or an index.
Superpriming of synaptic vesicles as a common basis for intersynapse variability and modulation of synaptic strength
Open accessAbstract
Significance: Short-term plasticity (STP) of synaptic connections underlies many basic signal processing capabilities of the brain, such as gain control, temporal filtering, and adaptation. Glutamatergic synapses, the predominant excitatory synapses in the brain, display large variability both in basal synaptic strength and in STP. We show that a small fraction of release-ready vesicles are released with much higher probability than other vesicles. The number of these “superprimed” vesicles is variable among synapses, but increases strongly after application of phorbol ester, an analogue of the second messenger diacylglycerol, and after inducing posttetanic potentiation. Thus, modulatory transmitter systems, acting through the phospholipase-C–diacylglycerol pathway, will be able to upregulate superprimed vesicles and thereby boost synaptic strength at the onset of burst-like activity.
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 cited source says what the claim attributes to it.
In the citing paper
“These might be “superprimed” vesicles [84,85].”
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 [85]
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
1 retracted
RETRACTED: Protein kinase C is a calcium sensor for presynaptic short-term plasticity
Fioravante, D., Chu, Y., de Jong, A. P. H., Leitges, M., Kaeser, P. S., & Regehr, W. G. (2014) · eLife · doi:10.7554/elife.03011 · Cited by 16
RetractedShort-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
Synaptic depression and cortical gain control
Abbott, L. F., Varela, J. A., Sen, K., & Nelson, S. B. (1997) · Science · doi:10.1126/science.275.5297.221 · Cited by 1,690
Synaptic theory of working memory
Mongillo, G., Barak, O., & Tsodyks, M. (2008) · Science · doi:10.1126/science.1150769 · Cited by 1,253
Heterogeneity of release probability, facilitation, and depletion at central synapses
Dobrunz, L. E., & Stevens, C. F. (1997) · Neuron · doi:10.1016/s0896-6273(00)80338-4 · Cited by 1,183
Südhof, T. C. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.012 · Cited by 1,062
An optimized fluorescent probe for visualizing glutamate neurotransmission
Marvin, J., Borghuis, B., Tian, L., Cichon, J., Harnett, M. T., Akerboom, J., Gordus, A., Renninger, S., Chen, T.-W., Bargmann, C., et al. (2013) · Nature Methods · doi:10.1038/nmeth.2333 · Cited by 965
Neuromodulation of Brain States
Lee, S., & Dan, Y. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.012 · Cited by 697
Schneggenburger, R., Meyer, A. C., & Neher, E. (1999) · Neuron · doi:10.1016/s0896-6273(00)80789-8 · Cited by 627
Self-citationThe probability of transmitter release at a mammalian central synapse
Hessler, N. A., Shirke, A. M., & Malinow, R. (1993) · Nature · doi:10.1038/366569a0 · Cited by 617
Cited by
Sorted by citations
Dynamically Primed Synaptic Vesicle States: Key to Understand Synaptic Short-Term Plasticity
Neher, E., & Brose, N. (2018) · Neuron · doi:10.1016/j.neuron.2018.11.024 · Cited by 210
Self-citationUltrafast glutamate sensors resolve high-frequency release at Schaffer collateral synapses
Helassa, N., Dürst, C. D., Coates, C., Kerruth, S., Arif, U., Schulze, C., Wiegert, J. S., Geeves, M. A., Oertner, T. G., & Török, K. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1720648115 · Cited by 149
The control of release probability at nerve terminals
Dittman, J. S., & Ryan, T. A. (2019) · Nature reviews. Neuroscience · doi:10.1038/s41583-018-0111-3 · Cited by 127
Vandael, D., Borges-Merjane, C., Zhang, X., & Jonas, P. (2020) · Neuron · doi:10.1016/j.neuron.2020.05.013 · Cited by 114
Munc13-1 and Munc18-1 together prevent NSF-dependent de-priming of synaptic vesicles
He, E., Wierda, K. D. B., van Westen, R., Broeke, J. H. P., Toonen, R. F. G., Cornelisse, L. N., & Verhage, M. (2017) · Nature Communications · doi:10.1038/ncomms15915 · Cited by 98
Lin, K., Taschenberger, H., & Neher, E. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2207987119 · Cited by 84
Self-citationMiki, T., Kaufmann, W. A., Malagón, G., Gomez, L. C., Tabuchi, K., Watanabe, M., Shigemoto, R., & Marty, A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1704470114 · Cited by 84
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
A C1–C2 Module in Munc13 Inhibits Calcium-Dependent Neurotransmitter Release
Michelassi, F., Liu, H.-W., Hu, Z.-T., & Dittman, J. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.015 · Cited by 72
Unc13: a multifunctional synaptic marvel
Dittman, J. S. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.12.011 · Cited by 78
Dong, W., Radulović, T., Goral, R. O., Thomas, C. I., Montesinos, M. S., Guerrero‐Given, D., Hagiwara, A., Putzke, T., Hida, Y., Abe, M., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.06.024 · Cited by 73
Fekete, Á., Nakamura, Y., Yang, Y., Herlitze, S., Mark, M. D., DiGregorio, D. A., & Wang, L. (2019) · Nature Communications · doi:10.1038/s41467-019-08452-2 · Cited by 71
Miki, T., Nakamura, Y., Malagon, G., Neher, E., & Marty, A. (2018) · Nature Communications · doi:10.1038/s41467-018-06336-5 · Cited by 53
Self-citationUltrastructural Correlates of Presynaptic Functional Heterogeneity in Hippocampal Synapses
Maus, L., Lee, C., Altas, B., Sertel, S. M., Weyand, K., Rizzoli, S. O., Rhee, J., Brose, N., Imig, C., & Cooper, B. H. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.02.083 · Cited by 68
Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmission
Lammertse, H. C. A., van Berkel, A. A., Iacomino, M., Toonen, R. F. G., Striano, P., Gambardella, A., Verhage, M., & Zara, F. (2019) · Brain · doi:10.1093/brain/awz391 · Cited by 64
Stange-Marten, A., Nabel, A. L., Sinclair, J. L., Fischl, M. J., Alexandrova, O., Wohlfrom, H., Kopp‐Scheinpflug, C., Pecka, M., & Grothe, B. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1702290114 · Cited by 61
Quantal Fluctuations in Central Mammalian Synapses: Functional Role of Vesicular Docking Sites
Pulido, C., & Marty, A. (2017) · Physiological Reviews · doi:10.1152/physrev.00032.2016 · Cited by 63
Elevated synaptic vesicle release probability in synaptophysin/gyrin family quadruple knockouts
Raja, M. K., Preobraschenski, J., Olmo-Cabrera, S. D., Martínez-Turrillas, R., Jahn, R., Pérez‐Otaño, I., & Wesseling, J. F. (2019) · eLife · doi:10.7554/elife.40744 · Cited by 57
Calcium 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
Kobbersmed, J. R., Grasskamp, A. T., Jusyte, M., Böhme, M. A., Ditlevsen, S., Sørensen, J. B., & Walter, A. M. (2020) · eLife · doi:10.7554/elife.51032 · Cited by 54
Munc13- and SNAP25-dependent molecular bridges play a key role in synaptic vesicle priming
Papantoniou, C., Laugks, U., Betzin, J., Capitanio, C., Ferrero, J. J., Sánchez‐Prieto, J., Schoch, S., Brose, N., Baumeister, W. P., Cooper, B. H., et al. (2023) · Science Advances · doi:10.1126/sciadv.adf6222 · Cited by 55
Some Subtle Lessons from the Calyx of Held Synapse
Neher, E. (2017) · Biophysical Journal · doi:10.1016/j.bpj.2016.12.017 · Cited by 46
Self-citationLipstein, N., Chang, S., Lin, K., López-Murcia, F. J., Neher, E., Taschenberger, H., & Brose, N. (2021) · Neuron · doi:10.1016/j.neuron.2021.09.054 · Cited by 53
Self-citationAldahabi, M., Balint, F., Holderith, N., Lorincz, A., Reva, M., & Nusser, Z. (2022) · Neuron · doi:10.1016/j.neuron.2022.09.035 · Cited by 50
The Cerebellar Mossy Fiber Synapse as a Model for High-Frequency Transmission in the Mammalian CNS
Delvendahl, I., & Hallermann, S. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.09.006 · Cited by 52
Heterogeneity of glutamatergic synapses: cellular mechanisms and network consequences
Wichmann, C., & Kuner, T. (2021) · Physiological Reviews · doi:10.1152/physrev.00039.2020 · Cited by 55
Ortega, J. M., Genç, Ö., & Davis, G. W. (2018) · eLife · doi:10.7554/elife.40385 · Cited by 40
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
Apparent calcium dependence of vesicle recruitment
Ritzau‐Jost, A., Jablonski, L., Viotti, J., Lipstein, N., Eilers, J., & Hallermann, S. (2018) · The Journal of Physiology · doi:10.1113/jp275911 · Cited by 39
Variability in the Munc13-1 content of excitatory release sites.
Karlocai, M. R., Heredi, J., Benedek, T., Holderith, N., Lorincz, A., & Nusser, Z. (2021) · eLife · doi:10.7554/elife.67468 · Cited by 37
High-speed imaging of glutamate release with genetically encoded sensors
Dürst, C. D., Wiegert, J. S., Helassa, N., Kerruth, S., Coates, C., Schulze, C., Geeves, M. A., Török, K., & Oertner, T. G. (2019) · Nature Protocols · doi:10.1038/s41596-019-0143-9 · Cited by 37
Doc2-mediated superpriming supports synaptic augmentation
Xue, R., Ruhl, D. A., Briguglio, J. S., Figueroa, A. G., Pearce, R., & Chapman, E. (2018) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1802104115 · Cited by 29
Neher, E. (2023) · The Journal of General Physiology · doi:10.1085/jgp.202313454 · Cited by 34
Self-citationNeurosecretion: what can we learn from chromaffin cells
Neher, E. (2017) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-017-2051-6 · Cited by 37
Self-citationA two-step docking site model predicting different short-term synaptic plasticity patterns
Pulido, C., & Marty, A. (2018) · The Journal of General Physiology · doi:10.1085/jgp.201812072 · Cited by 33
Sakmann, B. J. (2017) · Experimental Physiology · doi:10.1113/ep085776 · Cited by 32
Cognitive synaptopathy: synaptic and dendritic spine dysfunction in age-related cognitive disorders
Barrantes, F. J. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1476909 · Cited by 37
Presynaptic Diversity Revealed by Ca 2+ -Permeable AMPA Receptors at the Calyx of Held Synapse
Lujan, B., Dagostin, A., & von Gersdorff, H. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2565-18.2019 · Cited by 30
Advances in Engineering and Application of Optogenetic Indicators for Neuroscience
Piatkevich, K. D., Murdock, M. H., & Subach, F. V. (2019) · Applied Sciences · doi:10.3390/app9030562 · Cited by 30
“Kiss-shrink-run” unifies mechanisms for synaptic vesicle exocytosis and hyperfast recycling
Tao, C.-L., Tian, C.-L., Liu, Y.-T., Lu, Z.-H., Qi, L., Li, X., Li, C., Shen, X., Gu, M., Huang, W.-L., et al. (2025) · Science · doi:10.1126/science.ads7954 · Cited by 31
Morphofunctional changes at the active zone during synaptic vesicle exocytosis
Radecke, J., Seeger, R., Kádková, A., Laugks, U., Khosrozadeh, A., Goldie, K. N., Lučić, V., Sørensen, J. B., & Zuber, B. (2023) · EMBO Reports · doi:10.15252/embr.202255719 · Cited by 29
Single Bursts of Individual Granule Cells Functionally Rearrange Feedforward Inhibition
Neubrandt, M., Oláh, V. J., Brunner, J., Marosi, E. L., Soltész, I., & Szabadics, J. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1595-17.2018 · Cited by 28
Platzer, K., Sticht, H., Bupp, C. P., Ganapathi, M., Pereira, E. M., Guyader, G. L., Bilan, F., Henderson, L. B., Lemke, J. R., Taschenberger, H., et al. (2022) · Annals of Neurology · doi:10.1002/ana.26485 · Cited by 30
Self-citationJusyte, M., Blaum, N., Böhme, M. A., Berns, M. M. M., Bonard, A. E., Vámosi, Á. B., Pushpalatha, K. V., Kobbersmed, J. R., & Walter, A. M. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112541 · Cited by 26
Farsi, Z., Walde, M., Klementowicz, A. E., Paraskevopoulou, F., & Woehler, A. (2020) · iScience · doi:10.1016/j.isci.2020.101909 · Cited by 26
Self-citationTran, V., Miki, T., & Marty, A. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2114469119 · Cited by 27
Butola, T., Alvanos, T., Hintze, A., Koppensteiner, P., Kleindienst, D., Shigemoto, R., Wichmann, C., & Moser, T. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0586-21.2021 · Cited by 32
Neher, E., & Taschenberger, H. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.10.012 · Cited by 15
Self-citationFully-primed slowly-recovering vesicles mediate presynaptic LTP at neocortical neurons
Weichard, I., Taschenberger, H., Gsell, F., Bornschein, G., Ritzau‐Jost, A., Schmidt, H., Kittel, R. J., Eilers, J., Neher, E., Hallermann, S., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2305460120 · Cited by 24
Self-citationUnc13 Aligns SNAREs and Superprimes Synaptic Vesicles
Palfreyman, M. T., & Jørgensen, E. M. (2017) · Neuron · doi:10.1016/j.neuron.2017.07.017 · Cited by 23
Kinetics of transmitter release at the calyx of Held synapse
Sakaba, T. (2018) · Proceedings of the Japan Academy. Series B, Physical and biological sciences · doi:10.2183/pjab.94.010 · Cited by 17
Regulation of a subset of release-ready vesicles by the presynaptic protein Mover
Pofantis, E., Neher, E., & Dresbach, T. (2021) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.2022551118 · Cited by 9
Self-citationPresynaptic GCaMP expression decreases vesicle release probability at the calyx of Held
Singh, M., Lujan, B., & Renden, R. (2018) · Synapse · doi:10.1002/syn.22040 · Cited by 17
Aldahabi, M., Neher, E., & Nusser, Z. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2322550121 · Cited by 17
Self-citationGuzman, G. A., Guzman, R. E., Jordan, N., & Hidalgo, P. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00125 · Cited by 17
Kim, O., Okamoto, Y., Kaufmann, W. A., Brose, N., Shigemoto, R., & Jonas, P. (2024) · PLOS Biology · doi:10.1371/journal.pbio.3002879 · Cited by 15
Exact Distribution of the Quantal Content in Synaptic Transmission
Rijal, K., Müller, N. I. C., Friauf, E., Singh, A., Prasad, A., & Das, D. (2024) · Physical Review Letters · doi:10.1103/physrevlett.132.228401 · Cited by 15
Distinct temporal filters in mitral cells and external tufted cells of the olfactory bulb
Vaaga, C. E., & Westbrook, G. L. (2017) · The Journal of Physiology · doi:10.1113/jp274608 · Cited by 15
Bera, M., Grushin, K. S., Sundaram, R. V. K., Hinzen, J. S., Chen, J., Chatterjee, A., Radhakrishnan, A., Lee, S., Padmanarayana, M., Coleman, J., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-62420-7 · Cited by 15
Novel types of frequency filtering in the lateral perforant path projections to dentate gyrus
Quintanilla, J., Jia, Y., Lauterborn, J. C., Pruess, B. S., Le, A. A., Cox, C. D., Gall, C. M., LYNCH, G. S., & Gunn, B. G. (2022) · The Journal of Physiology · doi:10.1113/jp283012 · Cited by 13
Mechanistic insights into cAMP-mediated presynaptic potentiation at hippocampal mossy fiber synapses
Fukaya, R., Miyano, R., Hirai, H., & Sakaba, T. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1237589 · Cited by 13
Silva, M., Tran, V., & Marty, A. (2023) · eLife · doi:10.7554/elife.91087 · Cited by 14
Huson, V., Meijer, M., Dekker, M. P., ter Veer, M. J. T., Ruiter, M., van Weering, J. R. T., Verhage, M., & Cornelisse, L. N. (2020) · eLife · doi:10.7554/elife.55713 · Cited by 14
The M domain in UNC-13 regulates the probability of neurotransmitter release
Liu, H., Li, L., Sheoran, S., Yu, Y., Richmond, J. E., Xia, J., Tang, J., Liu, J., & Hu, Z. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108828 · Cited by 12
Gallimore, A. R., Hepburn, I., Georgiev, S. V., Rizzoli, S. O., & Schutter, E. D. (2025) · Science Advances · doi:10.1126/sciadv.adq6477 · Cited by 17
Molecular mechanisms of homeostatic plasticity in central pattern generator networks
Northcutt, A. J., & Schulz, D. J. (2019) · Developmental Neurobiology · doi:10.1002/dneu.22727 · Cited by 15
López-Murcia, F. J., Lin, K., Berns, M. M. M., Ranjan, M., Lipstein, N., Neher, E., Brose, N., Reim, K., & Taschenberger, H. (2024) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.2320505121 · Cited by 13
Self-citationHigh Entrainment Constrains Synaptic Depression Levels of an In vivo Globular Bushy Cell Model
Rudnicki, M., & Hemmert, W. (2017) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2017.00016 · Cited by 12
Quantum propensities in the brain cortex and free will
Georgiev, D. D. (2021) · Biosystems · doi:10.1016/j.biosystems.2021.104474 · Cited by 12
Chipman, P. H., Lee, U., Orr, B. O., Fetter, R. D., & Davis, G. W. (2025) · Neuron · doi:10.1016/j.neuron.2025.05.030 · Cited by 12
Lin, K., Ranjan, M., Lipstein, N., Brose, N., Neher, E., & Taschenberger, H. (2025) · The Journal of Physiology · doi:10.1113/jp286282 · Cited by 11
Self-citationHu, H., Wang, X., Li, C., Li, Y., Hao, J., Zhou, Y., Yang, X., Chen, P., Shen, X., & Zhang, S. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.10.020 · Cited by 10
Kádková, A., Murach, J., Østergaard, M., Malsam, A., Malsam, J., Lolicato, F., Nickel, W., Söllner, T. H., & Sørensen, J. B. (2024) · eLife · doi:10.7554/elife.88619 · Cited by 10
Nestvogel, D., Merino, R. M., Leon-Pinzon, C., Schottdorf, M., Lee, C., Imig, C., Brose, N., & Rhee, J. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.02.045 · Cited by 9
Morphofunctional changes at the active zone during synaptic vesicle exocytosisPreprint
Radecke, J., Seeger, R., Kádková, A., Laugks, U., Khosrozadeh, A., Goldie, K. N., Lučić, V., Sørensen, J. B., & Zuber, B. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.07.483217 · Cited by 10
SNARE Proteins in Synaptic Vesicle Fusion
Palfreyman, M. T., West, S. E., & Jørgensen, E. M. (2023) · Advances in neurobiology · doi:10.1007/978-3-031-34229-5_4 · Cited by 10
Gustafsson, B., Ma, R., & Hanse, E. (2019) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2019.00007 · Cited by 9
Wesseling, J. F. (2019) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2019.00032 · Cited by 9
Hain, P. J. H., & Moser, T. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1351280 · Cited by 8
Modulation of Neural Microcircuits That Control Complex Dynamics in Olfactory Networks
Huang, Z., Tatti, R., Loeven, A. M., Conde, D. R. L., & Fadool, D. A. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.662184 · Cited by 7
A two-subpopulation model that reflects heterogeneity of large dense core vesicles in exocytosis
Qin, N., Chen, Z., & Xue, R. (2022) · Cell Cycle · doi:10.1080/15384101.2022.2026576 · Cited by 8
Species-Specific Adaptation for Ongoing High-Frequency Action Potential Generation in MNTB Neurons
Kladisios, N., Wicke, K. D., Pätz, C., & Felmy, F. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.2320-22.2023 · Cited by 8
Martín, R., Suárez-Pinilla, A. S., García-Font, N., Laguna-Luque, M. L., López, J. C., Oset‐Gasque, M. J., Gruart, A., Delgado-Garcia, J. M., Torres, M., & Sánchez‐Prieto, J. (2023) · Molecular Autism · doi:10.1186/s13229-023-00547-4 · Cited by 9
Lin, K., Taschenberger, H., & Neher, E. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4075232 · Cited by 8
Self-citationThe intracellular Ca 2+ sensitivity of transmitter release in glutamatergic neocortical boutons
Bornschein, G., Brachtendorf, S., Reinert, A., Eshra, A., Kraft, R., Hirrlinger, J., Eilers, J., Hallermann, S., & Schmidt, H. (2025) · Science · doi:10.1126/science.adp0870 · Cited by 10
Meijer, M., Öttl, M., Yang, J., Subkhangulova, A., Kumar, A., Feng, Z., van Voorst, T. W., Groffen, A. J. A., van Weering, J. R. T., Zhang, Y., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-46828-1 · Cited by 7
Tuning auditory synapses for resilience, reliability and precision
Lujan, B., & von Gersdorff, H. (2017) · The Journal of Physiology · doi:10.1113/jp273496 · Cited by 3
Ultrafast glutamate sensors resolve high-frequency release at Schaffer collateral synapsesPreprint
Helassa, N., Dürst, C. D., Coates, C., Kerruth, S., Arif, U., Schulze, C., Wiegert, J. S., Geeves, M., Oertner, T. G., & Török, K. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/233494 · Cited by 4
Ranjan, M., Lin, K., Mueller, B. D., Wojcik, S. M., Lohse, M., Südhof, T. C., Jørgensen, E. M., Neher, E., Lipstein, N., Brose, N., et al. (2026) · Science Advances · doi:10.1126/sciadv.aea0449 · Cited by 3
Self-citationSilva, M., Tran, V., & Marty, A. (2024) · eLife · doi:10.7554/elife.91087.3 · Cited by 1
Xue, R., Zhang, E., & Wang, Y. (2024) · Acta Physiologica · doi:10.1111/apha.14115 · Cited by 1
Eichler, A., Kruse, P., Schob, C., & Lenz, M. (2025) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2025.1724377 · Cited by 2
Synaptic vesicle undocking induces low-frequency depression
Silva, M., Trigo, F. F., Llano, I., & Marty, A. (2026) · eLife · doi:10.64898/2026.01.15.699619 · Cited by 1
Shin, J., Lee, S. Y., Kim, Y., & Lee, S. (2026) · eLife · doi:10.7554/elife.102923.6 · Cited by 1
Synaptic Facilitation Enhances the Reliability and Precision of High-Frequency Neurotransmission
Bernal-Correa, A. M., Dagostin, A., von Gersdorff, H., & Kushmerick, C. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.0570-25.2026 · Cited by 1
Functioning of Synaptic Vesicle Pools: Diversity and Organizational Principles
Gafurova, C. R., & Petrov, A. M. (2026) · Biochemistry (Moscow) · doi:10.1134/s0006297926600535 · Cited by 1
Undoing of firing rate adaptation enables invariant population codes
Brandão, S. C., Ramirez, L., Züfle, P., Walter, A. M., Silies, M., & Martelli, C. (2026) · Science Advances · doi:10.1126/sciadv.aeg3535 · Cited by 1
Electrophysiological Analysis of the Synaptic Vesicle Priming Process
Nestvogel, D. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6444 · Cited by 1
Correlating Synaptic Ultrastructure and Function at the NanoscalePreprint
Maus, L., Altas, B., Rhee, J., Brose, N., Imig, C., & Cooper, B. H. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/588848 · Cited by 1
Metadata
- Authors
- Taschenberger, H., Woehler, A., & Neher, E.
- Affiliations
- Nanoscale Microscopy and Molecular Physiology of the Brain Cluster of Excellence 171 — DFG Research Center 103 (DE)
- Corresponding author
- Neher, Erwin
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2016-07-18
- Volume
- 113
- Issue
- 31
- Pages
- E4548-57
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC4978258
- OpenAlex
- W2477973977
- Cited by
- 128
- References
- 67
- Citations by year
- 2026: 10 · 2025: 12 · 2024: 13 · 2023: 18 · 2022: 10 · 2021: 12 · 2020: 8 · 2019: 15 · 2018: 13 · 2017: 16 · 2016: 1
- FWCI
- 8.44
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- MDC Repository (Max-Delbrueck-Center for Molecular Medicine) (submittedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion, other-oa)
- Funders
- Deutsche Forschungsgemeinschaft (CNMPB)
- European Commission Directorate-General for Research and Innovation (FP7-HEALTH-F2-2009-241498)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- synaptic vesicles, short-term plasticity, post-tetanic potentiation, short-term depression, synaptic facilitation, phospholipase C, diacylglycerol, phorbol ester, glutamatergic synapses
- MeSH terms
- Algorithms, Animals, Animals, Newborn, Cells, Cultured, Electric Stimulation, Female, Male, Models, Neurological, Synaptic Transmission, Neuronal Plasticity, Synapses, Synaptic Vesicles, Signal Transduction, Rats, Wistar, Glutamic Acid, Excitatory Postsynaptic Potentials
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