Synaptic plasticity at hippocampal mossy fibre synapses

Distinct short-term plasticity at two excitatory synapses in the hippocampus

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Activation of metabotropic glutamate receptor type 2/3 suppresses transmission at rat hippocampal mossy fibre synapses

Kamiya, H., Shinozaki, H., & Yamamoto, C. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021395 · Cited by 327 · see citing works

A genetic test of the effects of mutations in PKA on mossy fiber LTP and its relation to spatial and contextual learning

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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 · see citing works

Type I Adenylyl Cyclase Mutant Mice Have Impaired Mossy Fiber Long-Term Potentiation

Villacres, E. C., Wong, S. T., Chavkin, C., & Storm, D. R. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-09-03186.1998 · Cited by 187 · see citing works

Impaired Cerebellar Long-Term Potentiation in Type I Adenylyl Cyclase Mutant Mice

Storm, D. R., Hansel, C., Hacker, B., Parent, A., & Linden, D. J. (1998) · Neuron · doi:10.1016/s0896-6273(00)80500-0 · Cited by 159 · see citing works

Quantal transmission at mossy fibre targets in the CA3 region of the rat hippocampus

Lawrence, J. J., Grinspan, Z. M., & McBain, C. J. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2003.049551 · Cited by 125 · see citing works

Presynaptic R-type calcium channels contribute to fast excitatory synaptic transmission in the rat hippocampus

Gasparini, S., Kasyanov, A. M., Pietrobon, D., Voronin, L. L., & Cherubini, E. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-22-08715.2001 · Cited by 114 · see citing works

Central sensitization: a generator of pain hypersensitivity by central neural plasticity

Latremoliere, A., & Woolf, C. J. (2009) · The Journal of Pain · doi:10.1016/j.jpain.2009.06.012 · Cited by 3,913 · see citing works

Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels

Hansen, K. B., Wollmuth, L. P., Bowie, D., Furukawa, H., Menniti, F. S., Sobolevsky, A. I., Swanson, G. T., Swanger, S. A., Greger, I. H., Nakagawa, T., et al. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000131 · Cited by 686 · 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

BDNF and Hippocampal Synaptic Plasticity

Leal, G., Bramham, C. R., & Duarte, C. B. (2017) · Vitamins and Hormones · doi:10.1016/bs.vh.2016.10.004 · Cited by 425 · see citing works

Different Neuronal Activity Patterns Induce Different Gene Expression Programs

Tyssowski, K. M., DeStefino, N. R., Cho, J.-H., Dunn, C. J., Poston, R. G., Carty, C. E., Jones, R. D., Chang, S. M., Romeo, P., Wurzelmann, M. K., et al. (2018) · Neuron · doi:10.1016/j.neuron.2018.04.001 · Cited by 390 · see citing works

Presynaptic and Postsynaptic Amplifications of Neuropathic Pain in the Anterior Cingulate Cortex

Xu, H., Wu, L.-J., Wang, H., Zhang, X., Vadakkan, K. I., Kim, S. S., Steenland, H. W., & Zhuo, M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1812-08.2008 · Cited by 370 · see citing works

Neurobiology of local and intercellular BDNF signaling

Sasi, M., Vignoli, B., Canossa, M., & Blum, R. (2017) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-017-1964-4 · Cited by 324 · see citing works

The role of sleep in regulating structural plasticity and synaptic strength: implications for memory and cognitive function

Raven, F., Van der Zee, E. A., Meerlo, P., & Havekes, R. (2018) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2017.05.002 · Cited by 331 · see citing works

Tau-induced defects in synaptic plasticity, learning, and memory are reversible in transgenic mice after switching off the toxic Tau mutant

Sydow, A., Van der Jeugd, A., Zheng, F., Ahmed, T., Balschun, D., Petrova, O., Drexler, D., Zhou, L., Rune, G., Mandelkow, E., et al. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5245-10.2011 · Cited by 302 · see citing works

Pre- and postsynaptic twists in BDNF secretion and action in synaptic plasticity.

Edelmann, E., Leßmann, V., & Brigadski, T. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.05.043 · Cited by 248 · see citing works

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 · see citing works

Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons

Smrt, R. D., Eaves-Egenes, J., Barkho, B. Z., Santistevan, N. J., Zhao, C., Aimone, J. B., Gage, F. H., & Zhao, X. (2007) · Neurobiology of Disease · doi:10.1016/j.nbd.2007.04.005 · Cited by 239 · see citing works

Differential Gating and Recruitment of P/Q-, N-, and R-Type Ca²⁺Channels in Hippocampal Mossy Fiber Boutons

Li, L., Bischofberger, J., & Jonas, P. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1709-07.2007 · Cited by 206 · see citing works

Deconstructing complexity: serial block-face electron microscopic analysis of the hippocampal mossy fiber synapse

Wilke, S. A., Antonios, J. K., Bushong, E. A., Badkoobehi, A., Malek, E., Hwang, M., Terada, M., Ellisman, M. H., & Ghosh, A. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1600-12.2013 · Cited by 179 · see citing works

Neuronal Autophagy Regulates Presynaptic Neurotransmission by Controlling the Axonal Endoplasmic Reticulum

Kuijpers, M., Kochlamazashvili, G., Stumpf, A., Puchkov, D., Swaminathan, A., Lucht, M. T., Krause, E., Maritzen, T., Schmitz, D., & Haucke, V. (2021) · Neuron · doi:10.1016/j.neuron.2020.10.005 · Cited by 170 · see citing works

Molecular Mechanisms of Early and Late LTP

Baltaci, S. B., Mogulkoc, R., & Baltaci, A. K. (2019) · Neurochemical Research · doi:10.1007/s11064-018-2695-4 · Cited by 152 · see citing works

Mechanisms of Action and Persistent Neuroplasticity by Drugs of Abuse

Korpi, E. R., den Hollander, B., Farooq, U., Vashchinkina, E., Rajkumar, R., Nutt, D. J., Hyytiä, P., & Dawe, G. S. (2015) · Pharmacological Reviews · doi:10.1124/pr.115.010967 · Cited by 148 · see citing works

Mechanisms of Food Intake Repression in Indispensable Amino Acid Deficiency

Gietzen, D. W., Hao, S., & Anthony, T. G. (2007) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.27.061406.093726 · Cited by 143 · see citing works

<i>Fear Conditioning and Long‐term Potentiation in the Amygdala</i>: <i>What Really Is the Connection?</i>

Sah, P., Westbrook, R. F., & Lüthi, A. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1417.020 · Cited by 138 · see citing works

Radixin regulates synaptic GABAA receptor density and is essential for reversal learning and short-term memory

Hausrat, T. J., Muhia, M., Gerrow, K., Thomas, P., Hirdes, W., Tsukita, S., Heisler, F. F., Herich, L., Dubroqua, S., Breiden, P., et al. (2015) · Nature Communications · doi:10.1038/ncomms7872 · Cited by 138 · see citing works

Cognitive defects are reversible in inducible mice expressing pro-aggregant full-length human Tau

Van der Jeugd, A., Hochgräfe, K., Ahmed, T., Decker, J. M., Sydow, A., Hofmann, A., Wu, D., Messing, L., Balschun, D., D’Hooge, R., et al. (2012) · Acta Neuropathologica · doi:10.1007/s00401-012-0987-3 · Cited by 135 · see citing works

Functional dissection of circuitry in a neural integrator

Aksay, E., Olasagasti, I., Mensh, B. D., Baker, R., Goldman, M. S., & Tank, D. W. (2007) · Nature Neuroscience · doi:10.1038/nn1877 · Cited by 134 · see citing works

Synaptic memory and CaMKII

Nicoll, R. A., & Schulman, H. (2023) · Physiological Reviews · doi:10.1152/physrev.00034.2022 · Cited by 126 · see citing works

Neto1 Is an Auxiliary Subunit of Native Synaptic Kainate Receptors

Tang, M., Pelkey, K. A., Ng, D., Ivakine, E., McBain, C. J., Salter, M. W., & McInnes, R. R. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6617-10.2011 · Cited by 112 · see citing works

Compartmentalized Ca2+ Channel Regulation at Divergent Mossy-Fiber Release Sites Underlies Target Cell-Dependent Plasticity

Pelkey, K. A., Topolnik, L., Lacaille, J.-C., & McBain, C. J. (2006) · Neuron · doi:10.1016/j.neuron.2006.08.032 · Cited by 115 · see citing works

Short-Term Plasticity at Hippocampal Mossy Fiber Synapses Is Induced by Natural Activity Patterns and Associated with Vesicle Pool Engram Formation

Vandael, D., Borges-Merjane, C., Zhang, X., & Jonas, P. (2020) · Neuron · doi:10.1016/j.neuron.2020.05.013 · Cited by 114 · see citing works

High abundance of BDNF within glutamatergic presynapses of cultured hippocampal neurons

Andreska, T., Aufmkolk, S., Sauer, M., & Blum, R. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00107 · Cited by 100 · see citing works

Associative Plasticity at Excitatory Synapses Facilitates Recruitment of Fast-Spiking Interneurons in the Dentate Gyrus

Sambandan, S., Sauer, J.-F., Vida, I., & Bartos, M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2012-10.2010 · Cited by 82 · see citing works

Presynaptic plasticity: targeted control of inhibitory networks

McBain, C. J., & Kauer, J. A. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.05.008 · Cited by 79 · see citing works

Rab3B protein is required for long-term depression of hippocampal inhibitory synapses and for normal reversal learning

Tsetsenis, T., Younts, T. J., Chiu, C. Q., Kaeser, P. S., Castillo, P. E., & Südhof, T. C. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1112237108 · Cited by 81 · see citing works

State-Dependent cAMP Sensitivity of Presynaptic Function Underlies Metaplasticity in a Hippocampal Feedforward Inhibitory Circuit

Pelkey, K. A., Topolnik, L., Yuan, X.-Q., Lacaille, J.-C., & McBain, C. J. (2008) · Neuron · doi:10.1016/j.neuron.2008.11.018 · Cited by 69 · see citing works

Ultrastructural Imaging of Activity-Dependent Synaptic Membrane-Trafficking Events in Cultured Brain Slices

Imig, C., López-Murcia, F. J., Maus, L., García-Plaza, I. H., Mortensen, L. S., Schwark, M., Schwarze, V., Angibaud, J., Nägerl, U. V., Taschenberger, H., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.004 · Cited by 66 · see citing works

Bidirectional Hebbian Plasticity at Hippocampal Mossy Fiber Synapses on CA3 Interneurons

Galván, E. J., Calixto, E., & Barrionuevo, G. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4848-08.2008 · Cited by 63 · see citing works

Target‐cell‐dependent plasticity within the mossy fibre–CA3 circuit reveals compartmentalized regulation of presynaptic function at divergent release sites

Pelkey, K. A., & McBain, C. J. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2007.148635 · Cited by 58 · see citing works

Maintenance of long-term potentiation in hippocampal mossy fiber-CA3 pathway requires fine-tuned MMP-9 proteolytic activity

Wiera, G., Wozniak, G., Bajor, M., Kaczmarek, L., & Mozrzymas, J. W. (2013) · Hippocampus · doi:10.1002/hipo.22112 · Cited by 57 · see citing works

Joint CP-AMPA and group I mGlu receptor activation is required for synaptic plasticity in dentate gyrus fast-spiking interneurons

Hainmüller, T., Krieglstein, K., Kulik, A., & Bartos, M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1409394111 · Cited by 47 · see citing works

Structure, biophysics, and circuit function of a “giant” cortical presynaptic terminal

Vandael, D., & Jonas, P. (2024) · Science · doi:10.1126/science.adg6757 · Cited by 45 · see citing works

Differential regulation at functionally divergent release sites along a common axon

Pelkey, K. A., & McBain, C. J. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.04.008 · Cited by 43 · see citing works

Rapid Ca ²⁺ channel accumulation contributes to cAMP-mediated increase in transmission at hippocampal mossy fiber synapses

Fukaya, R., Maglione, M., Sigrist, S. J., & Sakaba, T. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2016754118 · Cited by 42 · see citing works

Calcium-stimulated adenylyl cyclase subtype 1 is required for presynaptic long-term potentiation in the insular cortex of adult mice

Miao, H.-H., Li, X.-H., Chen, Q.-Y., & Zhuo, M. (2019) · Molecular Pain · doi:10.1177/1744806919842961 · Cited by 30 · see citing works

Recruitment of release sites underlies chemical presynaptic potentiation at hippocampal mossy fiber boutons

Orlando, M., Dvorzhak, A., Bruentgens, F., Maglione, M., Rost, B. R., Sigrist, S. J., Breustedt, J., & Schmitz, D. (2021) · PLOS Biology · doi:10.1371/journal.pbio.3001149 · Cited by 30 · see citing works

The cellular and synaptic location of activated TrkB in mouse hippocampus during limbic epileptogenesis

Helgager, J., Liu, G., & McNamara, J. O. (2013) · Journal of Comparative Neurology · doi:10.1002/cne.23225 · Cited by 17 · see citing works

Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons

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 · see citing works

Ultrastructural analysis of wild-type and RIM1α knockout active zones in a large cortical synapse

Lichter, K., Paul, M. M., Pauli, M., Schoch, S., Kollmannsberger, P., Stigloher, C., Heckmann, M., & Sirén, A.-L. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111382 · Cited by 15 · see citing works