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Vasoactive Intestinal Polypeptide-Expressing Interneurons in the Hippocampus Support Goal-Oriented Spatial Learning
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Diverse computations in the neocortex are aided by specialized GABAergic interneurons (INs), which selectively target other INs. However, much less is known about how these canonical disinhibitory circuit motifs contribute to network operations supporting spatial navigation and learning in the hippocampus. Using chronic two-photon calcium imaging in mice performing random foraging or goal-oriented learning tasks, we found that vasoactive intestinal polypeptide-expressing (VIP+), disinhibitory INs in hippocampal area CA1 form functional subpopulations defined by their modulation by behavioral states and task demands. Optogenetic manipulations of VIP+ INs and computational modeling further showed that VIP+ disinhibition is necessary for goal-directed learning and related reorganization of hippocampal pyramidal cell population dynamics. Our results demonstrate that disinhibitory circuits in the hippocampus play an active role in supporting spatial learning. VIDEO ABSTRACT.
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“Place fields uniformly tiled the available space (Fig. 1c), with a slight over-representation of the reward’s position and of prominent tactile cues on the belt (see also refs. 39–41).”
From Place and behavioral modulation of hippocampal neurons during immobility (2026) · cites this paper as [41]
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Cites
Scikit-learn: Machine Learning in Python
Pedregosa, F., Varoquaux, G., Gramfort, A., Michel, V., Thirion, B., Grisel, O., Blondel, M., Müller, A., Nothman, J., Louppe, G., et al. (2012) · arXiv · doi:10.48550/arxiv.1201.0490 · Cited by 71,016
The mouse brain in stereotaxic coordinates
Konsman, J. (2003) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(03)00088-x · Cited by 16,796
The Mouse Brain in Stereotaxic Coordinates
Paxinos, G. (2001) · Cited by 12,859
The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat
O'Keefe, J., & Dostrovsky, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90358-1 · Cited by 6,151
Interneurons of the hippocampus
Freund, T. F., & Buzsáki, G. (1998) · Hippocampus · doi:10.1002/(sici)1098-1063(1996)6:4 · Cited by 3,478
The NEURON Simulation Environment
Hines, M. L., & Carnevale, N. T. (1997) · Neural Computation · doi:10.1162/neco.1997.9.6.1179 · Cited by 2,630
Dynamics of the Hippocampal Ensemble Code for Space
Wilson, M. A., & McNaughton, B. L. (1993) · Science · doi:10.1126/science.8351520 · Cited by 2,350
Neuronal Diversity and Temporal Dynamics: The Unity of Hippocampal Circuit Operations
Klausberger, T., & Somogyi, P. (2008) · Science · doi:10.1126/science.1149381 · Cited by 2,050
A cortical–hippocampal system for declarative memory
Eichenbaum, H. (2000) · Nature reviews. Neuroscience · doi:10.1038/35036213 · Cited by 1,817
Pfeffer, C. K., Xue, M., He, M., Huang, Z. J., & Scanziani, M. (2013) · Nature Neuroscience · doi:10.1038/nn.3446 · Cited by 1,353
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Self-citationTargeted Activation of Hippocampal Place Cells Drives Memory-Guided Spatial Behavior
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Humeau, Y., & Choquet, D. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0480-6 · Cited by 158
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Zhang, C., Zhu, H. L., Ni, Z., Xin, Q., Zhou, T., Wu, R., Gao, G., Gao, Z., Ma, H., Li, H., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.10.034 · Cited by 127
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Self-citationNeural dynamics underlying associative learning in the dorsal and ventral hippocampus
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Self-citationGoff, K. M., & Goldberg, E. M. (2019) · eLife · doi:10.7554/elife.46846 · Cited by 93
Cortical disinhibitory circuits: cell types, connectivity and function
Kullander, K., & Topolnik, L. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.04.009 · Cited by 86
Naskar, S., Qi, J., Pereira, F., Gerfen, C. R., & Lee, S. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108774 · Cited by 76
Guet-McCreight, A., Skinner, F. K., & Topolnik, L. (2020) · Frontiers in Neural Circuits · doi:10.3389/fncir.2020.00032 · Cited by 66
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Luo, X. M., Guet-McCreight, A., Villette, V., Francavilla, R., Marino, B., Chamberland, S., Skinner, F. K., & Topolnik, L. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz334 · Cited by 52
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Generation of Sharp Wave-Ripple Events by Disinhibition
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Structured inhibitory activity dynamics in new virtual environments
Arriaga, M. A., & Han, E. B. (2019) · eLife · doi:10.7554/elife.47611 · Cited by 49
Leroy, F., de Solis, C. A., Boyle, L. M., Bock, T., Lofaro, O. M., Buss, E. W., Asok, A., Kandel, E. R., & Siegelbaum, S. A. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01124-y · Cited by 53
Anxiety-related activity of ventral hippocampal interneurons
Forro, T., Volitaki, E., Malagon‐Vina, H., Klausberger, T., Nevian, T., & Ciocchi, S. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2022.102368 · Cited by 51
Bilash, O. M., Chavlis, S., Johnson, C. D., Poirazi, P., & Basu, J. (2023) · Cell Reports · doi:10.1016/j.celrep.2022.111962 · Cited by 52
Self-citationReorganization of CA1 dendritic dynamics by hippocampal sharp-wave ripples during learning
Rolotti, S. V., Blockus, H., Sparks, F. T., Priestley, J. B., & Losonczy, A. (2022) · Neuron · doi:10.1016/j.neuron.2021.12.017 · Cited by 50
Self-citationA hippocampal circuit mechanism to balance memory reactivation during sleep
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Mechanisms of memory-supporting neuronal dynamics in hippocampal area CA3
Li, Y., Briguglio, J. J., Romani, S., & Magee, J. C. (2024) · Cell · doi:10.1016/j.cell.2024.09.041 · Cited by 56
Inhibitory top-down projections from zona incerta mediate neocortical memory
Schroeder, A., Pardi, M. B., Keijser, J., Dalmay, T., Groisman, A. I., Schuman, E. M., Sprekeler, H., & Letzkus, J. J. (2023) · Neuron · doi:10.1016/j.neuron.2022.12.010 · Cited by 41
Cunha‐Reis, D., & Caulino‐Rocha, A. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00153 · Cited by 40
Distinct ventral hippocampal inhibitory microcircuits regulating anxiety and fear behaviors
Li, K., Koukoutselos, K., Sakaguchi, M., & Ciocchi, S. (2024) · Nature Communications · doi:10.1038/s41467-024-52466-4 · Cited by 44
Jeong, N., & Singer, A. C. (2022) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2022.102604 · Cited by 46
Albrecht, A., Redavide, E., Regev-Tsur, S., Stork, O., & Richter‐Levin, G. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.11.002 · Cited by 37
Ramos-Prats, A., Paradiso, E., Castaldi, F., Sadeghi, M., Mir, M. Y., Hörtnagl, H., Göbel, G., & Ferraguti, F. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.110893 · Cited by 39
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A local circuit-basis for spatial navigation and memory processes in hippocampal area CA1
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Self-citationGoff, K. M., Liebergall, S. R., Jiang, E., Somarowthu, A., & Goldberg, E. M. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112628 · Cited by 40
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Cell-type-specific responses to associative learning in the primary motor cortex
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Zemla, R., Moore, J. J., Hopkins, M. D., & Basu, J. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111700 · Cited by 29
Tuncdemir, S. N., Grosmark, A., Chung, H., Luna, V. M., Lacefield, C., Losonczy, A., & Hen, R. (2023) · Neuron · doi:10.1016/j.neuron.2023.09.016 · Cited by 29
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Raven, F., & Aton, S. J. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.750541 · Cited by 29
Offline memory replay in recurrent neuronal networks emerges from constraints on online dynamics
Milstein, A. D., Tran, S., Ng, G. Y., & Soltész, I. (2022) · The Journal of Physiology · doi:10.1113/jp283216 · Cited by 24
Brief synaptic inhibition persistently interrupts firing of fast-spiking interneurons
Chamberland, S., Nebet, E. R., Valero, M., Hanani, M., Egger, R., Larsen, S. B., Eyring, K. W., Buzsáki, G., & Tsien, R. W. (2023) · Neuron · doi:10.1016/j.neuron.2023.01.017 · Cited by 25
Rahmatullah, N., Schmitt, L., Stefano, L. A. D., Post, S., Robledo, J., Chaudhari, G., Pedapati, E. V., Erickson, C. A., Portera‐Cailliau, C., & Goel, A. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0571-23.2023 · Cited by 20
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Sun, Y., & Giocomo, L. M. (2022) · Nature Communications · doi:10.1038/s41467-022-34114-x · Cited by 19
Bidirectional synaptic plasticity rapidly modifies hippocampal representationsPreprint
Milstein, A. D., Li, Y., Bittner, K. C., Grienberger, C., Soltész, I., Magee, J. C., & Romani, S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.02.04.934182 · Cited by 20
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Liao, Z., & Losonczy, A. (2024) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-102423-100258 · Cited by 26
Self-citationSun, D., Unnithan, R. R., & French, C. R. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.640350 · Cited by 22
Alterations in Intrinsic and Synaptic Properties of Hippocampal CA1 VIP Interneurons During Aging
Francavilla, R., Guet-McCreight, A., Amalyan, S., Hui, C. W., Topolnik, D., Michaud, F., Marino, B., Tremblay, M., Skinner, F. K., & Topolnik, L. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.554405 · Cited by 18
Relationship Between Item and Source Memory: Explanation of Connection-Strength Model
Guo, J., Shubeck, K. T., & Hu, X. (2021) · Frontiers in Psychology · doi:10.3389/fpsyg.2021.691577 · Cited by 21
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Fischer, L. F., Soto-Albors, R. M., Tang, V. D., Bicknell, B. A., Grienberger, C., Francioni, V., Naud, R., Palmer, L. M., & Takahashi, N. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1132-22.2022 · Cited by 20
Cunha‐Reis, D., & Caulino‐Rocha, A. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.691978 · Cited by 20
Ultrafast simulation of large-scale neocortical microcircuitry with biophysically realistic neurons
Oláh, V. J., Pedersen, N. P., & Rowan, M. J. (2022) · eLife · doi:10.7554/elife.79535 · Cited by 15
VIPergic neuroprotection in epileptogenesis: challenges and opportunities
Cunha‐Reis, D., Caulino‐Rocha, A., & Correia‐de‐Sá, P. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.105356 · Cited by 16
Inhibitory and disinhibitory VIP IN-mediated circuits in neocortexPreprint
Dellal, S. S., Zurita, H., Kruglikov, I., Valero, M., Abad-Perez, P., Geron, E., Meng, J. H., Prönneke, A., Hanson, J. L., Mir, E., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.26.640383 · Cited by 24
Forro, T., & Klausberger, T. (2023) · Neuron · doi:10.1016/j.neuron.2023.05.007 · Cited by 18
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Bocchio, M., Vorobyev, A., Sadeh, S., Brustlein, S., Dard, R. F., Reichinnek, S., Emiliani, V., Baude, A., Clopath, C., & Cossart, R. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002837 · Cited by 20
Durá-Bernal, S., Griffith, E. Y., Barczak, A., O’Connell, M. N., McGinnis, T., Schroeder, C. E., Lytton, W. W., Lakatos, P., & Neymotin, S. A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.02.03.479036 · Cited by 16
Speigel, I. A., & Hemmings, H. C. (2022) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.812905 · Cited by 19
Fear memory recall involves hippocampal somatostatin interneurons
Zichó, K., Sos, K. E., Papp, P., Barth, A. M., Misák, E., Orosz, A., Mayer, M. I., Sebestény, R. Z., & Nyíri, G. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3002154 · Cited by 16
Troullinou, E., Tsagkatakis, G., Chavlis, S., Turi, G. F., Li, W., Losonczy, A., Tsakalides, P., & Poirazi, P. (2020) · IEEE Transactions on Emerging Topics in Computational Intelligence · doi:10.1109/tetci.2020.3028581 · Cited by 16
Self-citationSong, C., Kang, X., Yang, F., Du, W., Zhang, J., Liu, L., Kang, J., Jia, N., Yue, H., Fan, L., et al. (2021) · Reviews in the Neurosciences · doi:10.1515/revneuro-2020-0134 · Cited by 15
Self-citationHighly unstable heterogeneous representations in VIP interneurons of the anterior cingulate cortex
Johnson, C., Kretsge, L. N., Yen, W., Sriram, B., O’Connor, A., Liu, R. S., Jimenez, J., Phadke, R. A., Wingfield, K. K., Yeung, C., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01485-y · Cited by 15
Chatzikalymniou, A. P., Gumus, M., Lunyov, A. R., Rich, S., Lefebvre, J., & Skinner, F. K. (2021) · Hippocampus · doi:10.1002/hipo.23364 · Cited by 13
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Bigus, E. R., Lee, H., Bowler, J. C., Shi, J., & Heys, J. G. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01683-7 · Cited by 20
Katona, L., Hartwich, K., Tomioka, R., Somogyi, J., Roberts, J. D. B., Wagner, K., Joshi, A., Klausberger, T., Rockland, K. S., & Somogyi, P. (2020) · Brain Structure and Function · doi:10.1007/s00429-020-02029-2 · Cited by 14
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Gonkowski, S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21134692 · Cited by 12
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Caulino‐Rocha, A., Rodrigues, N. C., Ribeiro, J. A., & Cunha‐Reis, D. (2022) · Biology · doi:10.3390/biology11050627 · Cited by 12
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Metadata
- Authors
- Turi, G. F., Li, W.-K., Chavlis, S., Pandi, I., O’Hare, J., Priestley, J. B., Grosmark, A. D., Liao, Z., Ladow, M., Zhang, J. F., Zemelman, B. V., Poirazi, P., & Losonczy, A.
- Affiliations
- Columbia University (US)
- Mortimer B. Zuckerman Mind Brain Behavior Institute (US)
- FORTH Institute of Molecular Biology and Biotechnology (GR)
- University of Crete (GR)
- The University of Texas at Austin (US)
- Corresponding author
- Poirazi, Panayiota
- Losonczy, Attila
- ORCID
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2019-03
- Volume
- 101
- Issue
- 6
- Pages
- 1150-1165.e8
- ISSN
- 0896-6273 (ISSN-L)
- PMC
- PMC6428605
- OpenAlex
- W2913259775
- Cited by
- 218
- References
- 82
- Citations by year
- 2026: 26 · 2025: 35 · 2024: 34 · 2023: 33 · 2022: 30 · 2021: 27 · 2020: 22 · 2019: 9
- FWCI
- 12.79
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Mental Health (1R01MH100631)
- National Institute of Neurological Disorders and Stroke (1U19NS104590, 1R01NS094668)
- Zegar Family Foundation Award
- Kavli Foundation (NYSTEM-C029157, S10 OD018464)
- NIMH (F32MH118716)
- Revson Foundation
- NINDS (U01NS094330, U01NS099720)
- ERC Starting Grant dEMORY (ERC-2012-StG-311435)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- vasoactive intestinal peptide, GABAergic interneurons, hippocampal CA1, goal-directed learning, spatial learning, spatial navigation, two-photon calcium imaging, optogenetics, computational modeling, foraging behavior, behavioral state
- MeSH terms
- Animals, Appetitive Behavior, Goals, Hippocampus, Interneurons, Neural Inhibition, Vasoactive Intestinal Peptide, Pyramidal Cells, Neocortex, Mice, CA1 Region, Hippocampal, Optogenetics, Spatial Learning
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