The innervation of parvalbumin-containing interneurons by VIP-immunopositive interneurons in the primary somatosensory cortex of the adult rat
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γ‐Aminobutyric acid (GABA)ergic interneurons of neocortex consist of many subgroups with extremely heterogeneous morphological, physiological and molecular properties. To explore the putative effect of the vasoactive intestinal polypeptide‐immunopositive (VIP +) neurons on neocortical circuitry, the number and distribution of VIP + boutons were analysed on somatodendritic domains of 272 parvalbumin immunopositive (PV +) 3D‐reconstructed neurons. The synaptic nature of 91% of somatic and 76% of dendritic contacts was verified by electron microscopy. The target PV + neurons were separated in two significantly different groups by means of cluster analysis. The first group (Cluster 1, 26%) received on average five times more VIP + synapses than those of the second group. The second group (Cluster 2, 74%) contained cells that were poorly innervated by VIP + boutons or did not have either somatic or dendritic or any VIP innervation at all. The cells of Cluster 1 had a soma size and total dendritic length significantly smaller than that of Cluster 2, however, they received three times more dendritic synapses, which resulted in a five times higher VIP + synaptic density on dendrites. Our results showed that although most of the PV + cells are innervated by VIP + boutons at a varying degree, some 6% of PV + cells received no input from VIP + interneurons. This suggests a refined morphological basis to influence the majority of the PV + interneurons, which are very effectively controlling pyramidal cell firing. Together with metabolic and neuromodulatory effects of VIP, this would probably result in an enhanced responsiveness of the latter cell type to tactile stimuli.
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At least a portion of Vip interneurons form perisomatic basket terminals on their postsynaptic targets, with Vip-containing boutons found on both pyramidal cells and interneurons.
“At least a portion of Vip INs seems to form perisomatic basket terminals on their postsynaptic targets. Vip containing boutons have been found on both PCs and INs (David et al., 2007; Freund et al., 1986; Hioki et al., 2013; Kawaguchi and Kubota, 1996; Peters, 1990; Staiger et al., 2004).”
From GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits (2016) · cites this paper as David et al., 2007
The discussion (Technical considerations; page not supplied) describes VIP-positive boutons arranged like baskets around PV-positive interneuron cell bodies, and the correlated microscopy analysis verifies somatic synapses on those cells. The paper discusses VIP effects on pyramidal cells but does not show VIP-containing boutons on pyramidal cells, so it supports only the interneuron-target part of the claim. (LLM, conf=0.88)
Experimental — accuracy not yet measuredVIP cells contact the perisomatic region of PV interneurons and also contact calbindin interneurons.
“Work investigating the postsynaptic targets of VIP cells showed that these neurons contacted the perisomatic region of PV INs”
From GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits (2016) · cites this paper as David et al., 2007
VIP-containing cortical inhibitory interneurons project to both somatostatin and parvalbumin containing interneurons and have an inhibitory action on these cell types.
“VIP-containing cortical inhibitory interneurons project to both somatostatin (e.g. Martinotti) and parvalbumin (e.g. basket cells) containing interneurons and have an inhibitory action on these cell types (David et al., 2007; Jiang et al., 2013; Lee et al., 2013; Pi et al., 2013).”
From Waking state: rapid variations modulate neural and behavioral responses (2015) · cites this paper as David et al., 2007
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Cites
The structural organization of layer IV in the somatosensory region (S I) of mouse cerebral cortex
Woolsey, T. A., & Van der Loos, H. (1970) · Brain Research · doi:10.1016/0006-8993(70)90079-x · Cited by 2,254 · see citing works
Synchronization of neuronal activity in hippocampus by individual GABAergic interneurons
Cobb, S. R., Buhl, E. H., Halasy, K., Paulsen, O., & Somogyi, P. (1995) · Nature · doi:10.1038/378075a0 · Cited by 1,498 · see citing works
GABAergic cell subtypes and their synaptic connections in rat frontal cortex
Kawaguchi, Y. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.6.476 · Cited by 1,416 · see citing works
Cortical Map Reorganization Enabled by Nucleus Basalis Activity
Kilgard, M. P., & Merzenich, M. M. (1998) · Science · doi:10.1126/science.279.5357.1714 · Cited by 1,197 · see citing works
Parvalbumin in Most γ-Aminobutyric Acid-Containing Neurons of the Rat Cerebral Cortex
Celio, M. R. (1986) · Science · doi:10.1126/science.3945815 · Cited by 740 · see citing works
Molecular and Physiological Diversity of Cortical Nonpyramidal Cells
Cauli, B., Audinat, E., Lambolez, B., Angulo, M. C., Ropert, N., Tsuzuki, K., Hestrin, S., & Rossier, J. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-10-03894.1997 · Cited by 738 · see citing works
Cortex is driven by weak but synchronously active thalamocortical synapses
Bruno, R. M., & Sakmann, B. (2006) · Science · doi:10.1126/science.1124593 · Cited by 714 · see citing works
Sarter, M., Hasselmo, M. E., Bruno, J. P., & Givens, B. (2005) · Brain Research Reviews · doi:10.1016/j.brainresrev.2004.08.006 · Cited by 667 · see citing works
Interneuron Diversity series: Rhythm and mood in perisomatic inhibition
Freund, T. F. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00227-3 · Cited by 641 · see citing works
The ‘module-concept’ in cerebral cortex architecture
Szentágothai, J. (1975) · Brain Research · doi:10.1016/0006-8993(75)90122-5 · Cited by 614 · see citing works
Analysis of gamma rhythms in the rat hippocampus in vitro and in vivo
Traub, R. D., Whittington, M. A., Colling, S. B., Buzsáki, G., & Jefferys, J. G. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021397 · Cited by 607 · see citing works
Excitatory effect of GABAergic axo-axonic cells in cortical microcircuits
Szabadics, J., Varga, C., Molnár, G., Oláh, S., Barzó, P., & Tamás, G. (2006) · Science · doi:10.1126/science.1121325 · Cited by 598 · see citing works
Cortical GABA Interneurons in Neurovascular Coupling: Relays for Subcortical Vasoactive Pathways
Cauli, B., Tong, X., Rancillac, A., Serluca, N., Lambolez, B., Rossier, J., & Hamel, É. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3065-04.2004 · Cited by 568 · see citing works
Differential regulation of neocortical synapses by neuromodulators and activity
Gil, Z., Connors, B. W., & Amitai, Y. (1997) · Neuron · doi:10.1016/s0896-6273(00)80380-3 · Cited by 553 · see citing works
Kawaguchi, Y. (1995) · The Journal of Neuroscience · doi:10.1523/jneurosci.15-04-02638.1995 · Cited by 533 · see citing works
A specific ‘axo-axonal’ interneuron in the visual cortex of the rat
Somogyi, P. (1977) · Brain Research · doi:10.1016/0006-8993(77)90808-3 · Cited by 530 · see citing works
Three distinct families of GABAergic neurons in rat visual cortex
Gonchar, Y. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.4.347 · Cited by 481 · see citing works
Spike-timing-dependent synaptic plasticity depends on dendritic location
Froemke, R. C., Poo, M., & Dan, Y. (2005) · Nature · doi:10.1038/nature03366 · Cited by 403 · see citing works
Kawaguchi, Y., & Kondo, S. (2002) · Journal of Neurocytology · doi:10.1023/a:1024126110356 · Cited by 395 · see citing works
Hippocampal pyramidal cells excite inhibitory neurons through a single release site
Gulyás, A. I., Miles, R., Sik, A., Tóth, K., Tamamaki, N., & Freund, T. F. (1993) · Nature · doi:10.1038/366683a0 · Cited by 384 · see citing works
Kawaguchi, Y., & Kubota, Y. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-08-02701.1996 · Cited by 380 · see citing works
Three distinct subpopulations of GABAergic neurons in rat frontal agranular cortex
Kubota, Y., Hattori, R., & Yui, Y. (1994) · Brain Research · doi:10.1016/0006-8993(94)91060-x · Cited by 365 · see citing works
Porter, J. T., Johnson, C. K., & Agmon, A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-08-02699.2001 · Cited by 344 · see citing works
Classification of fusiform neocortical interneurons based on unsupervised clustering
Cauli, B., Porter, J. T., Tsuzuki, K., Lambolez, B., Rossier, J., Quenet, B., & Audinat, E. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.11.6144 · Cited by 316 · see citing works
Acsády, L., Görcs, T. J., & Freund, T. F. (1996) · Neuroscience · doi:10.1016/0306-4522(95)00609-5 · Cited by 310 · see citing works
DeFelipe, J. (1999) · Brain · doi:10.1093/brain/122.10.1807 · Cited by 297 · see citing works
Kawaguchi, Y., & Kubota, Y. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00685-4 · Cited by 294 · see citing works
Somogyi, P., Nunzi, M. G., Gorio, A., & Smith, A. D. (1983) · Brain Research · doi:10.1016/0006-8993(83)91076-4 · Cited by 273 · see citing works
Selective Excitation of Subtypes of Neocortical Interneurons by Nicotinic Receptors
Porter, J. T., Cauli, B., Tsuzuki, K., Lambolez, B., Rossier, J., & Audinat, E. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-13-05228.1999 · Cited by 262 · see citing works
Selective Cholinergic Modulation of Cortical GABAergic Cell Subtypes
Kawaguchi, Y. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.3.1743 · Cited by 250 · see citing works
Functional Properties of Electrical Synapses Between Inhibitory Interneurons of Neocortical Layer 4
Gibson, J. R., Beierlein, M., & Connors, B. W. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00520.2004 · Cited by 242 · see citing works
Quantitative Architecture Distinguishes Prefrontal Cortical Systems in the Rhesus Monkey
Dombrowski, S. M. (2001) · Cerebral Cortex · doi:10.1093/cercor/11.10.975 · Cited by 240 · see citing works
Innervation of different peptide-containing neurons in the hippocampus by gabaergic septal afferents
Gulyás, A. I., Görcs, T. J., & Freund, T. F. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90189-b · Cited by 234 · see citing works
Gioanni, Y., Rougeot, C., Clarke, P. B. S., Lepousé, C., Thierry, A. M., & Vidal, C. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00403.x · Cited by 191 · see citing works
Porter, J. T., Cauli, B., Staiger, J. F., Lambolez, B., Rossier, J., & Audinat, E. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00367.x · Cited by 173 · see citing works
Self-citationWhite, E. L., & Hersch, S. M. (1982) · Journal of Neurocytology · doi:10.1007/bf01258009 · Cited by 171 · see citing works
Processing in layer 4 of the neocortical circuit: new insights from visual and somatosensory cortex
Miller, K. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00239-7 · Cited by 170 · see citing works
Patz, S. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhg132 · Cited by 170 · see citing works
Krimer, L. S., & Goldman-Rakic, P. S. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-11-03788.2001 · Cited by 141 · see citing works
Cortical damping: analysis of thalamocortical response transformations in rodent barrel cortex
Pinto, D. J. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.1.33 · Cited by 137 · see citing works
Sensory-Motor Areas and Aspects of Cortical Connectivity
(1986) · Cerebral cortex · doi:10.1007/978-1-4613-2149-1 · Cited by 115 · see citing works
Voltage- and Site-Dependent Control of the Somatic Impact of Dendritic IPSPs
Williams, S. R., & Stuart, G. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-19-07358.2003 · Cited by 108 · see citing works
Toledo‐Rodriguez, M., Goodman, P. H., Illic, M., Wu, C., & Markram, H. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.089250 · Cited by 107 · see citing works
Vasoactive intestinal polypeptide-immunoreactive neurons in rat visual cortex.
Connor, J., & Peters, A. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90002-2 · Cited by 101 · see citing works
Bayraktar, T., Staiger, J. F., Acsady, L., Cozzari, C., Freund, T. F., & Zilles, K. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00218-7 · Cited by 99 · see citing works
Self-citationStaiger, J. F., Zilles, K., & Freund, T. F. (1996) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1996.tb01191.x · Cited by 98 · see citing works
Self-citationHuman fetal hippocampal development: II. The neuronal cytoskeleton
Arnold, S. E., & Trojanowski, J. Q. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960401)367:2 · Cited by 87 · see citing works
Termination of Thalamic Afferents in the Cerebral Cortex
White, E. L. (1986) · Cerebral cortex · doi:10.1007/978-1-4613-2149-1_8 · Cited by 74 · see citing works
Welker, E., Armstrong‐James, M., der Loos, H. V., & Kraftsik, R. (1993) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1993.tb00534.x · Cited by 74 · see citing works
Quantitative differences among the brains of cephalopods
Maddock, L., & Young, J. Z. (1987) · Journal of Zoology · doi:10.1111/j.1469-7998.1987.tb05967.x · Cited by 70 · see citing works
Ego‐Stengel, V., Shulz, D. E., Haidarliu, S., Sosnik, R., & Ahissar, E. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.1.422 · Cited by 65 · see citing works
Vasoactive intestinal polypeptide modulates neuronal excitability in hippocampal slices of the rat
Haas, H. L., & Gähwiler, B. H. (1992) · Neuroscience · doi:10.1016/0306-4522(92)90243-u · Cited by 61 · see citing works
Immunocytochemical analysis of basket cells in rat piriform cortex
Ekstrand, J. J., Domroese, M. E., Feig, S. L., Illig, K. R., & Haberly, L. B. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1179 · Cited by 58 · see citing works
Basal forebrain neurons provide major cholinergic innervation of primate neocortex
Struble, R. G., Lehmann, J. C., Mitchell, S. J., McKinney, M., Price, D. L., Coyle, J. T., & DeLong, M. R. (1986) · Neuroscience Letters · doi:10.1016/0304-3940(86)90193-x · Cited by 56 · see citing works
Staiger, J. F., Masanneck, C., Schleicher, A., & Zuschratter, W. (2004) · Journal of Comparative Neurology · doi:10.1002/cne.10953 · Cited by 53 · see citing works
Self-citationMagistretti, P. J., Cardinaux, J., & Martin, J. (1998) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1998.tb11181.x · Cited by 52 · see citing works
Sun, Q., Prince, D. A., & Huguenard, J. R. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-07-02751.2003 · Cited by 50 · see citing works
Görcs, T. J., Léránth, C., & MacLusky, N. J. (1986) · Journal of Histochemistry & Cytochemistry · doi:10.1177/34.11.2877022 · Cited by 48 · see citing works
Staiger, J. F., Freund, T. F., & Zilles, K. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01644.x · Cited by 44 · see citing works
Self-citationCunha‐Reis, D., Sebastião, A. M., Wirkner, K., Illés, P., & Ribeiro, J. A. (2004) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0705989 · Cited by 40 · see citing works
Ectopic action potential generation in cortical interneurons during synchronized GABA responses
Keros, S., & Hablitz, J. J. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2004.12.010 · Cited by 40 · see citing works
Staiger, J. F., Schubert, D., Zuschratter, W., Kötter, R., Luhmann, H. J., & Zilles, K. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02048.x · Cited by 34 · see citing works
Self-citationAndrásfalvy, B. K., & Módy, I. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.115428 · Cited by 34 · see citing works
Penschuck, S., Chen‐Bee, C. H., Prakash, N., & Frostig, R. D. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10361 · Cited by 30 · see citing works
Electrophysiological actions of VIP in rat somatosensory cortex
Sessler, F. M., Grady, S. M., Waterhouse, B. D., & Moises, H. C. (1991) · Peptides · doi:10.1016/0196-9781(91)90124-8 · Cited by 23 · see citing works
Bayraktar (2000) · doi:10.1002/(sici)1096-9861(20000508)420:3
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Tremblay, R., Lee, S., & Rudy, B. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.033 · Cited by 2,033 · see citing works
“neurons contacted the perisomatic region of PV INs (Dávid et al., 2007; Hioki et al., 2013) as well as CB INs (Staiger et al.”
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Taniguchi, H., He, M., Wu, P., Kim, S., Paik, R., Sugino, K., Kvitsani, D., Fu, Y., Lu, J., Lin, Y., et al. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.026 · Cited by 1,828 · see citing works
Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons
Rudy, B., Fishell, G., Lee, S., & Hjerling‐Leffler, J. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20853 · Cited by 1,420 · see citing works
Cortical interneurons that specialize in disinhibitory control
Pi, H.-J., Hangya, B., Kvitsiani, D., Sanders, J. I., Huang, Z. J., & Kepecs, A. (2013) · Nature · doi:10.1038/nature12676 · Cited by 1,136 · see citing works
Waking state: rapid variations modulate neural and behavioral responses
McGinley, M. J., Vinck, M., Reimer, J., Batista-Brito, R., Zagha, E., Cadwell, C. R., Tolias, A. S., Cardin, J. A., & McCormick, D. A. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.012 · Cited by 801 · see citing works
“VIP-containing cortical inhibitory interneurons project to both somatostatin (e.g. Martinotti) and parvalbumin (e.g. basket cells) containing interneurons and have an inhibitory action on these cell types (David et al., 2007; Jiang et al., 2013; Lee et al., 2013; Pi et al., 2013).”
A disinhibitory circuit mediates motor integration in the somatosensory cortex
Lee, S., Kruglikov, I., Huang, Z. J., Fishell, G., & Rudy, B. (2013) · Nature Neuroscience · doi:10.1038/nn.3544 · Cited by 758 · see citing works
Activation of specific interneurons improves V1 feature selectivity and visual perception
Lee, S.-H., Kwan, A. C., Zhang, S., Phoumthipphavong, V., Flannery, J. G., Masmanidis, S. C., Taniguchi, H., Huang, Z. J., Zhang, F., Boyden, E. S., et al. (2012) · Nature · doi:10.1038/nature11312 · Cited by 593 · see citing works
Lee, S., Hjerling-Leffler, J., Zagha, E., Fishell, G., & Rudy, B. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.1869-10.2010 · Cited by 600 · see citing works
Unique functional properties of somatostatin-expressing GABAergic neurons in mouse barrel cortex
Gentet, L. J., Kremer, Y., Taniguchi, H., Huang, Z. J., Staiger, J. F., & Petersen, C. C. H. (2012) · Nature Neuroscience · doi:10.1038/nn.3051 · Cited by 438 · see citing works
Self-citationMembrane potential dynamics of GABAergic neurons in the barrel cortex of behaving mice
Gentet, L. J., Avermann, M., Matyas, F., Staiger, J. F., & Petersen, C. C. H. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.006 · Cited by 429 · see citing works
Self-citationFeldmeyer, D., Brecht, M., Helmchen, F., Petersen, C. C. H., Poulet, J. F. A., Staiger, J. F., Luhmann, H. J., & Schwarz, C. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.11.002 · Cited by 354 · see citing works
“…been identified in the rodent barrel cortex (Bayraktar et al., 2000; Porter et al., 2001; Angulo et al., 2003; Staiger et al., 2004; Ma et al., 2006; Sun et al., 2006; David et al., 2007; Tan et al., 2008; Karagiannis et al., 2009; Sun, 2009; Staiger et al., 2009; Helmstaedter et al., 2009a,b,c).”
BackgroundSelf-citationFunctional and structural underpinnings of neuronal assembly formation in learning
Holtmaat, A., & Caroni, P. (2016) · Nature Neuroscience · doi:10.1038/nn.4418 · Cited by 239 · see citing works
Classification of NPY-Expressing Neocortical Interneurons
Karagiannis, A., Gallopin, T., Dávid, C., Battaglia, D., Geoffroy, H., Rossier, J., Hillman, E. M. C., Staiger, J. F., & Cauli, B. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.0058-09.2009 · Cited by 256 · see citing works
Self-citationInhibitory Interneurons Regulate Temporal Precision and Correlations in Cortical Circuits
Cardin, J. A. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.07.015 · Cited by 254 · see citing works
Prönneke, A., Scheuer, B., Wagener, R. J., Möck, M., Witte, M., & Staiger, J. F. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv202 · Cited by 204 · see citing works
Self-citationMechanisms of Inhibition within the Telencephalon: “Where the Wild Things Are”
Fishell, G., & Rudy, B. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113717 · Cited by 233 · see citing works
Tasks for inhibitory interneurons in intact brain circuits
Roux, L., & Buzsáki, G. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2014.09.011 · Cited by 218 · see citing works
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., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.01.009 · Cited by 218 · see citing works
Cooperative subnetworks of molecularly similar interneurons in mouse neocortex
Karnani, M. M., Jackson, J., Ayzenshtat, I., Tucciarone, J., Manoocheri, K., Snider, W. G., & Yuste, R. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.037 · Cited by 196 · see citing works
Neuronal circuits in barrel cortex for whisker sensory perception
Staiger, J. F., & Petersen, C. C. H. (2021) · Physiological Reviews · doi:10.1152/physrev.00019.2019 · Cited by 165 · see citing works
Self-citationInhibitory engrams in perception and memory
Barron, H. C., Vogels, T. P., Behrens, T. E., & Ramaswami, M. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1701812114 · Cited by 147 · see citing works
Vucurovic, K., Gallopin, T., Ferezou, I., Rancillac, A., Chameau, P., van Hooft, J. A., Geoffroy, H., Monyer, H., Rossier, J., & Vitalis, T. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhp310 · Cited by 139 · see citing works
Morpho‐physiological criteria divide dentate gyrus interneurons into classes
Hosp, J. A., Strüber, M., Yanagawa, Y., Obata, K., Vida, I., Jonas, P., & Bartos, M. (2014) · Hippocampus · doi:10.1002/hipo.22214 · Cited by 123 · see citing works
Inan, M., Zhao, M., Manuszak, M., Karakaya, C., Rajadhyaksha, A. M., Pickel, V. M., Schwartz, T. H., Goldstein, P. A., & Manfredi, G. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.04.004 · Cited by 118 · see citing works
Lodato, S., Tomassy, G. S., De Leonibus, E., Uzcategui, Y. G., Andolfi, G., Armentano, M., Touzot, A., Gaztelu, J. M., Arlotta, P., Menendez de la Prida, L., et al. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6580-10.2011 · Cited by 112 · see citing works
Genetic dissection of GABAergic neural circuits in mouse neocortex
Taniguchi, H. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00008 · Cited by 106 · see citing works
Hioki, H., Okamoto, S., Konno, M., Kameda, H., Sohn, J., Kuramoto, E., Fujiyama, F., & Kaneko, T. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.2255-12.2013 · Cited by 83 · see citing works
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Cauli, B., Zhou, X., Tricoire, L., Toussay, X., & Staiger, J. F. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00052 · Cited by 86 · see citing works
Self-citationLagler, M., Ozdemir, A. T., Lagoun, S., Malagon-Vina, H., Borhegyi, Z., Hauer, R., Jelem, A., & Klausberger, T. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.010 · Cited by 67 · see citing works
- Authors
- Dávid, C., Schleicher, A., Zuschratter, W., & Staiger, J. F.
- Affiliations
- University of Freiburg (DE)
- Heinrich Heine University Düsseldorf (DE)
- Leibniz Institute for Neurobiology (DE)
- Corresponding author
- Dávid, Csaba
- Venue
- European Journal of Neuroscience
- Publisher
- Wiley
- Published
- 2007-04
- Volume
- 25
- Issue
- 8
- Pages
- 2329-2340
- ISSN
- 0953-816X (ISSN-L)
- 1460-9568
- OpenAlex
- W1535045684
- Cited by
- 120
- References
- 66
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 4 · 2023: 6 · 2022: 3 · 2021: 7 · 2020: 8 · 2019: 6 · 2018: 11 · 2017: 8 · 2016: 8 · 2015: 6 · 2014: 10 · 2013: 12 · 2012: 5
- FWCI
- 1.19
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- European Journal of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- parvalbumin interneurons, vasoactive intestinal peptide, primary somatosensory cortex, GABAergic interneurons, synaptic innervation, dendritic synapses, interneuron heterogeneity
- MeSH terms
- Animals, Fluorescent Dyes, gamma-Aminobutyric Acid, Interneurons, Male, Parvalbumins, Somatosensory Cortex, Synapses, Vasoactive Intestinal Peptide, Cluster Analysis, Rats, Wistar, Cell Shape, Rats
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