The DOI matches its Crossref record; 338 of the 338 references it cites were found in a registry or an index.
Barrel cortex function
Open accessAbstract
Neocortex, the neuronal structure at the base of the remarkable cognitive skills of mammals, is a layered sheet of neuronal tissue composed of juxtaposed and interconnected columns. A cortical column is considered the basic module of cortical processing present in all cortical areas. It is believed to contain a characteristic microcircuit composed of a few thousand neurons. The high degree of cortical segmentation into vertical columns and horizontal layers is a boon for scientific investigation because it eases the systematic dissection and functional analysis of intrinsic as well as extrinsic connections of the column. In this review we will argue that in order to understand neocortical function one needs to combine a microscopic view, elucidating the workings of the local columnar microcircuits, with a macroscopic view, which keeps track of the linkage of distant cortical modules in different behavioral contexts. We will exemplify this strategy using the model system of vibrissal touch in mice and rats. On the macroscopic level vibrissal touch is an important sense for the subterranean rodents and has been honed by evolution to serve an array of distinct behaviors. Importantly, the vibrissae are moved actively to touch - requiring intricate sensorimotor interactions. Vibrissal touch, therefore, offers ample opportunities to relate different behavioral contexts to specific interactions of distant columns. On the microscopic level, the cortical modules in primary somatosensory cortex process touch inputs at highest magnification and discreteness - each whisker is represented by its own so-called barrel column. The cellular composition, intrinsic connectivity and functional aspects of the barrel column have been studied in great detail. Building on the versatility of genetic tools available in rodents, new, highly selective and flexible cellular and molecular tools to monitor and manipulate neuronal activity have been devised. Researchers have started to combine these with advanced and highly precise behavioral methods, on par with the precision known from monkey preparations. Therefore, the vibrissal touch model system is exquisitely positioned to combine the microscopic with the macroscopic view and promises to be instrumental in our understanding of neocortical function.
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
“Most information about whisker contact with objects is relayed through lemniscal pathway (8, 15, 43) (Fig. 5A).”
From Neural correlates of perceptual decision-making in the primary somatosensory cortex (2026) · cites this paper as [15]
Experimental — accuracy not yet measured
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
The Mouse Brain in Stereotaxic Coordinates
Paxinos, G. (2001) · Cited by 12,859
Distributed hierarchical processing in the primate cerebral cortex
Felleman, D. J., & Van Essen, D. C. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.1.1 · Cited by 7,783
Deep tissue two-photon microscopy
Helmchen, F., & Denk, W. T. (2005) · Nature Methods · doi:10.1038/nmeth818 · Cited by 4,288 · cited 1×
“Two-photon calcium imaging in L2/3 of barrel cortex in vivo (Helmchen and Denk, 2005; Wallace et al., 2008; Grewe and Helmchen, 2009) has provided additional insights into the spatiotemporal aspects of population reponses.”
BackgroundSelf-citationInterneurons of the neocortical inhibitory system
Markram, H., Toledo-Rodriguez, M., Wang, Y., Gupta, A., Silberberg, G., & Wu, C. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1519 · Cited by 2,954 · cited 2×
“This subcellular target structure specificity of the inhibitory neurons’ axon is the hallmark of many classifications and has been suggested to be independent of the laminar location of the cell body within a cortical column (Markram et al., 2004), but this view is far from unequivocal.”
BackgroundDriving fast-spiking cells induces gamma rhythm and controls sensory responses
Cardin, J. A., Carlén, M., Meletis, K., Knoblich, U., Zhang, F., Deisseroth, K., Tsai, L.-H., & Moore, C. I. (2009) · Nature · doi:10.1038/nature08002 · Cited by 2,603
Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators
Tian, L., Hires, S. A., Mao, T., Huber, D., Chiappe, M. E., Chalasani, S. H., Petreanu, L., Akerboom, J., McKinney, S. A., Schreiter, E. R., et al. (2009) · Nature Methods · doi:10.1038/nmeth.1398 · Cited by 1,967 · cited 1×
“Particular potential is offered further by in vivo calcium imaging using genetically-encoded calcium indicators (GECIs) such as GCaMP-3 (Tian et al., 2009) or Yellow Cameleon 3.60 (Nagai et al., 2004; Lütcke et al., 2010).”
MethodInfluentialNEURONAL CIRCUITS OF THE NEOCORTEX
Douglas, R. J., & Martin, K. A. C. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144152 · Cited by 1,886 · cited 3×
“From data obtained in cat visual cortex, Douglas and Martin defined a ‘canonical’ microcircuit of neocortex implying that most cortical areas have a rather similar basic neuronal network structure (Gilbert and Wiesel, 1983; Gilbert, 1983; Douglas and Martin, 1991, 2004).”
BackgroundA resource of Cre driver lines for genetic targeting of GABAergic neurons in cerebral cortex
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 · cited 1×
“…different molecules and their combinations, including oligopeptide co-transmitters, calcium binding proteins, and receptor subunits, suggesting a huge functional variability amongst cortical GABAergic neurons (Markram et al., 2004; Sugino et al., 2006; Ascoli et al., 2008; Taniguchi et al., 2011).”
BackgroundAmaral, D. G., Schumann, C. M., & Nordahl, C. W. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2007.12.005 · Cited by 1,492 · cited 1×
“Knowledge about its development may contribute important aspects needed to understand its mechanisms of operation in the adult, both under physiological as well as pathophysiological conditions, such as neurodevelopmental disorders (for review Amaral et al., 2008; Courchesne et al., 2007).”
BackgroundPetilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex
The Petilla Interneuron Nomenclature Group (PING) (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2402 · Cited by 1,491 · cited 2×
“The literature on neocortical GABAergic neurons is vast and many efforts have been made to describe their features and to characterize their synaptic connections (e.g. Ascoli et al., 2008).”
Background
Research works printed but not linked: 4
- Kölbl, 2010, Fast spiking inhibitory neurons in layer 4 of rat barrel cortex, Acta Physiologica (Oxford), 198, 90
- Oberlaender, 2011, Cell type-specific three-dimensional structure of thalamocortical circuits in a column of rat vibrissal cortex, Cerebral Cortex
- Ramon, 1921, Textura de la corteza visual del gato translation in: Cajal on the cerebral cortex, Archivos de Neurobiologiá, 2, 338
- Waiblinger, 2011, Physical cues used for discrimination of vibrotactile signals in the rat vibrissal system, Society for Neuroscience
Cited by
Sorted by citations
Sleep spindles: mechanisms and functions
Fernandez, L. M. J., & Lüthi, A. (2020) · Physiological Reviews · doi:10.1152/physrev.00042.2018 · Cited by 716
Membrane potential correlates of sensory perception in mouse barrel cortex
Sachidhanandam, S., Sreenivasan, V., Kyriakatos, A., Kremer, Y., & Petersen, C. C. H. (2013) · Nature Neuroscience · doi:10.1038/nn.3532 · Cited by 384
Self-citationA Cellular Resolution Map of Barrel Cortex Activity during Tactile Behavior
Peron, S., Freeman, J., Iyer, V., Guo, C., & Svoboda, K. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.027 · Cited by 334
“Tactile information from individual whiskers is processed in single barrel columns in vS1 (Feldmeyer et al., 2013; Simons, 1978).”
Excitatory neuronal connectivity in the barrel cortex
Feldmeyer, D. (2012) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2012.00024 · Cited by 298
Self-citationLuhmann, H. J., Sinning, A., Yang, J., Reyes‐Puerta, V., Stüttgen, M. C., Kirischuk, S., & Kilb, W. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00040 · Cited by 288
Self-citationMeredith, R. M. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.12.001 · Cited by 262
Bojarskaite, L., Bjørnstad, D. M., Pettersen, K. H., Cunen, C., Hermansen, G. H., Åbjørsbråten, K. S., Chambers, A. R., Sprengel, R., Vervaeke, K., Tang, W., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17062-2 · Cited by 228
Vélez‐Fort, M., Rousseau, C. V., Niedworok, C. J., Wickersham, I. R., Rancz, E. A., Brown, A. P. Y., Strom, M., & Margrie, T. W. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.001 · Cited by 188
“On the other hand, while this approach can provide an overview of connection likelihood and strength— bothwithin (Petersen and Sakmann, 2000) and between (Binzegger et al., 2004; Feldmeyer et al., 2013; Oberlaender et al., 2012) cortical layers and regions—such descriptions are often limited by their cellular and func…”
BackgroundType-I-interferon-responsive microglia shape cortical development and behavior
Escoubas, C. C., Dorman, L. C., Nguyen, P. T., Lagares-Linares, C., Nakajo, H., Anderson, S. R., Barron, J. J., Wade, S. D., Cuevas, B., Vainchtein, I. D., et al. (2024) · Cell · doi:10.1016/j.cell.2024.02.020 · Cited by 179
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
Self-citationBalasco, L., Provenzano, G., & Bozzi, Y. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2019.01016 · Cited by 209
Membrane Potential Dynamics of Neocortical Projection Neurons Driving Target-Specific Signals
Yamashita, T., Pala, A., Pedrido, L., Kremer, Y., Welker, E., & Petersen, C. C. H. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.059 · Cited by 185
“We focused on the primary somatosensory barrel cortex (S1) of mice, which contains a remarkable map of the mystacial vibrissae such that each whisker is individually represented in a well-defined cortical barrel column (Petersen, 2007; Diamond et al., 2008; Feldmeyer et al., 2013).”
Self-citationForli, A., Vecchia, D., Binini, N., Succol, F., Bovetti, S., Moretti, C., Nespoli, F., Mahn, M., Baker, C. A., Bolton, M. M., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.02.063 · Cited by 168
“, 2005) with extended shapes can be used to efficiently stimulate various cellular populations, including principal cells and different interneuron types, in cortical layer 2/3 and in layer 4, the main thalamorecipient lamina in sensory cortex (Feldmeyer et al., 2013).”
BackgroundA genuine layer 4 in motor cortex with prototypical synaptic circuit connectivity
Yamawaki, N., Borges, K., Suter, B. A., Harris, K. D., & Shepherd, G. M. G. (2014) · eLife · doi:10.7554/elife.05422 · Cited by 141
“The apparent absence of L4 in M1 and other agranular cortical areas has long been of interest for its implication that the circuit organization of these areas differs fundamentally from that of sensory areas (Shipp, 2005; Feldmeyer et al., 2013; Shipp et al., 2013; García-Cabezas and Barbas, 2014).”
BackgroundA Theory of How Columns in the Neocortex Enable Learning the Structure of the World
Hawkins, J., Ahmad, S., & Cui, Y. (2017) · Frontiers in Neural Circuits · doi:10.3389/fncir.2017.00081 · Cited by 152
“This type of well-defined structure is most clear in the rat barrel cortex (Lubke et al., 2000; Bureau et al., 2004; Feldmeyer et al., 2013) but Mountcastle and others have pointed out that although there are occasional discontinuities in physiological and anatomical properties, there is a diverse…”
BackgroundDepaulis, A., Olivier David, A., & Charpier, S. (2015) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2015.05.022 · Cited by 151
Neuronal activity patterns in the developing barrel cortex.
Luhmann, H. J., & Khazipov, R. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.025 · Cited by 132
“Although we will focus on a structurally and functionally well defined subregion of the somatosensory cortex, the barrel cortex (for review Petersen, 2007; Feldmeyer et al., 2013), we will also emphasize the role of subcortical structures and the motor system in the generation of activity patterns in the barrel cortex.”
Self-citationValiullina, F., Akhmetshina, D., Nasretdinov, A., Mukhtarov, M. R., Valeeva, G. R., Khazipov, R., & Rozov, A. V. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00001 · Cited by 147
“Layer 4 (L4) is the main input layer of the sensory cortex, which receives and pre-processes information from the thalamus and conveys it to other cortical layers (Petersen, 2007; Feldmeyer, 2012; Feldmeyer et al., 2013).”
BackgroundInhibitory Interneurons and their Circuit Motifs in the Many Layers of the Barrel Cortex
Feldmeyer, D., Qi, G., Emmenegger, V., & Staiger, J. F. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.027 · Cited by 140
Self-citationPOm Thalamocortical Input Drives Layer-Specific Microcircuits in Somatosensory Cortex
Audette, N. J., Urban‐Ciećko, J., Matsushita, M. T., & Barth, A. L. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx044 · Cited by 143
“In addition, weak and delayed inhibition from 5HT3a neurons—in combination with the silencing of SST interneurons—might enable L2 Pyr neurons to be particularly sensitive to delayed and convergent input from other brain areas, such as M1 or S2, or ascending inputs within the column (Feldmeyer et al. 2013; Kinnischtzke…”
El‐Boustani, S., Sermet, B. S., Foustoukos, G., Oram, T. B., Yizhar, O., & Petersen, C. C. H. (2020) · Nature Communications · doi:10.1038/s41467-020-17087-7 · Cited by 138
Self-citationSensory Processing Phenotypes in Fragile X Syndrome
Rais, M., Binder, D. K., Razak, K. A., & Ethell, I. M. (2018) · ASN NEURO · doi:10.1177/1759091418801092 · Cited by 143
“In mice, tactile information received through deflections of whiskers is processed in the somatosensory barrel cortex (Diamond et al., 2008; Diamond & Arabzadeh, 2013; Feldmeyer et al., 2013).”
BackgroundPathway-, layer- and cell-type-specific thalamic input to mouse barrel cortex
Sermet, B. S., Truschow, P., Feyerabend, M., Mayrhofer, J. M., Oram, T. B., Yizhar, O., Staiger, J. F., & Petersen, C. C. H. (2019) · eLife · doi:10.7554/elife.52665 · Cited by 132
Self-citationHow many neurons are sufficient for perception of cortical activity?
Dalgleish, H. W. P., Russell, L. E., Packer, A. M., Roth, A., Gauld, O. M., Greenstreet, F., Thompson, E., & Häusser, M. (2020) · eLife · doi:10.7554/elife.58889 · Cited by 117
Neural coding in barrel cortex during whisker-guided locomotion
Sofroniew, N., Vlasov, Y. A., Hires, S. A., Freeman, J., & Svoboda, K. (2015) · eLife · doi:10.7554/elife.12559 · Cited by 120
“Neurons in different layers are coupled through interlaminar connections which excite both excitatory neurons and inhibitory interneurons in the target layers (Lefort et al., 2009; Hooks et al., 2011; Feldmeyer et al., 2013; Pluta et al., 2015).”
BackgroundThe Cortical States of Wakefulness
Poulet, J. F. A., & Crochet, S. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2018.00064 · Cited by 126
“It is therefore considered to be a ‘‘higherorder’’ thalamic nucleus (Feldmeyer et al., 2013; Groh et al., 2014; Jouhanneau et al., 2014; Sherman, 2016).”
BackgroundSelf-citationCell Type-Specific Structural Organization of the Six Layers in Rat Barrel Cortex
Narayanan, R. T., Udvary, D., & Oberlaender, M. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00091 · Cited by 100
“though the cell types are purely defined by dendrite morphology, intrinsic properties (Feldmeyer et al., 2013), in vivo function (de Kock et al.”
BackgroundResultInfluentialActive touch and self-motion encoding by Merkel cell-associated afferents
Severson, K. S., Xu, D., de Loo, M. M. V., Bai, L., Ginty, D., & O'Connor, D. H. (2017) · Neuron · doi:10.1016/j.neuron.2017.03.045 · Cited by 108
“Yet these brainstem nuclei originate distinct pathways for somatosensory signals ascending to the cortex, with markedly different response properties (reviewed in: Bosman et al., 2011; Diamond et al., 2008; Feldmeyer et al., 2013; Kleinfeld andDeschênes, 2011).”
Narayanan, R. T., Egger, R., Johnson, A. S., Mansvelder, H. D., Sakmann, B. J., de Kock, C. P. J., & Oberlaender, M. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv053 · Cited by 104
“Our sample comprises all previously reported dendritic cell types of excitatory neurons in rat vS1 (Feldmeyer et al. 2013).”
Michaelson, S. D., Ozkan, E. D., Aceti, M., Maity, S., Llamosas, N., Weldon, M., Mizrachi, E., Vaissière, T., Gaffield, M. A., Christie, J. M., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0268-0 · Cited by 113
Sensory input drives rapid homeostatic scaling of the axon initial segment in mouse barrel cortex
Jamann, N., Dannehl, D., Lehmann, N., Wagener, R. J., Thielemann, C., Schultz, C., Staiger, J. F., Kole, M. H. P., & Engelhardt, M. (2021) · Nature Communications · doi:10.1038/s41467-020-20232-x · Cited by 101
“To explore AIS plasticity in a behaviorally-relevant context, we utilized the mouse whisker-to-barrel system (Feldmeyer et al., 2013; Stuttgen and Schwarz, 2018).”
BackgroundMethodInfluentialSelf-citationMulti-channel fiber photometry for population neuronal activity recording
Guo, Q., Zhou, J., Feng, Q., Lin, R., Gong, H., Luo, Q., Zeng, S., Luo, M., & Fu, L. (2015) · Biomedical Optics Express · doi:10.1364/boe.6.003919 · Cited by 107
Rapid Plasticity of Higher-Order Thalamocortical Inputs during Sensory Learning
Audette, N. J., Bernhard, S. M., Ray, A., Stewart, L. T., & Barth, A. L. (2019) · Neuron · doi:10.1016/j.neuron.2019.04.037 · Cited by 102
“VPM neurons receive ascending sensory information directly from the trigeminal brain stem nucleus and respond robustly to the deflection of a single whisker (Feldmeyer et al., 2013).”
High-speed low-light in vivo two-photon voltage imaging of large neuronal populations
Platiša, J., Ye, X., Ahrens, A. M., Liu, C., Chen, A., Davison, I. G., Tian, L., Pieribone, V. A., & Chen, J. L. (2023) · Nature Methods · doi:10.1038/s41592-023-01820-3 · Cited by 101
Diverse Long-Range Axonal Projections of Excitatory Layer 2/3 Neurons in Mouse Barrel Cortex
Yamashita, T., Vavladeli, A., Pala, A., Galan, K., Crochet, S., Petersen, S. S. A., & Petersen, C. C. H. (2018) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00033 · Cited by 100
“The mouse primary somatosensory barrel cortex (wS1) is an anatomically-defined brain region specialized in processing whisker sensory information (Woolsey and Van der Loos, 1970; Petersen, 2007; Diamond et al., 2008; Feldmeyer et al., 2013).”
BackgroundSelf-citationReyes‐Puerta, V., Sun, J., Kim, S., Kilb, W., & Luhmann, H. J. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu007 · Cited by 95
“The paralemniscar pathway could play a major role in the PC, where L5st cells showed an overrepresentation of intracolumnar activity; at the same time, the lemniscar pathway could be responsible for propagating the intracolumnar synchronization horizontally—thus attributing different but complementary roles to both pa…”
BackgroundResultInfluentialSelf-citationLayer-Specific Refinement of Sensory Coding in Developing Mouse Barrel Cortex
van der Bourg, A., Yang, J., Reyes‐Puerta, V., Laurenczy, B., Wieckhorst, M., Stüttgen, M. C., Luhmann, H. J., & Helmchen, F. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw280 · Cited by 98
“Although the formation and anatomical refinement of barrel cortex organization during development has been extensively studied (van der Loos and Woolsey 1973; Erzurumlu and Gaspar 2012; Feldmeyer et al. 2013), little is known about the corresponding functional changes, especially how whiskerevoked cortical activity de…”
BackgroundSelf-citationThalamic reticular control of local sleep in mouse sensory cortex
Fernandez, L. M. J., Vantomme, G., Osorio-Forero, A., Cardis, R., Béard, E., & Lüthi, A. (2018) · eLife · doi:10.7554/elife.39111 · Cited by 88
Cell-type-specific nicotinic input disinhibits mouse barrel cortex during active sensing
Gasselin, C., Hohl, B., Vernet, A., Crochet, S., & Petersen, C. C. H. (2021) · Neuron · doi:10.1016/j.neuron.2020.12.018 · Cited by 90
“In this study, we investigated functional roles of VIP neurons in the primary whisker somatosensory barrel cortex (wS1), a cortical region important for processing whisker-related sensorimotor information inmice (Bosmanet al., 2011; Diamond et al., 2008; Feldmeyer et al., 2013; Petersen, 2019).”
Self-citationDoll, C. A., & Broadie, K. S. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00030 · Cited by 86
“Furthermore, individual modalities develop progressively, as the critical periods of rodent somatosensory cortex begin at the subcortical level and then progress to cortical levels (Feldmeyer et al., 2013).”
BackgroundActivity-Dependent Axonal Plasticity in Sensory Systems
Jamann, N., Jordan, M., & Engelhardt, M. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.07.035 · Cited by 95
Pathophysiology of absence epilepsy: Insights from genetic models
Depaulis, A., & Charpier, S. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.02.035 · Cited by 86
A somatosensory circuit for cooling perception in mice
Milenkovic, N., Zhao, W., Walcher, J., Albert, T., Siemens, J., Lewin, G. R., & Poulet, J. F. A. (2014) · Nature Neuroscience · doi:10.1038/nn.3828 · Cited by 84
Self-citationThe fractal brain: scale-invariance in structure and dynamics
Grosu, G. F., Hopp, A. V., Moca, V. V., Bârzan, H., Ciuparu, A., Ercsey-Ravasz, M., Winkel, M., Linde, H., & Muresan, R. C. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac363 · Cited by 87
“Cortical minicolumns (Mountcastle 1997) and the barrel cortex (Petersen 2007; Feldmeyer et al. 2013) are good examples.”
BackgroundCrandall, S. R., Patrick, S. L., Cruikshank, S. J., & Connors, B. W. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.11.049 · Cited by 75
“The prevailing view of the barrel cortex is that it contains no cytoarchitectonic counterparts of barrels outside of L4 (Feldmeyer et al., 2013; Woolsey and Van der Loos, 1970).”
BackgroundInfluentialNaskar, S., Qi, J., Pereira, F., Gerfen, C. R., & Lee, S. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108774 · Cited by 76
“In the primary somatosensory cortex, for example, neurons that project to the primary motor cortex and the secondary somatosensory cortex mostly do not overlap, suggesting potential subpopulations of Pyr neurons within supragranular IT types, on the basis of their projection specificity (Feldmeyer et al., 2013; Sato a…”
Cortical Control of Whisker Movement
Petersen, C. C. H. (2014) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062012-170344 · Cited by 75
Self-citationHarding-Forrester, S., & Feldman, D. E. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63622-5.00004-8 · Cited by 77
Towards a “canonical” agranular cortical microcircuit
Beul, S. F., & Hilgetag, C. C. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00165 · Cited by 71
“J. Neurophysiol. 20, 408–434. Otsuka, T., and Kawaguchi, Y. (2008). Firing-Pattern-Dependent specificity of”
BackgroundInfluentialRomo, R., & Rossi-Pool, R. (2020) · Neuron · doi:10.1016/j.neuron.2019.11.033 · Cited by 72
Neural Circuits for Goal-Directed Sensorimotor Transformations
Crochet, S., Lee, S., & Petersen, C. C. H. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.08.011 · Cited by 69
Self-citationBrain-wide map of efferent projections from rat barrel cortex
Zakiewicz, I. M., Bjaalie, J. G., & Leergaard, T. B. (2014) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2014.00005 · Cited by 68
“…Lin, 1984; Dawson and Killackey, 1987; Welker et al., 1988; Fabri and Burton, 1991a) has made the rat barrel cortex a common model for anatomical and physiological investigations of sensory processing and brain plasticity (Petersen, 2007; Alloway, 2008; Wiest et al., 2008; Feldmeyer et al., 2013).”
BackgroundInfluentialCircuit organization of the excitatory sensorimotor loop through hand/forelimb S1 and M1
Yamawaki, N., Tapies, M. G. R., Stults, A. M., Smith, G. A., & Shepherd, G. M. (2021) · eLife · doi:10.7554/elife.66836 · Cited by 60
“In contrast, much is known about the circuit connections and structure-function relationships in corresponding transcortical pathways in the whisker-barrel system of rats and mice (Feldmeyer, 2012; Feldmeyer et al., 2013; Petersen, 2019; Staiger and Petersen, 2020).”
BackgroundBarrel Cortex Membrane Potential Dynamics in Social Touch
Lenschow, C., & Brecht, M. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.059 · Cited by 59
“They do so by their mobile whiskers, which also sense the environment, obstacles , gaps, and different textures or objects (Diamond et al., 2008; Feldmeyer et al., 2013).”
Self-citationHackett, T. A., de la Mothe, L. A., Camalier, C. R., Falchier, A., Lakatos, P., Kajikawa, Y., & Schroeder, C. E. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00072 · Cited by 64
“…cortex have since progressed toward defining the connections of morphologically and neurochemically distinct neuronal subpopulations in every layer and sublayer (Callaway, 2002; Thomson and Bannister, 2003; Bannister, 2005; Douglas and Martin, 2007; Briggs, 2010; Feldmeyer et al., 2013).”
BackgroundMethodInfluentialJuczewski, K., von Richthofen, H. J., Bagni, C., Celikel, T., Fisone, G., & Krieger, P. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.09.007 · Cited by 59
Staiger, J. F., Bojak, I., Miceli, S., & Schubert, D. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0726-8 · Cited by 60
“these neurons, as well as their functional diversity (Chen et al. 2013; Feldmeyer et al. 2013; Houweling and Brecht 2008; Oberlaender et al. 2012; Petersen and Crochet 2013; Sato and Svoboda 2010).”
Self-citationJarre, G., Altwegg‐Boussac, T., Williams, M. S., Studer, F., Chipaux, M., Olivier David, A., Charpier, S., Depaulis, A., Mahon, S., & Guillemain, I. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx174 · Cited by 57
“This could be caused by the rapid development of neocortical networks during the first weeks of life, including an increased synaptic connectivity between pyramidal neurons and a refinement of sensory maps, which results in an amplification of sensoryevoked depolarizing synaptic responses (Micheva and Beaulieu 1996; S…”
BackgroundCortical Output Is Gated by Horizontally Projecting Neurons in the Deep Layers
Egger, R., Narayanan, R. T., Guest, J. M., Bast, A., Udvary, D., Messore, L. F., Das, S., de Kock, C. P. J., & Oberlaender, M. (2019) · Neuron · doi:10.1016/j.neuron.2019.10.011 · Cited by 55
“Similar to L4SPs, which cluster around the dense terminal fields of VPM axons (Feldmeyer et al., 2013), we find that L6CCs cluster around the second innervation domain of VPM axons at the layer 5/6 border.”
Antonini, A., Sattin, A., Moroni, M., Bovetti, S., Moretti, C., Succol, F., Forli, A., Vecchia, D., Rajamanickam, V. P., Bertoncini, A., et al. (2020) · eLife · doi:10.7554/elife.58882 · Cited by 56
Spindle Bursts in Neonatal Rat Cerebral Cortex
Yang, J., Reyes‐Puerta, V., Kilb, W., & Luhmann, H. J. (2016) · Neural Plasticity · doi:10.1155/2016/3467832 · Cited by 55
“At this age a local, functionally defined lesion in the VPM blocks the whisker stimulationinduced cortical responses and also profoundly reduces the spontaneously occurring cortical burst activity [18], further demonstrating that the majority of the spontaneous spindle bursts in P0-P1 rat barrel cortex are generated i…”
BackgroundSelf-citationDomanski, A. P. F., Booker, S. A., Wyllie, D. J. A., Isaac, J. T. R., & Kind, P. C. (2019) · Nature Communications · doi:10.1038/s41467-019-12736-y · Cited by 59
Models of cortical malformation—Chemical and physical
Luhmann, H. J. (2015) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2015.03.034 · Cited by 54
Self-citationThalamic Drive of Cortical Parvalbumin-Positive Interneurons during Down States in Anesthetized Mice
Zucca, S., Pasquale, V., Roig, P. L. D. L., Panzeri, S., & Fellin, T. (2019) · Current Biology · doi:10.1016/j.cub.2019.04.007 · Cited by 51
The development of synaptic transmission is time-locked to early social behaviors in rats
Naskar, S., Narducci, R., Balzani, E., Cwetsch, A. W., Tucci, V., & Cancedda, L. (2019) · Nature Communications · doi:10.1038/s41467-019-09156-3 · Cited by 57
Inhibition in the auditory cortex
Studer, F., & Barkat, T. R. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.11.021 · Cited by 56
Jung, W. B., Jiang, H., Lee, S., & Kim, S. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2113313119 · Cited by 53
“In the current study, we adopted a widely investigated somatosensory network involving multiple brain regions, such as the first-order ventral posterior thalamic nucleus, higherorder posterior medial thalamic nucleus (POm), primary somatosensory cortex (S1), secondary somatosensory cortex (S2), and primary motor corte…”
MethodImprecise Whisker Map in the Neonatal Rat Barrel Cortex
Mitrukhina, O., Suchkov, D., Khazipov, R., & Minlebaev, M. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu169 · Cited by 52
Miceli, S., Negwer, M., van Eijs, F., Kalkhoven, C., van Lierop, I., Homberg, J., & Schubert, D. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00088 · Cited by 49
“…networks, which form the backbone of early intracortical processing of tactile sensory information (for review see Brecht, 2007; Petersen, 2007; Feldmeyer et al., 2013), we found (i) a reduced dendritic complexity of SpSt cells within the layer IV barrels, (ii) a decrease in the intracolumnar…”
BackgroundEmergent Exploration via Novelty Management
Gordon, G., Fonio, E., & Ahissar, E. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1872-14.2014 · Cited by 52
“, cerebellum (Lalazar and Vaadia, 2008; Shadmehr and Krakauer, 2008) and sensory perception areas, such as primary sensory cortices (Matyas et al., 2010; Bastos et al., 2012; Feldmeyer et al., 2013)].”
Backgroundde Kock, C. P. J., Pie, J. L., Pieneman, A. W., Mease, R. A., Bast, A., Guest, J. M., Oberlaender, M., Mansvelder, H. D., & Sakmann, B. J. (2021) · Communications Biology · doi:10.1038/s42003-021-02241-8 · Cited by 47
Qi, G., van Aerde, K. I., Abel, T. G., & Feldmeyer, D. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw243 · Cited by 47
Self-citationSurround Integration Organizes a Spatial Map during Active Sensation
Pluta, S. R., Lyall, E. H., Telian, G. I., Ryapolova-Webb, E. S., & Adesnik, H. (2017) · Neuron · doi:10.1016/j.neuron.2017.04.026 · Cited by 46
“The rodent whisker system is an advantageous system to address this question (Brecht, 2007; Feldmeyer et al., 2013; Petersen, 2007).”
BackgroundRollenhagen, A., Klook, K., Sätzler, K., Qi, G., Anstötz, M., Feldmeyer, D., & Lübke, J. H. R. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0850-5 · Cited by 54
“…studies of layer 4 connections (Feldmeyer et al. 1999, 2005, 2006; Egger et al. 1999; Silver et al. 2003; Ramirez et al. 2014; for review see Feldmeyer et al. 2013), relatively little is known about the quantitative geometry of intracortical synaptic boutons terminating on L4 excitatory…”
BackgroundSelf-citationCharacterization and Distribution of Reelin-Positive Interneuron Subtypes in the Rat Barrel Cortex
Pohlkamp, T., Dávid, C., Cauli, B., Gallopin, T., Bouché, E., Karagiannis, A., May, P., Herz, J., Frotscher, M., Staiger, J. F., et al. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht161 · Cited by 46
“It comprises a multitude of 43 additional molecular, electrophysiological, and morphological parameters of single neurons in the somatosensory barrel cortex, a major cortical model system to study the development of neurons and their assembly into functional circuits (Feldmeyer et al. 2012).”
BackgroundSelf-citationThe Posterior Parietal Cortex as Integrative Hub for Whisker Sensorimotor Information
Mohan, H., de Haan, R., Mansvelder, H. D., & de Kock, C. P. J. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.06.020 · Cited by 47
“are part of the lemniscal pathway, which is traditionally considered to carry exafferent sensory information (Feldmeyer et al., 2013).”
InfluentialBarrel Cortex: What is it Good for?
Stüttgen, M. C., & Schwarz, C. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.05.009 · Cited by 46
Self-citationGuy, J., Wagener, R. J., Möck, M., & Staiger, J. F. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu052 · Cited by 47
“ganizing principle in the otherwise disorganized reeler cortex (Mountcastle et al. 1955; Mountcastle 1957, 1997; Petersen and Sakmann 2001; Horton and Adams 2005; Feldmeyer et al. 2013).”
BackgroundSelf-citationKroon, T., Sierksma, M. C., & Meredith, R. M. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00075 · Cited by 45
“…observed in thalamocortical pathways: in Fmr1-KO mice, enhanced NMDA/AMPA synaptic ratios and altered plasticity occur during the first but not by the end of the second postnatal week, indicating developmental delays within the neurotypical critical period for this pathway (Harlow et al., 2010).”
BackgroundInfluentialOlfactory Development, Part 1: Function, From Fetal Perception to Adult Wine-Tasting
Sarnat, H. B., Flores‐Sarnat, L., & Wei, X. (2017) · Journal of Child Neurology · doi:10.1177/0883073817690867 · Cited by 42
“The synaptic organization of the olfactory bulb includes structural and functional columns,(43,44) similar to the barrels or radial units of the neocortex.(45,46) Lateral synaptic connectivity within the olfactory bulb is much sparser.”
BackgroundSensory coding is impaired in rat absence epilepsy
Studer, F., Laghouati, E., Jarre, G., Olivier David, A., Pouyatos, B., & Depaulis, A. (2018) · The Journal of Physiology · doi:10.1113/jp277297 · Cited by 42
“Accordingly, whisker-related information is processed by highlyorganized neuronal circuits from the barrel-field primary somatosensory cortex (S1Bf) (Feldmeyer et al. 2013; Crochet et al. 2018).”
BackgroundWhite matter structure and myelin-related gene expression alterations with experience in adult rats
Sampaio‐Baptista, C., Vallès, A., Khrapitchev, A. A., Akkermans, G., Winkler, A. M., Foxley, S., Sibson, N. R., Roberts, M. J., Miller, K. L., Diamond, M. E., et al. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101770 · Cited by 41
“These are relevant WM regions for the texture detection task in the light of the barrel cortex’s role in somatosensory information processing (for review see (Feldmeyer et al., 2013)).”
BackgroundFazlali, Z., Ranjbar‐Slamloo, Y., Adibi, M., & Arabzadeh, E. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00014 · Cited by 39
“…cortex, also known as the barrel cortex (BC) is a well-established model of cortical processing with an elegant cortical organization and high level of functional efficiency (Brecht et al., 1997; Petersen, 2007; Kleinfeld and Deschênes, 2011; Diamond and Arabzadeh, 2013; Feldmeyer et al., 2013).”
BackgroundDevelopment of the whisker-to-barrel cortex system
Yang, J., Kilb, W., Kirischuk, S., Unichenko, P., Stüttgen, M. C., & Luhmann, H. J. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.04.023 · Cited by 41
Self-citationŞencan, İ., Esipova, T., Kılıç, K., Li, B., Desjardins, M., Yaseen, M. A., Wang, H., Porter, J. E., Kura, S., Fu, B., et al. (2020) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x20928011 · Cited by 41
Lefort, S., & Petersen, C. C. H. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx094 · Cited by 38
“Here, we focus on the mouse C2 barrel column, a region of primary somatosensory cortex involved in processing tactile information relating to the C2 whisker (Petersen 2007; Feldmeyer et al. 2013).”
BackgroundSelf-citationRollenhagen, A., Ohana, O., Sätzler, K., Hilgetag, C. C., Kuhl, D., & Lübke, J. H. R. (2018) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2018.00024 · Cited by 45
“Multiple patch-clamp recordings in-vitro and in-vivo revealed a great diversity among cortical synapses with respect to their size, reliability, and temporal dynamics (reviewed by Lübke and Feldmeyer, 2007; Feldmeyer et al., 2013).”
BackgroundOptogenetic Stimulation of Cortex to Map Evoked Whisker Movements in Awake Head-Restrained Mice
Auffret, M., Ravano, V., Rossi, G. M. C., Hankov, N., Petersen, M. F. A., & Petersen, C. C. H. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.04.004 · Cited by 38
“Rodents use their array of mystacial whiskers to obtain tactile information about their immediate facial surroundings (Brecht, 2007; Petersen, 2007; Diamond et al., 2008; Bosman et al., 2011; Feldmeyer et al., 2013).”
Self-citationNeocortical dynamics during whisker-based sensory discrimination in head-restrained mice
Helmchen, F., Gilad, A., & Chen, J. L. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2017.09.003 · Cited by 38
“The rodent whisker-system has become a popular model system for studying tactile information processing due to is neuroethological relevance (Feldmeyer et al., 2013; Petersen, 2007).”
Self-citationAlmási, Z., Dávid, C., Witte, M., & Staiger, J. F. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2019.00045 · Cited by 38
Self-citationExcitatory neuronal CHD8 in the regulation of neocortical development and sensory-motor behaviors
Kweon, H., Jung, W. B., Im, G. H., Ryoo, J., Lee, J.-H., Do, H., Choi, Y., Song, Y.-H., Jung, H., Park, H., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108780 · Cited by 36
Castejon, C., Barros-Zulaica, N., & Núñez, Á. (2016) · PLoS ONE · doi:10.1371/journal.pone.0148169 · Cited by 38
Devilbiss, D. M. (2018) · Brain Research · doi:10.1016/j.brainres.2018.06.015 · Cited by 33
Developmental Switch in Neurovascular Coupling in the Immature Rodent Barrel Cortex
Zehendner, C. M., Tsohataridis, S., Luhmann, H. J., & Yang, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080749 · Cited by 36
“Sensory information in the mammalian cortex is processed in highly organized neuronal networks such as cortical columns[1,2].”
BackgroundSelf-citationCortical neurons and networks are dormant but fully responsive during isoelectric brain state
Altwegg‐Boussac, T., Schramm, A. E., Ballestero, J. A., Grosselin, F., Chávez, M., Lecas, S., Baulac, M., Naccache, L., Demeret, S., Navarro, V., et al. (2017) · Brain · doi:10.1093/brain/awx175 · Cited by 35
“4D, inset) and posteromedial nuclei, which are interconnected with S1 (Feldmeyer et al., 2013).”
Opposing Influence of Sensory and Motor Cortical Input on Striatal Circuitry and Choice Behavior
Lee, C. R., Yonk, A. J., Wiskerke, J., Paradiso, K. G., Tepper, J. M., & Margolis, D. J. (2019) · Current Biology · doi:10.1016/j.cub.2019.03.028 · Cited by 36
Simanaviciute, U., Ahmed, J., Brown, R. E., Connor‐Robson, N., Farr, T. D., Fertan, E., Gambles, N., Garland, H., Morton, A. J., Staiger, J. F., et al. (2019) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2019.108532 · Cited by 32
Self-citationA radial map of multi-whisker correlation selectivity in the rat barrel cortex
Estebanez, L., Bertherat, J., Shulz, D. E., Bourdieu, L., & Léger, J. (2016) · Nature Communications · doi:10.1038/ncomms13528 · Cited by 33
Response dynamics of rat barrel cortex neurons to repeated sensory stimulation
Kheradpezhouh, E., Adibi, M., & Arabzadeh, E. (2017) · Scientific Reports · doi:10.1038/s41598-017-11477-6 · Cited by 40
Organization of Sensory Feature Selectivity in the Whisker System
Bale, M. R., & Maravall, M. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.09.014 · Cited by 31
“Work on the structure and physiology of neuronal circuits across the whisker pathway has accumulated at an accelerating pace (Feldmeyer et al., 2013; Fox, 2017).”
Metadata
- Authors
- Feldmeyer, D., Brecht, M., Helmchen, F., Petersen, C. C. H., Poulet, J. F. A., Staiger, J. F., Luhmann, H. J., & Schwarz, C.
- Affiliations
- Forschungszentrum Jülich (DE)
- Humboldt-Universität zu Berlin (DE)
- University of Zurich (CH)
- École Polytechnique Fédérale de Lausanne (CH)
- Max Delbrück Center (DE)
- University of Göttingen (DE)
- University Medical Center of the Johannes Gutenberg University Mainz (DE)
- Hertie Institute for Clinical Brain Research (DE)
- Corresponding author
- Schwarz, Cornelius
- ORCID
- Venue
- Progress in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2013-04
- Volume
- 103
- Pages
- 3-27
- ISSN
- 0301-0082 (ISSN-L)
- OpenAlex
- W2119610099
- Cited by
- 354
- References
- 338
- Citations by year
- 2026: 15 · 2025: 22 · 2024: 14 · 2023: 15 · 2022: 18 · 2021: 31 · 2020: 31 · 2019: 35 · 2018: 26 · 2017: 37 · 2016: 32 · 2015: 32 · 2014: 29 · 2013: 16
- FWCI
- 1.98
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Progress in Neurobiology (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- MDC Repository (Max-Delbrueck-Center for Molecular Medicine) (acceptedVersion)
- GoeScholar The Publication Server of the Georg-August-Universität Göttingen (Georg-August-Universität Göttingen) (acceptedVersion, other-oa)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
- GRO (submittedVersion, cc-by-nc-nd)
- RWTH Publications (RWTH Aachen) (submittedVersion, other-oa)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion)
- Funders
- Swiss National Science Foundation (SNSF)
- Deutsche Forschungsgemeinschaft (FOR 1341)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Tactile and Sensory Interactions
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- barrel cortex, barrel columns, neocortex, whisker representation, primary somatosensory cortex, cortical microcircuits, sensorimotor integration, genetic instruments, rodent behavior, cortical connectivity
- MeSH terms
- Afferent Pathways, Animals, Somatosensory Cortex, Vibrissae, Neocortex, Mice, Rats, Touch Perception
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