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Long‐range connectivity of mouse primary somatosensory barrel cortex
Open accessAbstract
The primary somatosensory barrel cortex processes tactile vibrissae information, allowing rodents to actively perceive spatial and textural features of their immediate surroundings. Each whisker on the snout is individually represented in the neocortex by an anatomically identifiable ‘barrel’ specified by the segregated termination zones of thalamocortical axons of the ventroposterior medial nucleus, which provide the primary sensory input to the neocortex. The sensory information is subsequently processed within local synaptically connected neocortical microcircuits, which have begun to be investigated in quantitative detail. In addition to these local synaptic microcircuits, the excitatory pyramidal neurons of the barrel cortex send and receive long‐range glutamatergic axonal projections to and from a wide variety of specific brain regions. Much less is known about these long‐range connections and their contribution to sensory processing. Here, we review current knowledge of the long‐range axonal input and output of the mouse primary somatosensory barrel cortex. Prominent reciprocal projections are found between primary somatosensory cortex and secondary somatosensory cortex, motor cortex, perirhinal cortex and thalamus. Primary somatosensory barrel cortex also projects strongly to striatum, thalamic reticular nucleus, zona incerta, anterior pretectal nucleus, superior colliculus, pons, red nucleus and spinal trigeminal brain stem nuclei. These long‐range connections of the barrel cortex with other specific cortical and subcortical brain regions are likely to play a crucial role in sensorimotor integration, sensory perception and associative learning.
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“In contrast, sensory S1 and S2 cortices have strongly lateralized ipsilateral outputs (43, 59) and are densely and reciprocally interconnected (60) forming a top–down feedback loop that exhibits choice-related activity (10, 11, 22–25).”
From Neural correlates of perceptual decision-making in the primary somatosensory cortex (2026) · cites this paper as [60]
In the citing paper
“Similarly, the somatosensory pathway is composed of primary and secondary somatosensory cortical areas (SSp and SSs) and thalamic nuclei VPM, VPL and PO48,74”
From A mesoscale connectome of the mouse brain (2014) · cites this paper as [48]
Citations
Cites
The Mouse Brain in Stereotaxic Coordinates
Paxinos, G. (2001) · Cited by 12,859
Genome-wide atlas of gene expression in the adult mouse brain
Lein, E. S., Hawrylycz, M. J., Ao, N., Ayres, M., Bensinger, A., Bernard, A., Boe, A. F., Boguski, M. S., Brockway, K. S., Byrnes, E. J., et al. (2007) · Nature · doi:10.1038/nature05453 · Cited by 5,572
Generalized lacZ expression with the ROSA26 Cre reporter strain
Soriano, P. (1999) · Nature Genetics · doi:10.1038/5007 · Cited by 5,237
Millisecond-timescale, genetically targeted optical control of neural activity
Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G., & Deisseroth, K. A. (2005) · Nature Neuroscience · doi:10.1038/nn1525 · Cited by 5,015
Channelrhodopsin-2, a directly light-gated cation-selective membrane channel
Nagel, G., Szellas, T., Huhn, W., Kateriya, S., Adeishvili, N., Berthold, P. R., Ollig, D., Hegemann, P., & Bamberg, E. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1936192100 · Cited by 2,730
Parvalbumin neurons and gamma rhythms enhance cortical circuit performance
Sohal, V. S., Zhang, F., Yizhar, O., & Deisseroth, K. (2009) · Nature · doi:10.1038/nature07991 · Cited by 2,606
Driving 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
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
Transgenic strategies for combinatorial expression of fluorescent proteins in the nervous system
Livet, J., Weissman, T. A., Kang, H., Draft, R. W., Lu, J., Bennis, R. A., Sanes, J. R., & Lichtman, J. W. (2007) · Nature · doi:10.1038/nature06293 · Cited by 1,876
Cerebellum and nonmotor function
Strick, P. L., Dum, R. P., & Fiez, J. A. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125606 · Cited by 1,777
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Oh, S. W., Harris, J. A., Ng, L., Winslow, B., Cain, N., Mihalas, S., Wang, Q., Lau, C., Kuan, L., Henry, A. M., et al. (2014) · Nature · doi:10.1038/nature13186 · Cited by 2,612
Zingg, B., Chou, X.-L., Zhang, Z., Mesik, L., Liang, F., Tao, H. W., & Zhang, L. I. (2016) · Neuron · doi:10.1016/j.neuron.2016.11.045 · Cited by 775
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Mao, T., Kusefoglu, D., Hooks, B. M., Huber, D., Petreanu, L., & Svoboda, K. (2011) · Neuron · doi:10.1016/j.neuron.2011.07.029 · Cited by 538
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Mátyás, F., Sreenivasan, V., Marbach, F., Wacongne, C., Barsy, B., Matéo, C., Aronoff, R., & Petersen, C. C. H. (2010) · Science · doi:10.1126/science.1195797 · Cited by 428
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
“…exist with bilateral perirhinal cortex (Chakrabarti and Alloway, 2006; Ferezou et al., 2007; Sato and Svoboda, 2010; Aronoff et al., 2010), the contralateral somatosensory cortex (Petreanu et al., 2007), and contralateral motor cortex and ipsilateral orbitofrontal cortex (Aronoff et al., 2010).”
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Luhmann, 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
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Self-citationGong, H., Zeng, S., Yan, C., Lv, X., Yang, Z., Xu, T., Feng, Z., Ding, W., Qi, X., Li, A., et al. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.02.005 · Cited by 247
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Staiger, J. F., & Petersen, C. C. H. (2021) · Physiological Reviews · doi:10.1152/physrev.00019.2019 · Cited by 165
Self-citationPathway-specific reorganization of projection neurons in somatosensory cortex during learning
Chen, J. L., Margolis, D. J., Stankov, A. D., Sumanovski, L. T., Schneider, B. L., & Helmchen, F. (2015) · Nature Neuroscience · doi:10.1038/nn.4046 · Cited by 182
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Self-citationVanni, M. P., & Murphy, T. H. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.1818-14.2014 · Cited by 177
Comoli, E., Favaro, P. D., Vautrelle, N., Leriche, M., Overton, P. G., & Redgrave, P. (2012) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2012.00009 · Cited by 175
Merre, P. L., Esmaeili, V., Charrière, E., Galan, K., Salin, P. A., Petersen, C. C. H., & Crochet, S. (2017) · Neuron · doi:10.1016/j.neuron.2017.11.031 · Cited by 171
Self-citationShort- and long-latency afferent inhibition; uses, mechanisms and influencing factors
Turco, C. V., El‐Sayes, J., Savoie, M. J., Fassett, H. J., Locke, M. B., & Nelson, A. J. (2017) · Brain stimulation · doi:10.1016/j.brs.2017.09.009 · Cited by 162
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Niethard, N., Hasegawa, M., Itokazu, T., Oyanedel, C. N., Born, J., & Sato, T. R. (2016) · Current Biology · doi:10.1016/j.cub.2016.08.035 · Cited by 140
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Bergmann, E., Zur, G., Bershadsky, G., & Kahn, I. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw327 · Cited by 99
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Stehberg, J., Dang, P. T., & Frostig, R. D. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00093 · Cited by 78
Naskar, S., Qi, J., Pereira, F., Gerfen, C. R., & Lee, S. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.108774 · Cited by 76
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Self-citationPlomp, G., Quairiaux, C., Michel, C. M., & Astolfi, L. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.04.016 · Cited by 70
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Crochet, S., Lee, S., & Petersen, C. C. H. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.08.011 · Cited by 69
Self-citationFreyer, F., Reinacher, M., Nolte, G., Dinse, H. R., & Ritter, P. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00144 · Cited by 67
Grønli, J., Rempe, M. J., Clegern, W. C., Schmidt, M. A., & Wisor, J. P. (2016) · Journal of Sleep Research · doi:10.1111/jsr.12380 · Cited by 65
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Vinck, M. A., Bos, J. J., Mourik-Donga, L. A. V., Oplaat, K. T., Klein, G. A., Jackson, J. C., Gentet, L. J., & Pennartz, C. M. A. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00187 · Cited by 60
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Jung, W. B., Shim, H., & Kim, S. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.03.063 · Cited by 62
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Wang, D., Zhao, J. W., Gao, Z., Chen, N., Wen, B., Lu, W., Lei, Z., Chen, C., Liu, Y., Feng, J., et al. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00320 · Cited by 55
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Rahmati, N., Owens, C. B., Bosman, L. W. J., Spanke, J. K., Lindeman, S., Gong, W., Potters, J.-W., Romano, V., Voges, K., Moscato, L., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2966-13.2014 · Cited by 53
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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
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
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Cash, R. F. H., Isayama, R., Gunraj, C. A., Ni, Z., & Chen, R. E. (2015) · The Journal of Physiology · doi:10.1113/jphysiol.2014.286245 · Cited by 52
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Gao, Z., Chen, L., Fan, R., Lu, W., Wang, D., Cui, S., Huang, L. T., Zhao, S., Guan, S., Zhu, Y., et al. (2016) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2016.00285 · Cited by 47
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Guo, C., Peng, J., Zhang, Y., Li, A., Li, Y., Yuan, J., Xu, X., Ren, M., Gong, H., & Chen, S. (2017) · Scientific Reports · doi:10.1038/s41598-017-03000-8 · Cited by 47
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Haruta, M., Kitsumoto, C., Sunaga, Y., Takehara, H., Noda, T., Sasagawa, K., Tokuda, T., & Ohta, J. (2014) · Japanese Journal of Applied Physics · doi:10.7567/jjap.53.04el05 · Cited by 46
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Wang, Q., Henry, A. M., Harris, J. A., Oh, S. W., Joines, K. M., Nyhus, J., Hirokawa, K. E., Dee, N., Mortrud, M., Parry, S., et al. (2014) · Journal of Comparative Neurology · doi:10.1002/cne.23567 · Cited by 44
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Wolf, A. B., Lintz, M. J., Costabile, J. D., Thompson, J. A., Stubblefield, E. A., & Felsen, G. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00262.2015 · Cited by 45
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Ohara, S., Gianatti, M., Itou, K., Berndtsson, C. H., Doan, T. P., Kitanishi, T., Mizuseki, K., Iijima, T., Tsutsui, K., & Witter, M. P. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2019.00054 · Cited by 44
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Metadata
- Authors
- Aronoff, R., Matyas, F., Mateo, C., Ciron, C., Schneider, B., & Petersen, C. C. H.
- Affiliations
- École Polytechnique Fédérale de Lausanne (CH)
- Corresponding author
- Petersen, Carl C.H.
- Venue
- European Journal of Neuroscience
- Publisher
- Wiley
- Published
- 2010-06
- Volume
- 31
- Issue
- 12
- Pages
- 2221-2233
- ISSN
- 0953-816X (ISSN-L)
- 1460-9568
- OpenAlex
- W1954127107
- Cited by
- 323
- References
- 112
- Citations by year
- 2026: 16 · 2025: 17 · 2024: 19 · 2023: 19 · 2022: 17 · 2021: 27 · 2020: 26 · 2019: 20 · 2018: 26 · 2017: 31 · 2016: 23 · 2015: 22 · 2014: 20 · 2013: 15 · 2012: 12
- FWCI
- 0.94
- Type
- journal article
- Language
- en
- Open access
- green
- infoscience.epfl.ch
- Locations
- European Journal of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion)
- Infoscience (Ecole Polytechnique Fédérale de Lausanne) (submittedVersion, cc-by-nc-nd)
- Funders
- École Polytechnique Fédérale de Lausanne
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Tactile and Sensory Interactions
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- long-range connectivity, mice, whisker representation, thalamocortical connections, secondary somatosensory cortex, reciprocal projections, striatum, thalamic reticular nucleus, superior colliculus, sensorimotor integration, tactile perception, glutamatergic projections
- MeSH terms
- Animals, Brain Mapping, Humans, Neural Pathways, Somatosensory Cortex, Staining and Labeling, Thalamus, Touch, Vibrissae, Mice
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