A disinhibitory circuit motif and flexible information routing in the brain
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In the mammalian neocortex, an area typically receives inputs from, and projects to, dozens of other areas. Mechanisms are needed to flexibly route information to the right place at the right time, which we term 'pathway gating'. For instance, a region in your brain that receives signals from both visual and auditory pathways may want to 'gate in' the visual pathway while 'gating out' the auditory pathway when you try to read a book surrounded by people in a noisy café. In this review, we marshall experimental and computational evidence in support of a circuit mechanism for flexible pathway gating realized by a disinhibitory motif. Moreover, recent work shows an increasing preponderance of this disinhibitory motif from sensory areas to association areas of the mammalian cortex. Pathway input gating is briefly compared with alternative or complementary gating mechanisms. Predictions and open questions for future research on this puzzle about the complex brain system will be discussed.
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Animal studies using proxies for consciousness have highlighted certain neuron classes, layer-spanning elements, and cortical circuits.
“work in animal models using methods that can serve as proxies for consciousness (e.g. anesthesia, perceptual detection) has emphasized the importance of certain classes of neurons [7–9], layer-spanning neuronal elements [10], and cortical circuits [11].”
From Testing circuit-level theories of consciousness in humans (2026) · cites this paper as [11]
The section ‘A disinhibitory motif’ (page unavailable) reviews evidence from behaving mice for a cortical circuit involving distinct interneuron types, supporting the part attributed to [11] about cortical circuits. It does not characterize those experiments as using proxies for consciousness, such as anesthesia or perceptual detection. The neuron-class and layer-spanning claims are attached to other citations, not this one. (LLM, conf=0.78)
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Cites
A mechanism for cognitive dynamics: neuronal communication through neuronal coherence.
Fries, P. (2005) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.08.011 · Cited by 4,284 · see citing works
Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq
Zeisel, A., Muñoz-Manchado, A. B., Codeluppi, S., Lönnerberg, P., La Manno, G., Juréus, A., Marques, S., Munguba, H., He, L., Betsholtz, C., et al. (2015) · Science · doi:10.1126/science.aaa1934 · Cited by 3,124 · see citing works
A mesoscale connectome of the mouse brain
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 · see citing works
GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits
Tremblay, R., Lee, S., & Rudy, B. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.033 · Cited by 2,033 · see citing works
Neurophysiological and Computational Principles of Cortical Rhythms in Cognition
Wang, X.-J. (2010) · Physiological Reviews · doi:10.1152/physrev.00035.2008 · Cited by 1,939 · see citing works
Self-citationContext-dependent computation by recurrent dynamics in prefrontal cortex
Mante, V., Sussillo, D., Shenoy, K. V., & Newsome, W. T. (2013) · Nature · doi:10.1038/nature12742 · Cited by 1,807 · see citing works
Adult mouse cortical cell taxonomy revealed by single cell transcriptomics
Tasic, B., Menon, V., Nguyen, T. N., Kim, T. K., Jarsky, T., Yao, Z., Levi, B., Gray, L. T., Sorensen, S. A., Dolbeare, T., et al. (2016) · Nature Neuroscience · doi:10.1038/nn.4216 · Cited by 1,714 · 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
Pfeffer, C. K., Xue, M., He, M., Huang, Z. J., & Scanziani, M. (2013) · Nature Neuroscience · doi:10.1038/nn.3446 · Cited by 1,353 · 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
Interneuron cell types are fit to function
Kepecs, A., & Fishell, G. (2014) · Nature · doi:10.1038/nature12983 · Cited by 1,110 · see citing works
A Cortical Circuit for Gain Control by Behavioral State
Fu, Y., Tucciarone, J. M., Espinosa, J. S., Sheng, N., Darcy, D. P., Nicoll, R. A., Huang, Z. J., & Stryker, M. P. (2014) · Cell · doi:10.1016/j.cell.2014.01.050 · Cited by 937 · cited 3× · see citing works
“Similar concurrent changes of activity in pyramidal cells, SST and VIP cells are observed in primary visual cortex [38] and medial frontal cortex [36] of awake behaving mice.”
Principles of connectivity among morphologically defined cell types in adult neocortex
Jiang, X., Shen, S., Cadwell, C. R., Berens, P., Sinz, F., Ecker, A. S., Patel, S., & Tolias, A. S. (2015) · Science · doi:10.1126/science.aac9462 · Cited by 908 · see citing works
Interactions between frontal cortex and basal ganglia in working memory: A computational model
FRANK, M. J., LOUGHRY, B., & O'REILLY, R. C. (2001) · Cognitive, Affective, & Behavioral Neuroscience · doi:10.3758/cabn.1.2.137 · Cited by 879 · see citing works
A Weighted and Directed Interareal Connectivity Matrix for Macaque Cerebral Cortex
Markov, N. T., Ercsey-Ravasz, M. M., Ribeiro Gomes, A. R., Lamy, C., Magrou, L., Vezoli, J., Misery, P., Falchier, A., Quilodran, R., Gariel, M. A., et al. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhs270 · Cited by 857 · see citing works
Long-range and local circuits for top-down modulation of visual cortex processing
Zhang, S., Xu, M., Kamigaki, T., Hoang Do, J. P., Chang, W.-C., Jenvay, S., Miyamichi, K., Luo, L., & Dan, Y. (2014) · Science · doi:10.1126/science.1254126 · Cited by 804 · see citing works
Neural Networks of the Mouse Neocortex
Zingg, B., Hintiryan, H., Gou, L., Song, M. Y., Bay, M., Bienkowski, M. S., Foster, N. N., Yamashita, S., Bowman, I., Toga, A. W., et al. (2014) · Cell · doi:10.1016/j.cell.2014.02.023 · Cited by 797 · see citing works
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
A cellular mechanism for cortical associations: an organizing principle for the cerebral cortex
Larkum, M. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2012.11.006 · Cited by 755 · see citing works
A neural circuit for spatial summation in visual cortex
Adesnik, H., Bruns, W., Taniguchi, H., Huang, Z. J., & Scanziani, M. (2012) · Nature · doi:10.1038/nature11526 · Cited by 702 · see citing works
Canonical genetic signatures of the adult human brain
Hawrylycz, M., Miller, J. A., Menon, V., Feng, D., Dolbeare, T., Guillozet-Bongaarts, A. L., Jegga, A. G., Aronow, B. J., Lee, C.-K., Bernard, A., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4171 · Cited by 663 · see citing works
Sleep promotes branch-specific formation of dendritic spines after learning
Yang, G., Lai, C. S. W., Cichon, J., Ma, L., Li, W., & Gan, W.-B. (2014) · Science · doi:10.1126/science.1249098 · Cited by 616 · see citing works
Self-citationA Large-Scale Circuit Mechanism for Hierarchical Dynamical Processing in the Primate Cortex
Chaudhuri, R., Knoblauch, K., Gariel, M.-A., Kennedy, H., & Wang, X. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.008 · Cited by 582 · see citing works
Self-citationA synaptic and circuit basis for corollary discharge in the auditory cortex
Schneider, D. M., Nelson, A., & Mooney, R. (2014) · Nature · doi:10.1038/nature13724 · Cited by 580 · see citing works
Dense Inhibitory Connectivity in Neocortex
Fino, E., & Yuste, R. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.025 · Cited by 532 · see citing works
Thalamic control of sensory selection in divided attention
Wimmer, R. D., Schmitt, L. I., Davidson, T. J., Nakajima, M., Deisseroth, K., & Halassa, M. M. (2015) · Nature · doi:10.1038/nature15398 · Cited by 530 · see citing works
Gulyás, A. I., Hájos, N., & Freund, T. F. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-10-03397.1996 · Cited by 512 · see citing works
Branch-specific dendritic Ca2+ spikes cause persistent synaptic plasticity
Cichon, J., & Gan, W. (2015) · Nature · doi:10.1038/nature14251 · Cited by 509 · see citing works
Condé, F., Lund, J. S., Jacobowitz, D. M., Baimbridge, K. G., & Lewis, D. A. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903410109 · Cited by 500 · see citing works
Vogels, T. P., Rajan, K., & Abbott, L. F. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135637 · Cited by 497 · see citing works
A Predictive Network Model of Cerebral Cortical Connectivity Based on a Distance Rule
Ercsey-Ravasz, M., Markov, N. T., Lamy, C., Van Essen, D. C., Knoblauch, K., Toroczkai, Z., & Kennedy, H. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.036 · Cited by 487 · 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
Transcriptional Architecture of Synaptic Communication Delineates GABAergic Neuron Identity
Paul, A., Crow, M., Raudales, R., He, M., Gillis, J., & Huang, Z. J. (2017) · Cell · doi:10.1016/j.cell.2017.08.032 · Cited by 421 · see citing works
Wang, X.-J., Tegner, J. N., Constantinidis, C., & Goldman‐Rakic, P. S. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0305337101 · Cited by 405 · see citing works
Self-citationDisinhibition, a Circuit Mechanism for Associative Learning and Memory
Letzkus, J. J., Wolff, S. B. E., & Lüthi, A. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.024 · Cited by 401 · see citing works
Kim, Y., Yang, G. R., Pradhan, K., Venkataraju, K. U., Bota, M., García del Molino, L. C., Fitzgerald, G., Ram, K., He, M., Levine, J. M., et al. (2017) · Cell · doi:10.1016/j.cell.2017.09.020 · Cited by 389 · see citing works
Self-citationSomatostatin-expressing neurons in cortical networks
Urban-Ciecko, J., & Barth, A. L. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.53 · Cited by 374 · see citing works
Parallel processing by cortical inhibition enables context-dependent behavior
Kuchibhotla, K. V., Gill, J. V., Lindsay, G. W., Papadoyannis, E. S., Field, R. E., Sten, T. H., Miller, K. D., & Froemke, R. C. (2016) · Nature Neuroscience · doi:10.1038/nn.4436 · Cited by 350 · see citing works
Subtype-specific plasticity of inhibitory circuits in motor cortex during motor learning
Chen, S. X., Kim, A. N., Peters, A. J., & Komiyama, T. (2015) · Nature Neuroscience · doi:10.1038/nn.4049 · Cited by 317 · see citing works
Scaling down of balanced excitation and inhibition by active behavioral states in auditory cortex
Zhou, M., Liang, F., Xiong, X. R., Li, L., Li, H., Xiao, Z., Tao, H. W., & Zhang, L. I. (2014) · Nature Neuroscience · doi:10.1038/nn.3701 · Cited by 316 · see citing works
Layer-specific modulation of neocortical dendritic inhibition during active wakefulness
Muñoz, W., Tremblay, R., Levenstein, D., & Rudy, B. (2017) · Science · doi:10.1126/science.aag2599 · Cited by 305 · see citing works
Pakan, J. M., Lowe, S. C., Dylda, E., Keemink, S. W., Currie, S. P., Coutts, C. A., & Rochefort, N. L. (2016) · eLife · doi:10.7554/elife.14985 · Cited by 282 · cited 1× · see citing works
“[21 ,39] reported that, as mice made a transition from rest to movement, SST cells in L2/3 of V1 showed an increase of activity, instead of a previously reported decrease [38].”
Vision and Locomotion Shape the Interactions between Neuron Types in Mouse Visual Cortex
Dipoppa, M., Ranson, A., Krumin, M., Pachitariu, M., Carandini, M., & Harris, K. D. (2018) · Neuron · doi:10.1016/j.neuron.2018.03.037 · Cited by 280 · see citing works
Flexible information routing by transient synchrony
Palmigiano, A., Geisel, T., Wolf, F., & Battaglia, D. A. (2017) · Nature Neuroscience · doi:10.1038/nn.4569 · Cited by 275 · see citing works
Multiple gates on working memory
Chatham, C. H., & Badre, D. (2015) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2014.08.001 · Cited by 268 · see citing works
Orientation selectivity and the functional clustering of synaptic inputs in primary visual cortex
Wilson, D. E., Whitney, D. E., Scholl, B., & Fitzpatrick, D. (2016) · Nature Neuroscience · doi:10.1038/nn.4323 · Cited by 261 · see citing works
Mejias, J. F., Murray, J. D., Kennedy, H., & Wang, X.-J. (2016) · Science Advances · doi:10.1126/sciadv.1601335 · Cited by 227 · see citing works
Self-citationDelay activity of specific prefrontal interneuron subtypes modulates memory-guided behavior
Kamigaki, T., & Dan, Y. (2017) · Nature Neuroscience · doi:10.1038/nn.4554 · Cited by 208 · see citing works
Distinct Roles of Parvalbumin- and Somatostatin-Expressing Interneurons in Working Memory
Kim, D., Jeong, H., Lee, J., Ghim, J.-W., Her, E. S., Lee, S.-H., & Jung, M. W. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.023 · Cited by 201 · see citing works
A cortical disinhibitory circuit for enhancing adult plasticity
Fu, Y., Kaneko, M., Tang, Y., Álvarez-Buylla, A., & Stryker, M. P. (2015) · eLife · doi:10.7554/elife.05558 · Cited by 196 · 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
Meskenaïte, V. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970303)379:1 · Cited by 180 · see citing works
Brain-Wide Maps of Synaptic Input to Cortical Interneurons
Wall, N. R., Parra, M. D. L., Sorokin, J. M., Taniguchi, H., Huang, Z. J., & Callaway, E. M. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3967-15.2016 · Cited by 176 · see citing works
Gabbott, P. L. A., & Bacon, S. J. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960122)364:4 · Cited by 165 · see citing works
Joglekar, M. R., Mejias, J. F., Yang, G. R., & Wang, X.-J. (2018) · Neuron · doi:10.1016/j.neuron.2018.02.031 · Cited by 153 · see citing works
Self-citationA dendritic disinhibitory circuit mechanism for pathway-specific gating
Yang, G. R., Murray, J. D., & Wang, X.-J. (2016) · Nature Communications · doi:10.1038/ncomms12815 · Cited by 148 · see citing works
Self-citationFunctions and dysfunctions of neocortical inhibitory neuron subtypes
Hattori, R., Kuchibhotla, K. V., Froemke, R. C., & Komiyama, T. (2017) · Nature Neuroscience · doi:10.1038/nn.4619 · Cited by 142 · see citing works
Inhibitory stabilization and visual coding in cortical circuits with multiple interneuron subtypes
Litwin-Kumar, A., Rosenbaum, R., & Doiron, B. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00732.2015 · Cited by 138 · see citing works
Lu, J., Tucciarone, J., Padilla-Coreano, N., He, M., Gordon, J. A., & Huang, Z. J. (2017) · Nature Neuroscience · doi:10.1038/nn.4624 · Cited by 118 · see citing works
Connectivity of GABAergic Calretinin-immunoreactive Neurons in Rat Primary Visual Cortex
Gonchar, Y. (1999) · Cerebral Cortex · doi:10.1093/cercor/9.7.683 · Cited by 117 · see citing works
Spatial embedding of structural similarity in the cerebral cortex
Song, H. F., Kennedy, H., & Wang, X. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1414153111 · Cited by 101 · see citing works
Self-citationVIP+ interneurons control neocortical activity across brain states
Jackson, J., Ayzenshtat, I., Karnani, M., & Yuste, R. (2016) · Journal of Neurophysiology · doi:10.1152/jn.01124.2015 · Cited by 93 · see citing works
del Molino, L. C. G., Yang, G. R., Mejías, J. F., & Wang, X. (2017) · eLife · doi:10.7554/elife.29742 · Cited by 70 · see citing works
Self-citationLee, J. H., Christof Koch, A., & Mihalaş, Ş. (2017) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2017.00028 · Cited by 35 · see citing works
Comment on “Principles of connectivity among morphologically defined cell types in adult neocortex”
Barth, A. L., Burkhalter, A., Callaway, E. M., Connors, B. W., Cauli, B., DeFelipe, J., Feldmeyer, D., Freund, T., Kawaguchi, Y., Kisvarday, Z., et al. (2016) · Science · doi:10.1126/science.aaf5663 · Cited by 26 · see citing works
Sridharan, D., & Knudsen, E. I. (2014) · Vision Research · doi:10.1016/j.visres.2014.12.010 · Cited by 25 · see citing works
Jiang, X., Shen, S., Sinz, F., Reimer, J., Cadwell, C. R., Berens, P., Ecker, A. S., Patel, S., Denfield, G. H., Froudarakis, E., et al. (2016) · Science · doi:10.1126/science.aaf6102 · Cited by 13 · see citing works
Joglekar, M. R., Mejías, J. F., Yang, G. R., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/186007 · Cited by 4 · see citing works
Self-citationDefelipe (1999) · doi:10.1002/(sici)1096-9861(19990927)412:3
Flagged first, then by citations
Cited by
Sorted by citations
Miller, E. K., Lundqvist, M., & Bastos, A. M. (2018) · Neuron · doi:10.1016/j.neuron.2018.09.023 · Cited by 797 · see citing works
Artificial Neural Networks for Neuroscientists: A Primer
Yang, G. R., & Wang, X. (2020) · Neuron · doi:10.1016/j.neuron.2020.09.005 · Cited by 386 · see citing works
Self-citationMacroscopic gradients of synaptic excitation and inhibition in the neocortex
Wang, X. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-0262-x · Cited by 277 · see citing works
Self-citationMultidimensional processing in the amygdala
Gothard, K. M. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-0350-y · Cited by 166 · see citing works
Engagement of Pulvino-cortical Feedforward and Feedback Pathways in Cognitive Computations
Jaramillo, J., Mejías, J. F., & Wang, X. (2018) · Neuron · doi:10.1016/j.neuron.2018.11.023 · Cited by 160 · see citing works
Self-citationNajafi, F., Elsayed, G. F., Cao, R., Pnevmatikakis, E. A., Latham, P. E., Cunningham, J. P., & Churchland, A. K. (2019) · Neuron · doi:10.1016/j.neuron.2019.09.045 · Cited by 133 · see citing works
Kim, R., & B, T. J. S. A. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-00753-w · Cited by 130 · see citing works
A dopamine gradient controls access to distributed working memory in the large-scale monkey cortex
Froudist‐Walsh, S., Bliss, D. P., Ding, X., Rapan, L., Niu, M., Knoblauch, K., Zilles, K., Kennedy, H., Palomero‐Gallagher, N., & Wang, X. (2021) · Neuron · doi:10.1016/j.neuron.2021.08.024 · Cited by 115 · see citing works
Self-citationExperience shapes activity dynamics and stimulus coding of VIP inhibitory cells
Garrett, M., Manavi, S., Roll, K., Ollerenshaw, D. R., Groblewski, P. A., Ponvert, N. D., Kiggins, J. T., Casal, L., Mace, K. D., Williford, A., et al. (2020) · eLife · doi:10.7554/elife.50340 · Cited by 102 · see citing works
Neural Circuits That Mediate Selective Attention: A Comparative Perspective
Knudsen, E. I. (2018) · Trends in Neurosciences · doi:10.1016/j.tins.2018.06.006 · Cited by 92 · see citing works
Theory of the Multiregional Neocortex: Large-Scale Neural Dynamics and Distributed Cognition
Wang, X.-J. (2022) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-110920-035434 · Cited by 83 · see citing works
Self-citationRuff, D. A., & Cohen, M. R. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0477-1 · Cited by 73 · see citing works
Hertäg, L., & Sprekeler, H. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006999 · Cited by 68 · see citing works
Gomez, S. T., Blonde, J. D., Mendoza-Halliday, D., Kuebler, E. S., Everest, M., Wang, X., Inoue, W., Poulter, M. O., & Martínez-Trujillo, J. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa056 · Cited by 68 · see citing works
Self-citationdel Molino, L. C. G., Yang, G. R., Mejías, J. F., & Wang, X. (2017) · eLife · doi:10.7554/elife.29742 · Cited by 70 · see citing works
Self-citationGuet-McCreight, A., Skinner, F. K., & Topolnik, L. (2020) · Frontiers in Neural Circuits · doi:10.3389/fncir.2020.00032 · Cited by 64 · see citing works
A synaptic temperature sensor for body cooling
Kamm, G. B., Boffi, J. C., Zuza, K., Nencini, S., Campos, J., Schrenk-Siemens, K., Sonntag, I., Kabaoğlu, B., Hay, M. Y. A. E., Schwarz, Y. N., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.10.001 · Cited by 66 · see citing works
The generation of cortical novelty responses through inhibitory plasticity
Schulz, A., Miehl, C., Berry, M. J., & Gjorgjieva, J. (2021) · eLife · doi:10.7554/elife.65309 · Cited by 64 · see citing works
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Atapour, N., Majka, P., Wolkowicz, I. H., Malamanova, D., Worthy, K. H., & Rosa, M. G. P. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy263 · Cited by 57 · see citing works
Hierarchical timescales in the neocortex: Mathematical mechanism and biological insights
Li, S., & Wang, X. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2110274119 · Cited by 51 · see citing works
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Functional and pharmacological role of the dopamine D4 receptor and its polymorphic variants
Ferré, S., Belcher, A. M., Bonaventura, J., Quiroz, C., Sánchez‐Soto, M., Casadó-Anguera, V., Cai, N.-S., Moreno, E., Boateng, C. A., Keck, T. M., et al. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.1014678 · Cited by 45 · see citing works
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Roemschied, F. A., Pacheco, D. A., Aragon, M. J., Ireland, E. C., Li, X., Thieringer, K., Pang, R., & Murthy, M. (2023) · Nature · doi:10.1038/s41586-023-06632-1 · Cited by 39 · see citing works
Rhomberg, T., Rovira-Esteban, L., Vikór, A., Paradiso, E., Kremser, C., Nagy-Pál, P., Papp, O. I., Tasan, R. O., Erdélyi, F., Szabó, G., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2063-17.2018 · Cited by 43 · see citing works
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Doya, K., Ema, A., Kitano, H., Sakagami, M., & Russell, S. (2022) · Neural Networks · doi:10.1016/j.neunet.2022.05.012 · Cited by 45 · see citing works
Stability and learning in excitatory synapses by nonlinear inhibitory plasticity
Miehl, C., & Gjorgjieva, J. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010682 · Cited by 45 · see citing works
Lee, J. H., Christof Koch, A., & Mihalaş, Ş. (2017) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2017.00028 · Cited by 35 · see citing works
Stimulus novelty uncovers coding diversity in survey of visual cortexPreprint
Garrett, M., Groblewski, P. A., Piet, A. T., Ollerenshaw, D. R., Najafi, F., Yavorska, I., Amster, A., Bennett, C., Buice, M. A., Caldejon, S., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.14.528085 · Cited by 29 · see citing works
Untangling stability and gain modulation in cortical circuits with multiple interneuron classesPreprint
Bos, H., Miehl, C., Oswald, A.-M. M., & Doiron, B. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.15.148114 · Cited by 29 · see citing works
Liu, M., Liu, X., Hildebrandt, A., & Zhou, C. (2020) · Cerebral Cortex Communications · doi:10.1093/texcom/tgaa015 · Cited by 28 · see citing works
van den Brink, R. L., Hagena, K., Wilming, N., Murphy, P. R., Büchel, C., & Donner, T. H. (2022) · Neuron · doi:10.1016/j.neuron.2022.11.009 · Cited by 30 · see citing works
Top–down modulation in canonical cortical circuits with short-term plasticity
Waitzmann, F., Wu, Y. K., & Gjorgjieva, J. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2311040121 · Cited by 21 · see citing works
Rate and oscillatory switching dynamics of a multilayer visual microcircuit model
Hahn, G., Kumar, A., SCHMIDT, H. J., Knösche, T. R., & Deco, G. (2022) · eLife · doi:10.7554/elife.77594 · Cited by 18 · see citing works
Distinct burst properties contribute to the functional diversity of thalamic nuclei
Desai, N. V., & Varela, C. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25141 · Cited by 18 · see citing works
Cellular psychology: relating cognition to context-sensitive pyramidal cells
Phillips, W. A., Bachmann, T., Spratling, M. W., Muckli, L., Petro, L. S., & Zolnik, T. (2025) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2024.09.002 · Cited by 18 · see citing works
The spatial scale of somatostatin subnetworks increases from sensory to association cortex
Khoury, C. F., Fala, N. G., & Runyan, C. A. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111319 · Cited by 15 · see citing works
A Drosophila Circuit for Habituation Override
Trisal, S., Aranha, M. M., Chodankar, A., VijayRaghavan, K., & Ramaswami, M. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1842-21.2022 · Cited by 17 · see citing works
Antagonistic inhibitory subnetworks control cooperation and competition across cortical spacePreprint
Mossing, D. P., Veit, J., Palmigiano, A., Miller, K. D., & Adesnik, H. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.31.437953 · Cited by 16 · see citing works
The Cooperative Neuron: Cellular Foundations of Mental Life
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.001.0001 · Cited by 13 · see citing works
Cellular mechanisms of cooperative context-sensitive predictive inference
Marvan, T., & Phillips, W. A. (2024) · Current Research in Neurobiology · doi:10.1016/j.crneur.2024.100129 · Cited by 13 · see citing works
Wang, X., Pereira, U., Rosa, M. G. P., & Kennedy, H. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.11.002 · Cited by 12 · see citing works
Self-citationArousal and Locomotion Differently Modulate Activity of Somatostatin Neurons across Cortex
Khoury, C. F., Fala, N. G., & Runyan, C. A. (2023) · eNeuro · doi:10.1523/eneuro.0136-23.2023 · Cited by 10 · see citing works
Ruff, D. A., & Cohen, M. R. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/372888 · Cited by 12 · see citing works
Flexible control of representational dynamics in a disinhibition-based model of decision-making
Shen, B., Louie, K., & Glimcher, P. W. (2023) · eLife · doi:10.7554/elife.82426 · Cited by 9 · see citing works
AIM: A network model of attention in auditory cortex
Chou, K. F., & Sen, K. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009356 · Cited by 10 · see citing works
Dysfunctions of cellular context-sensitivity in neurodevelopmental learning disabilities
Granato, A., Phillips, W. A., Schulz, J. M., Mototaka Suzuki, A., & Larkum, M. E. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105688 · Cited by 8 · see citing works
Neuronal identity and cognitive control dynamics in the PFC
Nakajima, M. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.08.014 · Cited by 8 · see citing works
Hoftman, G. D., Bazmi, H. H., Ciesielski, A. J., Dinka, L. A., Chen, K., & Lewis, D. A. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa342 · Cited by 8 · see citing works
Key role of neuronal diversity in structured reservoir computing
Thivierge, J., Giraud, É., Lynn, M. B., & Charbonneau, A. T. (2022) · Chaos An Interdisciplinary Journal of Nonlinear Science · doi:10.1063/5.0111131 · Cited by 7 · see citing works
Graham, B. P., Kay, J., & Phillips, W. A. (2025) · Neural Computation · doi:10.1162/neco_a_01739 · Cited by 7 · see citing works
Dual counterstream architecture may support separation between vision and predictions
Marić, M., & Domijan, D. (2022) · Consciousness and Cognition · doi:10.1016/j.concog.2022.103375 · Cited by 7 · see citing works
Layer 3 Dynamically Coordinates Columnar Activity According to Spatial Context
Plomp, G., Larderet, I., Fiorini, M., & Busse, L. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1568-18.2018 · Cited by 7 · see citing works
van den Brink, R. L., Hagena, K., Wilming, N., Murphy, P. R., Calder-Travis, J. M., Finsterbusch, J., Büchel, C., & Donner, T. H. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.05.570327 · Cited by 10 · see citing works
Untangling stability and gain modulation in cortical circuits with multiple interneuron classes
Bos, H., Miehl, C., Oswald, A.-M. M., & Doiron, B. (2025) · eLife · doi:10.7554/elife.99808.4 · Cited by 6 · see citing works
Circumstantial evidence and explanatory models for synapses in large-scale spike recordings
Stevenson, I. H. (2023) · Neurons Behavior Data analysis and Theory · doi:10.51628/001c.90831 · Cited by 6 · see citing works
Si, H., & Sun, X. (2021) · Nonlinear Dynamics · doi:10.1007/s11071-020-06192-3 · Cited by 6 · see citing works
Untangling stability and gain modulation in cortical circuits with multiple interneuron classesPreprint
Bos, H., Miehl, C., Oswald, A.-M. M., & Doiron, B. (2024) · eLife · doi:10.7554/elife.99808 · Cited by 6 · see citing works
Disinhibition of a recurrent attractor gates a persistent goal signal for navigationPreprint
Lanz, A. J., Kathman, N. D., Hao, E., Ermentrout, B., & Nagel, K. I. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.07.681003 · Cited by 6 · see citing works
High-frequency bursts facilitate fast communication for human spatial attention
Boroujeni, K. B., Helfrich, R. F., Fiebelkorn, I. C., Bentley, J. N., Brunner, P., Lin, J. J., Knight, R. T., & Kästner, S. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-02160-5 · Cited by 5 · see citing works
Switching Operation Modes in the Neocortex via Cholinergic Neuromodulation
Puigbò, J.-Y., Arsiwalla, X. D., González‐Ballester, M. Á., & Verschure, P. F. M. J. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-01764-w · Cited by 5 · see citing works
Dendritic Kernel Convolutional Neural Network for Breast Ultrasound Images Segmentation
Zhang, H., Liu, Z., Zhang, Z., Lei, Z., Wang, Z., Hasegawa, H., & Gao, S. (2025) · IEEE Transactions on Systems Man and Cybernetics Systems · doi:10.1109/tsmc.2025.3615627 · Cited by 4 · see citing works
Neocortical inhibitory imbalance predicts successful sensory detection
Deister, C. A., Moore, A. I., Voigts, J., Bechek, S. C., Lichtin, R. D., Brown, T. C., & Moore, C. I. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114233 · Cited by 7 · see citing works
Compartmentalized pooling generates orientation selectivity in wide-field amacrine cells
Lei, W., Clark, D. A., & Demb, J. B. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2411130121 · Cited by 4 · see citing works
Soo, W. W. M., Goudar, V., & Wang, X.-J. (2023) · neural information processing systems · doi:10.52202/075280-1391 · Cited by 4 · see citing works
Self-citationKay, J. W., Phillips, W. A., Aru, J., Graham, B. P., & Larkum, M. E. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/604066 · Cited by 4 · see citing works
Testing circuit-level theories of consciousness in humans
Dykstra, A. R., Zhu, Y., Fernandez Pujol, C., Zhou, D. W., Jones, S. R., Marvan, T., & Bonaiuto, J. J. (2026) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2025.08.012 · Cited by 3 · see citing works
Biological detail and graph structure in network neuroscience
Papo, D., & Buldú, J. M. (2025) · Frontiers in Network Physiology · doi:10.3389/fnetp.2025.1667656 · Cited by 4 · see citing works
Epigenetics of neural networks in neurocognitive conditions: A review
Stolberg, V. B. (2025) · Brain Network Disorders · doi:10.1016/j.bnd.2025.08.001 · Cited by 3 · see citing works
Boroujeni, K. B., Balaram, P., Tiesinga, P. H. E., & Womelsdorf, T. (2025) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2025.102873 · Cited by 4 · see citing works
Si, H., & Sun, X. (2022) · Cognitive Neurodynamics · doi:10.1007/s11571-022-09914-y · Cited by 4 · see citing works
Zhao, S., Zhou, J., Zhang, Y., & Wang, D. (2023) · eNeuro · doi:10.1523/eneuro.0373-22.2023 · Cited by 3 · see citing works
Potter, C. T., Bassi, C. D., & Runyan, C. A. (2024) · iScience · doi:10.1016/j.isci.2024.110736 · Cited by 4 · see citing works
Yamauchi, N., Tawatsuji, Y., Suzuki, Y., Yamakawa, H., & Doya, K. (2025) · Neuroscience Research · doi:10.1016/j.neures.2025.105002 · Cited by 2 · see citing works
Phokhinanan, W., Obin, N., & Argentieri, S. (2024) · IEEE International Conference on Acoustics Speech and Signal Processing · doi:10.1109/icassp48485.2024.10446210 · Cited by 2 · see citing works
A genetic algorithm for self-supervised models of oscillatory neurodynamics
Nejat, H., Sherfey, J. S., & Bastos, A. M. (2026) · PLoS ONE · doi:10.1371/journal.pone.0354021 · Cited by 2 · see citing works
Potter, C. T., Bassi, C. D., & Runyan, C. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.09.523298 · Cited by 2 · see citing works
Communication subspaces align with training in ANNsPreprint
Poggi, P. G., Mihalaş, Ş., & Mastrovito, D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.11.623065 · Cited by 2 · see citing works
Untangling stability and gain modulation in cortical circuits with multiple interneuron classesPreprint
Bos, H., Miehl, C., Oswald, A.-M. M., & Doiron, B. (2025) · eLife · doi:10.7554/elife.99808.3 · Cited by 2 · see citing works
Introduction to The Cooperative Neuron
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.003.0001 · Cited by 1 · see citing works
Feyerabend, M., Witte, M., Möck, M., & Staiger, J. F. (2025) · iScience · doi:10.1016/j.isci.2025.112539 · Cited by 1 · see citing works
A synthetic resilience framework for stabilizing dynamical neural networks in neurodegeneration
Nirmal, A. K., Dayalan, H., Ayyar, G., Nithiananthan, G., & Thiruvengadam, H. (2026) · Discover Neuroscience · doi:10.1186/s13064-026-00301-5 · Cited by 1 · see citing works
Disinhibition as a canonical neural mechanism for flexible behavior
Standage, D., Paré, M., & Blohm, G. (2018) · Conference on Cognitive Computational Neuroscience (CCN) · doi:10.32470/ccn.2018.1165-0 · Cited by 1 · see citing works
Brain Connectomes Come of AgePreprint
Wang, X., Pereira, U., Rosa, M. G. P., & Kennedy, H. (2020) · arXiv (Cornell University) · doi:10.48550/arxiv.2008.03881 · Cited by 1 · see citing works
Self-citationFeature-based gating of cortical information transmissionPreprint
Ray, S. B., Kaping, D., & Treue, S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.08.463709 · Cited by 1 · see citing works
Larkum, M. E. (2023) · doi:10.1093/oso/9780198876984.002.0005
Evolution and Development of Cooperative Neurons
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.003.0007
An Information-theoretic View of Context-sensitive Computation
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.003.0009
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.003.0002
What Cooperative Neurons Do for Mental Life
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.003.0006
Pathologies of Cooperative Neuronal Processing
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.003.0008
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.002.0004
Cooperative Neurons in Various States of Mind and Brain
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.003.0005
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.003.0003
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.002.0003
Phillips, B. (2023) · doi:10.1093/oso/9780198876984.002.0006
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.002.0008
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.003.0011
Difficulties and Unresolved Issues
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.003.0010
Advance praise for The Cooperative Neuron
Phillips, W. A. (2023) · doi:10.1093/oso/9780198876984.002.0019
- Authors
- Wang, X.-J., & Yang, G. R.
- Affiliations
- New York University (US)
- Corresponding author
- Wang, Xiao-Jing
- Venue
- Current Opinion in Neurobiology
- Publisher
- Elsevier BV
- Published
- 2018-04
- Volume
- 49
- Pages
- 75-83
- ISSN
- 0959-4388 (ISSN-L)
- PMC
- PMC6599531
- OpenAlex
- W2793090406
- Cited by
- 113
- References
- 68
- Citations by year
- 2026: 7 · 2025: 16 · 2024: 12 · 2023: 28 · 2022: 13 · 2021: 10 · 2020: 12 · 2019: 5 · 2018: 8 · 2017: 2
- FWCI
- 1.17
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Current Opinion in Neurobiology (acceptedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIH (MH062349)
- ONR (N00014-17-1-2041)
- STCSM (14JC1404900, 15JC1400104)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Keywords
- information routing, neocortex, cortical circuits, sensory areas, association cortex, multisensory integration, computational modeling of neural circuits
- MeSH terms
- Animals, Cerebral Cortex, Dendrites, Humans, Interneurons, Models, Neurological, Neural Inhibition, Neural Pathways
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