Canonical cortical circuits: current evidence and theoretical implications

References

• Douglas RJ, Martin KA. Neuronal circuits of the neocortex. Annu Rev Neurosci. 2004;27(1):419–451.
   Google Scholar
• Heinzle J, Hepp K, Martin KA. A microcircuit model of the frontal eye fields. J Neurosci. 2007;27(35):9341–9353.
   PubMed Web of Science ®Google Scholar
• Douglas RJ, Martin KA, Whitteridge D. A canonical microcircuit for neocortex. Neural Comput. 1989;1(4):480–488.
   Web of Science ®Google Scholar
• Douglas RJ, Martin KA. Mapping the matrix: the ways of neocortex. Neuron. 2007;56(2):226–238.
   PubMed Web of Science ®Google Scholar
• Douglas RJ, Martin KA. A functional microcircuit for cat visual cortex. J Physiol (Lond). 1991;440:735–769.
   Google Scholar
• Binzegger T, Douglas RJ, Martin KA. A quantitative map of the circuit of cat primary visual cortex. J Neurosci. 2004;24(39):8441–8453.
   PubMed Web of Science ®Google Scholar
• Atencio CA, Sharpee TO, Schreiner CE. Hierarchical computation in the canonical auditory cortical circuit. Proc Natl Acad Sci U S A. 2009;106(51):21894–21899.
   Web of Science ®Google Scholar
• Atencio CA, Sharpee TO, Schreiner CE. Cooperative nonlinearities in auditory cortical neurons. Neuron. 2008;58(6):956–966.
   Web of Science ®Google Scholar
• Constantinidis C, Goldman-Rakic PS. Correlated discharges among putative pyramidal neurons and interneurons in the primate prefrontal cortex. J Neurophysiol. 2002;88(6):3487–3497.
   PubMed Web of Science ®Google Scholar
• Hussar CR, Pasternak T. Flexibility of sensory representations in prefrontal cortex depends on cell type. Neuron. 2009;64(5):730–743.
   Web of Science ®Google Scholar
• Wilson FA, O’Scalaidhe SP, Goldman-Rakic PS. Functional synergism between putative gamma-aminobutyrate-containing neurons and pyramidal neurons in prefrontal cortex. Proc Natl Acad Sci U S A. 1994;91(9):4009–4013.
   Web of Science ®Google Scholar
• Johnston K, DeSouza JF, Everling S. Monkey prefrontal cortical pyramidal and putative interneurons exhibit differential patterns of activity between prosaccade and antisaccade tasks. J Neurosci. 2009;29(17):5516–5524.
   Web of Science ®Google Scholar
• Karnani MM, Agetsuma M, Yuste R. A blanket of inhibition: functional inferences from dense inhibitory connectivity. Curr Opin Neurobiol. 2014;26:96–102.
   Web of Science ®Google Scholar
• Vogels TP, Abbott LF. Gating multiple signals through detailed balance of excitation and inhibition in spiking networks. Nat Neurosci. 2009;12(4):483–491.
   Web of Science ®Google Scholar
• Xue M, Atallah BV, Scanziani M. Equalizing excitation–inhibition ratios across visual cortical neurons. Nature. 2014;511(7511):596–600.
   Web of Science ®Google Scholar
• Hangya B, Pi HJ, Kvitsiani D, Ranade SP, Kepecs A. From circuit motifs to computations: mapping the behavioral repertoire of cortical interneurons. Curr Opin Neurobiol. 2014;26:117–124.
   Web of Science ®Google Scholar
• Kepecs A, Fishell G. Interneuron cell types are fit to function. Nature. 2014;505(7483):318–326.
   PubMed Web of Science ®Google Scholar
• Constantinidis C, Wang XJ. A neural circuit basis for spatial working memory. Neuroscientist. 2004;10(6):553–565.
   PubMed Web of Science ®Google Scholar
• Wang XJ, Tegner J, Constantinidis C, Goldman-Rakic PS. Division of labor among distinct subtypes of inhibitory neurons in a cortical microcircuit of working memory. Proc Natl Acad Sci U S A. 2004;101(5):1368–1373.
   Web of Science ®Google Scholar
• Ardid S, Vinck M, Kaping D, Marquez S, Everling S, Womelsdorf T. Mapping of functionally characterized cell classes onto canonical circuit operations in primate prefrontal cortex. J Neurosci. 2015;35(7):2975–2991.
   Web of Science ®Google Scholar
• Sanides F. Functional architecture of motor and sensory cortices in primates in the light of a new concept of neocortex evolution. In: Noback CR, Montagna W, editors. The Primate Brain: Advances in Primatology. New York, NY: Appleton-Century-Crofts; 1970.
   Google Scholar
• Economo von C. In: Triarhou LC, editor. Cellular Structure of the Human Cerebral Cortex. Basel, Switzerland: Karger Medical and Scientific Publishers; 2009.
   Google Scholar
• Zilles K, Amunts K. Architecture of the cerebral cortex. In: Mai JK, Paxinos G, editors. The Human Nervous System. San Diego, CA: Academic Press; 2012:836–895.
   Google Scholar
• Herculano-Houzel S, Watson C, Paxinos G. Distribution of neurons in functional areas of the mouse cerebral cortex reveals quantitatively different cortical zones. Front Neuroanat. 2013;7:35.
   Web of Science ®Google Scholar
• Collins CE, Airey DC, Young NA, Leitch DB, Kaas JH. Neuron densities vary across and within cortical areas in primates. Proc Natl Acad Sci U S A. 2010;107(36):15927–15932.
   Web of Science ®Google Scholar
• Kätzel D, Zemelman BV, Buetfering C, Wölfel M, Miesenböck G. The columnar and laminar organization of inhibitory connections to neocortical excitatory cells. Nat Neurosci. 2011;14(1):100–107.
   Web of Science ®Google Scholar
• Suzuki N, Bekkers JM. Two layers of synaptic processing by principal neurons in piriform cortex. J Neurosci. 2011;31(6):2156–2166.
   Web of Science ®Google Scholar
• Godlove DC, Maier A, Woodman GF, Schall JD. Microcircuitry of agranular frontal cortex: testing the generality of the canonical cortical microcircuit. J Neurosci. 2014;34(15):5355–5369.
   Web of Science ®Google Scholar
• Gilbert CD. Microcircuitry of the visual cortex. Annu Rev Neurosci. 1983;6(1):217–247.
   Google Scholar
• Callaway EM. Local circuits in primary visual cortex of the macaque monkey. Annu Rev Neurosci. 1998;21(1):47–74.
   Google Scholar
• Beul SF, Hilgetag CC. Towards a “canonical” agranular cortical microcircuit. Front Neuroanat. 2015;8:165.
   Web of Science ®Google Scholar
• Merton PA, Morton HB. Stimulation of the cerebral cortex in the intact human subject. Nature. 1980;285(5762):227.
   PubMed Web of Science ®Google Scholar
• Barker A, Freeston I, Jalinous R. Non-invasive stimulation of motor pathways within the brain using time-varying magnetic fields. Electroencephalogr Clin Neurophysiol. 1985;(61):S245.
   Google Scholar
• Di Lazzaro V, Ziemann U. The contribution of transcranial magnetic stimulation in the functional evaluation of microcircuits in human motor cortex. Front Neural Circuits. 2013;7:18.
   PubMed Web of Science ®Google Scholar
• Padoa-Schioppa C, Assad JA. Neurons in the orbitofrontal cortex encode economic value. Nature. 2006;441(7090):223–226.
   PubMed Web of Science ®Google Scholar
• Padoa-Schioppa C. Neuronal origins of choice variability in economic decisions. Neuron. 2013;80(5):1322–1336.
   Web of Science ®Google Scholar
• Rustichini A, Padoa-Schioppa C. A neuro-computational model of economic decisions. J Neurophysiol. 2015;114(3):1382–1398.
   Web of Science ®Google Scholar
• Mackey S, Petrides M. Architecture and morphology of the human ventromedial prefrontal cortex. Eur J Neurosci. 2014;40(5):2777–2796.
   Web of Science ®Google Scholar
• Binzegger T, Douglas RJ, Martin KA. Topology and dynamics of the canonical circuit of cat V1. Neural Netw. 2009;22(8):1071–1078.
   Web of Science ®Google Scholar
• Santos LR, Rosati AG. The evolutionary roots of human decision making. Annu Rev Psychol. 2015;66(1):321–347.
   Google Scholar