Parallel processing in the corticogeniculate pathway of the macaque monkey

Briggs, Farran; Usrey, W. Martin

doi:10.1016/j.neuron.2009.02.024

Cited by 139Visual perception and processing mechanismsNeural dynamics and brain functionNeuroscience and Neuropharmacology Research

Parallel processing in the corticogeniculate pathway of the macaque monkey

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Briggs, Farran, Usrey, W. Martin·2009·Neuron

DOI 10.1016/j.neuron.2009.02.024PMC PMC2789995

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Abstract

Summary Although corticothalamic feedback is ubiquitous across species and modalities, its role in sensory processing is unclear. This study provides the first detailed description of the visual physiology of corticogeniculate neurons in the primate. Using electrical stimulation to identify corticogeniculate neurons, we distinguish three groups of neurons with response properties that closely resemble those of neurons in the magnocellular, parvocellular and koniocellular layers of their target structure, the lateral geniculate nucleus (LGN) of the thalamus. Our results indicate that corticogeniculate feedback in the primate is stream-specific and provide strong evidence in support of the view that corticothalamic feedback can influence the transmission of sensory information from the thalamus to the cortex in a stream-selective manner.

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Canonical circuits have segregated parallel processing streams.
“A key property of canonical circuits is the segregation of parallel streams of processing.”
From Canonical Microcircuits for Predictive Coding (2012) · cites this paper as Briggs and Usrey, 2009
The Discussion section, “Feedforward and feedback pathways in the primate visual system” (page unavailable), calls separation into parallel streams a major hallmark of sensory processing and describes segregated streams in the primate visual system. The claim extends that property to canonical circuits generally, which this paper does not establish. (LLM, conf=0.82)
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The corticogeniculate feedback pathway from L6 preserves stream segregation: upper L6 cells preferentially synapse onto parvocellular LGN cells, and lower L6 cells target magnocellular LGN layers.
“The corticogeniculate feedback pathway from L6 maintains this segregation, as upper L6 cells preferentially synapse onto parvocellular cells in the LGN, while lower L6 cells target the magnocellular LGN layers (Fitzpatrick et al., 1994; Briggs and Usrey, 2009).”
From Canonical Microcircuits for Predictive Coding (2012) · cites this paper as Briggs and Usrey, 2009

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Segregation of Form, Color, Movement, and Depth: Anatomy, Physiology, and Perception
Livingstone, M. S., & Hubel, D. H. (1988) · Science · doi:10.1126/science.3283936 · Cited by 3,358 · see citing works
How parallel are the primate visual pathways?
Merigan, W. H., & Maunsell, J. H. R. (1993) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.16.030193.002101 · Cited by 1,597 · see citing works
The visual neurosciences
Chalupa, L. M., Werner, J. S., & Barnstable, C. J. (2004) · Cited by 1,020 · see citing works
Striate cortex of monkey and cat: contrast response function.
Albrecht, D. G., & Hamilton, D. B. (1982) · Journal of Neurophysiology · doi:10.1152/jn.1982.48.1.217 · Cited by 956 · see citing works
The primate retina contains two types of ganglion cells, with high and low contrast sensitivity.
Kaplan, E., & Shapley, R. M. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.8.2755 · Cited by 733 · see citing works
Attention modulates responses in the human lateral geniculate nucleus
O’Connor, D. H., Fukui, M. M., Pinsk, M. A., & Kästner, S. (2002) · Nature Neuroscience · doi:10.1038/nn957 · Cited by 730 · see citing works
The projections of cells in different layers of the cat's visual cortex
Gilbert, C. D., & Kelly, J. P. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901630106 · Cited by 724 · see citing works
The origin of efferent pathways from the primary visual cortex, area 17, of the macaque monkey as shown by retrograde transport of horseradish peroxidase
Lund, J. S., Lund, R. D., Hendrickson, A. E., Milam, A. H., & Fuchs, A. F. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901640303 · Cited by 681 · see citing works
Exploring the Thalamus and Its Role in Cortical Function
Sherman, S. M., & Guillery, R. W. (2005) · The MIT Press eBooks · doi:10.7551/mitpress/2940.001.0001 · Cited by 672 · see citing works
Orientation Selectivity in Macaque V1: Diversity and Laminar Dependence
Ringach, D. L., Shapley, R. M., & Hawken, M. J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-13-05639.2002 · Cited by 653 · see citing works
Contrast's effect on spatial summation by macaque V1 neurons
Sceniak, M. P., Ringach, D. L., Hawken, M. J., & Shapley, R. M. (1999) · Nature Neuroscience · doi:10.1038/11197 · Cited by 608 · see citing works
Classifying simple and complex cells on the basis of response modulation
SKOTTUN, B. C., Valois, R. L. D., Grosof, D. H., Movshon, J. A., Albrecht, D. G., & Bonds, A. B. (1991) · Vision Research · doi:10.1016/0042-6989(91)90033-2 · Cited by 608 · see citing works
X and Y cells in the lateral geniculate nucleus of macaque monkeys.
Kaplan, E., & Shapley, R. M. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014333 · Cited by 601 · see citing works
The Koniocellular Pathway in Primate Vision
Hendry, S. H. C., & Reid, R. C. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.127 · Cited by 591 · see citing works
Functional specificity of lateral geniculate nucleus laminae of the rhesus monkey
Schiller, P. H., & Malpeli, J. G. (1978) · Journal of Neurophysiology · doi:10.1152/jn.1978.41.3.788 · Cited by 548 · see citing works
Impact of Network Activities on Neuronal Properties in Corticothalamic Systems
Steriade, M. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.1.1 · Cited by 530 · see citing works
Guarding the gateway to cortex with attention in visual thalamus
McAlonan, K., Cavanaugh, J., & Wurtz, R. H. (2008) · Nature · doi:10.1038/nature07382 · Cited by 503 · see citing works
The organization of synaptic interconnections in the laminae of the dorsal lateral geniculate nucleus of the cat
Guillery, R. W. (1969) · Cell and Tissue Research · doi:10.1007/bf00321474 · Cited by 479 · see citing works
Sleep, epilepsy and thalamic reticular inhibitory neurons
Steriade, M. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.03.007 · Cited by 443 · see citing works
Parallel Pathways for Spectral Coding in Primate Retina
Dacey, D. M. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.743 · Cited by 442 · see citing works
The machinery of colour vision
Solomon, S. G., & Lennie, P. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2094 · Cited by 436 · see citing works
THE CIRCUITRY OF V1 AND V2: Integration of Color, Form, and Motion
Sincich, L. C., & Horton, J. C. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135731 · Cited by 433 · see citing works
The neurological organization of pathways between the dorsal lateral geniculate nucleus and visual cortex in old world and new world primates
Henderickson, A. E., Wilson, J. R., & Ogren, M. P. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901820108 · Cited by 423 · see citing works
Parallel Processing in the Visual System
Stone, J. (1983) · Springer eBooks · doi:10.1007/978-1-4684-4433-9 · Cited by 386 · see citing works
Multiparametric corticofugal modulation and plasticity in the auditory system
Suga, N., & Ma, X. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1222 · Cited by 380 · see citing works
Information Processing in the Primate Retina: Circuitry and Coding
Field, G. D., & Chichilnisky, E. J. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094252 · Cited by 364 · see citing works
Polyneuronal innervation of spiny stellate neurons in cat visual cortex
Ahmed, B., Anderson, J. C., Douglas, R. J., Martin, K. A. C., & Nelson, J. C. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903410105 · Cited by 338 · see citing works
The color-opponent and broad-band channels of the primate visual system
Schiller, P. H., & Logothetis, N. K. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90117-s · Cited by 311 · see citing works
Corticothalamic Inputs Control the Pattern of Activity Generated in Thalamocortical Networks
Blumenfeld, H., & McCormick, D. A. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-13-05153.2000 · Cited by 308 · see citing works
Visual response latencies of magnocellular and parvocellular LGN neurons in macaque monkeys
Maunsell, J. H. R., Ghose, G. M., Assad, J. A., McAdams, C. J., Boudreau, C. E., & Noerager, B. D. (1999) · Visual Neuroscience · doi:10.1017/s0952523899156177 · Cited by 298 · see citing works
Temporal-frequency selectivity in monkey visual cortex
Hawken, M. J., Shapley, R. M., & Grosof, D. H. (1996) · Visual Neuroscience · doi:10.1017/s0952523800008154 · Cited by 291 · see citing works
Emerging views of corticothalamic function
Briggs, F., & Usrey, W. M. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.09.002 · Cited by 268 · see citing works
Self-citation
The Afferent, Intrinsic, and Efferent Connections of Primary Visual Cortex in Primates
Casagrande, V. A., & Kaas, J. H. (1994) · Cerebral cortex · doi:10.1007/978-1-4757-9628-5_5 · Cited by 259 · see citing works
Corticofugal feedback influences the generation of length tuning in the visual pathway
Murphy, P. C., & Sillito, A. M. (1987) · Nature · doi:10.1038/329727a0 · Cited by 257 · see citing works
The Suppressive Field of Neurons in Lateral Geniculate Nucleus
Bonin, V., Mante, V., & Carandini, M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3562-05.2005 · Cited by 239 · see citing works
Relative numbers of cortical and brainstem inputs to the lateral geniculate nucleus
Erişir, A., Horn, S. C. V., & Sherman, S. M. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.4.1517 · Cited by 234 · see citing works
Laminar organization and contrast sensitivity of direction-selective cells in the striate cortex of the Old World monkey
Hawken, M. J., Parker, A. J., & Lund, J. S. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-10-03541.1988 · Cited by 224 · see citing works
Corticothalamic feedback and sensory processing
Alitto, H. J., & Usrey, W. M. (2003) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(03)00096-5 · Cited by 220 · see citing works
Self-citation
Contrast gain control in the primate retina: P cells are not X-like, some M cells are
Benardete, E. A., Kaplan, E., & Knight, B. W. (1992) · Visual Neuroscience · doi:10.1017/s0952523800004995 · Cited by 216 · see citing works
Extraclassical Receptive Field Properties of Parvocellular, Magnocellular, and Koniocellular Cells in the Primate Lateral Geniculate Nucleus
Solomon, S. G., White, A. J. R., & Martin, P. R. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-01-00338.2002 · Cited by 212 · see citing works
Immediate thalamic sensory plasticity depends on corticothalamic feedback
Krupa, D. J., Ghazanfar, A. A., & Nicolelis, M. A. L. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.14.8200 · Cited by 212 · see citing works
Structure and function of parallel pathways in the primate early visual system
Callaway, E. M. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.088047 · Cited by 209 · see citing works
Untitled work
Egner (2005) · doi:10.1038/nn1591 · Cited by 207 · see citing works
Cortically-induced coherence of a thalamic-generated oscillation
Alain Destexhe, A., Contreras, D., & Steriade, M. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00024-x · Cited by 194 · see citing works
Cortical Feedback Controls the Frequency and Synchrony of Oscillations in the Visual Thalamus
Bal, T., Debay, D., & Destexhe, A. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-19-07478.2000 · Cited by 183 · see citing works
Functional Topography of Corticothalamic Feedback Enhances Thalamic Spatial Response Tuning in the Somatosensory Whisker/Barrel System
Temereanca, S., & Simons, D. J. (2004) · Neuron · doi:10.1016/s0896-6273(04)00046-7 · Cited by 170 · see citing works
Stress-induced activation of nitric oxide-producing neurons in the rat brain
Krukoff, T. L., & Khalili, P. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970127)377:4 · Cited by 167 · see citing works
Chapter 2 The dynamics of primate retinal ganglion cells
Kaplan, E., & Benardete, E. A. (2001) · Progress in brain research · doi:10.1016/s0079-6123(01)34003-7 · Cited by 162 · see citing works
A quantitative study of synaptic interconnections in the dorsal lateral geniculate nucleus of the cat
G�illery, R. W. (1969) · Cell and Tissue Research · doi:10.1007/bf00321475 · Cited by 162 · see citing works
Attention-dependent Suppression of Metabolic Activity in the Early Stages of the Macaque Visual System
Vanduffel, W. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.2.109 · Cited by 161 · see citing works
Role of corticofugal feedback in hearing
Suga, N. (2008) · Journal of Comparative Physiology A · doi:10.1007/s00359-007-0274-2 · Cited by 156 · see citing works
Striate cortex increases contrast gain of macaque LGN neurons
Przybyszewski, A. W., Gaska, J., Foote, W. E., & Pollen, D. A. (2000) · Visual Neuroscience · doi:10.1017/s0952523800174012 · Cited by 153 · see citing works
Origin and dynamics of extraclassical suppression in the lateral geniculate nucleus of the macaque monkey
Alitto, H. J., & Usrey, W. M. (2008) · Neuron · doi:10.1016/j.neuron.2007.11.019 · Cited by 151 · see citing works
Self-citation
Segregation of Receptive Field Properties in the Lateral Geniculate Nucleus of a New-World Monkey, the Marmoset Callithrix jacchus
White, A. J. R., Wilder, H. D., Goodchild, A. K., Sefton, A. J., & Martin, P. R. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.4.2063 · Cited by 150 · see citing works
Thalamocortical Up States: Differential Effects of Intrinsic and Extrinsic Cortical Inputs on Persistent Activity
Rigas, P., & Castro‐Alamancos, M. A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0003-07.2007 · Cited by 147 · see citing works
Modulation of Responses and Frequency Tuning of Thalamic and Collicular Neurons by Cortical Activation in Mustached Bats
Zhang, Y. F., & Suga, N. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.1.325 · Cited by 145 · see citing works
Functional alignment of feedback effects from visual cortex to thalamus
Wang, W., Jones, H. E., Andolina, I. M., Salt, T. E., & Sillito, A. M. (2006) · Nature Neuroscience · doi:10.1038/nn1768 · Cited by 144 · see citing works
Orientation and Direction Selectivity of Neurons in V1 of Alert Monkeys: Functional Relationships and Laminar Distributions
Gur, M., Kagan, I., & Snodderly, D. M. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhi003 · Cited by 141 · see citing works
Looking back: corticothalamic feedback and early visual processing
Cudeiro, J., & Sillito, A. M. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.05.002 · Cited by 137 · see citing works
Spatial properties of koniocellular cells in the lateral geniculate nucleus of the marmoset Callithrix jacchus
White, A. J. R., Solomon, S. G., & Martin, P. R. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.0519a.x · Cited by 137 · see citing works
W-like response properties of interlaminar zone cells in the lateral geniculate nucleus of a primate (Galago crassicaudatus)
Irvin, G. E., Norton, T. T., Sesma, M. A., & Casagrande, V. A. (1986) · Brain Research · doi:10.1016/0006-8993(86)90450-6 · Cited by 132 · see citing works
The sublaminar organization of corticogeniculate neurons in layer 6 of macaque striate cortex
Fitzpatrick, D., Usrey, W. M., Schofield, B. R., & Einstein, G. (1994) · Visual Neuroscience · doi:10.1017/s0952523800001656 · Cited by 132 · see citing works
Self-citation
Three groups of cortico‐geniculate neurons and their distribution in binocular and monocular segments of cat striate cortex
Tsumoto, T., & Suda, K. (1980) · The Journal of Comparative Neurology · doi:10.1002/cne.901930115 · Cited by 122 · see citing works
Corticothalamic feedback enhances stimulus response precision in the visual system
Andolina, I. M., Jones, H. E., Wang, W., & Sillito, A. M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609318104 · Cited by 117 · see citing works
Spatial summation in lateral geniculate nucleus and visual cortex
Jones, H. E., Andolina, I. M., Oakely, N. M., Murphy, P. C., & Sillito, A. M. (2000) · Experimental Brain Research · doi:10.1007/s002210000574 · Cited by 108 · see citing works
Temporal contrast sensitivity in the lateral geniculate nucleus of a New World monkey, the marmoset Callithrix jacchus
Solomon, S. G., White, A. J. R., & Martin, P. R. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.0907s.x · Cited by 102 · see citing works
Efferent systems of the rabbit visual cortex: Laminar distribution of the cells of origin, axonal conduction velocities, and identification of axonal branches
Swadlow, H. A., & Weyand, T. G. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.902030415 · Cited by 100 · see citing works
Differential properties of cells in the feline primary visual cortex providing the corticofugal feedback to the lateral geniculate nucleus and visual claustrum
Grieve, K. L., & Sillito, A. M. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-07-04868.1995 · Cited by 100 · see citing works
Ordinal position and afferent input of neurons in monkey striate cortex
Bullier, J., & Henry, G. H. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901930407 · Cited by 99 · see citing works
Contributions of individual layer 6 pyramidal neurons to local circuitry in macaque primary visual cortex
Wiser, A., & Callaway, E. M. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-08-02724.1996 · Cited by 99 · see citing works
Corticogeniculate neurons, corticotectal neurons, and suspected interneurons in visual cortex of awake rabbits: receptive-field properties, axonal properties, and effects of EEG arousal
Swadlow, H. A., & Weyand, T. G. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.57.4.977 · Cited by 99 · see citing works
A Fast, Reciprocal Pathway between the Lateral Geniculate Nucleus and Visual Cortex in the Macaque Monkey
Briggs, F., & Usrey, W. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1035-07.2007 · Cited by 98 · see citing works
Self-citation
Contrast-sensitivity functions of W-, X-, and Y-like relay cells in the lateral geniculate nucleus of bush baby, Galago crassicaudatus
Norton, T. T., Casagrande, V. A., Irvin, G. E., Sesma, M. A., & Petry, H. M. (1988) · Journal of Neurophysiology · doi:10.1152/jn.1988.59.6.1639 · Cited by 94 · see citing works
Modelling corticothalamic feedback and the gating of the thalamus by the cerebral cortex
Alain Destexhe, A. (2000) · Journal of Physiology-Paris · doi:10.1016/s0928-4257(00)01093-7 · Cited by 92 · see citing works
Specificity in the axonal connections of layer VI neurons in tree shrew striate cortex: evidence for distinct granular and supragranular systems
Usrey, W., & Fitzpatrick, D. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-03-01203.1996 · Cited by 90 · see citing works
Self-citation
Visual physiology of the lateral geniculate nucleus in two species of New World monkey: Saimiri sciureus and Aotus trivirgatis
Usrey, W. M., & Reid, R. C. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00755.x · Cited by 90 · see citing works
Self-citation
Layer-Specific Input to Distinct Cell Types in Layer 6 of Monkey Primary Visual Cortex
Briggs, F., & Callaway, E. M. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-10-03600.2001 · Cited by 87 · see citing works
Self-citation
Feedback from V1 and inhibition from beyond the classical receptive field modulates the responses of neurons in the primate lateral geniculate nucleus
Webb, B. S., Tinsley, C. J., Barraclough, N. E., Easton, A., Parker, A. J., & Derrington, A. M. (2002) · Visual Neuroscience · doi:10.1017/s0952523802195046 · Cited by 87 · see citing works
Role of cortical feedback in the receptive field structure and nonlinear response properties of somatosensory thalamic neurons
Ghazanfar, A. A., Krupa, D. I., & Nicolelis, M. A. L. (2001) · Experimental Brain Research · doi:10.1007/s002210100849 · Cited by 82 · see citing works
Organization of the feedback pathway from striate cortex (V1) to the lateral geniculate nucleus (LGN) in the owl monkey (Aotus trivirgatus)
Ichida, J. M., & Casagrande, V. A. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10441 · Cited by 69 · see citing works
Completing the Corticofugal Loop: A Visual Role for the Corticogeniculate Type 1 Metabotropic Glutamate Receptor
Rivadulla, C., Martı́nez, L. M., Varela, C., & Cudeiro, J. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-07-02956.2002 · Cited by 62 · see citing works
Neural Coding of Color
Yokoyama, N., Shoda, K., & Tamori, Y. (2004) · Cited by 59 · see citing works
Corticofugal Output from the Primary Somatosensory Cortex Selectively Modulates Innocuous and Noxious Inputs in the Rat Spinothalamic System
Monconduit, L., López-Ávila, A., Molat, J.-L., Chalus, M., & Villanueva, L. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1293-06.2006 · Cited by 59 · see citing works
Cortical Modulation of Spatial and Angular Tuning Maps in the Rat Thalamus
Li, L., & Ebner, F. F. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4165-06.2007 · Cited by 58 · see citing works
Applications of parallel processing in vision
Brannan, J. R. (1992) · Cited by 55 · see citing works
Corticofugal feedback improves the timing of retino-geniculate signal transmission
Funke, K., Nelle, E., Li, B., & Wörgötter, F. (1996) · Neuroreport · doi:10.1097/00001756-199609020-00013 · Cited by 55 · see citing works
Corticofugal feedback influences the responses of geniculate neurons to moving stimuli
Guly�s, B., Lagae, L. G., Eysel, U. T., & Orban, G. A. (1990) · Experimental Brain Research · doi:10.1007/bf00608257 · Cited by 53 · see citing works
The M, P, and K Pathways of the Primate Visual System
Kaplan, E. (2003) · The MIT Press eBooks · doi:10.7551/mitpress/7131.003.0036 · Cited by 53 · see citing works
Modulation of the Receptive Fields of Midbrain Neurons Elicited by Thalamic Electrical Stimulation through Corticofugal Feedback
Wu, Y., & Yan, J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1320-07.2007 · Cited by 51 · see citing works
Corticothalamic Feedback for Sound-Specific Plasticity of Auditory Thalamic Neurons Elicited by Tones Paired with Basal Forebrain Stimulation
Zhang, Y., & Yan, J. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm188 · Cited by 51 · see citing works
Temporal properties of feedforward and feedback pathways between the thalamus and visual cortex in the ferret
Briggs, F., & Usrey, W. M. (2005) · Thalamus & Related Systems · doi:10.1017/s1472928807000131 · Cited by 48 · see citing works
Self-citation
Characteristics of corticothalamic neurons in area 17 of the cat
Harvey, A. R. (1978) · Neuroscience Letters · doi:10.1016/0304-3940(78)90164-7 · Cited by 46 · see citing works
Sublaminar organization within layer VI of the striate cortex in Galago
Conley, M., & Raczkowski, D. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903020218 · Cited by 41 · see citing works
Vibrissal responses of thalamic cells that project to the septal columns of the barrel cortex and to the second somatosensory area
Bokor, H., Acsády, L., & Deschênes, M. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0490-08.2008 · Cited by 36 · see citing works
Parallel Retinocortical Channels: X and Y and P and M
Shapley, R. M. (1992) · Advances in psychology · doi:10.1016/s0166-4115(08)61348-5 · Cited by 34 · see citing works
Suppression at High Spatial Frequencies in the Lateral Geniculate Nucleus of the Cat
Nolt, M. J., Kumbhani, R. D., & Palmer, L. A. (2007) · Journal of Neurophysiology · doi:10.1152/jn.01019.2006 · Cited by 32 · see citing works
Corticofugal influences on thalamic neurons during nociceptive transmission in awake rats
Wang, J., Chang, J., Woodward, D. J., Baccalá, L. A., Han, J., & Luo, F. (2007) · Synapse · doi:10.1002/syn.20375 · Cited by 29 · see citing works
Visual response augmentation in cat (and macaque) LGN: potentiation by corticofugally mediated gain control in the temporal domain
Cudeiro, J., Rivadulla, C., & Grieve, K. L. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00000.x · Cited by 17 · see citing works
Cell Types and Local Circuits in Primary Visual Cortex of the Macaque Monkey
Callaway, E. M. (2003) · The MIT Press eBooks · doi:10.7551/mitpress/7131.003.0050 · Cited by 17 · see citing works

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Canonical Microcircuits for Predictive Coding
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“The corticogeniculate feedback pathway from L6 maintains this segregation, as upper L6 cells preferentially synapse onto parvocellular cells in the LGN, while lower L6 cells target the magnocellular LGN layers (Fitzpatrick et al., 1994; Briggs and Usrey, 2009).”
BackgroundSelf-citation
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Self-citation
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Self-citation
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Self-citation
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Self-citation
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Self-citation
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Self-citation
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Self-citation
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Self-citation
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Self-citation
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Axonal Conduction Delays, Brain State, and Corticogeniculate Communication
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Distinct patterns of corticogeniculate feedback to different layers of the lateral geniculate nucleus
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Effects of cortical feedback on the spatial properties of relay cells in the lateral geniculate nucleus
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Self-citation
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Self-citation
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Self-citation
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Self-citation
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Self-citation
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Hawken, M. J., Shapley, R. M., Disney, A. A., García‐Marín, V., Henrie, J., Henry, C. A., Johnson, E. M., Joshi, S., Kelly, J. G., Ringach, D. L., et al. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1394-19.2020 · Cited by 19 · see citing works
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Self-citation
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Li, G., Ye, X., Song, T., Yang, Y., & Zhou, Y. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07781.x · Cited by 15 · see citing works
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Self-citation
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Self-citation
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Sherman, S. M. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.23897-2 · Cited by 8 · see citing works
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Li, Y., & Young, L.-S. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1008916 · Cited by 8 · see citing works
Distinct Mechanisms for Size Tuning in Primate Visual Cortex
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Self-citation
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Modulation of gamma-band activity across local cortical circuits
Brigg, F. (2009) · Frontiers in Integrative Neuroscience · doi:10.3389/neuro.07.015.2009 · Cited by 7 · see citing works
Robust effects of corticothalamic feedback and behavioral state on movie responses in mouse dLGNPreprint
Spacek, M. A., Crombie, D., Bauer, Y., Born, G., Liu, X., Katzner, S., & Busse, L. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/776237 · Cited by 7 · see citing works
Motor Control of Distinct Layer 6 Corticothalamic Feedback Circuits
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Self-citation
Patterned activity within the local cortical architecture
Briggs, F. (2010) · Frontiers in Neuroscience · doi:10.3389/fnins.2010.00018 · Cited by 6 · see citing works
Self-citation
A computational relationship between thalamic sensory neural responses and contrast perception
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Self-citation
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Visual Processing in the Primate Brain
Baker, C. I. (2012) · Wiley eBooks · doi:10.1002/9781118133880.hop203004 · Cited by 5 · see citing works
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Deshpande, G., & Wang, Y. (2022) · Brain Sciences · doi:10.3390/brainsci12101361 · Cited by 5 · see citing works
Estimating Neural Background Input with Controlled and Fast Perturbations: A Bandwidth Comparison between Inhibitory Opsins and Neural Circuits
Eriksson, D. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00058 · Cited by 4 · see citing works
Visual Corticotectal Neurons in Awake Rabbits: Receptive Fields and Driving Monosynaptic Thalamocortical Inputs
Su, C., Mendes-Platt, R. F., Alonso, J., Swadlow, H. A., & Bereshpolova, Y. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1945-23.2024 · Cited by 3 · see citing works
A connectomic approach to the lateral geniculate nucleus
Morgan, J. (2017) · Visual Neuroscience · doi:10.1017/s0952523817000116 · Cited by 3 · see citing works
Notice of Violation of IEEE Publication Principles: Tone Mapping Beyond the Classical Receptive Field
Gao, S., Tan, M.-J., He, Z., & Li, Y. (2020) · IEEE Transactions on Image Processing · doi:10.1109/tip.2020.2970541 · Cited by 3 · see citing works
Thalamocortical Interactions for Sensory Processing
Alonso, J. M., & Swadlow, H. A. (2017) · Oxford Research Encyclopedia of Neuroscience · doi:10.1093/acrefore/9780190264086.013.112 · Cited by 3 · see citing works
The Role of Layer 6 Corticothalamic Circuits in Vision: Plasticity, Sensory Processing, and Behavior
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Authors: Briggs, F., & Usrey, W. M.
Affiliations: University of California, Davis (US)
Corresponding author: Usrey, W. Martin
ORCID: Briggs, Farran
Usrey, W. Martin
Venue: Neuron
Publisher: Elsevier BV
Published: 2009-04
Volume: 62
Issue: 1
Pages: 135-146
ISSN: 0896-6273 (ISSN-L)
DOI: 10.1016/j.neuron.2009.02.024
PMC: PMC2789995
OpenAlex: W2087235763
Semantic Scholar: 8699c617077e0e61c6d83395314ee40c73de29e9
Cited by: 139
References: 99
Citations by year: 2026: 1 · 2025: 7 · 2024: 9 · 2023: 2 · 2022: 5 · 2021: 31 · 2020: 6 · 2019: 4 · 2018: 7 · 2017: 15 · 2016: 5 · 2015: 7 · 2014: 7 · 2013: 7 · 2012: 8
FWCI: 4.19
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
www.elsevier.com/legal/tdmrep-license (tdm)
www.elsevier.com/open-access/userlicense/1.0/ (vor, 1604 d)
doi.org/10.15223/policy-017 (stm-asf)
doi.org/10.15223/policy-037 (stm-asf)
doi.org/10.15223/policy-012 (stm-asf)
doi.org/10.15223/policy-029 (stm-asf)
doi.org/10.15223/policy-004 (stm-asf)
Locations: Neuron (publishedVersion)
PubMed (publishedVersion)
PubMed Central (acceptedVersion)
Funders: National Institutes of Health (EY12576, EY13588, EY15580)
McKnight Foundation
National Science Foundation (0727115)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: corticothalamic feedback, lateral geniculate nucleus, visual processing, magnocellular pathway, parvocellular pathway, koniocellular pathway, thalamocortical transmission, macaque, visual neurons
MeSH terms: Action Potentials, Animals, Biophysics, Brain Mapping, Electric Stimulation, Feedback, Geniculate Bodies, Macaca mulatta, Male, Models, Neurological, Neurons, Photic Stimulation, Reaction Time, Visual Cortex, Visual Pathways, Cluster Analysis

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Parallel processing in the corticogeniculate pathway of the macaque monkey

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