Cited by 1,602Visual perception and processing mechanismsMotor Control and AdaptationFace Recognition and Perception

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The connections of the middle temporal visual area (MT) and their relationship to a cortical hierarchy in the macaque monkey

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Maunsell, JH, van Essen, DC·1983·The Journal of Neuroscience

DOI 10.1523/jneurosci.03-12-02563.1983PMC PMC6564662

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Abstract

The cortical and subcortical connections of the middle temporal visual area (MT) of the macaque monkey were investigated using combined injections of [3H]proline and horseradish peroxidase within MT. Cortical connections were assigned to specific visual areas on the basis of their relationship to the pattern of interhemispheric connections, revealed by staining for degeneration following callosal transection. MT was shown to be reciprocally connected with many topographically organized cortical visual areas, including V1, V2, V3, and V4. These pathways link regions representing corresponding portions of the visual field in the different areas. In addition, MT has reciprocal connections with two previously unidentified cortical areas, which we have designated the medial superior temporal area (MST) and the ventral intraparietal area (VIP). The laminar distribution of terminals and cell bodies in cortical areas connected with MT follows a consistent pattern. In areas V1, V2, and V3, the projections to MT arise largely or exclusively from cells in supragranular layers, and the reciprocal connections from MT terminate mainly in supragranular and infragranular layers. In contrast, the projections to MST and VIP terminate mainly in layer IV, and the reciprocal pathways originate from cells in both superficial and deep layers. On the basis of this pattern, each connection can be designated as forward or feedback in nature, and a hierarchical arrangement of visual areas can be determined. In this hierarchy, MT is at a higher level than V1, V2, and V3, and at a lower level than MST and VIP. Subcortical projections were seen from MT to the claustrum, the putamen, the caudate nucleus, the inferior and lateral subdivisions of the pulvinar complex, the ventral lateral geniculate nucleus, the reticular nucleus of the thalamus, the superior colliculus, and the pontine nuclei.

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Hubel, D. H., & Wiesel, T. N. (1962) · The Journal of Physiology · doi:10.1113/jphysiol.1962.sp006837 · Cited by 13,680
Receptive fields and functional architecture of monkey striate cortex
Hubel, D. H., & Wiesel, T. N. (1968) · The Journal of Physiology · doi:10.1113/jphysiol.1968.sp008455 · Cited by 6,685
Tetramethyl benzidine for horseradish peroxidase neurohistochemistry: a non-carcinogenic blue reaction product with superior sensitivity for visualizing neural afferents and efferents.
Mesulam, M. M. (1978) · Journal of Histochemistry & Cytochemistry · doi:10.1177/26.2.24068 · Cited by 4,303
The autoradiographic demonstration of axonal connections in the central nervous system
Cowan, W. M., Gottlieb, D. I., Hendrickson, A. E., Price, J. L., & Woolsey, T. A. (1972) · Brain Research · doi:10.1016/0006-8993(72)90344-7 · Cited by 1,610
Functional properties of neurons in middle temporal visual area of the macaque monkey. I. Selectivity for stimulus direction, speed, and orientation
Maunsell, J. H. R., & Essen, D. C. V. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.49.5.1127 · Cited by 1,462
Self-citation
The representation of the visual field on the cerebral cortex in monkeys
Daniel, P. M., & Whitteridge, D. (1961) · The Journal of Physiology · doi:10.1113/jphysiol.1961.sp006803 · Cited by 1,147
Functional organization of a visual area in the posterior bank of the superior temporal sulcus of the rhesus monkey
Zeki, S. (1974) · The Journal of Physiology · doi:10.1113/jphysiol.1974.sp010452 · Cited by 982
Intracortical connectivity of architectonic fields in the somatic sensory, motor and parietal cortex of monkeys
Jones, E. G., Coulter, J. D., & Hendry, S. H. C. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901810206 · Cited by 977
Silver Staining of Myelin by Means of Physical Development
Gallyas, F. (1979) · Neurological Research · doi:10.1080/01616412.1979.11739553 · Cited by 936
Functional properties of neurons in middle temporal visual area of the macaque monkey. II. Binocular interactions and sensitivity to binocular disparity
Maunsell, J. H. R., & Essen, D. C. V. (1983) · Journal of Neurophysiology · doi:10.1152/jn.1983.49.5.1148 · Cited by 746
Self-citation

Show all 52 references

Research works printed but not linked: 1

Olszewski, J. (1952) The Thalamus of the Macaca mulatta, S. Karger AG, Basel.

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Impairment of vertical motion detection and downgaze palsy due to rostral midbrain infarction
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Eye Movements: Developmental Aspects
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Multiple Cortical Representations of Optic Flow Processing
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Authors: Maunsell, J., & van Essen, D.
Venue: The Journal of Neuroscience
Publisher: Society for Neuroscience
Published: 1983-12-01
Volume: 3
Issue: 12
Pages: 2563-2586
ISSN: 0270-6474 (ISSN-L)
1529-2401
DOI: 10.1523/jneurosci.03-12-02563.1983
PMC: PMC6564662
OpenAlex: W2145439642
Cited by: 1,602
References: 52
Citations by year: 2026: 14 · 2025: 19 · 2024: 16 · 2023: 17 · 2022: 21 · 2021: 31 · 2020: 52 · 2019: 30 · 2018: 33 · 2017: 34 · 2016: 30 · 2015: 31 · 2014: 40 · 2013: 49 · 2012: 39
FWCI: 30.40
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: cc-by-nc-sa
creativecommons.org/licenses/by-nc-sa/4.0/ (vor, 183 d)
Locations: Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: National Eye Institute (R01EY002091)
National Institute of General Medical Sciences (T32GM007737)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
Keywords: middle temporal area, MT, cortical hierarchy, visual cortex, interhemispheric connections, medial superior temporal area, ventral intraparietal area, visual area V1, visual area V2, area V4, subcortical projections, pulvinar, superior colliculus, macaque
MeSH terms: Animals, Brain Mapping, Horseradish Peroxidase, Macaca, Macaca fascicularis, Thalamus, Visual Cortex, Visual Fields, Visual Pathways

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The connections of the middle temporal visual area (MT) and their relationship to a cortical hierarchy in the macaque monkey

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