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Lateral division of the lateral posterior region: Connections with area 18 in cats

Published online by Cambridge University Press:  02 June 2009

Marcie W. Pospichal
Affiliation:
Department of Psychology, Vanderbilt University, Nashville
Iwona Stepniewska
Affiliation:
Department of Psychology, Vanderbilt University, Nashville
Brian M. Wimborne
Affiliation:
Research School for Biological Sciences, Australian National University, G.P.O. Box 334, Canberra, ACT 2601, Australia
Jon H. Kaas
Affiliation:
Department of Psychology, Vanderbilt University, Nashville

Abstract

To establish the topography of the lateral division of the lateral posterior region (LP1) projections to area 18, up to five different anatomical tracers were injected in separate rostrocaudal locations in area 18 of four adult cats, and patterns of retrogradely labeled LP1 cells were identified. LP1 inputs to area 18 arose from both caudal and rostral nuclei and were topological, organized in patterns that indicate that lower visual space is represented anteroventrally, and more central and upper visual space is represented caudodorsally. In the caudal LP1 nucleus, patches of labeled cells formed bands that ran parallel to the medial and lateral LPI borders and encompassed medial portions of the nucleus. In rostral LP1, the patches of labeled cells formed clusters giving the connections with area 18 a more modular appearance, and were nearer the lateral LP1 border. Injections made nearest area centralis representations in area 18 labeled more neurons than injections in cortex representing more peripheral visual space. Also, neighboring injections in area 18 labeled overlapping patches of cells, but no double-labeled cells were observed. These findings are consistent with previous conclusions based on electrophysiological mapping studies, that two retinotopically organized nuclei constitute LP1.

Type
Short Communications
Copyright
Copyright © Cambridge University Press 1996

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References

Abramson, B.P. & Chalupa, L.M. (1985). The laminar distribution of cortical connections with the tecto- and cortico-recipient zones in the cat's lateral posterior nucleus. Neuroscience 15, 8195.Google Scholar
Abramson, B.P. & Chalupa, L.M. (1988). Multiple pathways from the superior colliculus to the extrageniculate visual thalamus of the cat. Journal of Comparative Neurology 271, 397418.Google Scholar
Berson, D.M. & Graybiel, A.M. (1978). Parallel thalamic zones in the LP-pulvinar complex of the cat identified by their afferent and efferent connections. Brain Research 147, 39148.CrossRefGoogle ScholarPubMed
Birnbacher, D. & Albus, K. (1987). Divergence of single axons in afferent projections to the cat's visual cortical areas 17, 18, and 19: A parametric study. Journal of Comparative Neurology 261, 543561.CrossRefGoogle Scholar
Bullier, J., Kennedy, H. & Salinger, W. (1984). Bifurcation of sub-cortical afferents to visual areas 17, 18, and 19 in the cat cortex. Journal of Comparative Neurology 228, 309328.Google Scholar
Chalupa, L.M. & Abramson, B.P. (1989). Visual receptive fields in the striate-recipient zone of the lateral posterior-pulvinar complex. Journal of Neuroscience 9, 347357.Google Scholar
Humphrey, A.L., Sur, M., Uhlrich, D.J. & Sherman, S.M. (1985). Termination patterns of individual X- and Y-cell axons in the visual cortex of the cat: Projections to area 18, to the 17/18 border region, and to both areas 17 and 18. Journal of Comparative Neurology 233, 190211.CrossRefGoogle Scholar
Hutchins, B. & Updyke, B.V. (1989). Retinotopic organization within the lateral posterior complex of the cat. Journal of Comparative Neurology 285, 350398.Google Scholar
Kaas, J.H. (1990). Processing areas and modules in sensory-perceptual cortex. In Signal and Sense: Local and Global Order in Perceptual Maps, ed. Edelman, G.E. & Gall, W.O., pp. 6782. New York: Wiley-Liss.Google Scholar
Mesulam, M.M. (1978). Tetramethylbenzidine for horseradish peroxidase neurochemistry: A noncarcinogenic blue reaction product with superior sensitivity for visualizing neural afferents and efferents. Journal of Histochemical Cytochemistry 26, 106117.CrossRefGoogle Scholar
Miceli, D., Reperant, J., Marchand, L., Ward, R. & Vesselkin, N. (1991). Divergence and collateral axon branching in subsystems of visual cortical projections from the cat lateral posterior nucleus. Journal fur Hirnforschung 32, 165173.Google Scholar
Palestini, M., Guegan, M., Saavedra, H., Thomasset, M. & Batini, C. (1993). Glutamate, calbindin-D28k and parvalbumin immunoreactivity in the pulvinar-lateralis posterior complex of the cat: Relation to the projection to the Clare-Bishop area. Neuroscience Letters 160, 8992.CrossRefGoogle Scholar
Payne, B.R. & Siwek, D.F. (1990). Receptive fields of neurons at the confluence of cerebral cortical areas 17, 18, 20a and 20b in the cat. Visual Neuroscience 4, 475479.CrossRefGoogle ScholarPubMed
Pospichal, M.W., Wimborne, B.M., Stepniewska, I. & Kaas, J.H. (1996). Surface-view connectivity patterns of area 18 in cats. Acta Neurobiologicae Experimentalis (in press).CrossRefGoogle Scholar
Raczkowski, D. & Rosenquist, A.C. (1981). Retinotopic organization in the cat lateral posterior-pulvinar complex. Brain Research 221, 185191.Google Scholar
Raczkowski, D. & Rosenquist, A.C. (1983). Connections of the multiple visual cortical areas with the lateral posterior-pulvinar complex and adjacent thalamic nuclei in the cat. Journal of Neuroscience 3, 19121942.Google Scholar
Rosenquist, A.C. (1985). Connections of visual cortical areas in the cat. In Cerebral Cortex, ed. Peters, A. & Jones, E.G., pp. 81117. New York: Plenum Press.Google Scholar
Salin, P.A., Bullier, J. & Kennedy, H. (1989). Convergence and divergence in the afferent projections to cat area 17. Journal of Comparative Neurology 283, 486512.CrossRefGoogle ScholarPubMed
Tusa, R.J., Rosenquist, A.C. & Palmer, L.A. (1979). Retinotopic organization of area 18 and 19 in the cat. Journal of Comparative Neurology 185, 657678.Google Scholar
Updyke, B.V. (1977). Topographic organization of the projections from cortical areas 17, 18, and 19 onto the thalamus, pretectum, and superior colliculus in the cat. Journal of Comparative Neurology 173, 81122.Google Scholar
Updyke, B.V. (1983). A reevaluation of the functional organization and cytoarchitecture of the feline lateral posterior complex, with observations on adjoining cell groups. Journal of Comparative Neurology 219, 143181.CrossRefGoogle ScholarPubMed
Wimborne, B.M., Mccart, R.J. & Henry, G.H. (1993). Projections from the lateral division of the lateral posterior-pulvinar complex to area 21a and the striate cortex in the cat. Brain Research 603, 333337.CrossRefGoogle ScholarPubMed
Winans, S.S. (1967). Visual form discrimination after removal of the visual cortex in cats. Science 158, 944946.Google Scholar