Lagged Y cells in the cat lateral geniculate nucleus

We report on the existence of lagged Y (YL) cells in the A laminae of the cat lateral geniculate nucleus (LGN) and on criteria for identifying them using visual and electrical stimulation. Like the lagged X (XL) cells described previously (Mastronarde, 1987a; Humphrey & Weller, 1988a), YL cells responded to a spot stimulus with an initial dip in firing and a delayed latency to discharge after spot onset, and an anomalously prolonged firing after spot offset. However, the cells received excitatory input from retinal Y rather than X afferents, and showed nonlinear spatial summation and other Y-like receptive-field properties. Three YL cells tested for antidromic activation from visual cortex were found to be relay cells, with long conduction latencies similar to those of XL cells. Simultaneous recordings of a YL cell and its retinal Y afferents show striking parallels between lagged X and Y cells in retinogeniculate functional connectivity, and suggest that the YL-cell response profile reflects inhibitory processes occurring within the LGN. The YL cells comprised approximately 5% of Y cells and approximately 1% of all cells in the A laminae. Although infrequently encountered in the LGN, they may be roughly as numerous as Y cells in the retina, and hence could fulfill an important role in vision.

[1]  D N Mastronarde,et al.  Two classes of single-input X-cells in cat lateral geniculate nucleus. II. Retinal inputs and the generation of receptive-field properties. , 1987, Journal of neurophysiology.

[2]  M. J. Friedlander,et al.  Morphology of functionally identified neurons in lateral geniculate nucleus of the cat. , 1981, Journal of neurophysiology.

[3]  A. L. Humphrey,et al.  Functionally distinct groups of X‐cells in the lateral geniculate nucleus of the cat , 1988, The Journal of comparative neurology.

[4]  S. Lindström,et al.  Private inhibitory systems for the X and Y pathways in the dorsal lateral geniculate nucleus of the cat. , 1990, The Journal of physiology.

[5]  F. Hajdu,et al.  Quantitative histological studies on the lateral geniculate nucleus in the cat. II. Cell numbers and densities in the several layers. , 1978, Journal fur Hirnforschung.

[6]  S. Sherman,et al.  Brainstem control of response modes in neurons of the cat's lateral geniculate nucleus. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[7]  M. Dubin,et al.  Non‐uniform postnatal growth of the cat retina , 1984, The Journal of comparative neurology.

[8]  Interneurones in the lateral geniculate nucleus with monosynaptic excitation from retinal ganglion cells , 1983 .

[9]  P. Heggelund,et al.  Neurotransmitter receptors mediating excitatory input to cells in the cat lateral geniculate nucleus. I. Lagged cells. , 1990, Journal of neurophysiology.

[10]  A. L. Humphrey,et al.  Spatial and temporal response properties of lagged and nonlagged cells in cat lateral geniculate nucleus. , 1990, Journal of neurophysiology.

[11]  R E Weller,et al.  Structural correlates of functionally distinct X‐cells in the lateral geniculate nucleus of the cat , 1988, The Journal of comparative neurology.

[12]  D N Mastronarde,et al.  Two classes of single-input X-cells in cat lateral geniculate nucleus. I. Receptive-field properties and classification of cells. , 1987, Journal of neurophysiology.

[13]  A. Sillito,et al.  Dependence of retinogeniculate transmission in cat on NMDA receptors. , 1990, Journal of neurophysiology.

[14]  B. Cleland,et al.  Organization of visual inputs to interneurons of lateral geniculate nucleus of the cat. , 1977, Journal of neurophysiology.