Spatial summation and conduction latency classification of cells of the lateral geniculate nucleus of macaques

Cells in the lateral geniculate nucleus (LGN) of the macaque monkey were investigated with microelectrodes in an attempt to develop an overall classification scheme. We classified cells in the parvocellular (P) and magnocellular (M) layers according to (non)linearity of spatial summation, shock latency, and chromatic organization of center and surround. We also measured the spatial and temporal tuning to counterphasing and drifting sine wave gratings and tested for periphery effects. Our results showed that no strict laminar segregation existed for any cell property studied. Our results can be summarized as follows: 1. Most P layer cells showed a linear summation (98%) and color-opponent responses (80%), while other cells showed a nonlinear summation (Y-cells, 2%) and broad band responses (28%). In contrast, 37% of the M layer cells were linear summators and the remainder were nonlinear. Therefore, there are overlapping distributions of X- and Y- cells in P and M layers but not a strict segregation. 2. P layer cells had longer shock latencies than M layer cells. X-cells conducted more slowly (2.4 +/- 0.7 msec) than Y-cells (1.6 +/- 0.8 msec), but there were overlapping distributions. Latency shortened gradually, rather than abruptly, with increasing depth. 3. The first harmonic of X- and Y- cell responses was maximally sensitive to spatial frequencies of about 2 cycles/deg. Each type of cell modulated about a mean rate to a drifting grating, although Y-cells had higher distortion than X-cells. Response amplitudes to drifting gratings were higher for MX- and MY- than for PX-cells. No DC elevation to high spatial frequencies was seen. Spatial bandwidths averaged 2 to 5 octaves. X-cells were maximally tuned to temporal frequencies around 11 Hz, and Y-cells were tuned to about 19 Hz;. temporal bandwidths for both averaged 2.8 octaves. 4. Periphery effects were detected in 4% of the X-cells and 25% of the Y-cells. 5. These data indicate that gradual changes occur between dorsal and ventral layers: summation changes from linear to nonlinear; conduction latencies shorten; peak temporal tuning increases; response amplitudes increase; the periphery effect becomes more prevalent. Spatial tuning does not change. No strict laminar segregation or specificity exists for any of the properties that we studied.

[1]  W. Burke,et al.  Single‐unit recording from antidromically activated optic radiation neurones , 1962, The Journal of physiology.

[2]  J. Mcilwain RECEPTIVE FIELDS OF OPTIC TRACT AXONS AND LATERAL GENICULATE CELLS: PERIPHERAL EXTENT AND BARBITURATE SENSITIVITY. , 1964, Journal of neurophysiology.

[3]  W. Levick,et al.  EVIDENCE THAT MCILWAIN'S PERIPHERY EFFECT IS NOT A STRAY LIGHT ARTIFACT. , 1965, Journal of neurophysiology.

[4]  R. L. Valois,et al.  Analysis of response patterns of LGN cells. , 1966, Journal of the Optical Society of America.

[5]  C. Enroth-Cugell,et al.  The contrast sensitivity of retinal ganglion cells of the cat , 1966, The Journal of physiology.

[6]  C Blakemore,et al.  On the existence of neurones in the human visual system selectively sensitive to the orientation and size of retinal images , 1969, The Journal of physiology.

[7]  R. L. de Valois Contribution of different lateral geniculate cell types to visual behavior. , 1971, Vision research.

[8]  K Nakayama,et al.  Local adaptation in cat LGN cells: evidence for a surround antagonism. , 1971, Vision research.

[9]  H Ikeda,et al.  Receptive field organization of ‘sustained’ and ‘transient’ retinal ganglion cells which subserve different functional roles , 1972, The Journal of physiology.

[10]  W. Levick,et al.  Properties of sustained and transient ganglion cells in the cat retina , 1973, The Journal of physiology.

[11]  L. Maffei,et al.  The visual cortex as a spatial frequency analyser. , 1973, Vision research.

[12]  W. Levick,et al.  Properties of rarely encountered types of ganglion cells in the cat's retina and on overall classification , 1974, The Journal of physiology.

[13]  R. L. de Valois,et al.  Psychophysical studies of monkey vision. 3. Spatial luminance contrast sensitivity tests of macaque and human observers. , 1974, Vision research.

[14]  M. Cynader,et al.  Response characteristics of single cells in the monkey superior colliculus following ablation or cooling of visual cortex. , 1974, Journal of neurophysiology.

[15]  J. Stone,et al.  Retinal distribution and central projections of Y-, X-, and W-cells of the cat's retina. , 1974, Journal of neurophysiology.

[16]  P. Gouras,et al.  Functional properties of ganglion cells of the rhesus monkey retina. , 1975, The Journal of physiology.

[17]  J. Lund,et al.  Monkey retinal ganglion cells: Morphometric analysis and tracing of axonal projections, with a consideration of the peroxidase technique , 1975, The Journal of comparative neurology.

[18]  P. Padmos,et al.  Cone systems interaction in single neurons of the lateral geniculate nucleus of the macaque , 1975, Vision Research.

[19]  P. Gouras,et al.  Spatial summation, response pattern and conduction velocity of ganglion cells of the rhesus monkey retina , 1976, Vision Research.

[20]  R. Shapley,et al.  Quantitative analysis of retinal ganglion cell classifications. , 1976, The Journal of physiology.

[21]  R. W. Rodieck,et al.  Identification, classification and anatomical segregation of cells with X‐like and Y‐like properties in the lateral geniculate nucleus of old‐world primates. , 1976, The Journal of physiology.

[22]  M. Wright,et al.  Proceedings: Properties of sustained-X, transient-Y and transient-X cells in the cat's lateral geniculate nucleus. , 1976, The Journal of physiology.

[23]  R. Marrocco,et al.  Sustained and transient cells in monkey lateral geniculate nucleus: conduction velocites and response properties. , 1976, Journal of neurophysiology.

[24]  P. Schiller,et al.  Properties and tectal projections of monkey retinal ganglion cells. , 1977, Journal of neurophysiology.

[25]  F. de Monasterio,et al.  Properties of concentrically organized X and Y ganglion cells of macaque retina. , 1978, Journal of neurophysiology.

[26]  F M de Monasterio,et al.  Properties of ganglion cells with atypical receptive-field organization in retina of macaques. , 1978, Journal of neurophysiology.

[27]  F. M. D. Monasterio Center and surround mechanisms of opponent-color X and Y ganglion cells of retina of macaques. , 1978 .

[28]  J. Movshon,et al.  Spatial and temporal contrast sensitivity of neurones in areas 17 and 18 of the cat's visual cortex. , 1978, The Journal of physiology.

[29]  F M de Monasterio,et al.  Center and surround mechanisms of opponent-color X and Y ganglion cells of retina of macaques. , 1978, Journal of neurophysiology.

[30]  P. Schiller,et al.  Functional specificity of lateral geniculate nucleus laminae of the rhesus monkey. , 1978, Journal of neurophysiology.

[31]  F. M. D. Monasterio Properties of concentrically organized X and Y ganglion cells of macaque retina. , 1978 .

[32]  F. M. D. Monasterio Properties of ganglion cells with atypical receptive-field organization in retina of macaques. , 1978 .

[33]  J. Lythgoe,et al.  The visual pigments of rods and cones in the rhesus monkey, Macaca mulatta. , 1978, The Journal of physiology.

[34]  C. R. Michael,et al.  Columnar organization of color cells in monkey's striate cortex. , 1981, Journal of neurophysiology.

[35]  J W McClurkin,et al.  Modulation of lateral geniculate nucleus cell responsiveness by visual activation of the corticogeniculate pathway , 1982, The Journal of neuroscience : the official journal of the Society for Neuroscience.