Pietersen A N J, Cheong S K, Solomon S G, Tailby C, Martin P R
Australian Research Council Centre of Excellence for Integrative Brain Function, University of Sydney, Sydney, Australia; Save Sight Institute, University of Sydney, Sydney, Australia;
School of Medical Sciences, University of Sydney, Sydney, Australia; Department of Experimental Psychology, University College London, London, United Kingdom; and.
J Neurophysiol. 2014 Sep 15;112(6):1421-38. doi: 10.1152/jn.00077.2014. Epub 2014 Jun 11.
Visual perception requires integrating signals arriving at different times from parallel visual streams. For example, signals carried on the phasic-magnocellular (MC) pathway reach the cerebral cortex pathways some tens of milliseconds before signals traveling on the tonic-parvocellular (PC) pathway. Visual latencies of cells in the koniocellular (KC) pathway have not been specifically studied in simian primates. Here we compared MC and PC cells to "blue-on" (BON) and "blue-off" (BOF) KC cells; these cells carry visual signals originating in short-wavelength-sensitive (S) cones. We made extracellular recordings in the lateral geniculate nucleus (LGN) of anesthetized marmosets. We found that BON visual latencies are 10-20 ms longer than those of PC or MC cells. A small number of recorded BOF cells (n = 7) had latencies 10-20 ms longer than those of BON cells. Within all cell groups, latencies of foveal receptive fields (<10° eccentricity) were longer (by 3-8 ms) than latencies of peripheral receptive fields (>10°). Latencies of yellow-off inputs to BON cells lagged the blue-on inputs by up to 30 ms, but no differences in visual latency were seen on comparing marmosets expressing dichromatic ("red-green color-blind") or trichromatic color vision phenotype. We conclude that S-cone signals leaving the LGN on KC pathways are delayed with respect to signals traveling on PC and MC pathways. Cortical circuits serving color vision must therefore integrate across delays in (red-green) chromatic signals carried by PC cells and (blue-yellow) signals carried by KC cells.
视觉感知需要整合来自平行视觉流且到达时间不同的信号。例如,由相位性大细胞(MC)通路携带的信号比由持续性小细胞(PC)通路传播的信号提前几十毫秒到达大脑皮层通路。在猿猴灵长类动物中,尚未对侏儒细胞(KC)通路中细胞的视觉潜伏期进行专门研究。在这里,我们将MC和PC细胞与“蓝开”(BON)和“蓝关”(BOF)KC细胞进行了比较;这些细胞携带源自短波敏感(S)视锥细胞的视觉信号。我们在麻醉的狨猴的外侧膝状体核(LGN)中进行了细胞外记录。我们发现,BON视觉潜伏期比PC或MC细胞的潜伏期长10 - 20毫秒。少数记录的BOF细胞(n = 7)的潜伏期比BON细胞长10 - 20毫秒。在所有细胞组中,中央凹感受野(偏心度<10°)的潜伏期比外周感受野(偏心度>10°)的潜伏期长(3 - 8毫秒)。BON细胞的黄关输入潜伏期比蓝开输入滞后多达30毫秒,但在比较表达二色性(“红绿色盲”)或三色性色觉表型的狨猴时,未发现视觉潜伏期有差异。我们得出结论,相对于在PC和MC通路上传播的信号,通过KC通路离开LGN的S视锥细胞信号会延迟。因此,服务于色觉的皮层回路必须整合PC细胞携带的(红 - 绿)色信号和KC细胞携带的(蓝 - 黄)信号之间的延迟。