Layer-dependent loss and enhancement of geniculostriate and retinotectal pathways in adult human amblyopia

Abnormal visual experience during critical period leads to reorganization of neuroarchitectures in primate visual cortex. However, developmental plasticity of human subcortical visual pathways remains elusive. Using high-resolution fMRI and pathway-selective visual stimuli, we investigated layer-dependent response properties and connectivity of subcortical visual pathways of adult human amblyopia. Stimuli presented to the amblyopic eye showed selective response loss in the parvocellular layers of the lateral geniculate nucleus, and also reduced the connectivity to V1. Amblyopic eye's response to isoluminant chromatic stimulus was significantly reduced in the superficial layers of the superior colliculus, while the fellow eye's response robustly increased in the deeper layers associated with increased cortical feedbacks. Therefore, amblyopia led to selective reduction of parvocellular feedforward signals in the geniculostriate pathway, whereas loss and enhancement of parvocellular feedback signals in the retinotectal pathway. These findings shed light for future development of new tools for treating amblyopia and tracking the prognosis.

Distribution and specificity of S-cone (“blue cone”) signals in subcortical visual pathways

We review here the distribution of S-cone signals and properties of S-cone recipient receptive fields in subcortical pathways. Nearly everything we know about S-cone signals in the subcortical visual system comes from the study of visual systems in cats and primates (monkeys); in this review, we concentrate on results from macaque and marmoset monkeys. We discuss segregation of S-cone recipient (blue-on and blue-off) receptive fields in the dorsal lateral geniculate nucleus and describe their receptive field properties. We treat in some detail the question of detecting weak S-cone signals as an introduction for newcomers to the field. Finally, we briefly consider the question on how S-cone signals are distributed among nongeniculate targets.