Horizontal cell feedback without cone type-selective inhibition mediates "red-green" color opponency in midget ganglion cells of the primate retina.
Horizontal cell feedback without cone type-selective inhibition mediates "red-green" color opponency in midget ganglion cells of the primate retina.
复制标题
DOI:
10.1523/jneurosci.4385-10.2011
复制
发表时间:
2011-02-02
期刊:
影响因子:
--
通讯作者:
Dacey DM
中科院分区:
文献类型:
--
作者:
Crook JD;Manookin MB;Packer OS;Dacey DM
The distinctive red-green dimension of human and non-human primate color perception arose relatively recently in the primate lineage with the appearance of separate long (L) and middle (M) wavelength sensitive cone photoreceptor types. ‘Midget’ ganglion cells of the retina utilize center-surround receptive field structure to combine L and M cone signals antagonistically and thereby establish a ‘red-green, color-opponent’ visual pathway. However the synaptic origin of red-green opponency is unknown and conflicting evidence for either random or L vs M cone-selective inhibitory circuits have divergent implications for the developmental and evolutionary origins of trichromatic color vision. Here we directly measure the synaptic conductances evoked by selective L or M cone stimulation in the midget ganglion cell dendritic tree and show that L vs M cone opponency arises presynaptic to the midget cell and is transmitted entirely by modulation of an excitatory conductance. L and M cone synaptic inhibition is feedforward and thus occurs in-phase with excitation for both cone types. Block of GABAergic and glycinergic receptors does not attenuate or modify L vs M cone antagonism, discounting both pre- and postsynaptic inhibition as sources of cone opponency. In sharp contrast, enrichment of retinal pH buffering capacity, to attenuate negative feedback from horizontal cells that sum L and M cone inputs linearly and without selectivity, completely abolished both the midget cell surround and all chromatic opponency. Thus, red-green opponency appears to arise via outer retinal horizontal cell feedback that is not cone type-selective without recourse to any inner retinal L vs M cone inhibitory pathways.