Functional organization of the retina: receptive fields

Topographic projection: the anatomical picture

Retina, thalamus (LGN) and cortex; the visual field map in primary visual cortex.

Enlarged respresentation of the fovea.

Hemidecussation at the optic chiasm: two retinas, one cortical map, one  world (Newton).

An implication of topographic projection: receptive fields are small.

BUT the projection is not strictly one to one (dendritic trees have a spread), so neurons pick up from multiple receptors. Also: “gap junctions” connect adjacent receptors and horizontal cells.          

What is the role of horizontal cells and amacrine cells?

Electrophysiological measurement of receptive fields (Kuffler et al.)

Experimental setup

Results: a “Mexican hat” profile. Center-surround antagonism (= lateral inhibition)

Retinal microelectrode recording: RF is centered on cell body

Separate on- and off-systems respectively detect onset and offset of center stimulation at the bipolar cell and later levels

Structural basis of center-surround antagonism

Sign-conserving and sign-inverting synapses in the retina

Horizontal cells and (many) amacrine cells are agents of lateral inhibition, mediated by sign-inverting synapses

Perceptual consequences of center-surround antagonism: sensitivity to spatial contrast

Simultaneous contrast, Mach Bands, Hermann grid

Two reasons center-surround antagonism can be useful

Selective response to edges means economy of representation: a cartoon-like line drawing needs less information

The “trigger feature” concept, illustrated by “bug detector” retinal ganglion cells in frogs…rather than simply registering light or contrast, the firing of such a neuron may convey something important to the animal.

Neural diversity: X and Y (or P and M) cells for focal and ambient vision respectively

Diversity among bipolar cells: on- and off-center types for lighter, darker objects. Advantages of this over alternatives: each nerve impulse can be significant, a potential call to action.

More diversity among ganglion cells: anatomy(dendritic trees)

 X (=(i = P) and Y (= a = M) cells for focal,

        ambient vision respectively

X cells signal the total light falling in their receptive field, wherever it falls within the field, so an X cell may not respond when a light is shifted within its receptive field. Y cells detect any change (how?)

 X and Y cells are not truly specialized detectors (not like bug detectors): “ensemble coding”/”distributed representation” means the joint activity of many cells is needed to represent a useful message.

 

 

Supplementary material