Orientation Selectivity of Synaptic Input to Neurons in Mouse and Cat Primary Visual Cortex
Neurons
0301 basic medicine
Models, Neurological
Action Potentials
Excitatory Postsynaptic Potentials
Neural Inhibition
Mice, Inbred C57BL
Mice
03 medical and health sciences
Inhibitory Postsynaptic Potentials
Species Specificity
Orientation
Synapses
Cats
Animals
Photic Stimulation
Visual Cortex
DOI:
10.1523/jneurosci.2039-11.2011
Publication Date:
2011-08-24T16:54:58Z
AUTHORS (5)
ABSTRACT
Primary visual cortex (V1) is the site at which orientation selectivity emerges in mammals: visual thalamus afferents to V1 respond equally to all stimulus orientations, whereas their target V1 neurons respond selectively to stimulus orientation. The emergence of orientation selectivity in V1 has long served as a model for investigating cortical computation. Recent evidence for orientation selectivity in mouse V1 opens cortical computation to dissection by genetic and imaging tools, but also raises two essential questions: (1) How does orientation selectivity in mouse V1 neurons compare with that in previously described species? (2) What is the synaptic basis for orientation selectivity in mouse V1? A comparison of orientation selectivity in mouse and in cat, where such measures have traditionally been made, reveals that orientation selectivity in mouse V1 is weaker than in cat V1, but that spike threshold plays a similar role in narrowing selectivity between membrane potential and spike rate. To uncover the synaptic basis for orientation selectivity, we made whole-cell recordingsin vivofrom mouse V1 neurons, comparing neuronal input selectivity—based on membrane potential, synaptic excitation, and synaptic inhibition—to output selectivity based on spiking. We found that a neuron's excitatory and inhibitory inputs are selective for the same stimulus orientations as is its membrane potential response, and that inhibitory selectivity is not broader than excitatory selectivity. Inhibition has different dynamics than excitation, adapting more rapidly. In neurons with temporally modulated responses, the timing of excitation and inhibition was different in mice and cats.
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