Abstract
To investigate how the functional architecture is organized in layer 5 (L5) of the somatosensory cortex of a mouse in vivo, the input–output relationship was investigated using an all-optical approach. The neural activity in L5 was optically recorded using a Ca 2+ sensor, R-CaMP2, through a microprism inserted in the cortex under two-photon microscopy, while the L5 was regionally excited using optogenetics. The excitability was spread around the blue-light irradiated region, but the horizontal propagation was limited to within a certain distance (λ < 130 μm from the center of the illumination spot). When two regions were photostimulated with a short interval, the excitability of each cluster was reduced. Therefore, a column-like architecture had functionally emerged with reciprocal inhibition through a minimal number of synaptic relays. This could generate a synchronous output from a region of L5 with simultaneous enhancement of the signal-to-noise ratio by silencing of the neighboring regions.
| Original language | English |
|---|---|
| Pages (from-to) | 65-77 |
| Number of pages | 13 |
| Journal | Journal of Physiological Sciences |
| Volume | 69 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 22 2019 |
Keywords
- Ca imaging
- Column
- Optogenetics
- Reciprocal inhibition
- Self-organization
- Two-photon microscopy
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