(A) Blue light was delivered locally into V1 via optic fibers chronically implanted at a 45° angle to target the VEP recording site in layer 4 of binocular V1 of PV-Cre mice infected with AAV5-EF1α-DIO-hChR2(H134R)-eYFP. (B) Experimental timeline showing that after viral infection, electrode implantation, and ChR2 expression; mice were accustomed to head-fixation and gray screen viewing. Subsequently, they underwent a standard SRP induction protocol over 6 days. On day 7, mice viewed a novel oriented stimulus in addition to the familiar stimulus and, on 50% of presentations of each stimulus, blue light (473 nm) was delivered to cortex to optogenetically activate PV+ cells. (C) Significant SRP was induced over 6 days as VEPs underwent a typical potentiation. (D) On day 7, SRP was expressed through significantly larger VEP magnitude in response to the familiar Xo orientation than a novel X + 90° stimulus when blue light was not delivered (Black bars). In the presence of blue light (blue bars), VEPs were suppressed, and there was a significant reduction in the differential magnitude of VEPs driven by familiar and novel stimuli. (E) The ratio of VEP magnitude elicited by familiar/novel stimuli was significantly reduced by optogenetic activation of PV+ neurons, reflecting a decrement in SRP expression. Significant comparisons are marked with an asterisk and post hoc test p values are reported in D to emphasize the impact of laser stimulation on SRP selectivity. Error bars are standard error of the mean (S.E.M.).
DOI:
http://dx.doi.org/10.7554/eLife.11450.013
Figure 5—source data 1. PV-neuronal activation.