A. PV × Sncg double transgenic mice targeted distinct
genetically encoded reporters to INs.
B. Fluorescent intensity (FI) in IN somata (log scale). Markers show
individual cells, colored by FI ratio. N = 373 cells from 6 mice, 1 male, 5
females. Pearson’s R, p < .001.
C. Experimental strategy.
D. Example traces of a single Sncg and a PV IN. See also Fig. S3.
E. Event triggered average traces of Sncg and PV INs aligned to the
start of running, along with the pupil diameter, running speed and face movement
attributes. Traces show mean ± SEM values across all recorded cells.
F. PV IN responses to running (post-pre; pre = −10 to 0 s, post
= 0 to 5 s) were greater than Sncg IN responses by 46 ± 2% DF/F,
likelihood ratio test, χ2 = 294, p < .001, n = 469
cells from 3 male mice.
G. Response of Sncg and PV INs during run – stop events.
H. Sncg IN stop responses (post-pre; pre = −10 to 0 s, post = 0
to 5 s) were greater than in PV INs by 43 ± 2% DF/F, likelihood ratio
test, χ2 = 372, p < .001, n = 469 cells from 3 male
mice. See also Fig.
S3.
I. Response of Sncg and PV INs during SWRs.
J. The SWR response of PV INs (post-pre; pre = −1 to 0 s, post =
0 to 128 ms) was greater than the response of Sncg INs by 6 ± 0.7% DF/F,
likelihood ratio test, χ2 = 57, p < .001, n = 262 cells
from 2 male mice.
K. Response of Sncg and PV INs to face movements. The events shown here
were detected in the absence of running. Note that the value of the face
movement attribute was also high during running (panels e, g, different y axis
scale).
L. The response of PV INs to face movement events (post-pre; pre =
−10 to 0 s, post = 0 to 1 s) was greater than the response of Sncg INs by
15 ± 1% DF/F, likelihood ratio test, χ2 = 245, p
< .001, n = 469 cells from 3 male mice. Box plots show median ±
IQR, whiskers show range, notches represent CI.