Fig. 4 Whisker deprivation–induced remapping is stable beyond the deprivation period. Whisker deprivation–induced remapping is stable beyond the deprivation.

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Fig. 4 Whisker deprivation–induced remapping is stable beyond the deprivation period. Whisker deprivation–induced remapping is stable beyond the deprivation period. (A) WT mice were subjected to right S1FP (R. S1FP) photothrombosis. Half of the mice underwent right whisker trimming every other day for the first 8 weeks of the experiment; thereafter, trimming was halted and whiskers were allowed to regrow. (B) Limb behavior and OIS imaging were performed at the times indicated. (C to H) Activation density heat maps projected onto a white light cortical image show right S1FP maps, 8 (C and D) and 12 weeks (E and F) after photothrombosis, and right S1WB maps 12 weeks after photothrombosis (G and H) in WT-Control (C, E, and G) and WT-Depriv (D, F, and H) groups. RFP, right forepaw; WB, whisker barrel. (I to O) Activation heat maps projected onto a white light cortical image showing >65% density response for each map. Map identity is indicated by the label in each image, and dark blue represents overlap between the maps. The >65% threshold was used only for display; statistical comparisons were independent of any threshold. Spatial distribution difference: *P < 0.0071 (Bonferroni-corrected); n.s., not significant (see fig. S13 and Materials and Methods for more details). WT-Control, n = 11; WT-Depriv, n = 11. (P) Line graph showing the differences in limb use asymmetry before (Pre) and 1 (WK1), 3 (WK3), 5 (WK5), 7 (WK7), and 11 (WK11) weeks after right S1FP photothrombosis in WT-Control and WT-Depriv mice. *P ≤ 0.05, **P ≤ 0.01, ***, +++P ≤ 0.001; n.s., not significant compared to baseline time point (Pre), using repeated-measures ANOVA with Newman-Keuls multiple pairwise comparisons. WT-Control, n = 11; WT-Depriv, n = 8. Andrew W. Kraft et al., Sci Transl Med 2018;10:eaag1328 Published by AAAS