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. 2017 Feb 15;43(5):964–977. doi: 10.1038/npp.2017.12

Figure 1.

Figure 1

A2AR-CB1R heteromers are located on GABAergic neurons rather than glutamatergic projections in the mouse dorsal striatum. (a, b) PLA assays were performed in dorsal-striatum sections from 3–4-month-old mice of different genotypes. A2AR-CB1R heteromers are shown as green dots. Nuclei are colored in blue by DAPI staining. (a) Representative low-magnification image of tissue sections used for PLA assays. Left, DAPI-stained field; right, bright field. Scale bar: 1 mm. Representative pictures from control CB1R-floxed, GABA-CB1R−/−, Glu-CB1R−/−, and GABA-Glu-CB1R−/− mice. Scale bar: 20 μm. (b) Representative pictures from Stop-CB1R, GABA-CB1R-RS mice, Glu-CB1R-RS mice and CB1R-RS mice. Scale bar: 20 μm. (c) Quantification of the number of cells containing one or more dots expressed as the percentage of the total number of cells (blue nuclei). Data are the mean±SEM of counts in 5–14 different fields from three different animals of each type. One-way ANOVA followed by Dunnet post hoc test showed a significant (*p<0.05, ***p<0.001) decrease of heteromer expression compared to control CB1R-floxed mice (a) or to CB1R-RS mice (b). Further details of statistical analyses are given in Supplementary Table S2.