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. Author manuscript; available in PMC: 2016 Feb 6.
Published in final edited form as: Nature. 2015 Jul 1;524(7563):88–92. doi: 10.1038/nature14600

Extended Data Figure 8. Controls for LC cTRIO.

Extended Data Figure 8

a, Top, schematic for negative controls where AAVs expressing Flp-dependent TC and G were injected into the LC of Dbh-Cre mice, followed by RVdG injection into the LC, but the CAV-FLExloxP-Flp injection was omitted. Middle, coronal section of the LC stained with DAPI (blue) shows a small number of GFP+ neurons at the injection site. The dotted rectangle highlights GFP+ neurons magnified in the lower panel. b, Top, schematic for negative control where CAV-FLExloxP-Flp was injected into the olfactory bulb and AAVs expressing Flp-dependent TC and G were injected into the LC of wild-type mice, followed by RVdG injection; hence there was no Cre to mediate Flp expression in LC cells. Middle, coronal section of the LC stained with DAPI (blue) shows a small number of GFP+ neurons at the injection site. The dotted rectangle highlights GFP+ neurons magnified in the lower panel. c, Quantification of GFP+ background labeling in the LC (n=4 and 8). This labeling is likely caused by leaky TVA expression as discussed in Extended Data Fig. 1. In none of these control experiments did we observe GFP+ or TC+ neurons > 800 μm away from the injection site. Scale, 1 mm (middle panels), 100 μm (lower panels). Error bars, s.e.m.

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