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. 2017 Jun 6;8:15738. doi: 10.1038/ncomms15738

Figure 5. Serotonergic neurons signal onto mushroom body α- and γ-lobes to modulate the depression-like state.

Figure 5

(a) Blocking chemical synapses of serotonergic Trh493-GAL4 neurons by expressing TNT prevents the amelioration of the depression-like state by sucrose treatment overnight from day 3 (Test 1) to day 4 (Test 2), whereas driverless UAS-TNT controls recover by sucrose solution overnight. (b) Tonic depolarization of serotonergic Trh493-GAL4 neurons by expressing bacterial sodium-ion channels UAS-NaChBac prevents the depression-like state after 3 days vibration treatment; controls lack the driver. Sucrose overnight does not increase the effect of depolarizing Trh493 neurons. After blocking of 5-HT synthesis (α-MTP overnight), neither depolarization of Trh493 neurons nor sucrose treatment can ameliorate the depression-like state. (ce) Confocal stacks of 10.5 μm thickness, (c) immediately rostral to d. Anti-Fasciclin II staining (FASII, magenta) shows α-/β-lobes and (e) Anti-TRIO labelling the γ-lobes. Trh493-GAL4 driving UAS-mCD8::GFP shows co-localization with α- and γ-lobes, but not with β-lobes. The scale bar denotes 25 μm. (f) Blocking chemical synapses of the mushroom body Kenyon-cells in the mb247-GAL4 pattern (α-/β-/γ-lobes) prohibits the depression-like state even after 4 days of vibration treatment. Controls lack driver or effector. (g) Corresponding experiment to f but with γ-lobe Kenyon-cell driver H24-GAL4; γ-lobes are relevant for bringing about the depression-like state. (h) Blocking of α-/β-lobe Kenyon-cells in the pattern of c739-GAL4 cannot prevent the depression-like state after 3 days of vibration treatment; however, amelioration by sucrose overnight is abolished. Controls lack driver or effector. Black squares, medians; boxes, 25 and 75% quartiles; whiskers, 10 and 90% quantiles; numbers of animals are indicated below each box; NS, not significant; *, P<0.05; **, P<0.01; ***, P<0.001; Kruskal–Wallis test.