Figure 4. APL inhibits Kenyon cells.
(a–c) Stochastic transgene expression in neither (a), one (b), or both (c) APL neurons. Scale bars, 50 μm. (d–g) Impact of different APL manipulations on odor-evoked Ca2+ influx in the α lobe (see Supplementary Fig. 3 for all lobes). Black bars indicate 5 s pulses of ethyl acetate. (d) In control hemispheres of APL>shits1 flies where APL was unlabeled, odor-evoked Ca2+ influx in Kenyon cells declined slightly at 32 °C. (e) In hemispheres of APL>dTRPA1 flies where APL was labeled, odor-evoked Ca2+ influx in Kenyon cells was almost completely abolished at 32 °C. (f) In hemispheres of APL>shits1 flies where APL was labeled, odor-evoked Ca2+ influx in Kenyon cells increased greatly at 32 °C. (g) In APL-labeled hemispheres of APL>TeTx flies (red), odor-evoked Ca2+ influx in Kenyon cells was much higher than in APL-labeled hemispheres of APL>TeTx-inactive flies (blue) and APL-unlabeled hemispheres of APL>TeTx flies (green, lower panel). n, left to right, given as number of brain hemispheres [number of flies]: (d) n=24 [17.] (e) n=9 [5]. (f) n=30 [21]. (g) n=9 [7], 10 [8], 7 [6].* P<0.05, ** P<0.01, *** P<0.001, repeated-measures ANOVA with Geisser-Greenhouse correction and Holm-Sidak multiple comparisons test (d,e), Friedman test with Dunn’s multiple comparisons test (f), or one-way ANOVA with Tukey-Kramer post hoc test (g). § P<0.001, Mann-Whitney U test, comparing ratios of odor-evoked Ca2+ influx at 32 °C vs. 22 °C. See Supplementary Table 1 for full genotypes.
