Age, there were 4 cells each seen in the T1 and T

Age, there were 4 cells each seen in the T1 and T2 segments of TNTvif controls and TNT fliers with anti GFP (Fig. 7A, B). However, all the GFP positive cells were not always marked by anti-5-HT staining (Fig. 7C). Interestingly, nonfliers among the TNT expressing animals had significantlyFigure 6. Loss of synaptic activity in serotonergic neurons reduces 25033180 the cell numbers in thoracic ganglia. A) Immunohistochemistry of a thoracic ganglion expressing mCD8GFP and TNTvif in serotonergic neurons (sample S2, Fig. 7D). The thoracic segment has 4 cells (T1a ) in T1 region and 4 cells (T2a9 9) in the T2 region (antiGFP, green). Anti-5-HT staining (red) also follows the same pattern. B) Immunohistochemistry on TRH/TNTH thoracic ganglia collected from flies which passed the column flight test (fliers). Anti-GFP staining shows 4 cells in T1 and 5 cells, T2a9 9, in the T2 region. Anti-5-HT does not stain T2e9 (sample S6, Fig. 7C). C) Immunohistochemistry on TRH/ TNTH thoracic ganglia collected from non-fliers. Anti-GFP staining shows 4 cells (T1a ) in T1 and 3 cells (T2a9,b9,d9) in T2 region (sample S3, Fig. 7E). D) Schematic representation of serotonergic neurons as seen in T1 and T2 region of the thoracic ganglia. doi:10.1371/journal.pone.0046405.gSerotonergic Modulation of Drosophila FlightFigure 7. Distribution of serotonergic neurons in second thoracic segment across 10 samples. A) Schematic representation of the serotonergic neurons as seen in T1 and T2 region of the thoracic ganglia, showing the average number of T1 and T2 cells. B) Number of cells marked by anti-GFP in thoracic ganglia. Non-fliers of the genotype TRH/TNT have fewer GFP-positive neurons in T2 as compared with TNTvif controls (what about comparison with fliers also) (*p,0.05; Student’s t test). C) Number of cells marked by anti-GFP in thoracic ganglia. No significant difference is seen with anti-5-HT staining. D) TNTvif expression in TRHGAL4 shows 4 cells, T2a9 9, in the T2 region. An extra cell, T2e9 is seen in sample S1, which is marked by anti-GFP but not anti-5-HT. In samples S2 10 equal number of cells were marked by anti-GFP and anti-5-HT staining. E) Fliers of the genotype TRH/TNT show variation in T2c9,d9 cells, but the variation is not significantly different from TNTvif controls (Fig. 6D). F) TRH/TNT non-fliers lack T2c9,d9 in sample S1, S6 and S9. Sample S2 lacks all T2a9 9 cells. doi:10.1371/journal.pone.0046405.g(Fig. 7E, F) suggesting a reduced level of serotonin. In the abdominal segments of flies expressing either TNT or TNTvif, 7 pairs of GFP-positive cells were observed, all of which were 5-HT negative (Fig. 6).DiscussionThe importance of aminergic neurons in Drosophila air-puff stimulated flight has been shown previously in the context of IP3R signaling and SOCE [8,30]. However, these data are not straightforward. While itpr+ expression in DdCGAL4 expressing neurons can rescue flight defects in itpr mutants, knock down of the InsP3R in the DdCGAL4 domain by RNAi does not result in any observable flight defects, apart from hyper-excitability of the neural circuit. Interestingly, itpr mutant flight defects can also be rescued by itpr+ expression in the 317318-84-6 web Dilp2GAL4 neuronal domain, which does not overlap with DdCGAL4 [24]. Thus a possible explanation for the rescue of flight defects in itpr mutants by DdCGAL4 and Dilp2GAL4 could be non-cell autonomous mechanisms involving in one case neurohormonal release of serotonin and/or LED 209 site dopamine and in the other secreted neu.Age, there were 4 cells each seen in the T1 and T2 segments of TNTvif controls and TNT fliers with anti GFP (Fig. 7A, B). However, all the GFP positive cells were not always marked by anti-5-HT staining (Fig. 7C). Interestingly, nonfliers among the TNT expressing animals had significantlyFigure 6. Loss of synaptic activity in serotonergic neurons reduces 25033180 the cell numbers in thoracic ganglia. A) Immunohistochemistry of a thoracic ganglion expressing mCD8GFP and TNTvif in serotonergic neurons (sample S2, Fig. 7D). The thoracic segment has 4 cells (T1a ) in T1 region and 4 cells (T2a9 9) in the T2 region (antiGFP, green). Anti-5-HT staining (red) also follows the same pattern. B) Immunohistochemistry on TRH/TNTH thoracic ganglia collected from flies which passed the column flight test (fliers). Anti-GFP staining shows 4 cells in T1 and 5 cells, T2a9 9, in the T2 region. Anti-5-HT does not stain T2e9 (sample S6, Fig. 7C). C) Immunohistochemistry on TRH/ TNTH thoracic ganglia collected from non-fliers. Anti-GFP staining shows 4 cells (T1a ) in T1 and 3 cells (T2a9,b9,d9) in T2 region (sample S3, Fig. 7E). D) Schematic representation of serotonergic neurons as seen in T1 and T2 region of the thoracic ganglia. doi:10.1371/journal.pone.0046405.gSerotonergic Modulation of Drosophila FlightFigure 7. Distribution of serotonergic neurons in second thoracic segment across 10 samples. A) Schematic representation of the serotonergic neurons as seen in T1 and T2 region of the thoracic ganglia, showing the average number of T1 and T2 cells. B) Number of cells marked by anti-GFP in thoracic ganglia. Non-fliers of the genotype TRH/TNT have fewer GFP-positive neurons in T2 as compared with TNTvif controls (what about comparison with fliers also) (*p,0.05; Student’s t test). C) Number of cells marked by anti-GFP in thoracic ganglia. No significant difference is seen with anti-5-HT staining. D) TNTvif expression in TRHGAL4 shows 4 cells, T2a9 9, in the T2 region. An extra cell, T2e9 is seen in sample S1, which is marked by anti-GFP but not anti-5-HT. In samples S2 10 equal number of cells were marked by anti-GFP and anti-5-HT staining. E) Fliers of the genotype TRH/TNT show variation in T2c9,d9 cells, but the variation is not significantly different from TNTvif controls (Fig. 6D). F) TRH/TNT non-fliers lack T2c9,d9 in sample S1, S6 and S9. Sample S2 lacks all T2a9 9 cells. doi:10.1371/journal.pone.0046405.g(Fig. 7E, F) suggesting a reduced level of serotonin. In the abdominal segments of flies expressing either TNT or TNTvif, 7 pairs of GFP-positive cells were observed, all of which were 5-HT negative (Fig. 6).DiscussionThe importance of aminergic neurons in Drosophila air-puff stimulated flight has been shown previously in the context of IP3R signaling and SOCE [8,30]. However, these data are not straightforward. While itpr+ expression in DdCGAL4 expressing neurons can rescue flight defects in itpr mutants, knock down of the InsP3R in the DdCGAL4 domain by RNAi does not result in any observable flight defects, apart from hyper-excitability of the neural circuit. Interestingly, itpr mutant flight defects can also be rescued by itpr+ expression in the Dilp2GAL4 neuronal domain, which does not overlap with DdCGAL4 [24]. Thus a possible explanation for the rescue of flight defects in itpr mutants by DdCGAL4 and Dilp2GAL4 could be non-cell autonomous mechanisms involving in one case neurohormonal release of serotonin and/or dopamine and in the other secreted neu.