Taste stimulation had no effect on the firing rate of PERin neurons in either fed or food-deprived animals

(Figure 3C). These studies argue that PERin neurons are not modulated by satiety state or gustatory cues. Because the dendrites of PERin neurons reside in the first leg neuromere, we wondered whether inputs into the first leg neuromere would activate PERin neurons. We therefore stimulated the major nerves of the ventral nerve cord and monitored responses of PERin by G-CaMP calcium imaging (Tian et al., 2009), using a dissected brain plus ventral nerve cord preparation and electrical nerve stimulation (10 V). PERin dendrites responded to stimulation of nerves of the first leg neuromere and were also excited by the stimulation of nerves from all legs, wings, and halteres, but not the abdominal nerve (Figures 4A–4C). Of these nerves, the posterior dorsal nerve in Selleck Epigenetics Compound Library segment 2 (PDN2) and the dorsal nerve in segment 3 (DN3) do not contain any gustatory neurons (Demerec, 1950), consistent

with the notion that nongustatory input activates PERin. Because mechanosensory neurons are a major sensory input carried by all nerves into the VNC, we tested whether PERin was activated by stimulation of mechanosensory neurons. The blue light-activated ion channel, channelrhodopsin-2 (ChR2), was expressed in mechanosensory neurons www.selleckchem.com/products/BKM-120.html under the control of the nompC promoter using the QF/QUAS transgenic system (Nagel et al., 2003, Petersen and Stowers, 2011 and Potter et al., 2010) and G-CaMP3 was expressed in PERin using the Gal4/UAS system. Light-induced activation of mechanosensory neurons in the legs produced robust calcium increases in PERin neurons (Figures 4D and 4E). Activating sugar, bitter, or water gustatory inputs with ChR2 did not elicit responses in PERin (Figure S3).

These results argue that PERin selectively responds to activation of mechanosensory neurons. In the adult, nompC-Gal4 drives expression in mechanosensory neurons in external sensory bristles and chordotonal organs ( Cheng et al., 2010 and Petersen and Stowers, 2011). through In larvae, NompC-positive neurons respond to touch, whereas different neurons detect noxious heat and harsh mechanosensory stimuli ( Cheng et al., 2010, Tracey et al., 2003 and Yan et al., 2013). As the repertoire of stimuli that activate NompC neurons in the adult has not been rigorously examined, we tested whether heat or mechanosensory cues would activate PERin similar to optogenetic stimulation of NompC neurons. Neither temperature increases nor an airpuff to a single leg activated PERin ( Figure S3). To test whether more rigorous movement would activate PERin, we monitored G-CaMP changes in PERin axons in animals that could freely move their legs ( Figure 5). Bouts of PERin activity were highly correlated with bouts of leg movement ( Figures 5A and 5C).