Neurotransmitter‐induced changes in the intracellular calcium concentration suggest a differential central modulation of CCAP neuron subsets in Drosophila

The complete sequencing of the Drosophila melanogaster genome allowed major progress in the research on invertebrate neuropeptide signaling. However, it is still largely unknown how the insect CNS exerts synaptic control over the secretory activity of peptidergic neurons; afferent pathways and employed chemical transmitters remain largely unidentified. In the present study, we set out to identify neurotransmitters mediating synaptic input onto CCAP‐expressing neurons (N CCAP ), which play an important role in the regulation of ecdysis‐related events. By in vitro and in situ calcium imaging with synthetic and genetically encoded calcium indicators, we provide evidence that differential neurotransmitter inputs control the activity of N CCAP subsets. In short‐term culture, almost all N CCAP showed increases of the free intracellular calcium concentration after application of acetylcholine (ACh) and nicotine, whereas only some N CCAP responded to glutamate and GABA. In the intact ventral ganglia of both larvae and adults, only few N CCAP showed intracellular calcium‐rises or calcium‐oscillations after application of cholinergic agonists indicating a prevailing central inhibition of most N CCAP during these developmental stages. In larvae, responding N CCAP were primarily located in the third thoracic neuromere. At least one N CCAP pair in this neuromere belonged to a morphologically distinct subset with neurohemal endings on the body wall muscles. Our results suggest that N CCAP express functional receptors for ACh, glutamate, and GABA, and indicate that these transmitters are involved in a context‐dependent regulation of functionally distinct N CCAP subsets. © 2007 Wiley Periodicals, Inc. Develop Neurobiol, 2007.