Emmy Noether Neuropeptide Group, Animal Physiology, Department of Biology, Philipps-University, Marburg, Germany.
PLoS One. 2007 Aug 1;2(8):e695. doi: 10.1371/journal.pone.0000695.
Recent studies on Drosophila melanogaster and other insects have revealed important insights into the functions and evolution of neuropeptide signaling. In contrast, in- and output connections of insect peptidergic circuits are largely unexplored. Existing morphological descriptions typically do not determine the exact spatial location of peptidergic axonal pathways and arborizations within the neuropil, and do not identify peptidergic in- and output compartments. Such information is however fundamental to screen for possible peptidergic network connections, a prerequisite to understand how the CNS controls the activity of peptidergic neurons at the synaptic level. We provide a precise 3D morphological description of peptidergic neurons in the thoracic and abdominal neuromeres of the Drosophila larva based on fasciclin-2 (Fas2) immunopositive tracts as landmarks. Comparing the Fas2 "coordinates" of projections of sensory or other neurons with those of peptidergic neurons, it is possible to identify candidate in- and output connections of specific peptidergic systems. These connections can subsequently be more rigorously tested. By immunolabeling and GAL4-directed expression of marker proteins, we analyzed the projections and compartmentalization of neurons expressing 12 different peptide genes, encoding approximately 75% of the neuropeptides chemically identified within the Drosophila CNS. Results are assembled into standardized plates which provide a guide to identify candidate afferent or target neurons with overlapping projections. In general, we found that putative dendritic compartments of peptidergic neurons are concentrated around the median Fas2 tracts and the terminal plexus. Putative peptide release sites in the ventral nerve cord were also more laterally situated. Our results suggest that i) peptidergic neurons in the Drosophila ventral nerve cord have separated in- and output compartments in specific areas, and ii) volume transmission is a prevailing way of peptidergic communication within the CNS. The data can further be useful to identify colocalized transmitters and receptors, and develop peptidergic neurons as new landmarks.
最近对黑腹果蝇和其他昆虫的研究揭示了神经肽信号的功能和进化的重要见解。相比之下,昆虫肽能电路的输入和输出连接在很大程度上尚未得到探索。现有的形态描述通常不能确定神经突间质中肽能轴突途径和分支的确切空间位置,也不能确定肽能的输入和输出隔室。然而,这些信息对于筛选可能的肽能网络连接是至关重要的,这是理解中枢神经系统如何在突触水平控制肽能神经元活性的前提。我们基于 Fasciclin-2(Fas2)免疫阳性轨迹作为标志物,提供了果蝇幼虫胸部和腹部神经节中肽能神经元的精确三维形态描述。将感觉神经元或其他神经元的 Fas2“坐标”与肽能神经元的 Fas2“坐标”进行比较,可以识别特定肽能系统的候选输入和输出连接。这些连接随后可以更严格地进行测试。通过免疫标记和 GAL4 指导的标记蛋白表达,我们分析了 12 种不同肽基因表达的神经元的投射和分区,这些基因编码了约 75%在果蝇中枢神经系统中鉴定出的神经肽。结果被组装成标准化的图谱,为识别具有重叠投射的候选传入或靶神经元提供了指导。一般来说,我们发现肽能神经元的假定树突隔室集中在中 Fas2 轨迹和末端丛周围。腹神经索中的假定肽释放部位也更侧向分布。我们的结果表明:i)果蝇腹神经索中的肽能神经元在特定区域具有分离的输入和输出隔室,ii)体积传递是中枢神经系统内肽能通讯的主要方式。这些数据还可用于鉴定共定位的递质和受体,并将肽能神经元开发为新的标志物。