, 2007), but little is known about how olfactory inputs are trans

, 2007), but little is known about how olfactory inputs are transformed from PNs to higher-order lateral horn neurons (Ruta et al., 2010). Thus far, most physiological and behavioral studies of Drosophila PNs have focused on the uniglomerular ePNs, which reside dorsal and lateral to the antennal lobe and whose axons form the inner antenno-cerebral selleck compound tract (iACT), innervating both the mushroom body and the lateral horn ( Figure 1A). However, a separate group of PNs reside ventral to the antennal lobe. Individual ventral PNs send dendrites to either single or multiple glomeruli and project their axons through the middle antenno-cerebral tract (mACT) to terminate only in the lateral horn,

bypassing the mushroom body altogether Palbociclib supplier ( Jefferis et al., 2007, Lai et al., 2008, Okada et al., 2009 and Stocker et al., 1990). In this study, we use the olfactory response of a specific set of higher-order neurons to show that these ventral PNs provide GABAergic inhibition in the lateral horn to route selective inputs to specific higher-order neurons.

Ventral PNs of the antennal lobe have previously been characterized using two GAL4 lines. GH146-GAL4 labels ∼6 ventral PNs ( Jefferis et al., 2001), all of which are GABAergic ( Jefferis et al., 2007), and all are uniglomerular except one that innervates all glomeruli ( Marin et al., 2002). Mz699-GAL4 labels >45 ventral PNs that are mostly complementary to those labeled by GH146-GAL4 ( Lai et al., 2008). Most Mz699-GAL4-positive (Mz699+ hereafter) ventral PNs project to multiple glomeruli ( Lai et al., 2008) and more than 80% are GABAergic ( Okada et al., 2009). Mz699-GAL4 also labels neurons in the ventrolateral protocerebrum (vlpr) that send processes into the lateral Cytidine deaminase horn ( Okada et al., 2009;

Figure 1B). To further characterize neurons labeled by Mz699-GAL4, we used mosaic analysis with a repressible cell marker (MARCM)-based clonal analysis ( Lee and Luo, 1999). Consistent with a previous study ( Lai et al., 2008), we found that Mz699+ ventral PNs were derived from a single neuroblast ( Figure 1C; Figure S1A). Most single-cell clones innervated a few glomeruli ( Figure S1B; n = 38 out of 39), which collectively covered the majority of glomeruli. We also introduced synaptotagmin-hemagglutinin (Syt-HA) as a synaptic vesicle marker in these MARCM clones and found that Syt-HA was highly enriched in the lateral horn but was largely absent from the antennal lobe in neuroblast and single-cell clones ( Figures S1A–S1C). This is consistent with a previous report based on the labeling of all Mz699+ neurons ( Okada et al., 2009). With single-cell resolution, we observed that the majority of the ventral PN (vPN) neural processes in the antennal lobe had fine terminal branches without Syt-HA signal ( Figure S1B), whereas Syt-HA puncta, likely representing presynaptic terminals of en passant synapses, were distributed throughout the branches in the lateral horn ( Figure S1C).

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