Biology subjects

Sizemore, T. R.

Publications and source records attributed to Sizemore, T. R..

4 recordsLinked to original sources

bioRxiv2025

Connectivity of serotonin neurons reveals a constrained inhibitory subnetwork within the olfactory system.

Inhibitory local interneurons (LNs) play an essential role in sensory processing by refining stimulus representations via a diverse collection of mechanisms. The morphological and physiological traits of individual LN types, as well as their connectivity within sensory networks, enable each LN type to support different computations such as lateral inhibition or gain control and are therefore ideal targets for modulatory neurons to have widespread impacts on network activity. In this study, we combined detailed connectivity analyses, serotonin receptor expression, neurophysiology, and computational modeling to demonstrate the functional impact of serotonin on a constrained LN network in the olfactory system of Drosophila. This subnetwork is composed of three LN types and we describe each of their distinctive morphology, connectivity, biophysical properties and odor response properties. We demonstrate that each LN type expresses different combinations of serotonin receptors and that serotonin differentially impacts the excitability of each LN type. Finally, by applying these serotonin induced changes in excitability to a computational model that simulates the impact of inhibition exerted by each LN-type, we predict a role for serotonin in adjusting the dynamic range of antennal lobe output neurons and in noise reduction in odor representations. Thus, a single modulatory system can differentially impact LN types that subserve distinct roles within the olfactory system. Significance StatementInhibitory interneurons refine information processing within sensory networks by enforcing distinct local computations. They are therefore ideal targets for modulatory neurons to efficiently alter sensory processing by up- or downregulating the computations each interneuron class subserves. We identify an interconnected network of three interneuron types in the olfactory system of Drosophila that receive a large amount of serotonergic synaptic input. Each interneuron type differs in their biophysical and response properties and serotonin differentially impacts their excitability. Finally, using a computational model, we predict that the combined effects of serotonin on these inhibitory neurons enables noise reduction in the olfactory system. Thus, modulation of individual cell types collectively adjusts distinct network computations to enable flexible sensory coding.

neuroscience↗

bioRxiv2023

Stimulus-Specific Modulation is Enabled by Differential Serotonin Receptor Expression

Neural networks must be able to flexibly process information under different conditions. To this end, networks frequently rely on uniform expression of modulatory receptors by distinct classes of neurons to fine tune the computations supported by each neuronal class. In this study, we explore the consequences of heterogeneous, rather than uniform, serotonin (5-HT) receptor expression within a cell class for olfactory processing in Drosophila melanogaster. Here, we demonstrate that two distinct populations of olfactory output neurons (projection neurons, PNs) display heterogeneous receptor co-expression of all 5-HT receptors. Moreover, the PN populations that express distinct 5-HT receptors innervate different combinations of glomeruli, implying that the effects of 5-HT on these PNs may vary with their odor tuning. Furthermore, connectomic analyses reveal that PN subsets with different receptor profiles have little convergence upon downstream synaptic partners. Finally, 5-HT differentially modulates the odor-evoked responses of PNs with distinct receptor expression profiles and odor tuning. Overall, this implies that heterogeneous modulatory receptor expression enables differential tuning of activity within a neuronal class depending on the odor scene to which individual neurons respond.

neuroscience↗

bioRxiv2022

A Neuropeptidergic Signaling Pathway for Olfactory Gain Modulation

Sensory systems are dynamically adjusted according to the animals ongoing needs by neuromodulators, such as neuropeptides. Although many neuropeptides are often widely-distributed throughout sensory networks, it is unclear whether such neuropeptides uniformly modulate network activity. Here, we leverage the numerically tractable primary olfactory center of Drosophila (the antennal lobe, AL) to resolve whether one such widely-distributed neuropeptide (myoinhibitory peptide, MIP) uniformly modulates AL processing. We find that despite being uniformly distributed across the AL, MIP decreases olfactory input to some glomeruli, while simultaneously increasing olfactory input to other glomeruli. We reveal that a heterogeneous ensemble of local interneurons (LNs) are the sole source of MIP within the AL. Through high-resolution connectomic analyses, as well as in vivo physiology, we find that the non-uniform effects of MIP are not likely due to MIPergic LN intrinsic properties (e.g., synaptic inputs/outputs, odor-evoked responses, etc.). Instead, we show that differential expression of the inhibitory MIP receptor (sex peptide receptor, SPR) across glomeruli allows MIP to act on distinct intraglomerular substrates, thus enabling differential modulation of olfactory input. Our findings demonstrate how even a seemingly simple case of modulation (i.e., a single neuropeptide acting through a single receptor) can have complex consequences on network processing by acting non-uniformly within different components of the overall network.

neuroscience↗

bioRxiv2019

Serotonergic Modulation of a Visual Microcircuit in Drosophila melanogaster

Sensory systems rely on neuromodulators, such as serotonin, to provide flexibility for information processing in the face of a highly variable stimulus space. Serotonergic neurons broadly innervate the optic ganglia of Drosophila melanogaster, a widely used model for studying vision. The role for serotonergic signaling in the Drosophila optic lobe and the mechanisms by which serotonin regulates visual neurons remain unclear. Here we map the expression patterns of serotonin receptors in the visual system, focusing on a subset of cells with processes in the first optic ganglion, the lamina, and show that serotonin can modulate visual responses. Serotonin receptors are expressed in several types of columnar cells in the lamina including 5-HT2B in lamina monopolar cell L2, required for the initial steps of visual processing, and both 5-HT1A and 5-HT1B in T1 cells, whose function is unknown. Subcellular mapping with GFP-tagged 5-HT2B and 5-HT1A constructs indicates that these receptors localize to layer M2 of the medulla, proximal to serotonergic boutons, suggesting that the medulla is the primary site of serotonergic regulation for these neurons. Serotonin increases intracellular calcium in L2 terminals in layer M2 and alters the kinetics of visually induced calcium transients in L2 neurons following dark flashes. These effects were not observed in flies without a functional 5-HT2B, which displayed severe differences in the amplitude and kinetics of their calcium response to both dark and light flashes. While we did not detect serotonin receptor expression in L1 neurons, they also undergo serotonin-induced calcium changes, presumably via cell non-autonomous signaling pathways. We provide the first functional data showing a role for serotonergic neuromodulation of neurons required for initiating visual processing in Drosophila and establish a new platform for investigating the serotonergic neuromodulation of sensory networks. Author SummarySerotonergic neurons innervate the Drosophila melanogaster eye, but the function of serotonergic signaling is not known. We found that serotonin receptors are expressed in all neuropils of the optic lobe and identify specific neurons involved in visual information processing that express serotonin receptors. We then demonstrate that activation of these receptors can alter how visual information is processed. These are the first data suggesting a functional role for serotonergic signaling in Drosophila vision. This study contributes to the understanding of serotonin biology and modulation of sensory circuits.

neuroscience↗