SIFa peptidergic neurons orchestrate the internal states and energy balance of male Drosophila melanogaster

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Title
SIFa peptidergic neurons orchestrate the internal states and energy balance of male Drosophila melanogaster
Author(s)
Y Song; T Zhang; Tae Hoon Ryu; K Zhang; Z Wu; Y Wei; J Schweizer; K N H Nguyen; A Kwan; X Zhang; Kweon Yu; W J Kim
Bibliographic Citation
PLoS Biology, vol. 23, no. 9, pp. e3003345-e3003345
Publication Year
2025
Abstract
Neuropeptide SIFamide (SIFa) neurons in Drosophila melanogaster have been characterized by their exceptionally elaborate arborization patterns, which extend from the brain into the ventral nerve cord (VNC). SIFa neurons are equipped to receive signals that integrate both internal physiological cues and external environmental stimuli. These signals enable the neurons to regulate energy balance, sleep patterns, metabolic status, and circadian timing. These peptidergic neurons are instrumental in orchestrating the animal's internal states and refining its behavioral responses, yet the precise molecular underpinnings of this process remain elusive. Here, we demonstrate that SIFa neurons coordinate a range of behavioral responses by selectively integrating inputs and outputs in a context-dependent manner. These neurons engage in a feedback loop with sNPF neurons in the VNC, modifying behaviors such as longer mating duration (LMD) and shorter mating duration (SMD). Additionally, SIFa neurons interact with dopamine and glutamate to differentially regulate sleep and mating duration. Activating SIFa neurons leads to reduced mating duration and increased food intake, while deactivating them reduces food intake. Overall, these findings demonstrate the importance of SIFa neurons in absorbing inputs and turning them into behavioral outputs, shedding light on animal's intricate behavioral orchestration.
ISSN
1544-9173
Publisher
Public Library of Science
Full Text Link
http://dx.doi.org/10.1371/journal.pbio.3003345
Type
Article
Appears in Collections:
Division of A.I. & Biomedical Research > Orphan Disease Therapeutic Target Research Center > 1. Journal Articles
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