Peptidergic signaling from clock neurons regulates reproductive dormancy in Drosophila melanogaster.
Dóra NagyPaola CusumanoGabriele AndreattaAne Martin AnduagaChristiane Hermann-LuiblNils ReinhardJoão GestoChristian WegenerGabriella MazzottaEzio RosatoCharalambos P KyriacouCharlotte Helfrich-FörsterRodolfo CostaPublished in: PLoS genetics (2019)
With the approach of winter, many insects switch to an alternative protective developmental program called diapause. Drosophila melanogaster females overwinter as adults by inducing a reproductive arrest that is characterized by inhibition of ovarian development at previtellogenic stages. The insulin producing cells (IPCs) are key regulators of this process, since they produce and release insulin-like peptides that act as diapause-antagonizing hormones. Here we show that in D. melanogaster two neuropeptides, Pigment Dispersing Factor (PDF) and short Neuropeptide F (sNPF) inhibit reproductive arrest, likely through modulation of the IPCs. In particular, genetic manipulations of the PDF-expressing neurons, which include the sNPF-producing small ventral Lateral Neurons (s-LNvs), modulated the levels of reproductive dormancy, suggesting the involvement of both neuropeptides. We expressed a genetically encoded cAMP sensor in the IPCs and challenged brain explants with synthetic PDF and sNPF. Bath applications of both neuropeptides increased cAMP levels in the IPCs, even more so when they were applied together, suggesting a synergistic effect. Bath application of sNPF additionally increased Ca2+ levels in the IPCs. Our results indicate that PDF and sNPF inhibit reproductive dormancy by maintaining the IPCs in an active state.
Keyphrases
- drosophila melanogaster
- spinal cord
- type diabetes
- cell cycle
- cell cycle arrest
- transcription factor
- white matter
- cell death
- glycemic control
- gene expression
- skeletal muscle
- cell proliferation
- oxidative stress
- adipose tissue
- minimally invasive
- binding protein
- blood brain barrier
- genome wide
- copy number
- dna methylation
- pi k akt
- subarachnoid hemorrhage
- deep brain stimulation
- brain injury