Litcius/Paper detail

AKH-FOXO pathway regulates starvation-induced sleep loss through remodeling of the small ventral lateral neuron dorsal projections

Qiankun He, Juan Du, Liya Wei, Zhangwu Zhao

2020PLoS Genetics30 citationsDOIOpen Access PDF

Abstract

Starvation caused by adverse feeding stresses or food shortages has been reported to result in sleep loss in animals. However, how the starvation signal interacts with the central nervous system is still unknown. Here, the adipokinetic hormone (AKH)-Fork head Box-O (FOXO) pathway is shown to respond to energy change and adjust the sleep of Drosophila through remodeling of the s-LNv (small ventral lateral neurons) dorsal projections. Our results show that starvation prevents flies from going to sleep after the first light-dark transition. The LNvs are required for starvation-induced sleep loss through extension of the pigment dispersing factor (PDF)-containing s-LNv dorsal projections. Further studies reveal that loss of AKH or AKHR (akh receptor) function blocks starvation-induced extension of s-LNv dorsal projections and rescues sleep suppression during food deprivation. FOXO, which has been reported to regulate synapse plasticity of neurons, acts as starvation response factor downstream of AKH, and down regulation of FOXO level considerably alleviates the influence of starvation on s-LNv dorsal projections and sleep. Taking together, our results outline the transduction pathways between starvation signal and sleep, and reveal a novel functional site for sleep regulation.

Topics & Concepts

Adipokinetic hormoneStarvationBiologySleep deprivationSignal transductionNeuroscienceSleep (system call)SynapseCell biologyStarvation responseEndocrinologyReceptorNeuropeptideGeneticsCircadian rhythmOperating systemComputer scienceNeurobiology and Insect Physiology ResearchCircadian rhythm and melatoninGenetics, Aging, and Longevity in Model Organisms