Control of lifespan and survival by Drosophila NF-κB signaling through neuroendocrine cells and neuroblasts

• Published in: Aging (Albany, NY.) NY.), 2020-11, Vol.12 (24), p.24604-24622
• Main Authors: Khor, Sinan, Cai, Dongsheng
• Format: Article
• Language: English
• Subjects: Aging - genetics; Aging - metabolism; Animals; Drosophila - genetics; Drosophila - metabolism; Drosophila Proteins - genetics; Drosophila Proteins - metabolism; Longevity - genetics; Neuroendocrine Cells - metabolism; Neurons - metabolism; NF-kappa B - genetics; NF-kappa B - metabolism; Research Paper; Signal Transduction - physiology
• ISSN: 1945-4589; 1945-4589
• DOI: 10.18632/aging.104196

We report a comparative analysis of the effects of immune activation in the fly nervous system using genetic activation models to target NF-κB within Toll versus Imd pathways. Genetic gain-of-function models for either pathway pan-neuronally as well as in discrete subsets of neural cells including neuroendocrine insulin-producing cells (IPCs) or neuroblasts reduce fly lifespan, however, these phenotypes in IPCs and neuroblasts are stronger with Toll activation than Imd activation. Of note, while aging is influenced more by Toll/NF-κB activation in IPCs during adulthood, neuroblasts influence aging more substantially during development. The study then focused on Toll/NF-κB inhibition, revealing that IPCs or neuroblasts are important for the effects of lifespan and healthspan extension but in a life stage-dependent manner while some of these effects display sexual dimorphism. Importantly, co-inhibition of Toll/NF-κB pathway in IPCs and neuroblasts increased fly lifespan greater than either cell population, suggesting that independent mechanisms might exist. Toll/NF-κB inhibition in IPCs was also sufficient to enhance survival under various fatal stresses, supporting the additional benefits to fly healthspan. In conclusion, IPCs and neuroblasts are important for NF-κB for controlling lifespan.