摘要：SummaryPrevious studies have revealed the importance of inter-tissue communications for lifespan regulation. However, the inter-tissue network responsible for lifespan regulation is not well understood, even in a simple organismCaenorhabditis elegans. To understand the mechanisms underlying systemic lifespan regulation, we focused on lifespan regulation by the insulin/insulin-like growth factor-1 signaling (IIS) pathway; IIS reduction activates the DAF-16/FOXO transcription factor, which results in lifespan extension. Our tissue-specific knockdown and knockout analyses demonstrated that IIS reduction in neurons and the intestine markedly extended lifespan. DAF-16 activation in neurons resulted in DAF-16 activation in the intestine and vice versa. Our dual gene manipulation method revealed that intestinal and neuronal DAF-16 mediate longevity induced bydaf-2knockout in neurons and the intestine, respectively. In addition, the systemic regulation of intestinal DAF-16 required the IIS pathway in intestinal and neurons. Collectively, these results highlight the importance of the neuronal DAF-16-to-intestinal DAF-16 communication for organismal lifespan regulation.Graphical abstractDisplay OmittedHighlights•Neurons and the intestine are important in the regulation of lifespan•Neuronaldaf-2KO activates not only neuronal DAF-16 but also intestinal DAF-16•Intestinaldaf-2KO activates not only intestinal DAF-16 but also neuronal DAF-16•DAF-16-to-DAF-16 communication between neurons and the intestine regulates lifespanBiological sciences; Genetics; Cell biology
