Kupffer cells control neonatal hepatic glucose metabolism via Igf1 signaling

During perinatal development, liver metabolism is tightly regulated to ensure energy supply for the newborn. Before birth, glycogen is stored in hepatocytes and later metabolized to glucose, meeting the energy demands of the neonate. Shortly after birth, lipogenesis begins, driven by the transcriptional activation of enzymes involved in fatty acid oxidation. These processes are thought to be largely regulated by systemic insulin and glucagon levels. However, the role of liver-derived local factors in neonatal hepatocyte metabolism remains unexplored. Kupffer cells (KCs), the liver's resident macrophages, colonize the fetal liver early in embryogenesis and support liver metabolism in adulthood. Yet, whether KCs influence neonatal hepatocyte metabolism is unknown. Here, using conditional knockout mouse models targeting macrophages, we demonstrate that yolk sac-derived KCs play a critical role in hepatocyte glycogen storage and function by regulating the TCA cycle - a role that monocyte-derived KC-like cells cannot substitute. Newborn pups lacking KCs mobilize glycogen more rapidly, a process regulated by insulin-like growth factor 1 (Igf1) production. Our findings reveal that macrophages are a major source of Igf1 at birth and that local Igf1 production by KCs is essential for balanced hepatocyte metabolism. Overall design: P0 livers from the Spiflox Tnfrsf11aeGFPCre mouse model were digested to form single cell suspension then 50g spin step was berformed to enrich hepatocytes cells in the pellet and liver immune cells in the supernatant.the pups were WT(Spi1f/f Tnfrsf11aeGFP+/+) and KO (Spif/f Tnfrsf11aeGFPCre/+) . 3' counting scRNAseq was performed on the cells using SeqWell ^s3. ). Full length scRNAseq libraries were generated via SmartSeq2.