Proteolytic activation of fatty acid synthase signals pan-stress resolution

Nat Metab. 2024 Jan;6(1):113-126. doi: 10.1038/s42255-023-00939-z. Epub 2024 Jan 2.

Abstract

Chronic stress and inflammation are both outcomes and major drivers of many human diseases. Sustained responsiveness despite mitigation suggests a failure to sense resolution of the stressor. Here we show that a proteolytic cleavage event of fatty acid synthase (FASN) activates a global cue for stress resolution in Caenorhabditis elegans. FASN is well established for biosynthesis of the fatty acid palmitate. Our results demonstrate FASN promoting an anti-inflammatory profile apart from palmitate synthesis. Redox-dependent proteolysis of limited amounts of FASN by caspase activates a C-terminal fragment sufficient to downregulate multiple aspects of stress responsiveness, including gene expression, metabolic programs and lipid droplets. The FASN C-terminal fragment signals stress resolution in a cell non-autonomous manner. Consistent with these findings, FASN processing is also seen in well-fed but not fasted male mouse liver. As downregulation of stress responses is critical to health, our findings provide a potential pathway to control diverse aspects of stress responses.

MeSH terms

  • Animals
  • Caenorhabditis elegans
  • Fatty Acid Synthase, Type I
  • Fatty Acid Synthases* / genetics
  • Fatty Acid Synthases* / metabolism
  • Fatty Acids*
  • Male
  • Mice
  • Palmitates
  • Proteolysis

Substances

  • Fatty Acid Synthases
  • Fatty Acids
  • Palmitates
  • Fasn protein, mouse
  • Fatty Acid Synthase, Type I