STING controls energy stress-induced autophagy and energy metabolism via STX17

J Cell Biol. 2022 Jul 4;221(7):e202202060. doi: 10.1083/jcb.202202060. Epub 2022 May 5.

Abstract

The stimulator of interferon genes (STING) plays a critical role in innate immunity. Emerging evidence suggests that STING is important for DNA or cGAMP-induced non-canonical autophagy, which is independent of a large part of canonical autophagy machineries. Here, we report that, in the absence of STING, energy stress-induced autophagy is upregulated rather than downregulated. Depletion of STING in Drosophila fat cells enhances basal- and starvation-induced autophagic flux. During acute exercise, STING knockout mice show increased autophagy flux, exercise endurance, and altered glucose metabolism. Mechanistically, these observations could be explained by the STING-STX17 interaction. STING physically interacts with STX17, a SNARE that is essential for autophagosome biogenesis and autophagosome-lysosome fusion. Energy crisis and TBK1-mediated phosphorylation both disrupt the STING-STX17 interaction, allow different pools of STX17 to translocate to phagophores and mature autophagosomes, and promote autophagic flux. Taken together, we demonstrate a heretofore unexpected function of STING in energy stress-induced autophagy through spatial regulation of autophagic SNARE STX17.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagosomes / metabolism
  • Autophagy*
  • Drosophila
  • Energy Metabolism*
  • Lysosomes* / genetics
  • Lysosomes* / metabolism
  • Membrane Proteins* / genetics
  • Membrane Proteins* / metabolism
  • Mice
  • Mice, Knockout
  • Physical Conditioning, Animal
  • Qa-SNARE Proteins* / genetics
  • Qa-SNARE Proteins* / metabolism

Substances

  • Membrane Proteins
  • Qa-SNARE Proteins
  • Sting1 protein, mouse
  • Stx17 protein, mouse