STING orchestrates the neuronal inflammatory stress response in multiple sclerosis

Cell. 2024 Jul 25;187(15):4043-4060.e30. doi: 10.1016/j.cell.2024.05.031. Epub 2024 Jun 14.

Abstract

Inflammation-induced neurodegeneration is a defining feature of multiple sclerosis (MS), yet the underlying mechanisms remain unclear. By dissecting the neuronal inflammatory stress response, we discovered that neurons in MS and its mouse model induce the stimulator of interferon genes (STING). However, activation of neuronal STING requires its detachment from the stromal interaction molecule 1 (STIM1), a process triggered by glutamate excitotoxicity. This detachment initiates non-canonical STING signaling, which leads to autophagic degradation of glutathione peroxidase 4 (GPX4), essential for neuronal redox homeostasis and thereby inducing ferroptosis. Both genetic and pharmacological interventions that target STING in neurons protect against inflammation-induced neurodegeneration. Our findings position STING as a central regulator of the detrimental neuronal inflammatory stress response, integrating inflammation with glutamate signaling to cause neuronal cell death, and present it as a tractable target for treating neurodegeneration in MS.

Keywords: STING; calcium signaling; cell death; excitotoxicity; ferroptosis; multiple sclerosis; neurodegeneration; neuroinflammation.

MeSH terms

  • Animals
  • Autophagy
  • Disease Models, Animal
  • Female
  • Ferroptosis
  • Glutamic Acid / metabolism
  • Humans
  • Inflammation* / metabolism
  • Male
  • Membrane Proteins* / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Multiple Sclerosis* / metabolism
  • Multiple Sclerosis* / pathology
  • Neurons* / metabolism
  • Neurons* / pathology
  • Phospholipid Hydroperoxide Glutathione Peroxidase / metabolism
  • Signal Transduction

Substances

  • Membrane Proteins
  • Sting1 protein, mouse
  • Phospholipid Hydroperoxide Glutathione Peroxidase
  • glutathione peroxidase 4, mouse
  • Glutamic Acid
  • STING1 protein, human