Involvement of endoplasmic reticulum stress in the necroptosis of microglia/macrophages after spinal cord injury

Neuroscience. 2015 Dec 17:311:362-73. doi: 10.1016/j.neuroscience.2015.10.049. Epub 2015 Oct 30.

Abstract

Microglia/macrophages play a crucial role in inflammation after spinal cord injury (SCI). Although extensive studies have been performed on the mechanisms of microglia/macrophage activation and recruitment, how microglia/macrophages are eliminated remains unclear. In the present study, we observed a high-level expression of mixed lineage kinase domain-like protein (MLKL), a key molecule in the execution of necroptosis, in microglia/macrophages after SCI in mice. In vivo PI-labeling and Necrostatin-1 treatment confirmed the necroptosis of microglia/macrophages. Interestingly, our electronic microscopic (EM) study revealed that MLKL localized not only at the membrane but also on the endoplasmic reticulum (ER) of necroptotic microglia/macrophages. Furthermore, receptor-interacting protein 3 (RIP3), another necrosome component, was also found on the ER of necroptotic microglia/macrophages. And Glucose-regulated protein 78 (GRP78), an ER stress sensor, was up-regulated in MLKL-positive microglia/macrophages after SCI, suggesting a possible link between necroptosis and ER stress. In vitro, oxygen-glucose deprivation (OGD) stress induced ER stress and necroptosis in microglia. Inhibiting ER stress by 4-phenylbutyrate (4-PBA) significantly blocked the OGD-induced necroptosis of microglia. In the end, our data showed that, GRP78 and phosphorylated MLKL were co-expressed by the microglia/macrophages in the injured human spinal cord. Taken together, these results suggested that microglia/macrophages undergo an ER-stress involved necroptosis after SCI, implying that ER stress and necroptosis could be manipulated for modulating inflammation post-SCI.

Keywords: ER stress; microglia/macrophage; necroptosis; spinal cord injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Disease Models, Animal
  • Endoplasmic Reticulum Chaperone BiP
  • Endoplasmic Reticulum Stress / drug effects
  • Endoplasmic Reticulum Stress / physiology*
  • Heat-Shock Proteins / metabolism
  • Humans
  • Macrophages / drug effects
  • Macrophages / pathology
  • Macrophages / physiology*
  • Male
  • Mice, Inbred C57BL
  • Microglia / drug effects
  • Microglia / pathology
  • Microglia / physiology*
  • Necrosis / drug therapy
  • Necrosis / pathology
  • Necrosis / physiopathology
  • Neuroprotective Agents / pharmacology
  • Phenylbutyrates / pharmacology
  • Protein Kinases / metabolism
  • Receptor-Interacting Protein Serine-Threonine Kinases / metabolism
  • Spinal Cord Injuries / drug therapy
  • Spinal Cord Injuries / pathology
  • Spinal Cord Injuries / physiopathology*

Substances

  • Endoplasmic Reticulum Chaperone BiP
  • HSPA5 protein, human
  • Heat-Shock Proteins
  • Hspa5 protein, mouse
  • Neuroprotective Agents
  • Phenylbutyrates
  • 4-phenylbutyric acid
  • MLKL protein, human
  • MLKL protein, mouse
  • Protein Kinases
  • Receptor-Interacting Protein Serine-Threonine Kinases
  • Ripk3 protein, mouse