Glutathione S-transferases promote proinflammatory astrocyte-microglia communication during brain inflammation.
Shin-Ichi KanoEric Y ChoiEisuke DohiSwati AgarwalDaniel J ChangAshley M WilsonBrian D LoIndigo V L RoseSantiago GonzalezTakashi ImaiAkira SawaPublished in: Science signaling (2019)
Astrocytes and microglia play critical roles in brain inflammation. Here, we report that glutathione S-transferases (GSTs), particularly GSTM1, promote proinflammatory signaling in astrocytes and contribute to astrocyte-mediated microglia activation during brain inflammation. In vivo, astrocyte-specific knockdown of GSTM1 in the prefrontal cortex attenuated microglia activation in brain inflammation induced by systemic injection of lipopolysaccharides (LPS). Knocking down GSTM1 in astrocytes also attenuated LPS-induced production of the proinflammatory cytokine tumor necrosis factor-α (TNF-α) by microglia when the two cell types were cocultured. In astrocytes, GSTM1 was required for the activation of nuclear factor κB (NF-κB) and the production of proinflammatory mediators, such as granulocyte-macrophage colony-stimulating factor (GM-CSF) and C-C motif chemokine ligand 2 (CCL2), both of which enhance microglia activation. Our study suggests that GSTs play a proinflammatory role in priming astrocytes and enhancing microglia activation in a microglia-astrocyte positive feedback loop during brain inflammation.
Keyphrases
- inflammatory response
- lps induced
- oxidative stress
- neuropathic pain
- toll like receptor
- nuclear factor
- white matter
- resting state
- rheumatoid arthritis
- functional connectivity
- cerebral ischemia
- prefrontal cortex
- spinal cord injury
- spinal cord
- stem cells
- multiple sclerosis
- transcription factor
- adipose tissue
- signaling pathway
- single cell
- anti inflammatory
- cell proliferation
- peripheral blood
- liver injury
- drug induced