Glutathione S-transferases promote proinflammatory astrocyte-microglia communication during brain inflammation

Shin Ichi Kano, Eric Y. Choi, Eisuke Dohi, Swati Agarwal, Daniel J. Chang, Ashley M. Wilson, Brian D. Lo, Indigo V.L. Rose, Santiago Gonzalez, Takashi Imai, Akira Sawa

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

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.

Original languageEnglish (US)
Article numbereaar2124
JournalScience signaling
Volume12
Issue number569
DOIs
StatePublished - 2019

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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