NF-kappaB-driven STAT2 and CCL2 expression in astrocytes in response to brain injury

J Immunol. 2008 Nov 15;181(10):7284-91. doi: 10.4049/jimmunol.181.10.7284.


Tissue response to injury includes expression of genes encoding cytokines and chemokines. These regulate entry of immune cells to the injured tissue. The synthesis of many cytokines and chemokines involves NF-kappaB and signal transducers and activators of transcription (STAT). Injury to the CNS induces glial response. Astrocytes are the major glial population in the CNS. We examined expression of STATs and the chemokine CCL2 and their relationship to astroglial NF-kappaB signaling in the CNS following axonal transection. Double labeling with Mac-1/CD11b and glial fibrillary acidic protein revealed that STAT2 up-regulation and phosphorylation colocalized exclusively to astrocytes, suggesting the involvement of STAT2 activating signals selectively in astroglial response to injury. STAT1 was also up-regulated and phosphorylated but not exclusively in astrocytes. Both STAT2 up-regulation and phosphorylation were NF-kappaB -dependent since they did not occur in the lesion-reactive hippocampus of transgenic mice with specific inhibition of NF-kappaB activation in astrocytes. We further showed that lack of NF-kappaB signaling significantly reduced injury-induced CCL2 expression as well as leukocyte infiltration. Our results suggest that NF-kappaB signaling in astrocytes controls expression of both STAT2 and CCL2, and thus regulates infiltration of leukocytes into lesion-reactive hippocampus after axonal injury. Taken together, these findings indicate a central role for astrocytes in directing immune-glial interaction in the CNS injury response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / immunology
  • Astrocytes / metabolism*
  • Axotomy
  • Blotting, Western
  • Brain Injuries / genetics
  • Brain Injuries / immunology
  • Brain Injuries / metabolism*
  • Chemokine CCL2 / biosynthesis*
  • Chemokine CCL2 / genetics
  • Female
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Gene Expression
  • Gene Expression Regulation
  • Hippocampus / immunology
  • Hippocampus / injuries
  • Hippocampus / metabolism
  • Immunohistochemistry
  • Mice
  • Mice, Knockout
  • NF-kappa B / immunology
  • NF-kappa B / metabolism*
  • Phosphorylation
  • RNA, Messenger / analysis
  • Reverse Transcriptase Polymerase Chain Reaction
  • STAT1 Transcription Factor / biosynthesis
  • STAT1 Transcription Factor / genetics
  • STAT2 Transcription Factor / biosynthesis*
  • STAT2 Transcription Factor / genetics


  • Ccl2 protein, mouse
  • Chemokine CCL2
  • NF-kappa B
  • RNA, Messenger
  • STAT1 Transcription Factor
  • STAT2 Transcription Factor
  • Stat1 protein, mouse