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Cell Rep. 2012 Apr 19;1(4):334-340. doi: 10.1016/j.celrep.2012.02.014. Epub 2012 Apr 5.

IRF8 is a critical transcription factor for transforming microglia into a reactive phenotype.

Author information

1
Department of Molecular and System Pharmacology, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, Fukuoka 812-8582, Japan.
2
Program in Genomics of Differentiation, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
3
Department of Immunology, Graduate School of Medicine, Yokohama City University, Yokohama 236-0004, Japan.
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Contributed equally

Abstract

Microglia become activated by multiple types of damage in the nervous system and play essential roles in neuronal pathologies. However, how microglia transform into reactive phenotypes is poorly understood. Here, we identify the transcription factor interferon regulatory factor 8 (IRF8) as a critical regulator of reactive microglia. Within the spinal cord, IRF8 expression was normally low; however, the expression was markedly upregulated in microglia, but not in neurons or astrocytes, after peripheral nerve injury (PNI). IRF8 overexpression in cultured microglia promoted the transcription of genes associated with reactive states; conversely, IRF8 deficiency prevented these gene expressions in the spinal cord following PNI. Furthermore, IRF8-deficient mice were resistant to neuropathic pain, a common sequela of PNI, and transferring IRF8-overexpressing microglia spinally to normal mice produced pain. Therefore, IRF8 may activate a program of gene expression that transforms microglia into a reactive phenotype. Our findings provide a newly observed mechanism for microglial activation.

PMID:
22832225
PMCID:
PMC4158926
DOI:
10.1016/j.celrep.2012.02.014
[Indexed for MEDLINE]
Free PMC Article

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