Department of Molecular and System Pharmacology, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, Fukuoka 812-8582, Japan.
Program in Genomics of Differentiation, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Cell Rep. 2012 Apr 19;1(4):334-340. doi: 10.1016/j.celrep.2012.02.014. Epub 2012 Apr 5.
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.
小胶质细胞被神经系统中的多种类型的损伤激活,并在神经元病变中发挥重要作用。然而,小胶质细胞如何转化为反应性表型尚不清楚。在这里,我们确定转录因子干扰素调节因子 8(IRF8)是反应性小胶质细胞的关键调节因子。在脊髓中,IRF8 的表达通常较低;然而,在外周神经损伤(PNI)后,IRF8 在小胶质细胞中显著上调,但在神经元或星形胶质细胞中没有上调。在培养的小胶质细胞中过表达 IRF8 会促进与反应性状态相关的基因的转录;相反,IRF8 缺陷可防止 PNI 后脊髓中这些基因的表达。此外,IRF8 缺陷型小鼠对神经病理性疼痛(PNI 的常见后遗症)具有抗性,并且将过表达 IRF8 的小胶质细胞脊柱转移到正常小鼠中会产生疼痛。因此,IRF8 可能激活了一个将小胶质细胞转化为反应性表型的基因表达程序。我们的发现为小胶质细胞激活提供了一个新的观察机制。