Aging‐like changes in the transcriptome of irradiated microglia
Abstract
Whole brain irradiation remains important in the management of brain tumors. Although necessary for improving survival outcomes, cranial irradiation also results in cognitive decline in long‐term survivors. A chronic inflammatory state characterized by microglial activation has been implicated in radiation‐induced brain injury. We here provide the first comprehensive transcriptional profile of irradiated microglia. Fluorescence‐activated cell sorting was used to isolate CD11b+ microglia from the hippocampi of C57BL/6 and Balb/c mice 1 month after 10 Gy cranial irradiation. Affymetrix gene expression profiles were evaluated using linear modeling and rank product analyses. One month after irradiation, a conserved irradiation signature across strains was identified, comprising 448 and 85 differentially up‐ and downregulated genes, respectively. Gene set enrichment analysis demonstrated enrichment for inflammation, including M1 macrophage‐associated genes, but also an unexpected enrichment for extracellular matrix and blood coagulation‐related gene sets, in contrast previously described microglial states. Weighted gene coexpression network analysis confirmed these findings and further revealed alterations in mitochondrial function. The RNA‐seq transcriptome of microglia 24‐h postradiation proved similar to the 1‐month transcriptome, but additionally featured alterations in apoptotic and lysosomal gene expression. Reanalysis of published aging mouse microglia transcriptome data demonstrated striking similarity to the 1‐month irradiated microglia transcriptome, suggesting that shared mechanisms may underlie aging and chronic irradiation‐induced cognitive decline. GLIA 2015;63:754–767Keywords
Funding Information
- NIH (R01 MH071472, California Institute of Regenerative Medicine Clinical Research Fellowship (to TCB), Stanford Medical Scholars Research Fellowships (to MDL and SK) and an American Brain Tumor Association Medical Student Summer Fellowship, supported by Dropping the Puck on Cancer at Indiana University)
This publication has 72 references indexed in Scilit:
- The microglial activation state regulates migration and roles of matrix-dissolving enzymes for invasionJournal of Neuroinflammation, 2013
- Hypothalamic programming of systemic ageing involving IKK-β, NF-κB and GnRHNature, 2013
- Genomic responses in mouse models poorly mimic human inflammatory diseasesProceedings of the National Academy of Sciences, 2013
- Essential role of cooperative NF-κB and Stat3 recruitment to ICAM-1 intronic consensus elements in the regulation of radiation-induced invasion and migration in gliomaOncogene, 2012
- The role of glial cells in synapse eliminationCurrent Opinion in Neurobiology, 2012
- Irradiation Alters MMP-2/TIMP-2 System and Collagen Type IV Degradation in BrainInternational Journal of Radiation Oncology - Biology - Physics (IJROBP), 2012
- Protective and pathogenic functions of macrophage subsetsNature Reviews Immunology, 2011
- The PPARα Agonist Fenofibrate Preserves Hippocampal Neurogenesis and Inhibits Microglial Activation After Whole-Brain IrradiationInternational Journal of Radiation Oncology - Biology - Physics (IJROBP), 2009
- Exploring the full spectrum of macrophage activationNature Reviews Immunology, 2008
- Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profilesProceedings of the National Academy of Sciences, 2005