Docosahexaenoic acid attenuates microglial activation and delays early retinal degeneration

J Neurochem. 2009 Sep;110(6):1863-75. doi: 10.1111/j.1471-4159.2009.06286.x. Epub 2009 Jul 17.

Abstract

Microgliosis is a common phenomenon in neurodegenerative disorders including retinal dystrophies. We performed a detailed characterization of activated microglia in the retinoschisin (Rs1h)-deficient (Rs1h(-/Y)) mouse model of inherited retinal degeneration. To visualize and isolate microglia, we crossed Rs1h(-/Y) animals with transgenic MacGreen mice, which express green fluorescent protein under the control of the macrophage-specific csf1r promoter. Activated microglia were detected in retinal sections and whole-mounts of early postnatal MacGreen/Rs1h(-/Y) mice before the onset of overt neuronal cell death. These activated microglia contained prominent lipid droplets and analysis of the retinal lipid composition showed decreased docosahexaenoic acid (DHA) levels in Rs1h(-/Y) retinas. To establish a link between microglia activation, reduced DHA levels, and neurodegeneration, a dietary intervention study was performed. Female Rs1h(-/-) mice and their Rs1h(-/Y) litter were either subjected to a diet enriched with DHA, or a control chow lacking DHA. Supplementation with DHA enhanced photoreceptor survival and converted activated microglia to a quiescent phenotype. Furthermore, DHA, but not docosapentaenoic acid or adrenic acid reduced pro-inflammatory gene expression, migration, and lipid accumulation of cultured BV-2 microglia. We conclude that retinal DHA levels control the activity of microglia and thereby may affect the progression and extent of retinal degeneration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Animals
  • Animals, Newborn
  • Cell Adhesion Molecules / deficiency
  • Cell Death / drug effects
  • Cell Movement / drug effects
  • Cells, Cultured
  • Dietary Supplements
  • Disease Models, Animal
  • Docosahexaenoic Acids / pharmacology*
  • Dose-Response Relationship, Drug
  • Eye Proteins
  • Fatty Acids / metabolism
  • Gene Expression Profiling / methods
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / physiology
  • Green Fluorescent Proteins / genetics
  • In Situ Nick-End Labeling / methods
  • Lipopolysaccharides / pharmacology
  • Mice
  • Mice, Transgenic
  • Microglia / drug effects*
  • Oligonucleotide Array Sequence Analysis / methods
  • Phospholipids / metabolism
  • Retina / drug effects*
  • Retina / pathology
  • Retinal Degeneration / genetics
  • Retinal Degeneration / pathology*
  • Time Factors
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cell Adhesion Molecules
  • Eye Proteins
  • Fatty Acids
  • Lipopolysaccharides
  • Phospholipids
  • RS1 protein, mouse
  • Tumor Necrosis Factor-alpha
  • Green Fluorescent Proteins
  • Docosahexaenoic Acids