4.6 Article

Diffusion magnetic resonance imaging-derived free water detects neurodegenerative pattern induced by interferon-γ

Journal

BRAIN STRUCTURE & FUNCTION
Volume 225, Issue 1, Pages 427-439

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00429-019-02017-1

Keywords

Interferon gamma; Diffusion MRI; Free water; White matter; Aging; Inflammation

Funding

  1. NIA NIH HHS [R01 AG055798, P30 AG066506, 1R01AG055798, P50 AG047266, P50AG047266] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS052318, P50NS091856, T32 NS082168, R21 NS065273, R01NS052318, R01 NS075012, P50 NS091856, R01NS075012, T32NS082168] Funding Source: Medline
  3. UF McKnight Brain Foundation [Postdoctoral Fellowship] Funding Source: Medline

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Imaging biomarkers for immune activation may be valuable for early-stage detection, therapeutic testing, and research on neurodegenerative conditions. In the present study, we determined whether diffusion magnetic resonance imaging-derived free water signal is a sensitive marker for neuroinflammatory effects of interferon-gamma (Ifn-gamma). Neonatal wild-type mice were injected in the cerebral ventricles with recombinant adeno-associated viruses expressing the inflammatory cytokine Ifn-gamma. Groups of mice expressing Ifn-gamma and age-matched controls were imaged at 1, 5 and 8 months. Mice deficient in Ifngr1(-/-) and Stat1(-/-) were scanned at 5 months as controls for the signaling cascades activated by Ifn-gamma. The results indicate that Ifn-gamma affected fractional anisotropy (FA), mean diffusivity (MD), and free water (FW) in white matter structures, midline cortical areas, and medial thalamic areas. In these structures, FA and MD decreased progressively from 1 to 8 months of age, while FW increased significantly. The observed reductions in FA and MD and increased FW with elevated brain Ifn-gamma was not observed in Ifngr1(-/-) or Stat1(-/-) mice. These results suggest that the observed microstructure changes involve the Ifn-gr1 and Stat1 signaling. Interestingly, increases in FW were observed in midbrain of Ifngr1(-/-) mice, which suggests alternative Ifn-gamma signaling in midbrain. Although initial evidence is offered in relation to the sensitivity of the FW signal to neurodegenerative and/or inflammatory patterns specific to Ifn-gamma, further research is needed to determine applicability and specificity across animal models of neuroinflammatory and degenerative disorders.

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