AI Article Synopsis

  • Imaging biomarkers like diffusion magnetic resonance imaging-derived free water signal could aid in early detection and research of neurodegenerative diseases.
  • The study examined the impact of the inflammatory cytokine Ifn-γ on brain microstructure in neonatal mice, revealing changes in fractional anisotropy, mean diffusivity, and free water in response to the cytokine over time.
  • Results suggest that traditional Ifn-γ signaling pathways are involved in these changes, while also indicating the need for further research to explore the sensitivity of these biomarkers across various neuroinflammatory conditions and animal models.

Article Abstract

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-γ). Neonatal wild-type mice were injected in the cerebral ventricles with recombinant adeno-associated viruses expressing the inflammatory cytokine Ifn-γ. Groups of mice expressing Ifn-γ 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-γ. The results indicate that Ifn-γ 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-γ 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-γ 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-γ, further research is needed to determine applicability and specificity across animal models of neuroinflammatory and degenerative disorders.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7003714PMC
http://dx.doi.org/10.1007/s00429-019-02017-1DOI Listing

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