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

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作者
Marcelo Febo
Pablo D. Perez
Carolina Ceballos-Diaz
Luis M. Colon-Perez
Huadong Zeng
Edward Ofori
Todd E. Golde
David E. Vaillancourt
Paramita Chakrabarty
机构
[1] University of Florida,Department of Psychiatry, College of Medicine
[2] University of Florida,Department of Neuroscience, College of Medicine
[3] University of Florida,Center for Translational Research in Neurodegenerative Diseases, College of Medicine
[4] University of Florida,Department of Applied Physiology and Kinesiology, College of Health and Human Performance
[5] University of Florida,Advanced Magnetic Resonance Imaging and Spectroscopy (AMRIS) Facility, College of Medicine
[6] University of Florida,McKnight Brain Institute, College of Medicine
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关键词
Interferon gamma; Diffusion MRI; Free water; White matter; Aging; Inflammation;
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摘要
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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页码:427 / 439
页数:12
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