TY - JOUR
T1 - Diffusion magnetic resonance imaging-derived free water detects neurodegenerative pattern induced by interferon-γ
AU - Febo, Marcelo
AU - Perez, Pablo D.
AU - Ceballos-Diaz, Carolina
AU - Colon-Perez, Luis M.
AU - Zeng, Huadong
AU - Ofori, Edward
AU - Golde, Todd E.
AU - Vaillancourt, David E.
AU - Chakrabarty, Paramita
N1 - Funding Information:
This work was supported by the National Institutes of Health (P50AG047266, R01NS052318, R01NS075012, T32NS082168, P50NS091856, 1R01AG055798).
Funding Information:
This work was supported by the National Institutes of Health (P50AG047266, R01NS052318, R01NS075012, T32NS082168, P50NS091856, 1R01AG055798). The authors thank the Advanced Magnetic Resonance Imaging and Spectroscopy (AMRIS) facility and National High Magnetic Field Laboratory (NHMFL) for their continued support (National Science Foundation Cooperative Agreement No. DMR-1157490 and the State of Florida).
Funding Information:
This work was supported by the National Institutes of Health (P50AG047266, R01NS052318, R01NS075012, T32NS082168, P50NS091856, 1R01AG055798). The authors thank the Advanced Magnetic Resonance Imaging and Spectroscopy (AMRIS) facility and National High Magnetic Field Laboratory (NHMFL) for their continued support (National Science Foundation Cooperative Agreement No. DMR-1157490 and the State of Florida).
Publisher Copyright:
© 2020, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - 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.
AB - 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.
KW - Aging
KW - Diffusion MRI
KW - Free water
KW - Inflammation
KW - Interferon gamma
KW - White matter
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U2 - 10.1007/s00429-019-02017-1
DO - 10.1007/s00429-019-02017-1
M3 - Article
C2 - 31894407
AN - SCOPUS:85077179741
SN - 1863-2653
VL - 225
SP - 427
EP - 439
JO - Brain Structure and Function
JF - Brain Structure and Function
IS - 1
ER -