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Gamma interferon signaling in oligodendrocytes is critical for protection from neurotropic coronavirus infection

Parra, G.I.; Bergmann, C.C.; Phares, T.W.; Hinton, D.R.; Atkinson, R.; Stohlman, S.A.

Journal of Virology 84(6): 3111-3115

2010


ISSN/ISBN: 1098-5514
PMID: 20042510
DOI: 10.1128/jvi.02373-09
Accession: 053348284

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Neurotropic coronavirus induces acute encephalomyelitis and demyelination in mice. Infection of BALB/c (H-2(d)) mice expressing a dominant negative gamma interferon (IFN-gamma) receptor specifically in oligodendrocytes was examined to determine the influence of IFN-gamma signaling on pathogenesis. Inhibition of IFN-gamma signaling in oligodendrocytes increased viral load, infection of oligodendrocytes, oligodendrocyte loss, demyelination, and axonal damage resulting in increased mortality. IFN-gamma levels and the inflammatory response were not altered, although the level of tumor necrosis factor (TNF) mRNA was increased. These data indicate that IFN-gamma signaling by oligodendroglia reduces viral replication but affects both demyelination and tissue destruction in a host-specific manner.

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