Journal of Neurochemistry · 2008 · 18 citations · 41 references
Life SciencesMolecular BiologyNeuroscienceGene ExpressionMolecular NeuroscienceTranscriptional RegulationCytokine BiologyCytokine RegulationCytokine SignalingInnate Immune ResponseInterferon ResponsesViral PathogenesisAntiviral Innate SignalingCytokine Expression RegulationCytokine MediatorsCytokine-induced Gene ExpressionInnate Cytokine ResponsesNeurotropic Viral InfectionNeurotropic Viral PathogenesisViral Infection Responses
We have previously shown that the protein tyrosine phosphatase SHP-1 is highly expressed in CNS glia and is an important modulator of cytokine signaling. As such, mice genetically lacking SHP-1 display constitutive myelin abnormalities, severe virus-induced demyelinating disease, and defects in innate anti-viral responses in the CNS. In this study, we show the differential distribution of the SHP-1 promoter-specific transcripts and demonstrate that several cytokines significantly induce SHP-1 expression in CNS glia. Consistent with these cytokine effects, infection with a neurotropic virus both in vitro and in vivo up-regulates SHP-1 transcripts and protein in CNS cells. Using CNS glial cultures of gene knockout mice, we show that interferons-beta and interferons-gamma act through STAT-1 and interferon regulatory factor-1 to induce the SHP-1 promoter I transcripts. Conversely, interferons-beta and IL-6 act through STAT-3 to induce SHP-1 promoter II transcripts. This study demonstrates that interferons and other cytokines associated with virus infections in the CNS can significantly induce the expression of SHP-1 through STAT-1/3 activity and provides a better understanding of the molecular mechanisms regulating cytokine-induced expression important for multiple homeostatic functions of SHP-1 in the CNS.
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Viral particles induce Ia antigen expression on astrocytes
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