We examined the gene expression and regulation of Type III interferon (IFN), IFN-λ, in human neuronal cells. Human neuronal cells expressed endogenous IFN-λ1 but not IFN-λ2/3. Upon the activation of Toll-like receptor (TLR)-3 expressed in the neuronal cells by polyriboinosinic polyribocytidylic acid (PolyI:C), both IFN-λ1 and IFN-λ2/3 expression was significantly induced. The activation of TLR-3 also exhibited antiviral activity against pseudotyped HIV-1 infection of the neuronal cells. Human neuronal cells also expressed functional IFN-λ receptor complex, interleukin-28 receptor α subunit (IL-28Rα) and IL-10Rβ, as evidenced by the observations that exogenous IFN-λ treatment inhibited pseudotyped HIV-1 infection of the neuronal cells and induced the expression of APOBEC3G/3F, the newly identified anti-HIV-1 cellular factors. These data provide direct and compelling evidence that there is intracellular expression and regulation of IFN-λ in human neuronal cells, which may have an important role in the innate neuronal protection against viral infections in the CNS. KeywordsInterferon (IFN); Toll-like receptor (TLR); NT2-N; Neuron; Virus; HIV Interferon lambda (IFN-λ), the newly discovered type III family of IFNs (Kotenko et al., 2003, Sheppard et al., 2003, comprises three structurally related cytokines, IFN-λ1, IFN-λ2 and IFN-λ3. A gene array experiment covering the whole human genome revealed that all the IFN-λinduced genes could also be activated by type I IFNs (Zhou et al., 2007). In addition,
Very little is known about the interactions between hepatitis C virus (HCV) and methamphetamine, which is a highly abused psychostimulant and a known risk factor for human immunodeficiency virus (HIV)/HCV infection. This study examined whether methamphetamine has the ability to inhibit innate immunity in the host cells, facilitating HCV replication in human hepatocytes. Methamphetamine inhibited intracellular interferon alpha expression in human hepatocytes, which was associated with the increase in HCV replication. In addition, methamphetamine also compromised the anti-HCV effect of recombinant interferon alpha. Further investigation of mechanism(s) responsible for the methamphetamine action revealed that methamphetamine was able to inhibit the expression of the signal transducer and activator of transcription 1, a key modulator in interferon-mediated immune and biological responses. Methamphetamine also down-regulated the expression of interferon regulatory factor-5, a crucial transcriptional factor that activates the interferon pathway. These in vitro findings that methamphetamine compromises interferon alpha-mediated innate immunity against HCV infection indicate that methamphetamine may have a cofactor role in the immunopathogenesis of HCV disease.
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