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. 2019 Feb 11;2019:2302835. doi: 10.1155/2019/2302835

Table 2.

Cytokine and chemokine expression in mixed glial primary cultures.

TNF-alpha IFN-alpha CXCL9 CXCL10
Control + NO donor 0.71 ± 0.03 0.45 ± 0.01 0.94 ± 0.02 1.27 ± 0.34
Control + iNOS inhibitor 1.01 ± 0.02 1.1 ± 0.45 0.17 ± 0.04 1.1 ± 0.03
sFasL 8.88 ± 1.89 4.5 ± 0.7 45.2 ± 0.54†† n.d.
HSV-1 86 ± 9.1†† 7422 ± 892†† 152 ± 29†† 424 ± 39††
HSV − 1 + NO donor 189±35∗∗ 1247±299∗∗ 95 ± 23 146±49∗∗
HSV − 1 + iNOS inhibitor 79 ± 12 10401±501∗∗ 294±51∗∗ 215±61∗∗
HSV − 1 + sFasL 43 ± 5 5673 ± 1329 445±91∗∗ 552 ± 59∗∗
HSV − 1 + NO donor + sFasL 49 ± 6.6 6427 ± 987 110 ± 23 150±45∗∗

Cytokine and chemokine expression changes in the mixed glial cultures at 24 h p.i. with HSV-1. Mixed glial cultures were subjected to treatment with the NO donor—SNP (100 μM)—or the inhibitor of iNOS—AMG (50 μM). mRNA levels of IFN-alpha, TNF-alpha, CXCL9, and CXCL10 are shown as expression relative to control on the basis of the 2∆∆Ct method. mRNA levels were counted from three PCR reactions for each sample. p ≤ 0.05 and ∗∗p ≤ 0.01 versus HSV-1-infected control and p ≤ 0.05 and ††p ≤ 0.01 versus uninfected control. n.d. means not detected.