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. 2002 Mar;76(6):2780–2788. doi: 10.1128/JVI.76.6.2780-2788.2002

FIG. 5.

FIG. 5.

Induction of RANTES production in the absence of PKR activity and specific viral proteins. RAW-pBK-CMV and RAW-PKR-M7 cells (a) or RAW 264.7 cells (b to e) were seeded and left overnight to settle. (a) The cells were mock infected or infected with 106 PFU of HSV-1 or HSV-2 per ml (MOI of 2). (b to e) The cells were treated with mock virus preparation or infected with 106 PFU of mutant virus (ICP0 mutant [b], ICP4 mutant [c], ICP22 mutant [d], or ICP27 mutant [e]) per ml (MOI or 2), wild-type HSV-1, or the reconstituted mutants. After 24 h of infection, supernatants were harvested and RANTES levels were measured by ELISA. Results are shown as means from three or four cultures ± SEMs. ND, not detectable. Similar results were seen in four independent experiments for panels a and b and two independent experiments for panels c to e.