PKR is required for maximal NF-κB activation but not IRF3 nuclear
localization. A, immunofluorescence images showing IRF3
(green) and 4′,6′-diamino-2-phenylindole (DAPI,
blue) staining following RNA transfection with CsiLUC20, PsiLUC50 or
pIpC. The cells were fixed at 4 h (top three rows) and 8 h
(bottom row) post-transfection. B, electrophoretic mobility
shift analysis using nuclear extracts from treated HeLa cells, parental
PKR+, or stable PKRkd, incubated with a NF-κB
oligonucleotide probe. C, Western blot analysis of IκB-α
and phosphorylated eIF-2α using PsiLUC50, pIpC, or TNF-α
transfected parental HeLa and PKRkd cells. Extracts were prepared
at the indicated time following treatment. Tubulin was used as a loading
control.