Abstract
UV irradiation of a continuous line of rabbit kidney cells (RK13) was used as a tool for the study of the mechanism of interferon induction. Irradiation of cells prior to their exposure to Newcastle disease virus (NDV) resulted in a dose-dependent decrease in interferon production. The inhibition of total cellular RNA synthesis by UV irradiation in uninduced cultures was similar to the inactivation curve of interferon production in NDV-induced cultures. In contrast, the production of interferon with polyinosinate-polycytidylate (poly[I].poly [C]) paradoxically was enhanced in cells irradiated with a wide range of doses of UV. However, in cells stimulated with poly(I).poly(C) and "superinduced" by the sequential addition of cycloheximide and actinomycin D, the rate of inactivation of interferon production by UV light was similar to that observed with NDV. These results are not inconsistent with the idea that both poly(I).poly(C) and NDV stimulate the same interferon gene(s), but indicate that the mechanism controlling its expression may be different for each inducer.
MeSH Terms
Cell Line/metabolism,radiation effects
Cycloheximide/pharmacology
Dactinomycin/pharmacology
Dose-Response Relationship, Radiation
Female
Genes
Interferons/biosynthesis
Kidney
Newcastle disease virus/growth & development
Poly I-C/pharmacology
Puromycin/pharmacology
RNA/biosynthesis
Radiation Effects
Time Factors
Tritium
Ultraviolet Rays
Uridine/metabolism
Virus Replication
Chemicals
Tritium
Dactinomycin
Puromycin
RNA
Interferons
Cycloheximide
Poly I-C
Uridine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Mozes L W
Vilcek J
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13 references, click to expand
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