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Mitogenic effect of double-stranded RNA in human fibroblasts: role of autogenous interferon

Journal Article · · J. Cell. Physiol.; (United States)
The synthetic double-stranded RNA polyinosinate-polycytidylate (poly(l).poly(C)) was mitogenic in cultures of human foreskin fibroblasts, as demonstrated by a stimulation of /sup 3/H-thymidine incorporation and an increase in cell density. Poly(l).poly(C) is a potent inducer of interferon (IFN)-beta in human fibroblasts. Single-stranded poly(l) or poly(C) were not mitogenic in human fibroblasts and did not stimulate IFN production. Antiserum to interferon (IFN)-beta, added to poly(l).poly(C)-stimulated cultures in order to neutralize endogenously generated IFN, markedly amplified the mitogenic action. Under similar experimental conditions, antiserum to IFN-beta did not enhance the mitogenic action of epidermal growth factor (EGF). Dexamethasone enhanced the mitogenic action of poly(l).poly(C) in a manner similar to antiserum against IFN-beta. This effect of dexamethasone correlated with its marked inhibitory action on poly(l).poly(C)-stimulated IFN production. Together with the results of other related studies, these findings support the notion of an evolutionary link between the generation of a mitogenic signal and IFN induction. In addition, these results support the concept that autocrine secretion of IFN-beta can exert negative feedback control of cell proliferation.
Research Organization:
New York Univ. Medical Center, NY
OSTI ID:
6618628
Journal Information:
J. Cell. Physiol.; (United States), Journal Name: J. Cell. Physiol.; (United States) Vol. 130:1; ISSN JCLLA
Country of Publication:
United States
Language:
English