There is general agreement that IFN-gamma is produced only by cells of
immune origin (T-cells, NK cells, and recently macrophages). However,
indirect evidence has suggested that undetectable, low levels of IFN-
gamma produced by cells of non-immune lineage, such as the murine line
L-929, enhanced the antiviral activity of IFNs-alpha and/or beta foll
owing induction by agents such as the double stranded RNA poly ICLC. S
ince L-929 cells were one of the prototypic cell lines for studying mu
rine IFN induction and action, we felt that it would be important to v
alidate this observation by detection of the mRNA for IFN-gamma. If co
nfirmed, it might indicate a role for IFN-gamma in non-immune cells. T
he present investigations revealed that mouse L-929 fibroblasts produc
e IFN-gamma message following exposure to conventional IFN-alpha/beta
inducers such as poly ICLC or Newcastle disease virus. In addition, we
found that IFN-gamma itself will induce its own message. We further s
how that this is not a phenomenon isolated to transformed cells since
we found that normal mouse embryo fibroblasts also produced the messag
e, however in a constitutive fashion.