AI Summary & Key Takeaways
AI InsightWe found that clones expressing the dominant negative form of the PKR gene were not only resistant to IFN-g-mediated killing, but were also incapable of inducing accumulation of IDO protein after IFN-g treatment.
📌 3 Key Takeaways
Abstract
We investigated whether the activity of double-stranded RNA activated kinase (p68/PKR) is necessary for induction of IDO (indolamine 2,3 -dioxygenase) gene by IFN-g. For this purpose, we planned to abrogate the function of cellular wt-PKR gene. Clones of ME180 cells expressing the dominant negative form of PKR were selected in the presence of neomycin. Then these cells were treated with IFN-g and accumulation of IDO protein was determined by Western blot analysis. We found that clones expressing the dominant negative form of the PKR gene were not only resistant to IFN-g-mediated killing, but were also incapable of inducing accumulation of IDO protein after IFN-g treatment.
Özet
We investigated whether the activity of double-stranded RNA activated kinase (p68/PKR) is necessary for induction of IDO (indolamine 2,3 -dioxygenase) gene by IFN-g. For this purpose, we planned to abrogate the function of cellular wt-PKR gene. Clones of ME180 cells expressing the dominant negative form of PKR were selected in the presence of neomycin. Then these cells were treated with IFN-g and accumulation of IDO protein was determined by Western blot analysis. We found that clones expressing the dominant negative form of the PKR gene were not only resistant to IFN-g-mediated killing, but were also incapable of inducing accumulation of IDO protein after IFN-g treatment.