bioRxiv · 10.1101/2020.11.02.365148
IL-12 signaling promotes TET2-mediated DNA demethylation during CD8 T cell effector differentiation
Abstract
CD8 T cell memory differentiation endows T cells with an ability to rapidly induce effector functions upon pathogen re-encounter. While it is well established that substantial epigenetic remodeling occurs during the effector stage of the immune response, the signaling events that imprint CD8 T cells with these stable epigenetic programs are not well-defined. To gain insight into the signaling determinants of effector-associated epigenetic programming among CD8 T cells, we explored the role of IL-12 in the imprinting of IFNg expression during human CD8 T cell priming. We observed that TCR-mediated stimulation of human naive CD8 T cells is not sufficient to induce substantial demethylation of the IFNg promotor. However, TCR stimulation in the presence of the inflammatory cytokine, IL-12, resulted in significant and stable demethylation of the IFNg locus that was commensurate with an increase in IFNg expression. We further show that IL-12-associated demethylation of the IFNg locus is coupled to cell division through TET2-dependent passive demethylation in an ex vivo human CAR T cell model system and an in vivo immunologically competent murine system. Collectively, these data illustrate that IL-12 signaling promotes TET2-mediated effector epigenetic programming in CD8 T cells during the primary immune response and serve as proof of concept that signal 3 cytokines can be used to guide the induction of epigenetically regulated traits among T cells used for adoptive immunotherapies.
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Zebley, C., Abdelsamed, H., Ghoneim, H., Alli, S., Haydar, D., Harris, T., Mcgargill, M., Krenciute, G., Youngblood, B.. 2020-11-02. IL-12 signaling promotes TET2-mediated DNA demethylation during CD8 T cell effector differentiation. https://doi.org/10.1101/2020.11.02.365148
Cite the original work for its findings. Save a collection to share your selection of sources.