Rroid2 regulates effector-to-memory CD8+ T cell differentiation during infection in vivo.
Journal Article
Overview
abstract
CD8+ T cell differentiation has been associated with changes in the expression of long noncoding RNAs (lncRNAs). Yet, which and how lncRNAs regulate CD8+ T cell responses following infection in vivo remains incompletely understood. We performed deep RNA-seq to map the lncRNA expression landscape of CD8+ T cell subsets during infection and generated lncRNA knockout mouse models to evaluate the in vivo relevance of six lncRNAs. We identified Rroid2 to regulate effector CD8+ T cell function and effector-to-memory differentiation. Rroid2-deficient mice displayed increased CD44dim Foxp3+ regulatory T cells while the development of other immune cells, such as natural killer cells, was not affected. In CD8+ T cells, Rroid2 deficiency resulted in a fine-tuned downregulation of transcription factors Id2 and T-bet and impaired KLRG1+ and KLRG1- effector CD8+ T cell proliferation and cytotoxicity as well as effector-to-memory CD8+ T cell differentiation. The human orthologue of Rroid2, LINC01814, is also upstream of the transcriptional regulator ID2 and is highly expressed in human memory CD8+ T cells. Taken together, Rroid2 represents a key regulatory layer that controls CD8+ T cell differentiation.
