Rroid2 regulates effector-to-memory CD8(+) T cell differentiation during infection in vivo.

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作者:Erber Julia, Stecher Carmen, Plajer Valerie, Braun Nina, Mallard William, Goff Loyal A, Barozzi Iros, Mohr Thomas, Rinn John L, Flavell Richard A, Herndler-Brandstetter Dietmar
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 CD44(dim) 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.

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