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The RNA-binding protein polypyrimidine tract binding protein 1 (PTBP1) has been found to have roles in CD4 T-cell activation, but its function in CD8 T cells remains untested. We show it is dispensable for the development of naïve mouse CD8 T cells, but is necessary for the optimal expansion and production of effector molecules by antigen-specific CD8 T cells in vivo. PTBP1 has an essential role in regulating the early events following activation of the naïve CD8 T cell leading to IL-2 and TNF production. It is also required to protect activated CD8 T cells from apoptosis. PTBP1 controls alternative splicing of over 400 genes in naïve CD8 T cells in addition to regulating the abundance of ∼200 mRNAs. PTBP1 is required for the nuclear accumulation of c-Fos, NFATc2, and NFATc3, but not NFATc1. This selective effect on NFAT proteins correlates with PTBP1-promoted expression of the shorter Aβ1 isoform and exon 13 skipped Aβ2 isoform of the catalytic A-subunit of calcineurin phosphatase. These findings reveal a crucial role for PTBP1 in regulating CD8 T-cell activation.

Original publication

DOI

10.1002/eji.202149781

Type

Journal article

Journal

Eur J Immunol

Publication Date

07/2022

Volume

52

Pages

1058 - 1068

Keywords

CD8 T cells, RNA binding proteins, cellular activation, gene regulation, Alternative Splicing, Animals, CD8-Positive T-Lymphocytes, Heterogeneous-Nuclear Ribonucleoproteins, Mice, Polypyrimidine Tract-Binding Protein, Protein Isoforms