| First Author | O'Sullivan JA | Year | 2023 |
| Journal | Int J Mol Sci | Volume | 24 |
| Issue | 4 | PubMed ID | 36835342 |
| Mgi Jnum | J:355319 | Mgi Id | MGI:7441128 |
| Doi | 10.3390/ijms24043930 | Citation | O'Sullivan JA, et al. (2023) Memory Precursors and Short-Lived Effector T cell Subsets Have Different Sensitivities to TGFbeta. Int J Mol Sci 24(4) |
| abstractText | After exposure to an antigen, CD8 T cells reach a decision point about their fate: to become either short-lived effector cells (SLECs) or memory progenitor effector cells (MPECs). SLECs are specialized in providing an immediate effector function but have a shorter lifespan and lower proliferative capacity compared to MPECs. Upon encountering the cognate antigen during an infection, CD8 T cells rapidly expand and then contract to a level that is maintained for the memory phase after the peak of the response. Studies have shown that the contraction phase is mediated by TGFbeta and selectively targets SLECs, while sparing MPECs. The aim of this study is to investigate how the CD8 T cell precursor stage determines TGFbeta sensitivity. Our results demonstrate that MPECs and SLECs have differential responses to TGFbeta, with SLECs being more sensitive to TGFbeta than MPECs. This difference in sensitivity is associated with the levels of TGFbetaRI and RGS3, and the SLEC-related transcriptional activator T-bet binding to the TGFbetaRI promoter may provide a molecular basis for increased TGFbeta sensitivity in SLECs. |
