An autonomous TCR signal-sensing switch influences CD4/CD8 lineage choice in mice

Abstract

How multipotential cells initiate distinct gene expression programs in response to external cues to instruct cell fate choice remains a fundamental question in biology. Establishment of CD4 and CD8 T cell fates during thymocyte development is critically regulated by T cell receptor (TCR) signals, which in turn control expression of the CD4-determining transcription factor ThPOK. However, the mechanism whereby differential TCR signals are molecularly interpreted to promote or antagonize ThPOK expression, and thereby CD4 versus CD8 lineage fates remains unknown. Here we show, using reverse genetic and molecular approaches that an autonomous, position-independent TCR-sensing switch is embedded within the ThPOK locus. Further, using an in vivo mutagenesis approach, we demonstrate that differential TCR signals are interpreted during lineage commitment by relative binding of EGR, NFAT and Ebox factors to this bistable switch. Collectively our study reveals the central molecular mechanism whereby TCR signaling influences differential lineage choice. Ultimately, these findings may provide an important new tool for skewing T cell fate to treat cancer and autoimmune diseases.

The TCR assigns naive T cells to a preferred lymph node

“…Apparently, the CD4/CD8 lineage choice of T cells is completely TCR driven, and this choice is made consistently within and between mice. In other words, the CD4/CD8 fate choice is principally deterministic, in line with TCR restriction for class II or class I MHC, respectively (22)(23)(24)(25). Training a neural network on the data (see Materials and Methods), the prediction of a CD8 fate based on TCRα sequence achieved an area under the curve (AUC) of 0.8.…”