| Literature DB >> 27668801 |
Motoko Y Kimura1, Julien Thomas1, Xuguang Tai1, Terry I Guinter1, Miho Shinzawa1, Ruth Etzensperger1, Zhenhu Li2, Paul Love2, Toshinori Nakayama3, Alfred Singer1.
Abstract
Major histocompatibility complex class I (MHC I) positive selection of CD8+ T cells in the thymus requires that T cell antigen receptor (TCR) signaling end in time for cytokines to induce Runx3d, the CD8-lineage transcription factor. We examined the time required for these events and found that the overall duration of positive selection was similar for all CD8+ thymocytes in mice, despite markedly different TCR signaling times. Notably, prolonged TCR signaling times were counter-balanced by accelerated Runx3d induction by cytokines and accelerated differentiation into CD8+ T cells. Consequently, lineage errors did not occur except when MHC I-TCR signaling was so prolonged that the CD4-lineage-specifying transcription factor ThPOK was expressed, preventing Runx3d induction. Thus, our results identify a compensatory signaling mechanism that prevents lineage-fate errors by dynamically modulating Runx3d induction rates during MHC I positive selection.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27668801 PMCID: PMC6691722 DOI: 10.1038/ni.3560
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606