T cell self-reactivity during thymic development dictates the timing of positive selection.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 33884954.
- Also identified by DOI 10.7554/eLife.65435 and PMC identifier 8116051.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Functional tuning of T cells based on their degree of self-reactivity is established during positive selection in the thymus, although how positive selection differs for thymocytes with relatively low versus high self-reactivity is unclear. In addition, preselection thymocytes are highly sensitive to low-affinity ligands, but the mechanism underlying their enhanced T cell receptor (TCR) sensitivity is not fully understood. Here we show that murine thymocytes with low self-reactivity experience briefer TCR signals and complete positive selection more slowly than those with high self-reactivity. Additionally, we provide evidence that cells with low self-reactivity retain a preselection gene expression signature as they mature, including genes previously implicated in modulating TCR sensitivity and a novel group of ion channel genes. Our results imply that thymocytes with low self-reactivity downregulate TCR sensitivity more slowly during positive selection, and associate membrane ion channel expression with thymocyte self-reactivity and progress through positive selection.
Medical subject headings
- Cell Differentiation
- Histocompatibility Antigens Class I
- Receptors, Antigen, T-Cell
- Self Tolerance
- Thymocytes
- Thymus Gland