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Examination of Thymic Positive and Negative Selection by Flow Cytometry
Published on: October 8, 2012
Thymic OX40 expression discriminates cells undergoing strong responses to selection ligands
Mark Klinger1, Joong Kyu Kim, Stephen A Chmura
1Department of Microbiology and Immunology and.
Journal of Immunology (Baltimore, Md. : 1950)
|April 4, 2009
Summary
Researchers discovered that OX40 (tumor necrosis factor receptor superfamily member 18) is expressed on some naive T cells in the thymus. This indicates a subset of T cells, including regulatory T (Treg) cell precursors, are selected via strong thymic signaling.
Area of Science:
- Immunology
- T cell biology
- Thymic selection
Background:
- OX40 (tumor necrosis factor receptor superfamily member 18) is a receptor primarily found on activated and regulatory T (Treg) cells.
- Its expression pattern suggests a potential role beyond activated T cells.
Purpose of the Study:
- To investigate the expression of OX40 on naive T cells within the thymus.
- To determine if OX40 expression in the thymus is linked to specific T cell populations or signaling events.
Main Methods:
- Utilized an Ox40-cre allele for lineage tracing in thymocytes.
- Analyzed OX40 expression in conjunction with T cell markers like CD25.
- Correlated OX40 expression with thymic positive selection signaling strength.
Main Results:
- A subpopulation of naive T cells was identified to have previously expressed OX40 in the thymus.
- Thymic OX40 expression was observed in CD25(high) regulatory T (Treg) cell precursors.
- Previous OX40 expression on naive T cells correlated with a partially activated phenotype, distinct from other naive T cells.
- Thymic OX40 expression marked thymocytes that received strong positive selection signals.
Conclusions:
- The findings suggest that thymic OX40 expression identifies T cells, including Treg precursors and a distinct naive T cell subset, selected through robust signaling.
- This highlights a role for strong thymic self-ligand interactions in shaping specific T cell populations.

