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A model of preferential pairing between epithelial and dendritic cells in thymic antigen transfer

Matouš Vobořil, Jiří Březina, Tomáš Brabec, Jan Dobeš, Ondřej Ballek, Martina Dobešová, Jasper Manning, Richard S Blumberg, Dominik Filipp

2022eLife25 citationsDOIOpen Access PDF

Abstract

Medullary thymic epithelial cells (mTECs), which produce and present self-antigens, are essential for the establishment of central tolerance. Since mTEC numbers are limited, their function is complemented by thymic dendritic cells (DCs), which transfer mTEC-produced self-antigens via cooperative antigen transfer (CAT). While CAT is required for effective T cell selection, many aspects remain enigmatic. Given the recently described heterogeneity of mTECs and DCs, it is unclear whether the antigen acquisition from a particular TEC subset is mediated by preferential pairing with a specific subset of DCs. Using several relevant Cre -based mouse models that control for the expression of fluorescent proteins, we have found that, in regards to CAT, each subset of thymic DCs preferentially targets a distinct mTEC subset(s). Importantly, XCR1 + -activated DC subset represented the most potent subset in CAT. Interestingly, thymic DCs can also acquire antigens from more than one mTEC, and of these, monocyte-derived dendritic cells (moDCs) were determined to be the most efficient. moDCs also represented the most potent DC subset in the acquisition of antigen from other DCs. These findings suggest a preferential pairing model for the distribution of mTEC-derived antigens among distinct populations of thymic DCs.

Topics & Concepts

Cell biologyAntigenDendritic cellChemistryAntigen presentationAntigen-presenting cellBiologyFunction (biology)T cellCentral toleranceAntigen processingIn vitroCellFörster resonance energy transferImmunologyAdoptive cell transferCaenorhabditis elegansCytotoxic T cellHEK 293 cellsT-cell receptorImmunotherapy and Immune ResponsesT-cell and B-cell ImmunologyImmune Response and Inflammation
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