| Literature DB >> 35172142 |
Junko Morimoto1, Minoru Matsumoto2, Ryuichiro Miyazawa1, Hideyuki Yoshida3, Koichi Tsuneyama4, Mitsuru Matsumoto5.
Abstract
Impaired production of thymic regulatory T cells (Tregs) is implicated in the development of Aire-dependent autoimmunity. Because Tregs require agonistic T cell receptor stimuli by self-antigens to develop, reduced expression of self-antigens from medullary thymic epithelial cells (mTECs) has been considered to play a major role in the reduced Treg production in Aire deficiency. Here, we show that mTECs abnormally express co-inhibitory receptor CTLA-4 if Aire is non-functional. Upon binding with CD80/CD86 ligands expressed on thymic dendritic cells (DCs), the ectopically expressed CTLA-4 from Aire-deficient mTECs removes the CD80/CD86 ligands from the DCs. This attenuates the ability of DCs to provide co-stimulatory signals and to present self-antigens transferred from mTECs, both of which are required for Treg production. Accordingly, impaired production of Tregs and organ-specific autoimmunity in Aire-deficient mice are rescued by the depletion of CTLA-4 expression from mTECs. Our studies illuminate the significance of mTEC-DC interaction coordinated by Aire for the establishment of thymic tolerance.Entities:
Keywords: Treg; aire-dependent autoimmunity; antigen transfer; ectopic CTLA-4 expression; mTEC; self-antigen; single-cell analysis; thymic DC; thymic tolerance; trans-endocytosis
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Year: 2022 PMID: 35172142 DOI: 10.1016/j.celrep.2022.110384
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423