| Literature DB >> 29321275 |
Jaehak Oh1, Nan Wu1, Andrea J Barczak2, Rebecca Barbeau2, David J Erle2, Jeoung-Sook Shin3.
Abstract
Thymic dendritic cells (tDCs) play an important role in central tolerance by eliminating self-reactive thymocytes or differentiating them to regulatory T (Treg) cells. However, the molecular and cellular mechanisms underlying these functions are not completely understood. We found that mouse tDCs undergo maturation following cognate interaction with self-reactive CD4+ thymocytes and that this maturation is dependent on CD40 signaling. Ablation of CD40 expression in tDCs resulted in a significant reduction in the number of Treg cells in association with a significant reduction in the number of mature tDCs. In addition, CD40-deficient DCs failed to fully mature upon cognate interaction with CD4+ thymocytes in vitro and failed to differentiate them into Treg cells to a sufficient number. These findings suggest that tDCs mature and potentiate Treg cell development in feedback response to self-reactive CD4+ thymocytes.Entities:
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Year: 2018 PMID: 29321275 PMCID: PMC5809249 DOI: 10.4049/jimmunol.1700768
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422