| Literature DB >> 29752065 |
Justin S A Perry1, Emilie V Russler-Germain1, You W Zhou1, Whitney Purtha2, Matthew L Cooper3, Jaebok Choi3, Mark A Schroeder3, Vanessa Salazar1, Takeshi Egawa4, Byeong-Chel Lee5, Nada A Abumrad6, Brian S Kim7, Mark S Anderson2, John F DiPersio3, Chyi-Song Hsieh8.
Abstract
The development of T cell tolerance in the thymus requires the presentation of host proteins by multiple antigen-presenting cell (APC) types. However, the importance of transferring host antigens from transcription factor AIRE-dependent medullary thymic epithelial cells (mTECs) to bone marrow (BM) APCs is unknown. We report that antigen was primarily transferred from mTECs to CD8α+ dendritic cells (DCs) and showed that CD36, a scavenger receptor selectively expressed on CD8α+ DCs, mediated the transfer of cell-surface, but not cytoplasmic, antigens. The absence of CD8α+ DCs or CD36 altered thymic T cell selection, as evidenced by TCR repertoire analysis and the loss of allo-tolerance in murine allogeneic BM transplantation (allo-BMT) studies. Decreases in these DCs and CD36 expression in peripheral blood of human allo-BMT patients correlated with graft-versus-host disease. Our findings suggest that CD36 facilitates transfer of mTEC-derived cell-surface antigen on CD8α+ DCs to promote tolerance to host antigens during homeostasis and allo-BMT.Entities:
Keywords: CD36; antigen transfer; apoptotic cell clearance; efferocytosis; medullary thymic epithelial cells; regulatory T cells; scavenger receptor; thymic dendritic cells; tolerance
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Year: 2018 PMID: 29752065 PMCID: PMC5986080 DOI: 10.1016/j.immuni.2018.04.007
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745