| Literature DB >> 28461569 |
Cassie-Marie Peigné1,2, Alexandra Léger1, Marie-Claude Gesnel1, Fabienne Konczak1, Daniel Olive3, Marc Bonneville1,2, Richard Breathnach1, Emmanuel Scotet4,2.
Abstract
Vγ9Vδ2 T lymphocytes are the major human peripheral γδ T cell subset, with broad reactivity against stressed human cells, including tumor cells. Vγ9Vδ2 T cells are specifically activated by small phosphorylated metabolites called phosphoantigens (PAg). Stress-induced changes in target cell PAg levels are specifically detected by butyrophilin (BTN)3A1, using its intracellular B30.2 domain. This leads to the activation of Vγ9Vδ2 T cells. In this study, we show that changes in the juxtamembrane domain of BTN3A1, but not its transmembrane domain, induce a markedly enhanced or reduced γδ T cell reactivity. There is thus a specific requirement for BTN3A1's juxtamembrane domain for correct γδ T cell-related function. This work identified, as being of particular importance, a juxtamembrane domain region of BTN3A molecules identified as a possible dimerization interface and that is located close to the start of the B30.2 domain.Entities:
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Year: 2017 PMID: 28461569 DOI: 10.4049/jimmunol.1601910
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422