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Structural determination of lipid antigens captured at the CD1d--T-cell receptor interface.

Authors :
Brennan, Patrick J.
Tan-Yun Cheng
Pellicci, Daniel G.
Watts, Gerald F. M.
Veerapen, Natacha
Young, David C.
Rossjohn, Jamie
Besra, Gurdyal S.
Godfrey, Dale I.
Brenner, Michael B.
Moody, D. Branch
Source :
Proceedings of the National Academy of Sciences of the United States of America. 8/1/2017, Vol. 114 Issue 31, p8348-8353. 6p.
Publication Year :
2017

Abstract

Glycolipid antigens recognized by αβ T-cell receptors (TCRs) drive the activation of invariant natural killer T (iNKT) cells, a specialized subset of innate T lymphocytes. Glycolipids with α-linked anomeric carbohydrates have been identified as potent microbial lipid anti- gens for iNKT cells, and their unusual α-anomeric linkage has been thought to define a "foreign" lipid antigen motif. However, mammals use endogenous lipids to select iNKT cells, and there is compelling evidence for iNKT cell responses in various types of sterile inflammation. The nature of endogenous or environmental lipid antigens encountered by iNKT cells is not well defined. Here, we sought to identify lipid antigens in cow's milk, a prominent part of the human diet. We developed a method to directly capture lipid antigens within CD1d-lipid--TCR complexes, while excluding CD1d bound to nonantigenic lipids, followed by direct biochemical analysis of the lipid antigens trapped at the TCR--CD1d interface. The specific antigens captured by this "TCR trap" method were identified as α-linked monohexosylceramides by mass spectrometry fragmentation patterns that distinguished α- from β-anomeric monohexosylceramides. These data provide direct biochemical evidence for α-linked lipid antigens from a common dietary source. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00278424
Volume :
114
Issue :
31
Database :
Academic Search Index
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
124445608
Full Text :
https://doi.org/10.1073/pnas.1705882114