Your browser doesn't support javascript.
loading
Structural determination of lipid antigens captured at the CD1d-T-cell receptor interface.
Brennan, Patrick J; Cheng, Tan-Yun; 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.
Affiliation
  • Brennan PJ; Department of Medicine, Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115; pbrennan3@bwh.harvard.edu mbrenner@research.bwh.harvard.edu bmoody@bwh.harvard.edu.
  • Cheng TY; Department of Medicine, Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.
  • Pellicci DG; Department of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, VIC 3010, Australia.
  • Watts GFM; Australian Research Council Centre of Excellence in Advanced Molecular Imaging, University of Melbourne, Parkville, VIC 3010, Australia.
  • Veerapen N; Department of Medicine, Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.
  • Young DC; School of Biosciences, University of Birmingham, Birmingham B15 2TT, United Kingdom.
  • Rossjohn J; Department of Medicine, Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.
  • Besra GS; Infection and Immunity Program, Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia.
  • Godfrey DI; Institute of Infection and Immunity, Cardiff University School of Medicine, Cardiff CF14 4XN, United Kingdom.
  • Brenner MB; Australian Research Centre of Excellence in Advanced Molecular Imaging, Monash University, Clayton, VIC 3800, Australia.
  • Moody DB; School of Biosciences, University of Birmingham, Birmingham B15 2TT, United Kingdom.
Proc Natl Acad Sci U S A ; 114(31): 8348-8353, 2017 08 01.
Article in En | MEDLINE | ID: mdl-28716901
Glycolipid antigens recognized by αß 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 antigens 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 ß-anomeric monohexosylceramides. These data provide direct biochemical evidence for α-linked lipid antigens from a common dietary source.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Lymphocyte Activation / Receptors, Antigen, T-Cell, alpha-beta / Natural Killer T-Cells / Antigens, CD1d / Galactosylceramides Limits: Animals / Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2017 Type: Article

Full text: 1 Database: MEDLINE Main subject: Lymphocyte Activation / Receptors, Antigen, T-Cell, alpha-beta / Natural Killer T-Cells / Antigens, CD1d / Galactosylceramides Limits: Animals / Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2017 Type: Article