Published October 27, 2009 | Version v1
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Recognition of Lyso-Phospholipids by Human Natural Killer T Lymphocytes

Description

Natural killer T (NKT) cells are a subset of T lymphocytes with potent immunoregulatory properties. Recognition of self-antigens presented by CD1d molecules is an important route of NKT cell activation; however, the molecular identity of specific autoantigens that stimulate human NKT cells remains unclear. Here, we have analyzed human NKT cell recognition of CD1d cellular ligands. The most clearly antigenic species was lyso-phosphatidylcholine (LPC). Diacylated phosphatidylcholine and lyso-phosphoglycerols differing in the chemistry of the head group stimulated only weak responses from human NKT cells. However, lyso-sphingomyelin, which shares the phosphocholine head group of LPC, also activated NKT cells. Antigen-presenting cells pulsed with LPC were capable of stimulating increased cytokine responses by NKT cell clones and by freshly isolated peripheral blood lymphocytes. These results demonstrate that human NKT cells recognize cholinated lyso-phospholipids as antigens presented by CD1d. Since these lyso-phospholipids serve as lipid messengers in normal physiological processes and are present at elevated levels during inflammatory responses, these findings point to a novel link between NKT cells and cellular signaling pathways that are associated with human disease pathophysiology.

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Additional details

Identifiers

DOI
10.1371/journal.pbio.1000228
Other
oai:uchicago.tind.io:10198

Funding

National Institutes of Health
AI60777
National Institutes of Health
AI074940
National Institutes of Health
HHSN266200400027C
National Institutes of Health
AI073922
National Institutes of Health
AI057519
Medical Research Council and The Wellcome Trust
Royal Society Wolfson Research Merit Award

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Biochemistry and Molecular Biology