Recognition of Lyso-Phospholipids by Human Natural Killer T Lymphocytes

• DOI: 10.1371/journal.pbio.1000228
• Publication Date: 2009-10-26T21:49:48Z
• Authors: Lisa M. Fox; Daryl G. Cox; Jennifer L. Lockr...; Xiaohua Wang; Xiuxu Chen; Louise Scharf; David L. Trott; Rachel M. Ndonye; Natacha Veerapen; Gurdyal S. Besra; Amy R. Howell; Mark E. Cook; Erin J. Adams; William H. Hildeb...; Jenny E. Gumperz
• Keywords: Inflammation; Antigen Presentation; QH301-705.5; Phosphorylcholine; 610; Antigen-Presenting Cells; Lysophosphatidylcholines; Lymphocyte Activation; Autoantigens; Cell Line; 3. Good health; 03 medical and health sciences; 0302 clinical medicine; Sphingosine; Cytokines; Humans; Natural Killer T-Cells; Biology (General); Antigens, CD1d; Research Article; Signal Transduction

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.