Recognition of lyso-phospholipids by human natural killer T lymphocytes.

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 u...

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Main Authors: Lisa M Fox, Daryl G Cox, Jennifer L Lockridge, 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 Hildebrand, Jenny E Gumperz
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-10-01
Series:PLoS Biology
Online Access:http://europepmc.org/articles/PMC2760207?pdf=render
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author Lisa M Fox
Daryl G Cox
Jennifer L Lockridge
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 Hildebrand
Jenny E Gumperz
author_facet Lisa M Fox
Daryl G Cox
Jennifer L Lockridge
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 Hildebrand
Jenny E Gumperz
author_sort Lisa M Fox
collection DOAJ
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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spelling doaj.art-3f5a22c8a7f44061b89d85e01ac33a7a2022-12-21T18:33:51ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852009-10-01710e100022810.1371/journal.pbio.1000228Recognition of lyso-phospholipids by human natural killer T lymphocytes.Lisa M FoxDaryl G CoxJennifer L LockridgeXiaohua WangXiuxu ChenLouise ScharfDavid L TrottRachel M NdonyeNatacha VeerapenGurdyal S BesraAmy R HowellMark E CookErin J AdamsWilliam H HildebrandJenny E GumperzNatural 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.http://europepmc.org/articles/PMC2760207?pdf=render
spellingShingle Lisa M Fox
Daryl G Cox
Jennifer L Lockridge
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 Hildebrand
Jenny E Gumperz
Recognition of lyso-phospholipids by human natural killer T lymphocytes.
PLoS Biology
title Recognition of lyso-phospholipids by human natural killer T lymphocytes.
title_full Recognition of lyso-phospholipids by human natural killer T lymphocytes.
title_fullStr Recognition of lyso-phospholipids by human natural killer T lymphocytes.
title_full_unstemmed Recognition of lyso-phospholipids by human natural killer T lymphocytes.
title_short Recognition of lyso-phospholipids by human natural killer T lymphocytes.
title_sort recognition of lyso phospholipids by human natural killer t lymphocytes
url http://europepmc.org/articles/PMC2760207?pdf=render
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