CD1c presentation of synthetic glycolipid antigens with foreign alkyl branching motifs

被引:53
作者
de Jong, Annemieke
Arce, Eva Casas
Cheng, Tan-Yun
van Summeren, Ruben P.
Feringa, Ben L.
Dudkin, Vadim
Crich, David
Matsunaga, Isamu
Minnaard, Adriaan J.
Moody, D. Branch
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med,Div Rheumatol Immunol & Allergy, Boston, MA 02115 USA
[2] Univ Groningen, Stratingh Inst, NL-9747 AG Groningen, Netherlands
[3] Merck Res Labs, Dept Med Chem, West Point, PA 19486 USA
[4] Univ Illinois, Dept Chem, Chicago, IL 60607 USA
[5] Kyoto Univ, Inst Virus Res, Dept Viral Oncol, Lab Cell Regulat,Sakyo Ku, Kyoto 6068507, Japan
来源
CHEMISTRY & BIOLOGY | 2007年 / 14卷 / 11期
关键词
D O I
10.1016/j.chembiol.2007.09.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human CD1c is a protein that activates alpha beta T cells by presenting self antigens, synthetic mannosyl phosphodolichols, and mycobacterial mannosyl phosphopolyketides. To determine which molecular features of antigen structure confer a T cell response, we measured activation by structurally divergent Mycobacterium tuberculosis mannosyl-beta 1-phosphomycoketides and synthetic analogs with either stereorandom or stereospecific methyl branching patterns. T cell responses required both a phosphate and a beta-linked mannose unit, and they showed preference for C30-34 lipid units with methyl branches in the S-configuration. Thus, T cell responses were strongest for synthetic compounds that mimicked the natural branched lipids produced by mycobacterial polyketide synthase 12. Incorporation of methylmalonate to form branched lipids is a common bacterial lipid-synthesis pathway that is absent in vertebrates. Therefore, the preferential recognition of branched lipids may represent a new lipidbased pathogen.-associated molecular pattern.
引用
收藏
页码:1232 / 1242
页数:11
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