Role of lipid trimming and CD1 groove size in cellular antigen presentation

被引:43
作者
Cheng, Tan-Yun
Relloso, Miguel
Van Rhijn, Ildiko
Young, David C.
Besra, Gurdyal S.
Briken, Volker
Zajonc, Dirk M.
Wilson, Ian A.
Porcelli, Steven
Moody, D. Branch
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Rheumatol Immunol & Allergy, Boston, MA 02115 USA
[2] Univ Utrecht, Fac Vet Med, Dept Infect & Immun, Utrecht, Netherlands
[3] Univ Birmingham, Sch Biosci, Birmingham, W Midlands, England
[4] Albert Einstein Coll Med, Dept Immunol & Microbiol, Bronx, NY 10467 USA
[5] Inst Allergy & Immunol, Div Cellular Biol, La Jolla, CA USA
[6] Scripps Res Inst, Dept Mol Biol, La Jolla, CA USA
[7] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA USA
基金
英国医学研究理事会;
关键词
antigen processing; CD1; T cells; tuberculosis;
D O I
10.1038/SJ.EMBOJ.7601185
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
Cellular CD1 proteins bind lipids that differ in length (C12-80), including antigens that exceed the capacity of the CD1 groove. This could be accomplished by trimming lipids to a uniform length before loading or by inserting each lipid so that it penetrates the groove to a varying extent. New assays to detect antigen fragments generated within human dendritic cells showed that bacterial antigens remained intact, even after delivery to lysosomes, where control lipids were cleaved. Further, recombinant CD1b proteins could bind and present C-80 lipid antigens using a mechanism that did not involve cellular enzymes or lipid cleavage, but was regulated by pH in the physiologic range. We conclude that endosomal acidification acts directly, rather than through enzymatic trimming, to insert lipids into CD1b. Lipids are loaded in an intact form, so that they likely protrude through a portal near the bottom of the groove, which represents an escape hatch for long lipids from mycobacterial pathogens.
引用
收藏
页码:2989 / 2999
页数:11
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