Natural ligand of mouse CD1d1: Cellular glycosylphosphatidylinositol

被引:350
作者
Joyce, S [1 ]
Woods, AS
Yewdell, JW
Bennink, JR
De Silva, AD
Boesteanu, A
Balk, SP
Cotter, RJ
Brutkiewicz, RR
机构
[1] Penn State Univ, Milton S Hershey Med Ctr, Coll Med, Dept Microbiol & Immunol, Hershey, PA 17033 USA
[2] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
[4] NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
[5] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Div Hematol Oncol, Boston, MA 02215 USA
关键词
D O I
10.1126/science.279.5356.1541
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mouse CD1d1, a member of the CD1 family of evolutionarily conserved major histocompatibility antigen-like molecules, controls the differentiation and function of a T lymphocyte subset, NK1(+) natural T cells, proposed to regulate immune responses. The CD1d1 crystal structure revealed a large hydrophobic binding site occupied by a ligand of unknown chemical nature. Mass spectrometry and metabolic radiolabeling were used to identify cellular glycosylphosphatidylinositol as a major natural ligand of CD1d1. CD1d1 bound glycosylphosphatidylinositol through its phosphatidylinositol aspect with high affinity. Glycosylphosphatidylinositol or another glycolipid could be a candidate natural ligand for CD1d1-restricted T cells.
引用
收藏
页码:1541 / 1544
页数:4
相关论文
共 27 条
[1]   AN NK1.1+ CD4+8- SINGLE-POSITIVE THYMOCYTE SUBPOPULATION THAT EXPRESSES A HIGHLY SKEWED T-CELL ANTIGEN RECEPTOR-V-BETA FAMILY [J].
ARASE, H ;
ARASE, N ;
OGASAWARA, K ;
GOOD, RA ;
ONOE, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6506-6510
[2]   Association between alpha beta TCR(+)CD4(-)CD8(-) T-cell deficiency and IDDM in NOD/Lt mice [J].
Baxter, AG ;
Kinder, SJ ;
Hammond, KJL ;
Scollay, R ;
Godfrey, DI .
DIABETES, 1997, 46 (04) :572-582
[3]   CD1 RECOGNITION BY MOUSE NK1(+) T-LYMPHOCYTES [J].
BENDELAC, A ;
LANTZ, O ;
QUIMBY, ME ;
YEWDELL, JW ;
BENNINK, JR ;
BRUTKIEWICZ, RR .
SCIENCE, 1995, 268 (5212) :863-865
[4]   HUMAN T-CELL RECEPTOR (TCR) ALPHA/BETA+ CD4-CD8- T-CELLS EXPRESS OLIGOCLONAL TCRS, SHARE JUNCTIONAL MOTIFS ACROSS TCR V(BETA)-GENE FAMILIES, AND PHENOTYPICALLY RESEMBLE MEMORY T-CELLS [J].
BROOKS, EG ;
BALK, SP ;
AUPEIX, K ;
COLONNA, M ;
STROMINGER, JL ;
GROHSPIES, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11787-11791
[5]   TAP-INDEPENDENT, BETA(2)-MICROGLOBULIN-DEPENDENT SURFACE EXPRESSION OF FUNCTIONAL-MOUSE CD1.1 [J].
BRUTKIEWICZ, RR ;
BENNINK, JR ;
YEWDELL, JW ;
BENDELAC, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (06) :1913-1919
[6]   PEPTIDE BINDING AND PRESENTATION BY MOUSE CD1 [J].
CASTANO, AR ;
TANGRI, S ;
MILLER, JEW ;
HOLCOMBE, HR ;
JACKSON, MR ;
HUSE, WD ;
KRONENBERG, M ;
PETERSON, PA .
SCIENCE, 1995, 269 (5221) :223-226
[7]   Impaired NK1(+) T cell development and early IL-4 production in CD1-deficient mice [J].
Chen, YH ;
Chiu, NM ;
Mandal, M ;
Wang, N ;
Wang, CR .
IMMUNITY, 1997, 6 (04) :459-467
[8]   Requirements for CD1d recognition by human invariant V alpha 24(+) CD4(-)CD8(-) T cells [J].
Exley, M ;
Garcia, J ;
Balk, SP ;
Porcelli, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (01) :109-120
[9]   CONSTANT NEUTRAL LOSS SCANNING FOR THE CHARACTERIZATION OF BACTERIAL PHOSPHOLIPIDS DESORBED BY FAST ATOM BOMBARDMENT [J].
HELLER, DN ;
MURPHY, CM ;
COTTER, RJ ;
FENSELAU, C ;
UY, OM .
ANALYTICAL CHEMISTRY, 1988, 60 (24) :2787-2791
[10]   PROFILING OF BACTERIA BY FAST-ATOM-BOMBARDMENT MASS-SPECTROMETRY [J].
HELLER, DN ;
COTTER, RJ ;
FENSELAU, C .
ANALYTICAL CHEMISTRY, 1987, 59 (23) :2806-2809