CD1a-binding glycosphingolipids stimulating human autoreactive T-cells: synthesis of a family of sulfatides differing in the acyl chain moiety

被引:30
作者
Compostella, F
Franchini, L
De Libero, G
Palmisano, G
Ronchetti, F
Panza, L
机构
[1] Univ Piemonte Orientale, Dipartimento Sci Chim Alimentari Farmaceut & Farm, I-28100 Novara, Italy
[2] Univ Milan, Dipartimento Chim & Biochim Med, I-20133 Milan, Italy
[3] Univ Basel Hosp, CH-4031 Basel, Switzerland
[4] Univ Insubria, Dipartimento Sci Chim Fisiche & Matemat, I-22100 Como, Italy
关键词
azidosphingosine; antigens; glycolipids; biologically active compounds;
D O I
10.1016/S0040-4020(02)01092-X
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Native sulfatide (a mixture of 3-sulfated beta-D-galactopyranosylceramides with different fatty acids at the ceramide moiety) is an antigen presented by CD1a proteins. Herein the preparation of four sulfatides, which are constituents of the natural mixture and bear palmitic, stearic, behenic or nervonic fatty acid chains, is described. Azidosphingosine was stereoselectively synthesized through a CuCN-catalyzed allylic alkylation of a hexenitol dimesylate derived from D-xylose; beta-glycosylation of azidosphingosine, with a suitable D-galactosyl trichloroacetimidate led, after reduction of the azido, group, to the galactosylsphingosine skeleton, which was derivatized with the different fatty acids. Final regioselective 3-sulfation gave the desired sulfatides, which were tested for activation of sulfatide-specific and CD1a-restricted T-cell clones. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:8703 / 8708
页数:6
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