Matsumoto N, Ribaudo R K, Abastado J P, Margulies D H, Yokoyama W M
Howard Hughes Medical Institute, Rheumatology Division, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Immunity. 1998 Feb;8(2):245-54. doi: 10.1016/s1074-7613(00)80476-8.
The mouse NK inhibitory Ly-49A receptor specifically interacts with a peptide-induced conformational determinant on its MHC class I ligand, H-2Dd. In addition, it binds the polysaccharide fucoidan, consistent with its C-type lectin homology and the hypothesis that Ly-49A interacts with carbohydrates on Dd. Herein, however, we demonstrate that Ly-49A recognizes Dd mutants lacking N-glycosylation. Fucoidan competes for binding with anti-Ly-49A antibodies that inhibit Ly-49A-Dd interaction, and blocks apparent Ly-49A binding to unglycosylated Dd. We confirm that Ly-49A recognizes the alpha1 and amino-terminal alpha2 domains of Dd by analysis of recombinant H-2Kd-H-2Dd molecules. These studies indicate that Ly-49A recognizes carbohydrate-independent epitope(s) on Dd and suggest that Ly-49A has two distinct ligands, carbohydrate and MHC class I.
小鼠NK抑制性Ly-49A受体特异性地与其MHC I类配体H-2Dd上的肽诱导构象决定簇相互作用。此外,它还结合岩藻依聚糖,这与其C型凝集素同源性以及Ly-49A与Dd上碳水化合物相互作用的假设一致。然而,在此我们证明Ly-49A可识别缺乏N-糖基化的Dd突变体。岩藻依聚糖与抑制Ly-49A-Dd相互作用的抗Ly-49A抗体竞争结合,并阻断Ly-49A与未糖基化Dd的明显结合。通过对重组H-2Kd-H-2Dd分子的分析,我们证实Ly-49A识别Dd的α1和氨基末端α2结构域。这些研究表明,Ly-49A识别Dd上不依赖碳水化合物的表位,并提示Ly-49A有两种不同的配体,即碳水化合物和MHC I类分子。