Department of Microbiology and Immunology and the National Institute for Biotechnology in the Negev, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.
J Virol. 2010 Apr;84(8):3789-97. doi: 10.1128/JVI.01815-09. Epub 2010 Feb 10.
Natural killer (NK) cells serve as a crucial first-line defense against tumors and virus-infected cells. We previously showed that lysis of influenza virus (IV)-infected cells is mediated by the interaction between the NK receptor, NKp46, and the IV hemagglutinin (HA) type 1 expressed by the infected cells. This interaction requires the presence of sialyl groups on the NKp46-T225 O-glycoforms. In the current study, we analyzed the O-glycan sequences that are imperative for the interaction between recombinant NKp46 (rNKp46) and IV H1N1 strains. We first showed that rNKp46 binding to IV H1N1 is not mediated by a glycoform unique to the Thr225 site. We then characterized the O-glycan sequences that mediate the interaction of rNKp46 and IV H1N1; we employed rNKp46s with dissimilar glycosylation patterns and IV H1N1 strains with different sialic acid alpha2,3 and alpha2,6 linkage preferences. The branched alpha2,3-sialylated O-glycoform Neu5NAcalpha2,3-Galbeta1,4-GlcNAcbeta1,6[Neu5NAcalpha2,3-Galbeta1,3]GalNAc competently mediated the interaction of rNKp46 with IV H1N1, manifesting a preference for alpha2,3 linkage. In contrast, the linear alpha2,3-sialylated O-glycoform Neu5NAcalpha2,3-Galbeta1,3-GalNAc was not correlated with enhanced interaction between rNKp46 and IV H1N1 or a preference for alpha2,3 linkage. The branched alpha2,3- and alpha2,6-sialylated O-glycoform Neu5NAcalpha2,3-Galbeta1,3[Neu5NAcalpha2,6]GalNAc competently mediated the interaction of rNKp46 with IV H1N1, manifesting a preference for alpha2,6 linkage. Previous viral HA-binding-specificity studies were performed with glycopolymer conjugates, free synthetic sialyl oligosaccharides, and sialidase-treated cells. This study shed light on the O-glycan sequences involved in the interaction of glycoprotein and viral hemagglutinins and may help in the design of agents inhibitory to hemagglutinin for influenza treatment.
自然杀伤 (NK) 细胞是抵抗肿瘤和病毒感染细胞的第一道防线。我们之前的研究表明,流感病毒 (IV) 感染细胞的裂解是由 NK 受体 NKp46 与感染细胞表达的 IV 血凝素 (HA) 1 型之间的相互作用介导的。这种相互作用需要 NKp46-T225 O-糖基化形式上的唾液酸基团的存在。在本研究中,我们分析了对重组 NKp46 (rNKp46) 与 IV H1N1 株相互作用至关重要的 O-聚糖序列。我们首先表明,rNKp46 与 IV H1N1 的结合不是由 Thr225 位点特有的糖基化形式介导的。然后,我们对介导 rNKp46 与 IV H1N1 相互作用的 O-聚糖序列进行了表征;我们使用具有不同糖基化模式的 rNKp46 和具有不同唾液酸 α2,3 和 α2,6 键合偏好的 IV H1N1 株。分支的 α2,3-唾液酸化 O-糖基化形式 Neu5NAcalpha2,3-Galbeta1,4-GlcNAcbeta1,6[Neu5NAcalpha2,3-Galbeta1,3]GalNAc 能够介导 rNKp46 与 IV H1N1 的相互作用,表现出对 α2,3 键合的偏好。相比之下,线性的 α2,3-唾液酸化 O-糖基化形式 Neu5NAcalpha2,3-Galbeta1,3-GalNAc 与 rNKp46 与 IV H1N1 之间增强的相互作用无关,也没有对 α2,3 键合的偏好。分支的 α2,3-和 α2,6-唾液酸化 O-糖基化形式 Neu5NAcalpha2,3-Galbeta1,3[Neu5NAcalpha2,6]GalNAc 能够介导 rNKp46 与 IV H1N1 的相互作用,表现出对 α2,6 键合的偏好。以前的病毒 HA 结合特异性研究是使用糖聚合物缀合物、游离合成的唾液酸寡糖和唾液酸酶处理的细胞进行的。本研究阐明了参与糖蛋白与病毒血凝素相互作用的 O-聚糖序列,这可能有助于设计抑制流感病毒血凝素的药物。