Avril Tony, North Simon J, Haslam Stuart M, Willison Hugh J, Crocker Paul R
Wellcome Trust Biocentre, University of Dundee, Dow Street, Dundee DD1 5EH, UK.
J Leukoc Biol. 2006 Oct;80(4):787-96. doi: 10.1189/jlb.1005559. Epub 2006 Jul 20.
Siglec-7 is a CD33-related sialic acid-binding Ig-like lectin expressed strongly on NK cells, where it can function as an inhibitory receptor. Its sialic acid-binding activity on NK cells is masked by cis interactions with sialylated glycans, which are likely to be important for regulating the inhibitory function of Siglec-7, which exhibits an unusual preference for alpha2,8-linked disialic acids, a motif found in "b-series" gangliosides and some glycoproteins. To investigate the presence of alpha2,8-linked disialic acids on NK cells, T cells, monocytes, and B cells, we first analyzed their expression of all known alpha2,8-sialyltransferase genes by quantitative PCR. Unlike T cells, B cells, and monocytes, NK cells consistently expressed mRNA encoding ST8Sia VI, which creates alpha2,8-linked disialic acids on O-linked glycans of glycoproteins. All blood leukocytes expressed ST8Sia IV, implicated in polysialic acid synthesis, and NK cells variably expressed high levels of ST8Sia V mRNA required for GT3 expression. Two human IgM antibodies, Ha1 and Pi1, with specificity for the alpha2,8-disialyl motif reacted strongly with NK cells in a sialic acid-dependent manner and less strongly with T cells and monocytes. Antibody-induced clustering of Siglec-7 on NK cells resulted in partial colocalization with anti-Ha1. Finally, MALDI-TOF mass spectrometric analysis of isolated NK cell O-glycans revealed the presence of a peak at mass-to-charge ratio of 1619.4 mass units, corresponding to a putative alpha2,8-disialylated glycan. Together, these results suggest that NK cells are decorated with alpha2,8-disialic acid structures implicated in regulation of cellular activation via interactions with Siglec-7.
唾液酸结合免疫球蛋白样凝集素7(Siglec-7)是一种与CD33相关的唾液酸结合免疫球蛋白样凝集素,在自然杀伤细胞(NK细胞)上高表达,可作为抑制性受体发挥作用。其在NK细胞上的唾液酸结合活性被与唾液酸化聚糖的顺式相互作用所掩盖,这可能对调节Siglec-7的抑制功能很重要,Siglec-7对α2,8连接的二唾液酸具有不寻常的偏好,这种基序存在于“b系列”神经节苷脂和一些糖蛋白中。为了研究NK细胞、T细胞、单核细胞和B细胞上α2,8连接的二唾液酸的存在情况,我们首先通过定量PCR分析了它们所有已知的α2,8-唾液酸转移酶基因的表达。与T细胞、B细胞和单核细胞不同,NK细胞持续表达编码ST8Sia VI的mRNA,ST8Sia VI可在糖蛋白上O连接聚糖上产生α2,8连接的二唾液酸。所有血液白细胞都表达参与多唾液酸合成的ST8Sia IV,NK细胞可变地表达GT3表达所需的高水平ST8Sia V mRNA。两种对α2,8-二唾液酸基序具有特异性的人IgM抗体Ha1和Pi1以唾液酸依赖的方式与NK细胞强烈反应,与T细胞和单核细胞的反应较弱。抗体诱导的NK细胞上Siglec-7的聚集导致与抗Ha1部分共定位。最后,对分离的NK细胞O聚糖进行基质辅助激光解吸电离飞行时间质谱分析,发现质荷比为1619.4质量单位处有一个峰,对应于一个假定的α2,8-二唾液酸化聚糖。总之,这些结果表明NK细胞装饰有α2,8-二唾液酸结构,这些结构通过与Siglec-7相互作用参与细胞活化的调节。