Inoue Sadako, Poongodi Geetha L, Suresh Nimmagadda, Chang Tschining, Inoue Yasuo
Institute of Biological Chemistry, Academia Sinica, Taipei 115-29, Taiwan.
Glycoconj J. 2006 Jul;23(5-6):401-10. doi: 10.1007/s10719-006-6125-5.
KDN (Deaminoneuraminic acid, or deaminated neuraminic acid) is a minor but biosynthetically independent member of the sialic acid. Human occurrence of KDN has already been established, although its level is so little that it is often undetectable by conventional sialic acid analysis. Elevated expression of KDN in fetal cord blood cells and some malignant tumor cells have been reported. However, in mammalian cells and tissues KDN mostly occurs as the free sugar and little occurred conjugated to glycolipids and/or glycoproteins. A positive correlation between the ratio of free KDN/free Neu5Ac in ovarian adenocarcinomas and the stage of malignancy has been noted for diagnostic use. We hypothesized that elevated expression of KDN in mammalian systems may be closely related to elevated activities of enzymes involved in the formation of sialoglycoconjugates and/or aberrant supply of the precursor sugar, mannose, used in the biosynthesis of KDN. In this study we used human ovarian teratocarcinoma cells PA-1 to further analyze KDN expression in human cells. Major findings reported in this paper are, (i) a 30 kDa KDN-glycoprotein immunostainable with monoclonal antibody, mAb.kdn3G, (specific for the KDNalpha2 --> 3Galbeta1--> epitope) and sensitive to KDNase was identified in the membrane fraction of the cell: (ii) a 49 kDa KDN-glycoprotein that is not reactive with mAb.kdn3G but is sensitive to KDNase was identified in the soluble fraction: and (iii) PA-1 cells showed unique response to mannose added to the growth medium in that the levels of both free and bound forms of KDN are elevated. This is the first report on the identification of mammalian KDN-glycoproteins by chemical and biochemical methods.
KDN(脱氨神经氨酸,或去氨基神经氨酸)是唾液酸中含量较少但生物合成独立的成员。KDN在人体内的存在已得到证实,尽管其含量极低,常规唾液酸分析往往无法检测到。已有报道称,胎儿脐带血细胞和一些恶性肿瘤细胞中KDN表达升高。然而,在哺乳动物细胞和组织中,KDN大多以游离糖的形式存在,很少与糖脂和/或糖蛋白结合。卵巢腺癌中游离KDN/游离Neu5Ac的比例与恶性程度呈正相关,可用于诊断。我们推测,哺乳动物系统中KDN表达升高可能与参与唾液酸糖缀合物形成的酶活性升高和/或KDN生物合成中使用的前体糖甘露糖供应异常密切相关。在本研究中,我们使用人卵巢畸胎瘤细胞PA-1进一步分析人细胞中KDN的表达。本文报道的主要发现如下:(i)在细胞的膜部分鉴定出一种30 kDa的KDN糖蛋白,可被单克隆抗体mAb.kdn3G免疫染色(对KDNalpha2 --> 3Galbeta1-->表位具有特异性),且对KDN酶敏感;(ii)在可溶性部分鉴定出一种49 kDa的KDN糖蛋白,它与mAb.kdn3G无反应,但对KDN酶敏感;(iii)PA-1细胞对添加到生长培养基中的甘露糖表现出独特的反应,即游离和结合形式的KDN水平均升高。这是首次通过化学和生化方法鉴定哺乳动物KDN糖蛋白的报告。