Nakashima Koki, Hoshino Hitomi, Zhang Zui, Akama Tomoya O, Kondo Nobuyuki, Hasegawa Seiki, Sekido Yoshitaka, Fukushima Mana, Ishizuka Tamotsu, Kobayashi Motohiro
Department of Pathology, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.
Department of Respiratory Medicine, Faculty of Medical Sciences, University of Fukui, Eiheiji, Japan.
Pathol Int. 2025 Jun 17. doi: 10.1111/pin.70033.
The glycoform of heart development protein with EGF-like domains 1 (HEG1) recognized by the SKM9-2 monoclonal antibody is a useful diagnostic marker for malignant pleural mesothelioma (MPM). The putative glycoform includes core 2 O-glycans carrying sialyl poly-N-acetyllactosamine (LacNAc), but sulfation modifications are undetermined. Since sialyl 6-sulfo LacNAc-capped core 2 O-glycans are expressed in MPM and their structure overlaps with low-sulfated keratan sulfate (KS), we asked whether low-sulfated KS is expressed in MPM and whether HEG1 is decorated with low-sulfated KS. We performed immunohistochemical analysis of 41 MPM cases using anti-KS monoclonal antibodies and endoglycosidases, reversed-phase ion-pair high-performance liquid chromatography analysis of KS/sulfated LacNAc isolated from human pleural tissue, and western blot analysis of HEG1·IgG recombinant fusion proteins secreted from low-sulfated KS-expressing human embryonic kidney cells. Most MPM tissues were stained with anti-low-sulfated KS antibodies and staining was eliminated by endo-β-galactosidase and keratanase II but not by peptide-N-glycosidase F. Disaccharide composition analysis revealed that mono-sulfated LacNAc disaccharide and di-sulfated LacNAc disaccharide accounted for 83.1% and 16.9% of pleural KS/sulfated LacNAc, respectively. Western blot analysis of HEG1·IgG glycoforms indicated that HEG1 functions as a core protein for low-sulfated KS. Thus, HEG1 protein decorated with low-sulfated KS is expressed in MPM.
被SKM9-2单克隆抗体识别的含表皮生长因子样结构域的心脏发育蛋白1(HEG1)糖型是恶性胸膜间皮瘤(MPM)的一种有用诊断标志物。推定的糖型包括携带唾液酸化多聚N-乙酰乳糖胺(LacNAc)的核心2 O-聚糖,但硫酸化修饰尚未确定。由于唾液酸化6-硫酸化LacNAc封端的核心2 O-聚糖在MPM中表达,且其结构与低硫酸化硫酸角质素(KS)重叠,我们询问低硫酸化KS是否在MPM中表达以及HEG1是否被低硫酸化KS修饰。我们使用抗KS单克隆抗体和内切糖苷酶对41例MPM病例进行了免疫组织化学分析,对从人胸膜组织中分离的KS/硫酸化LacNAc进行了反相离子对高效液相色谱分析,并对从表达低硫酸化KS的人胚肾细胞分泌的HEG1·IgG重组融合蛋白进行了蛋白质印迹分析。大多数MPM组织用抗低硫酸化KS抗体染色,且染色被内切β-半乳糖苷酶和角质素酶II消除,但未被肽-N-糖苷酶F消除。二糖组成分析显示,单硫酸化LacNAc二糖和二硫酸化LacNAc二糖分别占胸膜KS/硫酸化LacNAc的83.1%和16.9%。对HEG1·IgG糖型的蛋白质印迹分析表明,HEG1作为低硫酸化KS的核心蛋白发挥作用。因此,在MPM中表达了被低硫酸化KS修饰的HEG1蛋白。