Lin Bei, Hao Ying-Ying, Wang Dong-Dong, Zhu Lian-Cheng, Zhang Shu-Lan, Saito Makiko, Iwamori Masao
Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang 110004, China.
Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2008 Jun;30(3):284-9.
To transfect human alpha1, 2-fucosyltransferase (alpha1, 2-FT) gene to ovarian cancer cell line RMG-I and investigate the antigenic expression change of Lewis y and the other related oligosaccharides.
The expression vector pcDNA3.1(-)-HFUT-H was constructed by polymerase chain reaction (PCR) to clone human alpha1, 2-FT gene coding region. The alpha1, 2-FT gene stable high-expression cell line RMG-I-H was established by transfecting pcDNA3.1(-)-HFUT-H to ovarian cell line RMG-I. The change of alpha1, 2-FT activity in the cell line before and after the tranfection was confirmed by the determination of enzymatic activity. The changes of cell lipid and glucolipid, especially the change of type II oligosaccharide, in the cell line before and after the transfection was determined by Thin-Layer Chromatography (TLC) and TLC immunostaining method, respectively.
The H-1 antigen and Lewis y antigen were obviously increased in the cell line RMG-1-H, especially the latter one, which was 20 times higher than before, and the type I saccharide chain Lewis b was decreased significantly. The main lipid components on the cell membrane, cholesterol and phosphatides, showed no change in the cell lines before and after the transfection, and the neutral glycolipid also showed no obvious change.
The transfection of alpha1, 2-FT gene can increase the activity of alpha1, 2-FT in the cell line RMG-I and mainly increase the expression of Lewis y antigen simultaneously. The construction of RMG-I Lewis y high expression cell line provides a cell model for further study on the relationship between Lewis y antigen and biological behaviors in the ovarian cancer.
将人α1,2-岩藻糖基转移酶(α1,2-FT)基因转染至卵巢癌细胞系RMG-I,研究Lewis y及其他相关寡糖的抗原表达变化。
通过聚合酶链反应(PCR)构建表达载体pcDNA3.1(-)-HFUT-H,克隆人α1,2-FT基因编码区。将pcDNA3.1(-)-HFUT-H转染至卵巢癌细胞系RMG-I,建立α1,2-FT基因稳定高表达细胞系RMG-I-H。通过酶活性测定确认转染前后细胞系中α1,2-FT活性的变化。分别采用薄层层析(TLC)和TLC免疫染色法测定转染前后细胞系中细胞脂质和糖脂的变化,尤其是II型寡糖的变化。
RMG-1-H细胞系中H-1抗原和Lewis y抗原明显增加,尤其是后者,比转染前高20倍,I型糖链Lewis b显著降低。细胞膜上的主要脂质成分胆固醇和磷脂在转染前后的细胞系中无变化,中性糖脂也无明显变化。
α1,2-FT基因转染可增加RMG-I细胞系中α1,2-FT的活性,同时主要增加Lewis y抗原的表达。RMG-I Lewis y高表达细胞系的构建为进一步研究卵巢癌中Lewis y抗原与生物学行为之间的关系提供了细胞模型。