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首页> 外文期刊>The international journal of biochemistry and cell biology >Differential expression of alpha-2,3-sialyltransferases and alpha-1,3/4-fucosyltransferases regulates the levels of sialyl Lewis a and sialyl Lewis x in gastrointestinal carcinoma cells.
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Differential expression of alpha-2,3-sialyltransferases and alpha-1,3/4-fucosyltransferases regulates the levels of sialyl Lewis a and sialyl Lewis x in gastrointestinal carcinoma cells.

机译:α-2,3-唾液酸转移酶和α-1,3/ 4-岩藻糖基转移酶的差异表达调节胃肠癌细胞中唾液酸化的路易斯a和唾液酸化的Lewis x的水平。

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摘要

Sialyl Lewis x and sialyl Lewis a expression depends on sialyltransferases and fucosyltransferases. In this study, we screened for major variations of sialyltransferases and fucosyltransferases involved in the synthesis and regulation of sialyl Lewis x and sialyl Lewis a epitopes in gastrointestinal carcinoma cells. Our results show that expression of ST3Gal IV in several gastrointestinal cell lines is correlated with the expression of sialyl Lewis x at the cell surface. ST3Gal IV overexpressed in the gastric MKN45 cell line, showed exclusive enzymatic activity towards glycoproteins containing terminal Galbeta1-4GlcNAc structure. On the other hand, when ST3Gal III was overexpressed in MKN45, an increase in the expression levels of both sialyl Lewis epitopes was observed. ST3Gal III and ST3Gal IV lead to de novo synthesis of sialyl Lewis x determinant on different molecular weight glycoproteins of MKN45 cells suggesting that each enzyme used different substrates within the available glycoproteome. The final glycosylation step in sialyl Lewis x and sialyl Lewis a biosynthesis in MKN45 cell line was shown to be associated to FUT5, which efficiently fucosylated sialyl Lewis precursors on glycoproteins. Moreover we demonstrate that the expression of sialyl Lewis epitopes in the MKN45 was induced by cell confluence, which can be regarded as a model to study altered glycosylation during tumour progression. This increase was observed together with an increase in mRNA levels of ST3GAL3, FUT5 and FUT6, and a decrease in FUT4 transcript levels in MKN45 confluent cells, suggesting a possible control at the transcriptional level.
机译:唾液酸化Lewis X和唾液酸化Lewis的表达取决于唾液酸化转移酶和岩藻糖基转移酶。在这项研究中,我们筛选了唾液酸转移酶和岩藻糖基转移酶的主要变异,这些变异涉及胃肠道癌细胞中唾液酸化的路易斯x和唾液酸化的Lewis a表位的合成和调控。我们的结果表明,ST3Gal IV在几种胃肠道细胞系中的表达与唾液酸化的Lewis x在细胞表面的表达相关。在胃MKN45细胞系中过表达的ST3Gal IV对含有末端Galbeta1-4GlcNAc结构的糖蛋白显示出独家的酶促活性。另一方面,当ST3Gal III在MKN45中过表达时,观察到两个唾液酸化的路易斯表位的表达水平增加。 ST3Gal III和ST3Gal IV导致在MKN45细胞的不同分子量糖蛋白上从头合成唾液酸化的Lewis x决定簇,表明每种酶在可用的糖蛋白组中使用了不同的底物。唾液酸化的Lewis x和唾液酸化的Lewis a在MKN45细胞系中的生物合成中的最终糖基化步骤显示与FUT5相关,FUT5有效地将糖蛋白上的唾液酸化唾液酸化的Lewis前体。此外,我们证明了MKN45中唾液酸化的路易斯表位的表达是由细胞融合诱导的,它可以被认为是研究肿瘤进展过程中糖基化改变的模型。在MKN45融合细胞中,观察到这种增加以及ST3GAL3,FUT5和FUT6的mRNA水平的增加以及FUT4转录水平的降低,表明可能在转录水平进行了控制。

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