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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道癌细胞中唾液酸化 Lewis a 和唾液酸化 Lewis x 的水平。

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.

机构信息

Instituto de Patologia e Imunologia Molecular da Universidade do Porto (IPATIMUP), Porto, Portugal.

出版信息

Int J Biochem Cell Biol. 2010 Jan;42(1):80-9. doi: 10.1016/j.biocel.2009.09.010. Epub 2009 Sep 23.

Abstract

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.

摘要

唾液酸化 Lewis x 和唾液酸化 Lewis a 的表达取决于唾液酸转移酶和岩藻糖基转移酶。在这项研究中,我们筛选了参与胃肠道癌细胞中唾液酸化 Lewis x 和唾液酸化 Lewis a 表位合成和调节的主要唾液酸转移酶和岩藻糖基转移酶的变异体。我们的结果表明,几种胃肠道细胞系中 ST3Gal IV 的表达与细胞表面唾液酸化 Lewis x 的表达相关。在胃癌 MKN45 细胞系中过表达 ST3Gal IV 时,对含有末端 Galβ1-4GlcNAc 结构的糖蛋白具有独特的酶活性。另一方面,当 ST3Gal III 在 MKN45 中过表达时,观察到两种唾液酸化表位的表达水平均增加。ST3Gal III 和 ST3Gal IV 导致 MKN45 细胞不同分子量糖蛋白上新合成的唾液酸化 Lewis x 决定簇,表明每种酶在可用糖蛋白组内使用不同的底物。在 MKN45 细胞系中唾液酸化 Lewis x 和唾液酸化 Lewis a 生物合成的最后糖基化步骤与 FUT5 相关联,FUT5 有效地在糖蛋白上糖基化唾液酸化 Lewis 前体。此外,我们证明 MKN45 中唾液酸化表位的表达受细胞汇合的诱导,这可以作为研究肿瘤进展过程中糖基化改变的模型。这种增加与 MKN45 汇合细胞中 ST3GAL3、FUT5 和 FUT6 的 mRNA 水平增加以及 FUT4 转录物水平降低同时发生,表明可能在转录水平上进行了控制。

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