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Glycosaminoglycan model glass substrates and cancer cell interactions

机译:糖胺聚糖模型玻璃基材和癌细胞相互作用

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We have analyzed the the static adhesion of three cancer cell lines of varying metastatic potential to surfaces functionalized with glycosaminoglycans (GAGs) in relation to GAG charge per dimer and GAG chain length. Four different GAGs (heparan sulfate (HS), chondroitin sulfate A (CSA), chondroitin sulfate C (CSC) and keratan sulfate (KS)) were deposited on glass surfaces that had been previously coated with 3-aminopropyltriethoxy-silane (APTES), and the substrates were used in static adhesion experiments. GAGs were strongly bonded to the silanized glass cover slips. The best substrate for adhesion was HS while KS was the least preferred substrate. The observed adhesion of whole cancer cells showed that a functional dependence may exist with the number of charges per dimer of the polyelectrolyte to which they are attaching and that this dependence takes the form of a linear function that increases with the number of charges per dimer.
机译:我们已经分析了三种癌细胞系的静态粘附,不同的转移电位与糖胺聚糖(GAG)相对于每二聚体的GAG电荷相对于GAG电荷和GAG链长度的表面官能化的表面。沉积在先前涂覆3-氨基丙基三乙氧基 - 硅烷(Aptes)的玻璃表面上沉积在预先涂覆的玻璃表面上的四种不同的Gag(Heperan硫酸盐A(CSA),软骨素硫酸盐C(CSC)和角蛋白硫酸盐(Ks)),并且基材用于静态粘合实验。 Gags强烈地粘合到硅烷化玻璃盖滑轮上。用于粘合性的最佳基材是HS,而Ks是最少于优选的基材。观察到的全癌细胞的粘附表明,具有它们附着的聚电解质的每二聚体的电荷的数量可以存在功能依赖性,并且该依赖性采用线性函数的形式随着每二聚体的电荷的数量而增加。

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