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培养的C6胶质瘤细胞表面糖决定簇的生长相关变化:一项细胞化学凝集素结合研究。

Growth related changes in sugar determinants on the surface of C6 glioma cells in culture: a cytochemical lectin-binding study.

作者信息

Berezovskaya O L, Mares V, Skibo G G

机构信息

A.A. Bogomoletz Institute of Physiology, Ukrainian Academy of Science, Kiev, Ukraine.

出版信息

J Neurosci Res. 1995 Oct 1;42(2):192-8. doi: 10.1002/jnr.490420206.

Abstract

The cell surface sugar determinants (CSSD) were examined in C6 glioma cells in cultures at different conditions of growth by peroxidase conjugates of the lectins: peanut agglutinin (PNA), Ricinus communis agglutinin (RCA), Helix pomatia agglutinin (HPA), wheat germ agglutinin (WGA), lentil agglutinin (LCA), laburnum bork agglutinin (LABA), and lotus agglutinin (TPA). It was found that the cells bound more intensively WGA, LCA, and RCA compared to PNA, HPA; the weakest staining was provided by LABA and TPA. Binding intensity for PNA significantly increased after pretreatment of the cells with neuraminidase. This indicates that a part of the beta-D-galactose residues on the surface membrane of C6 glioma cells is covered by sialic acid. The process of sialization was increased during the culturing of C6 glioma cells. Addition of cis-DDP or dBcAMP to cultures growing in medium with 10% of CS increased the number of Gal residues which are not covered by sialic acid. The expression of beta-D-galactose (Gal), N-acetyl-D-galactosamine (NAcDGal), and fucose (Fuc) residues appeared to be most responsive to changes in growth conditions and degree of cell differentiation. The expressions of N-acetyl-D-glucosamine (NAcDGlc) and mannose (Man) residues were high and seems did not depend on changing of the conditions of culturing. In C6 glioma cells cultures in which the rate of cell division, formation of the cell processes, and adhesiveness of the cells to the substratum were reduced by growing cells in MEM+, expression of beta-Gal, NAcDGal, and Fuc was considerably reduced. The decrease of expression of beta-Gal, NAcDGal, and Fuc on the surface of cell membrane was more pronounced in MEM+ with 1% of CS than in MEM+ with 10% of CS. In DbcAMP and cis-DDP treated cultures, grown in medium with 1% serum, in which cell division was inhibited without obvious changes in cell adhesiveness to the substratum, binding of PNA and HPA was increased due to higher expression of beta-Gal and NAcDGal. From these observations it was concluded that the pattern of expression of sugar residues on the cell surface varies according to the biological state of the cells and are easily affected by tissue culture conditions.

摘要

通过凝集素的过氧化物酶缀合物

花生凝集素(PNA)、蓖麻凝集素(RCA)、蜗牛凝集素(HPA)、麦胚凝集素(WGA)、扁豆凝集素(LCA)、金链花凝集素(LABA)和莲凝集素(TPA),在不同生长条件下培养的C6胶质瘤细胞中检测细胞表面糖决定簇(CSSD)。结果发现,与PNA、HPA相比,细胞与WGA、LCA和RCA的结合更强烈;LABA和TPA的染色最弱。用神经氨酸酶预处理细胞后,PNA的结合强度显著增加。这表明C6胶质瘤细胞表面膜上的一部分β-D-半乳糖残基被唾液酸覆盖。在C6胶质瘤细胞培养过程中,唾液酸化过程增强。向含10%胎牛血清的培养基中生长的培养物中添加顺铂或二丁酰环磷腺苷(dBcAMP),可增加未被唾液酸覆盖的半乳糖残基数量。β-D-半乳糖(Gal)、N-乙酰-D-半乳糖胺(NAcDGal)和岩藻糖(Fuc)残基的表达似乎对生长条件和细胞分化程度的变化最敏感。N-乙酰-D-葡萄糖胺(NAcDGlc)和甘露糖(Man)残基的表达较高,似乎不依赖于培养条件的改变。在MEM+培养基中培养细胞,使细胞分裂速率、细胞突起形成以及细胞与基质的粘附性降低,C6胶质瘤细胞培养物中β-Gal、NAcDGal和Fuc的表达显著降低。在含1%胎牛血清的MEM+培养基中,细胞膜表面β-Gal、NAcDGal和Fuc表达的降低比在含10%胎牛血清的MEM+培养基中更明显。在含1%血清的培养基中培养的经二丁酰环磷腺苷和顺铂处理的培养物中,细胞分裂受到抑制,而细胞与基质的粘附性无明显变化,由于β-Gal和NAcDGal的表达增加,PNA和HPA的结合增加。从这些观察结果得出结论,细胞表面糖残基的表达模式根据细胞的生物学状态而变化,并且容易受到组织培养条件的影响。

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