Seftor R E, Seftor E A, Grimes W J, Liotta L A, Stetler-Stevenson W G, Welch D R, Hendrix M J
Department of Anatomy, University of Arizona College of Medicine, Tucson 85724.
Melanoma Res. 1991 Apr-May;1(1):43-54. doi: 10.1097/00008390-199104000-00006.
A 48 h pretreatment of two malignant and invasive human melanoma cell lines with either swainsonine (an inhibitor of Golgi alpha-mannosidase II) or deoxymannojirimycin (a Golgi alpha-mannosidase I inhibitor) resulted in a dose-dependent decrease in the cells' ability to invade a reconstituted basement membrane in vitro. This effect was reversible within 48 h of removing the drugs. Treatment with either drug resulted in both cell lines being more resistant to the cytotoxic effects of the lectin leukoagglutinin (PHA-L) and more sensitive to the lectin concanavalin A which indirectly indicated a change in the cell surface oligosaccharide composition and structure consistent with the known effects of these drugs on N-linked oligosaccharide processing. A 25-33% decrease was noted in the adhesion of treated cells to either a reconstituted basement membrane or human umbilical vein endothelial cell monolayer while no change was measured in the cells' proliferative rates. A correlative decrease was observed, however, in the expression of human type IV collagenase mRNA which was recovered within 48 h of removing the drugs. These results suggest that a correlation exists between the drug-induced changes in the cell surface oligosaccharide composition and structure with a concomitant decrease in the mRNA and secreted levels of type IV collagenase and the ability of these cells to invade.
用苦马豆素(一种高尔基体α-甘露糖苷酶II抑制剂)或脱氧甘露诺吉霉素(一种高尔基体α-甘露糖苷酶I抑制剂)对两种恶性侵袭性人类黑色素瘤细胞系进行48小时预处理,导致细胞体外侵袭重组基底膜的能力呈剂量依赖性下降。在去除药物后的48小时内,这种效应是可逆的。用这两种药物处理均导致两种细胞系对凝集素白细胞凝集素(PHA-L)的细胞毒性作用更具抗性,而对凝集素伴刀豆球蛋白A更敏感,这间接表明细胞表面寡糖组成和结构发生了变化,与这些药物对N-连接寡糖加工的已知作用一致。观察到处理后的细胞与重组基底膜或人脐静脉内皮细胞单层的黏附力下降了25%-33%,而细胞增殖率没有变化。然而,在去除药物后的48小时内,观察到人类IV型胶原酶mRNA的表达呈相关下降。这些结果表明,药物诱导的细胞表面寡糖组成和结构变化与IV型胶原酶的mRNA和分泌水平的相应下降以及这些细胞的侵袭能力之间存在相关性。