Sato C, Kojima K, Nishizawa K, Ikawa Y
Cancer Res. 1979 Mar;39(3):1113-7.
Early membrane events in erythroid differentiation were investigated by means of cell electrophoresis utilizing cultured Friend erythroleukemia cell clones of different inducibility. The cell electrophoretic mobility decreased by 18% within 30 min of treatment with 1.5% dimethyl sulfoxide (DMSO) in highly inducible clones but not in noninducible clones. The reduced mobility persisted for 5 days of incubation with DMSO until hemoglobin synthesis. DMSO treatment for less than 16 hr and subsequent incubation without the drug resulted in the complete recovery of the mobility and no hemoglobin synthesis. Longer exposure to DMSO resulted in the loss of recovery of mobility and an increasing fraction of benzidine-positive cells seen on Day 5. Measurement of the electrophoretic mobility after the removal of acidic sugars by their specific enzymes suggested that hyaluronidase-sensitive negative charges were lost from the cell surface only in highly inducible clones. The mobility reduction associated with hyaluronic acid was also caused by other potent inducers (sodium butyrate, N-methylacetamide, and N,N-dimethylacetamide). These results suggest that the decrease in cell surface glycocalyx might be an early step in the induction of differentiation of Friend erythroleukemia cells.
利用不同诱导性的培养弗氏红白血病细胞克隆,通过细胞电泳研究红系分化早期的膜事件。在高诱导性克隆中,用1.5%二甲基亚砜(DMSO)处理30分钟内,细胞电泳迁移率下降了18%,而在非诱导性克隆中则没有下降。迁移率降低在与DMSO孵育5天直至血红蛋白合成期间持续存在。用DMSO处理少于16小时,随后在无药物情况下孵育,迁移率完全恢复且无血红蛋白合成。长时间暴露于DMSO导致迁移率恢复丧失,且在第5天观察到联苯胺阳性细胞比例增加。用特定酶去除酸性糖后测量电泳迁移率表明,仅在高诱导性克隆中,细胞表面对透明质酸酶敏感的负电荷丢失。与透明质酸相关的迁移率降低也由其他强效诱导剂(丁酸钠、N-甲基乙酰胺和N,N-二甲基乙酰胺)引起。这些结果表明,细胞表面糖萼的减少可能是诱导弗氏红白血病细胞分化的早期步骤。