Seibicke S, Zimmermann H P, Haeffner E W
Institut für Zell- und Tumorbiologie, Deutsches Krebsforschungszentrum, Heidelberg, F.R.G.
Biochim Biophys Acta. 1988 Oct 20;944(3):487-96. doi: 10.1016/0005-2736(88)90520-2.
Cultured ascites tumor cells and their lipid-depleted variants, which contained 35-40% less membrane phospholipid and cholesterol, were used for fusion experiments with unilamellar lipid vesicles which were between 300 and 600 nm in diameter. Vesicle-cell interaction was followed by tracer studies using vesicles double-labeled in the lipid moiety, by vesicle-encapsulated [3H] dextran, and by measurements of energy transfer between N-(10-[1-pyrene]decanoyl)sphingomyelin-labeled vesicles and alpha-parinaric acid-labeled cells in the presence of poly(ethylene glycol) (PEG) as fusogen. The reaction rates measured with the radiolabeled vesicles were found to follow patterns similar to those obtained with the resonance energy transfer assay. This latter method revealed a vesicle-cell membrane fusion reaction, which was substantiated by radiolabeling the internal cellular compartment after treatment of the cells with [3H]dextran-encapsulated vesicles as shown by electron microscopic autoradiography on semi-thin sections. Endocytosis as a reaction mechanism can be excluded, since no energy transfer was observed at 25 degrees C in the absence of PEG. Investigations of vesicle bilayer order and fluidity on vesicle-cell interaction revealed optimal reactivity, with intermediate fluidity corresponding to cholesterol/phospholipid ratios between 0.7 and 1.0 and fluorescence depolarization (P) values of 0.18 and 0.21. Lipid depletion decreased the reaction velocity between cells and vesicles by about 20%, exhibiting V values of 33.2 mumol/min, as compared to the control of 41.4 mumol/min determined for 10(7) cells. The affinity constants for vesicle lipid were affected only slightly with Km values of 0.195 mM (0.210 mM). The activation energies for the reaction were calculated to give values of EA = 22.44 kJ/mol for the control and of EA = 20.4 kJ/mol for the modified cells. These data indicate that the decrease in membrane lipid content apparently has no major influence on the extent of the interaction.
培养的腹水肿瘤细胞及其脂质耗尽变体(其膜磷脂和胆固醇含量减少35 - 40%)用于与直径在300至600纳米之间的单层脂质囊泡进行融合实验。通过使用脂质部分双重标记的囊泡、囊泡包封的[³H]葡聚糖进行示踪研究,以及在聚乙二醇(PEG)作为融合剂存在的情况下测量N-(10-[1-芘]癸酰)鞘磷脂标记的囊泡与α-紫罗酮酸标记的细胞之间的能量转移,来跟踪囊泡与细胞的相互作用。发现用放射性标记囊泡测量的反应速率遵循与共振能量转移测定法获得的模式相似的模式。后一种方法揭示了囊泡 - 细胞膜融合反应,在用[³H]葡聚糖包封的囊泡处理细胞后,通过对超薄切片进行电子显微镜放射自显影显示细胞内区室被放射性标记,从而证实了这一点。由于在25℃且不存在PEG的情况下未观察到能量转移,因此可以排除内吞作用作为反应机制。对囊泡双层有序性和流动性对囊泡 - 细胞相互作用的研究表明,具有最佳反应性,中间流动性对应于胆固醇/磷脂比在0.7至1.0之间,荧光去极化(P)值为0.18和0.21。脂质耗尽使细胞与囊泡之间的反应速度降低约20%,V值为33.2 μmol/min,而对于10⁷个细胞,对照测定值为41.4 μmol/min。囊泡脂质的亲和常数仅受到轻微影响,Km值为0.195 mM(0.210 mM)。计算出该反应的活化能,对照的EA值为22.44 kJ/mol,修饰细胞的EA值为20.4 kJ/mol。这些数据表明膜脂质含量的降低显然对相互作用的程度没有重大影响。