A. Tkachenko, A. Onishchenko, V. Prokopyuk, S. Yefimova, V. Klochkov, P. Maksimchuk, N. Kavok, Y. Posokhov
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引用次数: 0
摘要
的目标。目的:评价GdYVO4:Eu3+纳米粒子直接暴露后对白细胞细胞膜状态的影响。材料和方法。将2-(2′- oh -苯基)-5-(4′-联苯)-1,3-oxazole致膜性荧光探针与经不同浓度GdYVO4:Eu3+纳米颗粒(0 μg/ml、20 μg/ml、40 μg/ml、80 μg/ml)直接处理的血液白细胞悬浮液直接孵育24 h,用FL8500型荧光分光光度计记录探针正常形态和互变异构体形态的荧光。我们的研究结果表明,仅在使用最高浓度纳米颗粒的悬浮液中,才观察到互变异构体形式的荧光强度与正常形式的荧光强度比(IT*/ in *)的值有统计学意义的升高,而在低浓度纳米颗粒时,探针所在的膜区域磷脂双分子层的状态没有改变。低浓度的GdYVO4:Eu3+纳米颗粒不会改变白细胞细胞膜的脂质秩序,而其高浓度会促进脂质秩序的增加,这表明探针所在的磷脂双分子层区域的流动性降低,微粘度增加。
High Concentrations of GdYVO4:Eu3+ Nanoparticles Alter the State of White Blood Cell Membranes by Increasing Their Microviscosity
Aim. To evaluate the effects of GdYVO4:Eu3+ nanoparticles on the state of leukocyte cell membranes upon direct exposure.Materials and methods. The membranotropic fluorescent probe 2-(2’-OH-phenyl)-5-(4’-biphenyl)-1,3-oxazole was incubated directly with leukocyte suspensions obtained from blood treated directly with different concentrations of GdYVO4:Eu3+ nanoparticles (0 μg/ml, 20 μg/ml, 40 μg/ml, 80 μg/ml) during 24 h. The fluorescence of normal and tautomeric forms of the probe was registered using a FL8500 Fluorescence Spectrophotometer (Perkin Elmer, USA).Results. Our findings indicate that the statistically significant elevation in values of the tautomeric form fluorescence intensity-to-normal form fluorescence intensity ratio (IT*/IN*) was observed only for suspensions with the highest concentration of nanoparticles used, while at low concentrations nanoparticles did not alter the state of phospholipid bilayer in the region of membranes where the probe locates.Conclusions. Low concentrations of GdYVO4:Eu3+ nanoparticles don’t alter the lipid order of leukocyte cell membranes, while their high concentrations promote an increase in lipid order suggesting a decrease in fluidity and an increase in microviscosity of the area of phospholipid bilayer where the probe locates.