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Influence of zinc deficiency on cell-membrane fluidity in Jurkat, 3T3 and IMR-32 cells

机译:锌缺乏对Jurkat,3T3和IMR-32细胞膜流动性的影响

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pWe investigated whether zinc deficiency can affect plasma membrane rheology. Three cell lines, human leukaemia T-cells (Jurkat), rat fibroblasts (3T3) and human neuroblastoma cells (IMR-32), were cultured for 48 h in control medium, in zinc-deficient medium (1.5 μM zinc; 1.5 Zn), or in the zinc-deficient medium supplemented with 15 μM zinc (15 Zn). The number of viable cells was lower in the 1.5 Zn group than in the control and 15 Zn groups. The frequency of apoptosis was higher in the 1.5 Zn group than in the control and 15 Zn groups. Membrane fluidity was evaluated using the 6-(9-anthroyloxy)stearic acid and 16-(9-anthroyloxy)palmitic acid probes. Membrane fluidity was higher in 1.5 Zn cells than in the control cells; no differences were observed between control cells and 15 Zn cells. The effect of zinc deficiency on membrane fluidity at the water/lipid interface was associated with a higher phosphatidylserine externalization. The higher membrane fluidity in the hydrophobic region of the bilayer was correlated with a lower content of arachidonic acid. We suggest that the increased fluidity of the membrane secondary to zinc deficiency is in part due to a decrease in arachidonic acid content and the apoptosis-related changes in phosphatidylserine distribution./p
机译:>我们调查了锌缺乏症是否会影响质膜流变性。在缺锌培养基(1.5μM锌; 1.5 Zn)中,将三种细胞系,人类白血病T细胞(Jurkat),大鼠成纤维细胞(3T3)和人类神经母细胞瘤细胞(IMR-32)培养48小时。 ,或在补充15μM锌(15 Zn)的缺锌培养基中。 1.5 Zn组的活细胞数低于对照组和15 Zn组。 1.5 Zn组的凋亡频率高于对照组和15 Zn组。使用6-(9-蒽氧基)硬脂酸和16-(9-蒽氧基)棕榈酸探针评估膜的流动性。 1.5 Zn细胞的膜流动性高于对照细胞。在对照细胞和15个Zn细胞之间没有观察到差异。锌缺乏对水/脂质界面膜流动性的影响与较高的磷脂酰丝氨酸外在作用有关。双层疏水区域中较高的膜流动性与较低的花生四烯酸含量相关。我们认为,锌缺乏引起的膜流动性增加部分归因于花生四烯酸含量的减少以及磷脂酰丝氨酸分布的凋亡相关变化。

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