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首页> 外文期刊>Bioelectromagnetics. >Morphofunctional study of 12-O-tetradecanoyl-13-phorbol acetate (TPA)-induced differentiation of U937 cells under exposure to a 6 mT static magnetic field.
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Morphofunctional study of 12-O-tetradecanoyl-13-phorbol acetate (TPA)-induced differentiation of U937 cells under exposure to a 6 mT static magnetic field.

机译:暴露于6 mT静磁场下的12-O-十四烷酰基13-佛波醇乙酸酯(TPA)诱导的U937细胞分化的形态功能研究。

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This study deals with the morphofunctional influence of 72 h exposure to a 6 mT static magnetic field (SMF) during differentiation induced by 50 ng/ml 12-O-tetradecanoyl-13-phorbol acetate (TPA) in human leukaemia U937 cells. The cell morphology of U937 cells was investigated by optic and electron microscopy. Specific antibodies and/or molecules were used to label CD11c, CD14, phosphatidylserine, F-actin and to investigate the distribution and activity of lysosomes, mitochondria and SER. [Ca(2+)](i) was evaluated with a spectrophotometer. The degree of differentiation in SMF-exposed cells was lower than that of non-exposed cells, the difference being exposure time-dependent. SMF-exposed cells showed cell shape and F-actin modification, inhibition of cell attachment, appearance of membrane roughness and large blebs and impaired expression of specific macrophagic markers on the cell surface. The intracellular localization of SER and lysosomes was only partially affected by exposure. A significant localization of mitochondria with an intact membrane potential at the cell periphery in non-exposed, TPA-stimulated cells was observed; conversely, in the presence of SMF, mitochondria were mainly localised near the nucleus. In no case did SMF exposure affect cell viability. The sharp intracellular increase of [Ca(2+)](i) could be one of the causes of the above-described changes.
机译:这项研究处理了在人类白血病U937细胞中由50 ng / ml 12-O-十四烷酰-13-佛波醇乙酸酯(TPA)诱导的分化过程中,暴露于6 mT静磁场(SMF)72 h对形态功能的影响。通过光学和电子显微镜研究了U937细胞的细胞形态。特定的抗体和/或分子被用来标记CD11c,CD14,磷脂酰丝氨酸,F-肌动蛋白,并研究溶酶体,线粒体和SER的分布和活性。用分光光度计评价[Ca(2 +)](i)。 SMF暴露的细胞的分化程度低于未暴露的细胞,其分化程度取决于暴露时间。暴露于SMF的细胞表现出细胞形状和F-肌动蛋白修饰,抑制细胞附着,出现膜粗糙和大气泡以及损害细胞表面特定的巨噬细胞标记物的表达。 SER和溶酶体的细胞内定位仅部分受到暴露的影响。在未暴露的,受TPA刺激的细胞中,观察到线粒体明显定位于完整的膜电位。相反,在SMF的存在下,线粒体主要位于细胞核附近。在任何情况下,SMF暴露均不会影响细胞活力。细胞内[Ca(2 +)](i)的急剧增加可能是上述变化的原因之一。

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