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首页> 外文期刊>Cytometry: The Journal of the Society for Analytical Cytology >Chronology of cellular alterations during 7-ketocholesterol-induced cell death on A7R5 rat smooth muscle cells: Analysis by time lapse-video microscopy and conventional fluorescence microscopy
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Chronology of cellular alterations during 7-ketocholesterol-induced cell death on A7R5 rat smooth muscle cells: Analysis by time lapse-video microscopy and conventional fluorescence microscopy

机译:A7R5大鼠平滑肌细胞在7-酮胆固醇诱导的细胞死亡过程中细胞改变的时间顺序:通过延时视频显微镜和常规荧光显微镜分析

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摘要

Background: Time-lapse video microscopy was used to determine whether mitochondrial and nuclear changes (decrease in mitochondrial transmembrane potential, condensation, and/or fragmentation of the nuclei, morphologic features typical of apoptosis) occurring during 7-ketocholesterol-induced cell death on A7R5 rat smooth muscle cells took place before or after the loss of cell adhesion. In addition, changes in actin organization were followed by conventional fluorescence microscopy. Methods: Morphologic, functional, and spatial changes at the mitochondrial level were investigated with 3,3'-dihexyloxacarbocyanine iodide and/or MitoTracker Red, and nuclear morphology was characterized by staining with Hoechst 33342. Actin fibers, which are major components of the filament network of the cytoskeleton, were visualized with phalloidin linked to fluorescein. The numbers of adherent and nonadherent cells were determined by cell counting. Results: 7-Ketocholesterol-induced cell death was associated with a rapid alteration of actin fibers, a loss of intercellular junctions, and cell shape modifications. Analysis of mitochondrial transmembrane potential showed successively a hyperpolarization and a more or less pronounced progressive decrease followed by a dramatic drop associated with an increase in Hoechst 33342 staining, reflecting chromatin condensation and morphologic changes in the nuclei. Conclusions: During cell death induced by 7-ketocholesterol in A7R5 rat smooth muscle cells, the different methods of microscopy allowed us to establish that alterations of actin fibers and mitochondrial dysfunctions occurred before condensation and/or fragmentation of the nuclei, which preceded the loss of cell adhesion. (C) 2003 Wiley-liss, Inc. [References: 67]
机译:背景:延时视频显微镜用于确定在7酮胆固醇诱导的A7R5细胞死亡期间是否发生线粒体和核的变化(线粒体跨膜电位的降低,核的凝聚和/或碎裂,典型的细胞凋亡的形态学特征)大鼠平滑肌细胞发生在细胞粘附丧失之前或之后。另外,肌动蛋白组织的变化随后是常规的荧光显微镜检查。方法:使用3,3'-二己基氧杂碳菁花青碘化物和/或MitoTracker Red研究线粒体水平的形态,功能和空间变化,并用Hoechst 33342染色来表征核形态。肌动蛋白纤维是长丝的主要成分用与荧光素连接的鬼笔环肽可以看到细胞骨架的网络。粘附细胞和非粘附细胞的数目通过细胞计数来确定。结果:7-酮胆固醇诱导的细胞死亡与肌动蛋白纤维的快速改变,细胞间连接的丧失和细胞形状的改变有关。线粒体跨膜电位的分析显示,超极化和或多或少明显的进行性降低,接着是与Hoechst 33342染色增加相关的急剧下降,反映了染色质浓缩和细胞核形态变化。结论:在A7R5大鼠平滑肌细胞中由7-酮胆固醇诱导的细胞死亡期间,不同的显微镜方法使我们能够确定肌动蛋白纤维的改变和线粒体功能障碍发生在核的凝结和/或断裂之前,先于核的丧失。细胞粘附。 (C)2003 Wiley-liss,Inc. [参考:67]

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