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首页> 外文期刊>Analytical and quantitative cytology and histology >Flow cytometry and factor analysis evaluation of confocal image sequences of morphologic and functional changes occurring at the mitochondrial level during 7-ketocholesterol-induced cell death.
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Flow cytometry and factor analysis evaluation of confocal image sequences of morphologic and functional changes occurring at the mitochondrial level during 7-ketocholesterol-induced cell death.

机译:流式细胞仪和因子分析评估共焦图像序列的形态和功能变化发生在7-酮胆固醇诱导的细胞死亡过程中的线粒体水平。

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摘要

OBJECTIVE: To analyze functional and morphologic alterations that occur at the mitochondrial level by flow cytometry and laser scanning confocal microscopy (CLSM) combined with factor analysis of biomedical image sequences (FAMIS). STUDY DESIGN: Under treatment of U937 cells with 7-ketocholesterol, functional alterations that occur at the mitochondrial level (especially loss of transmembrane mitochondrial potential [delta psi m]) were assessed with 3,3'-dihexyloxacarbocyanine iodide (DiOC6(3)) and mitotracker red (CMXRos), whereas morphologic changes were analyzed with nonyl acridine orange (NAO). By flow cytometry, these different dyes were excited at 488 nm, whereas on CLSM, excitation of NAO and CMXRos was performed by lines of an argon laser. By CLSM, spectral sequences were performed to characterize NAO and CMXRos. FAMIS was used to transform the image sequences in factor images. RESULTS: By flow cytometry, rapid loss of delta psi m induced by 7-ketocholesterol was detected with both DiOC6(3) and CMXRos, which gave similar results. Morphologic alterations of mitochondria were revealed with NAO. The factor images obtained from confocal image sequences confirmed these results. CONCLUSION: The simultaneous use of NAO, CMXRos and FAMIS constitutes a new method to detect morphologic and functional alterations occurring at the mitochondrial level during cell death.
机译:目的:通过流式细胞仪和激光扫描共聚焦显微镜(CLSM)结合生物医学图像序列(FAMIS)的因子分析,分析在线粒体水平发生的功能和形态变化。研究设计:在用7-酮胆固醇对U937细胞进行处理的情况下,使用3,3'-二己基氧杂羰基花青碘碘化物(DiOC6(3))评估了线粒体水平发生的功能改变(尤其是跨膜线粒体电位[δpsi m]的损失)。和线粒体红色(CMXRos),而形态变化则用壬基a啶橙(NAO)进行分析。通过流式细胞术,这些不同的染料在488 nm激发,而在CLSM上,通过氩激光线激发NAO和CMXRos。通过CLSM,执行光谱序列以表征NAO和CMXRos。 FAMIS用于转换因子图像中的图像序列。结果:通过流式细胞术,DiOC6(3)和CMXRos均检测到7-酮胆固醇引起的psim的快速损失,结果相似。 NAO显示线粒体的形态改变。从共焦图像序列获得的因子图像证实了这些结果。结论:同时使用NAO,CMXRos和FAMIS构成了一种检测细胞死亡过程中线粒体形态和功能变化的新方法。

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