首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Laser-stimulated fluorescence of submicrometer regions within single mitochondria of rhodamine-treated myocardial cells in culture.
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Laser-stimulated fluorescence of submicrometer regions within single mitochondria of rhodamine-treated myocardial cells in culture.

机译:激光刺激若丹明处理过的心肌细胞单个线粒体内亚微米区域的荧光。

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摘要

A focused laser beam of 442 nm was used to stimulate fluorescence in 0.5-micrometer spots in single mitochondria of myocardial and endothelial cells in culture. Cells were treated with rhodamine 6G or 123 in order to render the mitochondria fluorescent. Rhodamine 123-treated cells exhibited a gradual decrease in fluorescence over several minutes, whereas the rhodamine 6G-treated myocardial cells exhibited three distinct patterns of variable fluorescence intensity. These patterns were detected at different points within the same mitochondrion or in different mitochondria. Mitochondria from nonmyocardial endothelial cells did not exhibit any variable intensity patterns of fluorescence. Electron microscopy revealed no ultrastructural damage attributable to laser exposure of the mitochondria. The variable fluorescence patterns are hypothesized to be indicative of localized alterations in molecules or ions at the suborganelle level.
机译:使用442 nm聚焦激光束刺激培养的心肌和内皮细胞单个线粒体中0.5微米点的荧光。用罗丹明6G或123处理细胞以使线粒体发荧光。罗丹明123处理的细胞在几分钟内显示出逐渐降低的荧光,而若丹明6G处理的心肌细胞则显示出三种不同的荧光强度变化模式。在同一线粒体内或不同线粒体中的不同点检测到这些模式。来自非心肌内皮细胞的线粒体未显示任何可变强度的荧光模式。电子显微镜显示没有线粒体激光暴露引起的超微结构损伤。假设可变荧光模式指示亚细胞器水平的分子或离子的局部改变。

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