首页> 外文会议>Conference on Optical Biopsy and Tissue Optics 5-6 July 2000 Amsterdam, the Netherlands >Endogenous fluorescence of normal and malignant fibroblast cultures
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Endogenous fluorescence of normal and malignant fibroblast cultures

机译:正常和恶性成纤维细胞培养物的内源性荧光

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Light-induced fluorescence (LIF) technique is based on fluorescence emitted from intracellular chromophores upon illumination fo cells by monochromatic light. We compared LIF emitted from a pair of normal and malignant murine cell lines, differing in H-ras expression. The malignant cells fluoresced significantly less than the normal cells, upon excitation at 290+-10 nm. For both cell types, fluorescence decreased with decreasing cell conentration, but at each concentration, the normal cells fluoresced more than the malignant cells. The effect of viability and metabolic stage of the cells on this pattern was compared. The difference among the cells was not due to a difference in protein or DNA content. Thus, this model system demonstrates the specific contribution of H-ras to sub-cellular chromophores, resulting in a significant difference in their autofluorescence intensity, while measuring both emission and excitation scans. This study suggests a potential use of the LIF technique to distinguish between normal and malignant cells and tissues.
机译:光诱导荧光(LIF)技术基于细胞内发色团在单色光照射下细胞发出的荧光。我们比较了从一对正常和恶性鼠细胞系发出的LIF,它们的H-ras表达有所不同。在290 + -10 nm激发后,恶性细胞的荧光显着少于正常细胞。对于两种细胞类型,荧光都随着细胞浓度的降低而降低,但是在每种浓度下,正常细胞的荧光都比恶性细胞多。比较了细胞活力和代谢阶段对该模式的影响。细胞之间的差异不是由于蛋白质或DNA含量的差异。因此,该模型系统证明了H-ras对亚细胞发色团的特定贡献,从而在测量发射扫描和激发扫描时导致了其自发荧光强度的显着差异。这项研究表明,LIF技术可用于区分正常和恶性细胞与组织。

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