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Endogenous fluorescence of normal and malignant fibroblast cultures

机译:内源性荧光正常和恶性成纤维细胞培养物

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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:光诱导的荧光(LiF)技术基于通过单色光照射的细胞内发色团发射的荧光。我们比较了从一对正常和恶性鼠细胞系发射的LiF,不同于H-Ras表达。在290 + -10nm的激发时,恶性细胞荧光显着小于正常细胞。对于两种细胞类型,荧光随着细胞夹持剂的降低而降低,但在每种浓度下,正常细胞比恶性细胞更荧光。比较了细胞对该模式的活力和代谢阶段的影响。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-RA对亚细胞发色团的特定贡献,导致其自发荧光强度的显着差异,同时测量发射和激发扫描。该研究表明,潜在使用LIF技术区分正常和恶性细胞和组织。

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