首页> 外文期刊>Toxicology: An International Journal Concerned with the Effects of Chemicals on Living Systems >Expression of Fas antigen and apoptosis caused by 5,10,15, 20-tetra(4-methoxyphenyl)porphyrin (TMP) on carcinoma cells: implication for photodynamic therapy.
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Expression of Fas antigen and apoptosis caused by 5,10,15, 20-tetra(4-methoxyphenyl)porphyrin (TMP) on carcinoma cells: implication for photodynamic therapy.

机译:5,10,15,20-四(4-甲氧基苯基)卟啉(TMP)引起的Fas抗原表达和凋亡在癌细胞上的意义:对光动力疗法的意义。

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摘要

The photodynamic effects of 5,10,15, 20-tetra(4-methoxyphenyl)porphyrin (TMP) on a Hep-2 cell line were investigated. TMP toxicity in the dark and in relation to illumination with visible light was examined. Hep-2 cells were treated with different TMP concentrations (1, 5 and 10 microM). The uptake of TMP by Hep-2 cells increased with TMP concentration and an increase of the initial uptake rate was observed with increasing TMP concentrations. However, after 24 h of incubation, a similar value of intracellular TMP concentration was reached at all three concentrations of TMP added. Cell toxicity induced by TMP was analyzed in the dark at different concentrations of the photosensitizer and at several incubation periods. The cell mortality obtained after exposure of the cell cultures to visible light was exclusively due to the photosensitization effect of TMP produced by light irradiation. Staining with the hematoxylin-eosin method demonstrated that treatment with TMP, followed by exposure to visible light, notably increased the apoptotic figures. Fas antigen was only expressed in these conditions. The results contribute to the understanding of the photodynamic therapy (PDT) mechanism produced by TMP on Hep-2 carcinoma cell line.
机译:研究了5,10,15,20-四(4-甲氧基苯基)卟啉(TMP)对Hep-2细胞系的光动力作用。检查了TMP在黑暗中以及与可见光照明相关的毒性。 Hep-2细胞用不同的TMP浓度(1、5和10 microM)处理。 Hep-2细胞对TMP的摄取随TMP浓度的增加而增加,并且随着TMP浓度的增加,观察到初始摄取率的增加。但是,孵育24小时后,在所有三种添加的TMP浓度下,细胞内TMP浓度均达到了相似的值。在黑暗中,在不同浓度的光敏剂和几个潜伏期中,分析了由TMP诱导的细胞毒性。将细胞培养物暴露于可见光后获得的细胞死亡率完全是由于光照射产生的TMP的光敏作用。用苏木精-曙红法染色表明,用TMP处理,然后再暴露于可见光下,可显着增加细胞凋亡率。 Fas抗原仅在这些条件下表达。该结果有助于了解TMP对Hep-2癌细胞系产生的光动力疗法(PDT)机制。

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