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Effect of indocyanine green and illumination on gene expression in human retinal pigment epithelial cells.

机译:吲哚菁绿和光照对人视网膜色素上皮细胞基因表达的影响。

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PURPOSE: To investigate the biological effects of indocyanine green (ICG) and acute illumination on human retinal pigment epithelial (RPE) cells. METHODS: Three concentrations (0, 0.25, and 2.5 mg/mL) of ICG were applied to ARPE19 cells for 1 minute. After isotonic rinsing, the cells were irradiated with a light beam with a wavelength spectrum from 400 to 800 nm and an output of 1850 lumens for 15 minutes. The cells were collected at timed intervals for the investigation of cell death and expression of stress-response genes by reverse transcription-polymerase chain reaction, immunofluorescence, and Western blot analysis. RESULTS: After ICG incubation, photoreactive changes were observed in the RPE cells. A reduction in cellular viability and considerable shrinkage of the cells were observed. The expressions of the apoptosis-related genes p53 and bax and the cell cycle arrest protein p21 were upregulated in cells treated with both ICG and light. Of the early-response genes, the expression of c-fos was specifically enhanced by light, with additive effects from the presence of ICG. Such stimulatory effects on these gene expressions were greater at 2.5 mg/mL than at 0.25 mg/mL ICG. CONCLUSIONS: ICG in the presence of acute illumination can elicit cell-cycle arrest and even apoptosis in RPE cells. The establishment of a safety level in the application of ICG in the region of 0.25 mg/mL is recommended.
机译:目的:研究吲哚菁绿(ICG)和急性光照对人视网膜色素上皮细胞(RPE)的生物学影响。方法:将三种浓度(0、0.25和2.5 mg / mL)的ICG应用于ARPE19细胞1分钟。等渗漂洗后,用波长光谱为400至800nm且输出为1850流明的光束照射细胞15分钟。定时收集细胞,通过逆转录-聚合酶链反应,免疫荧光和蛋白质印迹分析研究细胞死亡和应激反应基因的表达。结果:ICG孵育后,在RPE细胞中观察到光反应性变化。观察到细胞活力的降低和细胞的显着收缩。在用ICG和光处理的细胞中,凋亡相关基因p53和bax的表达以及细胞周期阻滞蛋白p21的表达上调。在早期反应基因中,光会特别增强c-fos的表达,而ICG的存在会产生附加作用。对这些基因表达的这种刺激作用在2.5 mg / mL时比在0.25 mg / mL ICG时更大。结论:ICG在急性光照下可以引起RPE细胞的细胞周期停滞甚至凋亡。建议在应用ICG时将安全水平确定为0.25 mg / mL。

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