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Protective effect of a laser-induced sub-lethal temperature rise on RPE cells from oxidative stress

机译:激光诱导的亚致死温度升高对氧化应激的RPE细胞的保护作用

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Recently introduced new technologies that enable temperature-controlled laser irradiation on the RPE allowed us to investigate temperature-resolved RPE cell responses. In this study we aimed primarily to establish an experimental setup that can realize laser irradiation on RPE cell culture with the similar temperature distribution as in the clinical application, with a precise time/temperature history. With this setup, we conducted investigations to elucidate the temperature-dependent RPE cell biochemical responses and the effect of transient hyperthermia on the responses of RPE cells to the secondary-exposed oxidative stress. Porcine RPE cells cultivated in a culture dish (inner diameter = 30 mm) with culture medium were used, on which laser radiation (A = 1940 nm, spot diameter = 30 mm) over 10 s was applied as a heat source. The irradiation provides a radially decreasing temperature profile which is close to a Gaussian shape with the highest temperature in the center. Power setting for irradiation was determined such that the peak temperature (T_(max)) in the center of the laser spot at the cells reaches from 40 degC to 58 degC (40,43,46, 50, 58 degC). Cell viability was investigated with ethidium homodimer III staining at the time points of 3 and 24 h following laser irradiation. Twenty four hours after laser irradiation the cells were exposed to hydrogen peroxide (H2O2) for 5 h, followed by the measurement of intracellular glutathione, intracellular 4-hydroxynonenal (HNE) protein adducts, and secreted vascular endothelial growth factor (VEGF). The mean temperature threshold for RPE cell death after 3 h was found to be around 52 degC, and for 24 h around 50 degC with the current irradiation setting. A sub-lethal preconditioning on T_(max) = 43 degC significantly induced the reduced glutathione (GSH)/oxidized glutathione (GSSG) ratio, and decreased H_2O_2-induced increase of intracellular 4-HNE protein adducts. Although sub-lethal hyperthermia (T_(max) = 40 degC, 43 degC, and 46 degC) caused a slight increase of VEGF secretion in 6 h directly following irradiation, secondary exposed H_2O_2-induced VEGF secretion was significantly reduced in the sub-lethally preheated groups, where the largest effect was seen following the irradiation with T_(max) = 43 degC. In summary, the current results suggest that sub-lethal thermal laser irradiation on the RPE at T_(max) = 43 degC for 10 s enhances cell defense system against oxidative stress, with increasing the GSH/ GSSG ratio. Together with the results that the decreased amount of H_2O_2-induced 4-HNE in sub-lethally preheated RPE cells was accompanied by the lower secretion of VEGF, it is also strongly suggested that-the sub-lethal hyperthermia may modify RPE cell functionality to protect RPE cells, from oxidative stress and associated functional decrease, which are considered to play a significant role in the pathogenesis of age-related macular degeneration and other chorioretinal degenerative diseases.
机译:最近推出了能够在RPE上实现温度控制的激光照射的新技术,使我们能够研究温度分辨的RPE细胞应答。在该研究中,我们主要针对建立一种实验设置,可以实现与临床应用中类似温度分布的RPE细胞培养对RPE细胞培养的激光辐射,具有精确的时间/温度历史。通过该设置,我们进行了调查,以阐明温度依赖性RPE细胞生化反应和短暂热疗对RPE细胞对二次暴露氧化应激的反应的影响。使用在培养基(内径= 30mm)中培养的猪RPE细胞,其作为热源施加超过10秒的激光辐射(A = 1940nm,点直径= 30mm)。辐射提供径向降低的温度曲线,其靠近具有中心的最高温度的高斯形状。确定照射的电源设置使得细胞中激光斑点中心的峰值温度(T_(最大))达到40℃至58degc(40,43,46,50,58degc)。在激光照射之后,用在3和24小时的时间点的乙锭同源III染色研究细胞活力。激光照射后二十四小时细胞暴露于过氧化氢(H 2 O 2)5小时,然后测量细胞内谷胱甘肽,细胞内4-羟基(HNE)蛋白质加合物,分泌的血管内皮生长因子(VEGF)。在3小时后RPE细胞死亡的平均温度阈值约为52℃,并且24小时约50℃,电流照射设定。 T_(MAX)= 43 degc上的亚致死预处理显着诱导降低的谷胱甘肽(GSH)/氧化谷胱甘肽(GSSG)比,降低H_2O_2诱导的细胞内4-HNE蛋白质加合物的增加。虽然亚致死的热疗(T_(max)= 40degc,43 degc和46 degc)在照射后直接导致6小时的VEGF分泌略微增加,但在妊娠中,继发暴露的H_2O_2诱导的VEGF分泌显着降低预热组,在用T_(max)= 43 degc辐照后看到最大效果。总之,目前的结果表明,T_(MAX)= 43℃的RPE上的亚致死热激光照射10S增强细胞防御系统,随着GSH / GSSG比率的增加。与结果一起伴随着VEGF分泌的次致命预热的RPE细胞中的降低的H_2O_2诱导的4-HNE的结果,也强烈建议 - 亚致死的热疗可以改变RPE细胞功能以保护来自氧化应激和相关功能降低的RPE细胞被认为在年龄相关黄斑变性和其他潜冲性退化疾病的发病机制中发挥着重要作用。

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