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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RPE细胞氧化应激的保护作用

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摘要

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:最近引入的能够在RPE上进行温度控制的激光辐照的新技术使我们能够研究温度分辨的RPE细胞反应。在这项研究中,我们的主要目的是建立一个实验装置,该装置可以在RPE细胞培养上实现激光照射,并具有与临床应用相似的温度分布,并具有精确的时间/温度历史记录。通过这种设置,我们进行了研究,以阐明温度依赖性RPE细胞的生化反应以及瞬时高温对RPE细胞对二次暴露的氧化应激反应的影响。使用在具有培养基的培养皿(内径= 30mm)中培养的猪RPE细胞,在其上施加超过10s的激光辐射(A = 1940nm,斑点直径= 30mm)作为热源。辐照提供了一个径向降低的温度曲线,该曲线接近于中心温度最高的高斯形状。确定辐照的功率设置,以使单元处激光点中心的峰值温度(T_(max))达到40摄氏度至58摄氏度(40、43、46、50、58摄氏度)。在激光照射后3小时和24小时的时间点用乙二胺均二聚体III染色研究细胞活力。激光照射后二十四小时,将细胞暴露于过氧化氢(H2O2)中5小时,然后测量细胞内谷胱甘肽,细胞内4-羟基壬烯(HNE)蛋白加合物和分泌的血管内皮生长因子(VEGF)。发现3小时后RPE细胞死亡的平均温度阈值约为52摄氏度,在当前照射设置下约为50摄氏度24小时。在T_(max)= 43摄氏度下进行亚致死预处理可显着降低谷胱甘肽(GSH)/氧化谷胱甘肽(GSSG)的比例,并降低H_2O_2诱导的细胞内4-HNE蛋白加合物的增加。尽管亚致死性高热(T_(max)= 40 degC,43 degC和46 degC)导致在照射后6小时内VEGF分泌略有增加,但是次暴露的H_2O_2诱导的VEGF的分泌在亚致命预热的组,在用T_(max)= 43℃辐照后效果最大。总而言之,当前结果表明,在T_(max)= 43℃的RPE上亚致死热激光辐照10 s可以增强细胞防御系统抵抗氧化应激的能力,同时增加GSH / GSSG比。连同在亚致死的预热RPE细胞中H_2O_2诱导的4-HNE的减少伴随着VEGF分泌降低的结果一起,也强烈建议-亚致死高温可以修饰RPE细胞功能以保护RPE细胞由于氧化应激和相关功能降低而被认为在与年龄有关的黄斑变性和其他脉络膜视网膜变性疾病的发病机理中起重要作用。

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