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Upregulated epidermal growth factor receptor expression following near-infrared irradiation simulating solar radiation in a three-dimensional reconstructed human corneal epithelial tissue culture model

机译:在三维重建的人类角膜上皮组织培养模型中,模拟太阳辐射的近红外辐射后表皮生长因子受体表达上调

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Background and objective: Humans are increasingly exposed to near-infrared (NIR) radiation from both natural (eg, solar) and artificial (eg, electrical appliances) sources. Although the biological effects of sun and ultraviolet (UV) exposure have been extensively investigated, the biological effect of NIR radiation is still unclear. We previously reported that NIR as well as UV induces photoaging and standard UV-blocking materials, such as sunglasses, do not sufficiently block NIR. The objective of this study was to investigate changes in gene expression in three-dimensional reconstructed corneal epithelial tissue culture exposed to broad-spectrum NIR irradiation to simulate solar NIR radiation that reaches human tissues. Materials and methods: DNA microarray and quantitative real-time polymerase chain reaction analysis were used to assess gene expression levels in a three-dimensional reconstructed corneal epithelial model composed of normal human corneal epithelial cells exposed to water-filtered broad-spectrum NIR irradiation with a contact cooling (20°C). The water-filter allowed 1,000–1,800?nm wavelengths and excluded 1,400–1,500?nm wavelengths. Results: A DNA microarray with >62,000 different probes showed 25 and 150 genes that were up- or downregulated by at least fourfold and twofold, respectively, after NIR irradiation. In particular, epidermal growth factor receptor (EGFR) was upregulated by 19.4-fold relative to control cells. Quantitative real-time polymerase chain reaction analysis revealed that two variants of EGFR in human corneal epithelial tissue were also significantly upregulated after five rounds of 10?J/cm2 irradiation ( P <0.05). Conclusion: We found that NIR irradiation induced the upregulated expression of EGFR in human corneal cells. Since over half of the solar energy reaching the Earth is in the NIR region, which cannot be adequately blocked by eyewear and thus can induce eye damage with intensive or long-term exposure, protection from both UV and NIR radiation may prevent changes in gene expression and in turn eye damage.
机译:背景和目的:人类越来越多地暴露于来自自然(例如太阳能)和人工(例如电器)源的近红外(NIR)辐射。尽管已经广泛研究了暴露于阳光和紫外线(UV)的生物学效应,但NIR辐射的生物学效应仍不清楚。我们以前曾报道过NIR和紫外线会引起光老化,而标准的紫外线阻隔材料(例如太阳镜)并不能充分阻隔NIR。这项研究的目的是调查暴露于广谱NIR辐射下的三维重建角膜上皮组织培养物中基因表达的变化,以模拟到达人体组织的太阳NIR辐射。材料和方法:DNA微阵列和定量实时聚合酶链反应分析被用于评估三维重建的角膜上皮模型中的基因表达水平,该模型由暴露于水过滤的广谱NIR照射下的正常人角膜上皮细胞组成。接触冷却(20°C)。滤水器允许使用1,000–1,800?nm波长,而排除1,400–1,500?nm波长。结果:具有> 62,000种不同探针的DNA微阵列显示出25个和150个基因在近红外照射后分别被上调或下调了至少四倍和两倍。特别地,表皮生长因子受体(EGFR)相对于对照细胞被上调了19.4倍。实时定量聚合酶链反应分析表明,在五轮10?J / cm 2 照射后,人角膜上皮组织中的两个EGFR变体也显着上调(P <0.05)。结论:我们发现,近红外辐射可诱导人角膜细胞中EGFR的表达上调。由于到达地球的太阳能有一半以上位于近红外区域,因此不能被眼镜充分遮挡,因此长时间或长期暴露在眼内会导致眼睛受损,因此,抵御紫外线和近红外辐射可能会阻止基因表达的变化进而损害眼睛。

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