首页> 外文期刊>The Journal of investigative dermatology. >Evidence that ferritin is UV inducible in human skin: part of a putative defense mechanism.
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Evidence that ferritin is UV inducible in human skin: part of a putative defense mechanism.

机译:铁蛋白在人体皮肤中可被紫外线诱导的证据:推测的防御机制的一部分。

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摘要

As ferritin has been identified as an important factor in antioxidant defense in cultured human skin cells we evaluated the presence of ferritin in human skin in vivo and the modifications following irradiation with UVA I, UVA I + II, and solar simulating light by immunohistochemical analysis. We report that the putative protective protein ferritin is regularly present in the basal layer of unirradiated epidermis in vivo and that the induction of ferritin was dependent on wavelength and cell type. Following UVA I radiation, ferritin increased both in epidermal and in dermal tissue. The same response occurred, although to a lesser extent, with UVA I + II but did not occur following solar simulating radiation. Quantitative analysis for ferritin in cultured keratinocytes and fibroblasts from seven individuals following each UV spectra were also assessed by enzyme-linked immunosorbent assay. The induction of ferritin by UV was highly dependent on the waveband and cell type. UVA I and UVA I + II radiations induced ferritin expression in dermal fibroblasts up to 260% and 200% over basal levels, respectively. Solar simulating radiation produced only a small induction of approximately 130% over basal ferritin levels in dermal fibroblasts. Ferritin increased in cultured fibroblasts as early as 3 h post-UVA with a peak at 6 h that remained until 48 h; there was no observable qualitative or quantitative increase seen in the undifferentiated cultured epidermal keratinocytes. Our findings indicate that the putative defense system of ferritin exists in human skin in vivo and its induction is dependent on UV spectra and cell type. The increased concentrations of this antioxidant in human skin following acute UV radiation could afford increased protection against subsequent oxidative stress.
机译:由于铁蛋白已被确定为培养的人类皮肤细胞中抗氧化防御的重要因素,我们通过免疫组化分析评估了体内人类皮肤中铁蛋白的存在以及经UVA I,UVA I + II和太阳模拟光照射后的修饰。我们报告说,推定的保护性蛋白铁蛋白经常存在于体内未辐照表皮的基底层中,并且铁蛋白的诱导取决于波长和细胞类型。 UVA I辐射后,铁蛋白在表皮和真皮组织中均增加。 UVA I + II发生了相同的反应,尽管程度较小,但在太阳模拟辐射后并未发生。还通过酶联免疫吸附测定法评估了每个紫外光谱后来自七个个体的培养的角质形成细胞和成纤维细胞中铁蛋白的定量分析。紫外线对铁蛋白的诱导高度依赖于波段和细胞类型。 UVA I和UVA I + II辐射分别导致真皮成纤维细胞中铁蛋白的表达超过基础水平的260%和200%。太阳模拟辐射仅比真皮成纤维细胞的基础铁蛋白水平产生了约130%的少量诱导。最早在UVA后3 h,培养的成纤维细胞中铁蛋白增加,在6 h达到峰值,一直持续到48 h。在未分化培养的表皮角质形成细胞中没有观察到定性或定量的增加。我们的发现表明,铁蛋白的假定防御系统存在于人体皮肤的体内,其诱导取决于紫外线光谱和细胞类型。急性紫外线辐射后,人体皮肤中这种抗氧化剂的浓度增加,可以增强抵抗后续氧化应激的能力。

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