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Protective effect of geranylgeranylacetone against radiation-induced delayed effects on human keratinocytes

机译:香叶基香叶基丙酮对辐射诱导的人类角质形成细胞延迟作用的保护作用

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摘要

Skin exposure to ionizing radiation affects the normal wound healing process. We investigated the beneficial effects of a pharmacological treatment with geranylgeranylacetone (GGA) on keratinocytes using in vitro scratch wound injury assay in nonirradiated and irradiated conditions. Irradiation affected the wound closure of keratinocytes 24 h after scratch injury, whereas re-epithelialization was markedly accelerated after GGA treatment when compared to nontreated keratinocytes. We demonstrated that GGA treatment increased migration of human epidermal keratinocytes and this migratory property was not related to RhoA signaling. Interestingly, Western blot analysis revealed that GGA treatment down-regulated caspase 3 active form expression and up-regulated the activated phenotype by inducing both keratin 6 (K6) expression and interleukin-1β (IL-1β) release without modification of the differentiate phenotype. Finally, the proteomic profiling was performed on keratinocytes, showing that global protein changes occurred after irradiation of keratinocytes treated or untreated with GGA.
机译:皮肤暴露于电离辐射会影响正常的伤口愈合过程。我们在体外和非辐射条件下,采用体外刮擦伤口损伤试验,研究了香叶基香叶基丙酮(GGA)对角质形成细胞的药物治疗的有益作用。划痕损伤后24小时,辐照会影响角质形成细胞的伤口闭合,而与未处理的角质形成细胞相比,GGA处理后再上皮形成明显加快。我们证明了GGA治疗增加了人类表皮角质形成细胞的迁移,而这种迁移特性与RhoA信号传导无关。有趣的是,蛋白质印迹分析显示,GGA处理通过诱导角蛋白6(K6)表达和白介素1β(IL-1β)释放而下调了caspase 3活性形式的表达,并上调了激活的表型,而没有改变分化表型。最后,对角质形成细胞进行了蛋白质组学分析,表明在用GGA处理或未处理的角质形成细胞照射后,总蛋白质发生了变化。

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