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香叶基丙酮对人角质形成细胞辐射延迟效应的防护作用。

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

机构信息

IRSN, Institut de Radioprotection et de Sureté Nucléaire, Laboratoire de Radio Pathologie et de Thérapie Expérimentale, BP 17, 92262 Fontenay-aux-Roses Cedex, France.

出版信息

Radiat Res. 2013 Feb;179(2):232-42. doi: 10.1667/RR2717.1. Epub 2013 Jan 4.

Abstract

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.

摘要

皮肤暴露于电离辐射会影响正常的伤口愈合过程。我们使用非照射和照射条件下的体外划痕伤口损伤测定法,研究了香叶基丙酮(GGA)对角质形成细胞的药理治疗的有益作用。照射会影响划痕损伤后 24 小时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,用 GGA 处理后再上皮化明显加快。我们证明 GGA 处理增加了人表皮角质形成细胞的迁移,并且这种迁移特性与 RhoA 信号无关。有趣的是,Western blot 分析表明,GGA 处理通过诱导角蛋白 6(K6)表达和白细胞介素 1β(IL-1β)释放而下调 caspase 3 活性形式的表达,并上调激活表型,而不改变分化表型。最后,对角质形成细胞进行蛋白质组学分析,结果表明,用或不用 GGA 处理的照射角质形成细胞后会发生整体蛋白质变化。

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