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首页> 外文期刊>Annals of Dermatology >Epigallocatechin Gallate-Mediated Alteration of the MicroRNA Expression Profile in 5α-Dihydrotestosterone-Treated Human Dermal Papilla Cells
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Epigallocatechin Gallate-Mediated Alteration of the MicroRNA Expression Profile in 5α-Dihydrotestosterone-Treated Human Dermal Papilla Cells

机译:表没食子儿茶素没食子酸酯介导的5α-二氢睾丸酮处理的人真皮乳头细胞中MicroRNA表达谱的改变。

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Background Dihydrotestosterone (DHT) induces androgenic alopecia by shortening the hair follicle growth phase, resulting in hair loss. We previously demonstrated how changes in the microRNA (miRNA) expression profile influenced DHT-mediated cell death, cell cycle arrest, cell viability, the generation of reactive oxygen species (ROS), and senescence. Protective effects against DHT have not, however, been elucidated at the genome level. Objective We showed that epigallocatechin gallate (EGCG), a major component of green tea, protects DHT-induced cell death by regulating the cellular miRNA expression profile. Methods We used a miRNA microarray to identify miRNA expression levels in human dermal papilla cells (DPCs). We investigated whether the miRNA expression influenced the protective effects of EGCG against DHT-induced cell death, growth arrest, intracellular ROS levels, and senescence. Results EGCG protected against the effects of DHT by altering the miRNA expression profile in human DPCs. In addition, EGCG attenuated DHT-mediated cell death and growth arrest and decreased intracellular ROS levels and senescence. A bioinformatics analysis elucidated the relationship between the altered miRNA expression and EGCG-mediated protective effects against DHT. Conclusion Overall, our results suggest that EGCG ameliorates the negative effects of DHT by altering the miRNA expression profile in human DPCs.
机译:背景二氢睾丸激素(DHT)通过缩短毛囊生长期诱导雄激素性脱发,导致脱发。我们先前证明了microRNA(miRNA)表达谱的变化如何影响DHT介导的细胞死亡,细胞周期停滞,细胞生存力,活性氧(ROS)的产生和衰老。然而,尚未在基因组水平上阐明对DHT的保护作用。目的我们证明了表没食子儿茶素没食子酸酯(EGCG)是绿茶的主要成分,它通过调节细胞miRNA表达谱来保护DHT诱导的细胞死亡。方法我们使用miRNA芯片来鉴定人真皮乳头细胞(DPC)中的miRNA表达水平。我们调查了miRNA表达是否影响EGCG对DHT诱导的细胞死亡,生长停滞,细胞内ROS水平和衰老的保护作用。结果EGCG通过改变人DPC中的miRNA表达谱来保护免受DHT的影响。此外,EGCG减弱了DHT介导的细胞死亡和生长停滞,并降低了细胞内ROS水平和衰老。生物信息学分析阐明了改变的miRNA表达与EGCG介导的DHT保护作用之间的关系。结论总体而言,我们的结果表明EGCG可通过改变人DPC中的miRNA表达谱来减轻DHT的负面影响。

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