Wu Zhuoxia, Zhang Lianbo
Department of Plastic and Reconstructive Surgery, China-Japan Union Hospital of Jilin University, Changchun, Jilin 130033, P.R. China.
Exp Ther Med. 2017 Sep;14(3):2554-2562. doi: 10.3892/etm.2017.4807. Epub 2017 Jul 19.
Epigenetic repressor polycomb group (PcG) proteins are thought to serve a role in a number of cellular processes, including carcinogenesis, senescence, apoptosis and DNA repair. In the present study, long-wave ultraviolet A (UVA) was used to irradiate human skin fibroblasts (HSFs) and embryonic skin fibroblasts (ESFs) in order to simulate photoaging of the skin. The results of cell proliferation, apoptosis, hyaluronic acid (HA) content and reverse transcription-quantitative polymerase chain reaction assays revealed that the expression levels of genes encoding key PcG proteins ( and ) were altered. In addition, the expression levels of these genes were associated with the expression of enzymes that regulate HA synthesis. Furthermore, the expression levels of PcG proteins differed between HSFs and ESFs, suggesting that PcG proteins serve a role in altering HA synthesis during the UVA-induced fibroblast aging process. This signaling pathway may represent a novel molecular mechanism regulating the photoaging of the skin. The findings of the present study provide important insights into the underlying mechanisms of photoaging of the human skin. Further studies are required to clarify the molecular mechanisms underling skin aging and to identify targets for the clinical treatment of photoaging.
表观遗传抑制性多梳蛋白家族(PcG)被认为在包括致癌作用、衰老、细胞凋亡和DNA修复在内的许多细胞过程中发挥作用。在本研究中,使用长波紫外线A(UVA)照射人皮肤成纤维细胞(HSF)和胚胎皮肤成纤维细胞(ESF),以模拟皮肤的光老化。细胞增殖、凋亡、透明质酸(HA)含量及逆转录-定量聚合酶链反应分析结果显示,编码关键PcG蛋白(和)的基因表达水平发生了改变。此外,这些基因的表达水平与调节HA合成的酶的表达相关。此外,HSF和ESF中PcG蛋白的表达水平不同,这表明PcG蛋白在UVA诱导的成纤维细胞衰老过程中在改变HA合成方面发挥作用。该信号通路可能代表一种调节皮肤光老化的新分子机制。本研究结果为人类皮肤光老化的潜在机制提供了重要见解。需要进一步研究以阐明皮肤衰老的分子机制,并确定光老化临床治疗的靶点。