Dipartimento di Scienze della Vita e dell'Ambiente, Università Politecnica delle Marche, Ancona, Italy.
Dipartimento di Scienze Cliniche, Specialistiche ed Odontostomatologiche, Università Politecnica delle Marche, Ancona, Italy.
Oxid Med Cell Longev. 2018 Sep 23;2018:5469159. doi: 10.1155/2018/5469159. eCollection 2018.
Reactive oxygen species (ROS) production in the skin is among the highest compared to other organs, and a clear correlation exists between ROS production and skin aging. Many attempts are underway to reduce oxidative stress in the skin by topical treatment or supplementation with antioxidants/cosmeceuticals, and cultures of human dermal fibroblasts (HDF) are widely used for these studies. Here, we examined the influence of oxygen tension on cell aging in HDF and how this impacted ROS production, the enzymatic and nonenzymatic antioxidant response system, and the efficacy of this defense system in limiting DNA damage and in modulating gene expression of proteins involved in the extracellular matrix, linked to skin aging. We investigated a selection of parameters that represent and reflect the behavior of cellular responses to aging and oxygen tension. Serial passaging of HDF under normoxia (21%) and hypoxia (5%) leads to cell aging as confirmed by -galactosidase activity, p16 expression, and proliferation rate. However, in HDF under 21% O, markers of aging were significantly increased compared to those under 5% O at matched cell passages despite having lower levels of intracellular ROS and higher levels of CoQ, total GSH, SOD1, SOD3, and mitochondrial superoxide anion. miRNA-181a, which is known to be upregulated in HDF senescence, was also analyzed, and indeed, its expression was significantly increased in old cells at 21% O compared to those at 5% O. Upregulation of MMP1 and downregulation of COL1A1 along with increased DNA damage were also observed under 21% O vs 5% O. The data highlight that chronic exposure to atmospheric 21% O is able to trigger hormetic adaptive responses in HDF that however fail, in the long term, to prevent cellular aging. This information could be useful in further investigating molecular mechanisms involved in adaptation of skin fibroblasts to oxidative stress and may provide useful hints in addressing antiaging strategies.
皮肤中的活性氧(ROS)产生量与其他器官相比是最高的,ROS 产生与皮肤衰老之间存在明显的相关性。人们正在尝试通过局部治疗或补充抗氧化剂/化妆品来减少皮肤中的氧化应激,并且广泛使用人真皮成纤维细胞(HDF)培养物进行这些研究。在这里,我们研究了氧张力对 HDF 细胞衰老的影响,以及这如何影响 ROS 产生、酶和非酶抗氧化反应系统,以及该防御系统在限制 DNA 损伤和调节与皮肤衰老相关的细胞外基质蛋白表达中的功效。我们研究了一系列代表和反映细胞对衰老和氧张力反应的参数。在常氧(21%)和低氧(5%)下对 HDF 进行连续传代导致细胞衰老,这通过β-半乳糖苷酶活性、p16 表达和增殖率得到证实。然而,在 21%O 下的 HDF 中,与在 5%O 下的 HDF 相比,尽管细胞内 ROS 水平较低,CoQ、总 GSH、SOD1、SOD3 和线粒体超氧阴离子水平较高,但衰老标志物明显增加。还分析了已知在 HDF 衰老中上调的 miRNA-181a,事实上,与在 5%O 下相比,在 21%O 下的衰老细胞中其表达显著增加。与 5%O 相比,在 21%O 下还观察到 MMP1 的上调和 COL1A1 的下调以及 DNA 损伤增加。数据表明,长期暴露于大气 21%O 能够在 HDF 中引发 hormetic 适应性反应,但长期来看,这些反应无法防止细胞衰老。这些信息对于进一步研究皮肤成纤维细胞对氧化应激的适应的分子机制可能是有用的,并为解决抗衰老策略提供有用的线索。