Programmed gene expression change in mouse skin after ultraviolet radiation damage.
Kaibin YangShiting SongYafei ZhangSiting ShenXingzhi XuZhicao YuePublished in: Experimental dermatology (2022)
Ultraviolet (UV) radiation is a major cause of skin damage and carcinogenesis. Here, we systematically analyse the acute gene expression change in skin in vivo after UV exposure, aiming to establish the common C57BL/6 mouse strain as a convenient model for future pathological research and drug discovery. The back fur of C57BL/6 mice was depilated, and a mixed UV light source was used to irradiate the skin. Full-thickness skin samples were collected at 0, 0.5, 2, 6, 12 and 24 h. Total RNAs were extracted and subjected to RNA sequencing analysis. We found that the gene expression change in mouse skin is highly similar to previous reports in human skin. These include down-regulation of differentiation-related genes and extracellular matrix genes, and up-regulation of cytokine/chemokine genes. An early wave of activator protein 1 (AP-1) expression is induced, whereas activation of the p53 pathway is not significant. The impact of the AP-1 transcription factors and the antioxidant tea polyphenols is discussed. The analysis of acute gene expression change in skin after UV irradiation provides a starting point to investigate how the skin responds to genotoxic stress.
Keyphrases
- gene expression
- soft tissue
- wound healing
- dna methylation
- extracellular matrix
- transcription factor
- oxidative stress
- liver failure
- emergency department
- drug induced
- metabolic syndrome
- type diabetes
- genome wide
- single cell
- radiation induced
- binding protein
- optical coherence tomography
- intensive care unit
- endothelial cells
- dna binding