Combined Transcriptomic and Proteomic Analyses Reveal the Different Responses to UVA and UVB Radiation in Human Keratinocytes.
Qinqin ZhaoYueyue ChenLi-Ping QuPublished in: Photochemistry and photobiology (2022)
Ultraviolet (UV) radiation from sunlight is a major risk factor for many cutaneous pathologies including skin aging and cancers. Despite decades of research, the different responses to UVA and UVB in human keratinocytes have not been systemically investigated. Here, we performed multi-omics to characterize the common and different changes in gene transcription and protein expression after exposure to UVB and UVA, respectively. Keratinocyte cells, treated with or without UV, were analyzed by TMT-labeled MS/MS spectra and RNA-sequencing. A common set of genes/proteins was found to be impacted by both UVA and UVB and the other differential genes/proteins showed wavelength specificity. The common set of genes/proteins were mainly involved in keratinization, lipid metabolic processes and stimulus response. The UVB specifically responsive genes/proteins were mainly related to RNA processing, gene silencing regulation and cytoskeleton organization. The UVA specifically responsive genes/proteins were mainly involved in vesicle-mediated transport and oxygen-containing compound response. Meanwhile, the hub differential genes/proteins in each set were identified by protein-protein interaction networks and cluster analysis. This work provided a global view of the similar and differential molecular mechanisms of UVB- and UVA-induced cell damage in keratinocytes, which would be beneficial for further studies in the prevention or treatment of UV-related pathologies.
Keyphrases
- ms ms
- genome wide
- genome wide identification
- single cell
- bioinformatics analysis
- endothelial cells
- protein protein
- genome wide analysis
- stem cells
- dna methylation
- transcription factor
- small molecule
- induced apoptosis
- wound healing
- induced pluripotent stem cells
- computed tomography
- radiation therapy
- cancer therapy
- fatty acid
- soft tissue
- high glucose
- cell proliferation
- radiation induced
- nucleic acid