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Combined Transcriptomic and Proteomic Analyses Reveal the Different Responses to UVA and UVB Radiation in Human Keratinocytes
被引:2
|作者:
Zhao, Qinqin
[1
]
Chen, Yueyue
[1
,2
]
Qu, Liping
[1
,2
,3
]
机构:
[1] Shanghai Jiyan Biopharmaceut Dev Co Ltd, Botanee Res Inst, Characterist Plants Res & Dev Ctr, Shanghai, Peoples R China
[2] Yunnan Yunke Characterist Plant Extract Lab Co Lt, Yunnan Characterist Plant Extract Lab, Kunming, Yunnan, Peoples R China
[3] Yunnan Botanee Biotechnol Grp Co Ltd, Kunming, Yunnan, Peoples R China
关键词:
INDUCED DNA-DAMAGE;
ULTRAVIOLET-LIGHT;
MECHANISMS;
UBIQUITINATION;
FIBROBLASTS;
IRRADIATION;
DEGRADATION;
SENESCENCE;
EXPRESSION;
PROTEIN;
D O I:
10.1111/php.13658
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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.
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页码:137 / 152
页数:16
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