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Updated: Feb 16, 2026

Parallel Measurement of Circadian Clock Gene Expression and Hormone Secretion in Human Primary Cell Cultures
Published on: November 11, 2016
UVA1 exposures change gene expression and circadian time-related protein CRY2 in human skin
Annina Haapasalo1, Olivia Liong2, Juha Jernman3
1Department of Dermatology, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland; Department of Allergology and Dermatology, Tampere University Hospital, Tampere, Finland.
Background:
The molecular effects involved in the cellular response to ultraviolet A1 (UVA1) exposures in human skin are incompletely understood.
Objectives:
We examined the molecular mechanisms underlying the physiological effects of low-dose UVA1 exposures in human skin in vivo by observing especially the contribution of diurnal preference and circadian clock-related genes and proteins.
Methods:
Healthy volunteers (n = 21) were exposed to a cumulative dose of 30 J/cm2 of UVA1 (340-400 nm) or 0.42 J/cm2 of violet light (390-440 nm, n = 20). Immunohistochemistry, transcriptomics, real-time quantitative PCR (RT-qPCR), gene enrichment analyses, and cellular deconvolution were performed from buttock skin samples at the start and after three days of consecutive morning exposures.
Results:
UVA1 exposures significantly increased CRY2 and P53 protein staining in the IHC and yielded 16 differentially expressed genes (DEGs) involved in melanogenesis (Pmel, Tyr, Tyrp1), cytotoxic protection (Aldh3a2/a1, Cdk7, Nampt, Bcl2a1, Ackr4, Rpa3, Ube2q2) and circadian rhythm (Csnk1e, Nampt) in the skin compared to unexposed skin samples. RT-qPCR was performed for Aldh3a1, Aldh3a2, Tyr, Tyrp1 and Nampt to strengthen the transcriptomic results. No DEGs were found when exploring the underlying adipose tissue or the violet light-exposed group. In cellular deconvolution analysis, the fraction of eosinophils and M0 macrophages was increased after UVA1 exposures, with M0 macrophages especially among morning-types.
Conclusion:
Low-dose UVA1 exposures caused changes in gene expression, P53 and CRY2 protein production, and cell type fractions in the skin, but the effects did not reach the subcutaneous adipose tissue. Since the solar UVR dominates in UVA, it is essential to continue to protect the skin from harmful solar agents, regardless of the diurnal preference.
Insights
Low-dose ultraviolet A1 (UVA1) exposure alters skin gene expression and protein levels, including circadian clock genes, but does not affect deeper tissues. Continued skin protection from solar UVR is essential.
Area of Science:
- Dermatology
- Molecular Biology
- Chronobiology
Background:
- The molecular mechanisms of skin response to ultraviolet A1 (UVA1) are not fully understood.
- Investigating the role of circadian clock genes in UVA1-induced skin changes is crucial.
Purpose of the Study:
- To investigate the molecular mechanisms of low-dose UVA1 exposure on human skin.
- To assess the contribution of diurnal preference and circadian clock genes to UVA1 effects.
Main Methods:
- Healthy volunteers received UVA1 or violet light exposure.
- Skin biopsies were analyzed using immunohistochemistry, transcriptomics, and RT-qPCR.
- Gene enrichment and cellular deconvolution analyses were performed.
Main Results:
- UVA1 exposure increased CRY2 and P53 protein levels.
- 16 differentially expressed genes related to melanogenesis, cytotoxic protection, and circadian rhythm were identified.
- UVA1 increased eosinophils and M0 macrophages, particularly in morning-type individuals.
Conclusions:
- Low-dose UVA1 impacts skin gene expression, protein production, and cell fractions.
- Effects of UVA1 exposure were limited to the skin and did not reach subcutaneous adipose tissue.
- Protection against solar UVR remains vital regardless of diurnal preference.
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