Abstract
Simple SummaryZebrafish is a good in vivo model to study how skin responds to Ultraviolet B (UVB) irradiation at the cellular, molecular, and whole organism levels. Previous studies showed that zebrafish embryo fin undergoes extensive shrinkage after exposure to UVB irradiation, and this phenotypic change can be assessed using antioxidant drugs. To provide more detailed chronological changes for zebrafish embryos after receiving UVB irradiation, sequential alterations of zebrafish embryos at morphological (fin), cellular (cell death, oxidative stress, immune-response, and marker gene expression) and molecular (microarray screen and real-time RT-PCR assay) levels were examined in this study. The results showed that junbb gene expression was activated as early as 3 h post-UVB irradiation, followed by significant elevation of apoptosis around 9 h post-UVB irradiation, neutrophil migration to the wound area approximately 14 h post-UVB irradiation, and activation of mmp gene expression at around 24 h post-UVB irradiation. These chronological cellular and molecular responses after UVB irradiation in zebrafish provide a basic and fundamental foundation for future line construction and UVB-associated gene validation.Ultraviolet B (UVB) radiation has drawn more attention over these past few decades since it causes severe DNA damage and induces inflammatory response. Serial gene profiling and high throughput data in UVB-associated phenomenon in human cultured cells or full rack of human skin have been investigated. However, results using different tissue models lead to ambiguity in UVB-induced pathways. In order to systematically understand the UVB-associated reactions, the zebrafish model was used, and whole organism gene profiling was performed to identify a novel biomarker which can be used to generate a new mechanistic approach for further screening on a UVB-related system biology. In this study, detailed morphological assays were performed to address biological response after receiving UVB irradiation at morphological, cellular, and molecular levels. Microarray screening and whole genome profiling revealed that there is an early onset expression of junbb in zebrafish embryos after UVB irradiation. Also, the identified novel biomarker junbb is more sensitive to UVB response than mmps which have been used in mouse models. Moreover, cellular and molecular response chronology after UVB irradiation in zebrafish provide a solid and fundamental mechanism for use in a UV radiation-associated study in the future.
Highlights
Ultraviolet radiation, categorized by wavelengths into UVC (200–280 nm), Ultraviolet B (UVB) (280–320 nm), and UVA (320–400 nm), has the ability to ionize molecules and induces a series of chemical reactions [1].Generally, about 95% of the UV light reaching the ground is UVA
Zebrafish 3 dpf embryos were irradiated at different doses of UVB
The results showed that the size of caudal fin was significantly reduced when irradiated with UVB higher than 300 J/m2 (Figure 1C–E and statistically compared to Figure 1F) compared to the control (Figure 1A)
Summary
Ultraviolet radiation, categorized by wavelengths into UVC (200–280 nm), UVB (280–320 nm), and UVA (320–400 nm), has the ability to ionize molecules and induces a series of chemical reactions [1]. About 95% of the UV light reaching the ground is UVA Both UVC and UVB are mostly filtered and absorbed by Earth’s atmosphere, such as the ozone, oxygen, and water, during light transmission. Due to the fact of ozone layer depletion, an increase in exposure of the Earth’s surface to UVB and UVC radiation has been observed [2,3]. Cells produce reactive oxygen species (ROS) after prolonged exposure to UVA which causes DNA damage, unbalances the immune system, and, leads to skin cancer [9].
Sign-in/Register to view highlights & summary 
Published Version (
Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call