Near-infrared radiation causes sebaceous gland enlargement along with an ROS-dependent augmentation of epidermal growth factor receptor expression in hamsters.
Shiho TanakaHiroaki SakaueToshikazu KoiwaiNatsuki OkudaKatsuki OkuyamaYoshihiko HoriokaYasunari HiramatsuMakoto KawashimaNaoko IshiguroTakashi SatoPublished in: Experimental dermatology (2023)
As near-infrared radiation (NIR), which is a composition of sunlight with an 780-1400 nm wavelength, is associated with skin aging such as wrinkles and slacks, the biological actions of NIR with high dermal penetration remains unclear. In the present study, we found that NIR irradiation (40 J/cm 2 ) at different levels of irradiance (95-190 mW/cm 2 ) using a laboratory device with a xenon flash lamp (780-1700 nm) caused sebaceous gland enlargement concomitantly with skin thickening in the auricle skin of hamsters. The sebaceous gland enlargement resulted from the proliferation of sebocytes due to an increase in the number of proliferating cell nuclear antigen (PCNA)- and lamin B1-positive cells in vivo. In addition, NIR irradiation transcriptionally augmented the production of epidermal growth factor receptor (EGFR) accompanied with an increase in the reactive oxygen species (ROS) level in hamster sebocytes in vitro. Furthermore, the administration of hydrogen peroxide increased the level of EGFR mRNA in the sebocytes. Therefore, these results provide novel evidence that NIR irradiation causes the hyperplasia of sebaceous glands in hamsters by mechanisms in which EGFR production is transcriptionally augmented through ROS-dependent pathways in sebocytes.
Keyphrases
- epidermal growth factor receptor
- photodynamic therapy
- reactive oxygen species
- tyrosine kinase
- growth factor
- hydrogen peroxide
- drug release
- wound healing
- fluorescence imaging
- advanced non small cell lung cancer
- fluorescent probe
- soft tissue
- small cell lung cancer
- cell death
- dna damage
- radiation induced
- nitric oxide
- cell cycle arrest
- induced apoptosis
- single cell
- cell therapy
- stem cells
- cell proliferation
- mesenchymal stem cells
- loop mediated isothermal amplification