Related Experiment Video
Updated: Mar 13, 2026

Studying Chronic Exposure of Mice to Ultraviolet B Radiation
Published on: August 19, 2025
UVB Exposure Prevents Atherosclerosis by Regulating Immunoinflammatory Responses
Naoto Sasaki1, Tomoya Yamashita2, Kazuyuki Kasahara2
1From the Division of Cardiovascular Medicine, Department of Internal Medicine (N.S., T. Yamashita., K.K., T.E., K.Y., T. Matsumoto, K.N., T.K., M.T., T. Mizoguchi, T.H., Y.S., K.-i.H.) and Division of Dermatology, Department of Internal Related (A.F., M.H., K.T., K.W., C.N.), Kobe University Graduate School of Medicine, Japan; Department of Medical Pharmaceutics, Kobe Pharmaceutical University, Japan (N.S.); Department of Single Molecule Imaging (T. Yamaguchi) and Department of Experimental Immunology (S.S.), World Premier International Immunology Frontier Research Center, Osaka University, Japan; Department of Cell Growth and Differentiation, Center for iPS Cell Research and Application (CiRA), Kyoto University, Japan (M.T.); and Centre d'Immunologie de Marseille-Luminy and the Centre d'Immunophénomique, UM2 Aix-Marseille Université, Marseille, France (B.M.). n-sasaki@kobepharma-u.ac.jp tomoya@med.kobe-u.ac.jp.
Ultraviolet B (UVB) irradiation prevents atherosclerosis development in mice by boosting regulatory T cells. This suggests the skin immune system could be a new target for treating cardiovascular disease.
Area of Science:
- Immunology
- Dermatology
- Cardiovascular Research
Background:
- Ultraviolet B (UVB) irradiation effectively treats inflammatory skin conditions by modulating adaptive immunity.
- Its role in preventing arterial inflammatory diseases like atherosclerosis is not well understood.
Purpose of the Study:
- To investigate whether UVB irradiation can prevent the development and progression of atherosclerosis.
- To explore the underlying immune mechanisms involved in UVB's potential anti-atherosclerotic effects.
Main Methods:
- UVB exposure was administered to atherosclerosis-prone mice.
- Immune cell populations, specifically CD4+ forkhead box P3+ regulatory T cells, were analyzed.
- Studies involved epidermal Langerhans cell-depleted mice to assess their role.
Main Results:
- UVB exposure significantly inhibited atherosclerosis development and progression in mice.
- This was associated with expanded and functionally enhanced CD4+ forkhead box P3+ regulatory T cells.
- Epidermal Langerhans cells were found to be critical for UVB-induced regulatory T cell expansion and atheroprotection.
Conclusions:
- The skin immune system represents a novel therapeutic target for atherosclerosis.
- UVB irradiation offers a potential new strategy for preventing and treating atherosclerosis by modulating skin immunity.
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