UVB radiation mediates inflammatory responses causing skin damage and defects in epidermal differentiation. 1α,25-Dihydroxyvitamin D3 (
1,25(OH)2D3) interacts with the
vitamin D3 receptor (VDR) to regulate inflammatory responses. Additionally,
1,25(OH)2D3/VDR signaling represents a potential therapeutic target in the treatment of skin disorders associated with
inflammation and poor differentiation of keratinocytes. Since the protective effect of
1,25(OH)2D3 against UVB-induced skin damage and
inflammation is recognized, CYP11A1-derived
vitamin D3-hydroxyderivatives including
20(OH)D3,
1,20(OH)2D3, 20,23(
OH)2D3 and 1,20,23(
OH)3D3 were tested for their anti-inflammatory and skin protection properties in UVB-irradiated human epidermal keratinocytes (HEKn). HEKn were treated with
secosteroids for 24 h pre- and post-UVB (50 mJ/cm2) irradiation.
Secosteroids modulated the expression of the inflammatory response genes (IL-17, NF-κB p65, and IκB-α), reducing nuclear-NF-κB-p65 activity and increasing cytosolic-IκB-α expression as well as that of pro-inflammatory mediators,
IL-17, TNF-α, and IFN-γ. They stimulated the expression of
involucrin (IVL) and
cytokeratin 10 (CK10), the major markers of epidermal differentiation, in UVB-irradiated cells. We conclude that CYP11A1-derived hydroxyderivatives inhibit UVB-induced epidermal inflammatory responses through activation of IκB-α expression and suppression of NF-kB-p65 activity and its downstream signaling
cytokines, TNF-α, and IFN-γ, as well as by inhibiting
IL-17 production and activating epidermal differentiation.