IL-6 Negatively Regulates IL-22RExpression on Epidermal Keratinocytes: Implications for Irritant Contact Dermatitis.

Abstract

Irritant Contact Dermatitis (ICD) is characterized by epidermal hyperplasia and inflammatory cytokine release. IL-6 has been shown to be involved in the pathogenesis of ICD; however, the involvement of the IL-22/IL-22Raxis and its relation to IL-6 in the inflammatory response following irritant exposure are unknown. Using a chemical model of ICD, it was observed that mice with a keratinocyte-specific knockout of IL-6R(IL-6R) presented with increased inflammation and IL-22Rand IL-22 protein expression relative to WT following irritant exposure, indicating that IL-6Rdeficiency in epidermal keratinocytes leads to the upregulation of IL-22Rand its ligand during ICD. Furthermore, it was shown that IL-6 negatively regulates the expression of IL-22Ron epidermal keratinocytes. This effect is functional as the effects of IL-22 on keratinocyte proliferation and differentiation were markedly reduced when keratinocytes were pretreated with IL-6 prior to IL-22 treatment. These results show that IL-6 modulates the IL-22/IL-22Raxis in the skin and suggest that this occurrence may be associated with the increased epidermal hyperplasia and exacerbated inflammatory response observed in IL-6Rmice during ICD.