IL-1 receptor antagonist attenuates MAP kinase/AP-1 activation and MMP1 expression in UVA-irradiated human fibroblasts induced by culture medium from UVB-irradiated human skin keratinocytes
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作者:
Wang, XY
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机构:Nanjing Med Univ, Affiliated Hosp, Dept Dermatol, Nanjing 210029, Peoples R China
Wang, XY
Bi, ZG
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机构:Nanjing Med Univ, Affiliated Hosp, Dept Dermatol, Nanjing 210029, Peoples R China
Bi, ZG
Chu, WM
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机构:Nanjing Med Univ, Affiliated Hosp, Dept Dermatol, Nanjing 210029, Peoples R China
Chu, WM
Wan, YS
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Nanjing Med Univ, Affiliated Hosp, Dept Dermatol, Nanjing 210029, Peoples R ChinaNanjing Med Univ, Affiliated Hosp, Dept Dermatol, Nanjing 210029, Peoples R China
Wan, YS
[1
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机构:
[1] Nanjing Med Univ, Affiliated Hosp, Dept Dermatol, Nanjing 210029, Peoples R China
[2] Brown Univ, Dept Mol Microbiol & Immunol, Providence, RI 02912 USA
[3] Providence Coll, Dept Biol, Providence, RI 02918 USA
Solar UV light comprises UVB wavelengths (290-320 nm) and UVA wavelengths (320-400 nm). UVB radiation reaches the epidermis and, to a lesser extent, the upper part of the dermis, while UVA radiation penetrates more deeply into human skin. Existing studies have demonstrated that UV-irradiated epidermal keratinocytes release cytokines that indirectly promote MMP-1 production in dermal fibroblasts. In this study, we first investigated the effect of IL-1 on MAPK activity, c-Jun and c-Fos mRNA expression, and MMP-1 and MMP-2 production in UVA-irradiated human dermal fibroblasts. The results showed that UVA irradiation dose-dependently increased MMP-1 but not MMP-2 production in human skin fibroblasts. IL-1 alpha and IL-1 beta promoted MMP-1 but not MMP-2 production in UVA-irradiated fibroblasts. Both IL-1 alpha and IL-1 beta activated MAP kinase, significantly elevating c-Jun and c-Fos mRNA expression. We then investigated the indirect effect of UVB-irradiated keratinocyte culture medium on MMP-1 production in UVA-irradiated primary cultured human dermal fibroblasts and the effect of IL-1R alpha. The results showed that cell culture medium from UVB-irradiated keratinocytes increased MMP-1 production in UVA-irradiated fibroblasts, and IL-1R alpha dose-dependently inhibited MMP-1 production. IL-1R alpha dose-dependently inhibited c-Jun mRNA expression of fibroblasts with no significant effect on c-Fos mRNA expression. These results demonstrate that UVB-irradiated keratinocytes promoted MMP-1 production in UVA-irradiated fibroblasts in a paracrine manner while IL-1R alpha reduced MMP-1 production through inhibiting c-Jun mRNA expression. Collectively, our data suggest that IL-1 plays an important role in the dermal collagen degradation associated with UV-induced premature aging of the skin and IL-1Ra may be applied for the prevention and treatment of photoaging.