Interleukin (IL)-1 family comprise 11 members that plays an important role in immune regulation and inflammatory process. Retinoids exert complex effects on the immune system, having anti-inflammatory effects in chronic dermatological diseases. Vitamin D (vitD) and analogs have been shown to suppress TNF-?-induced IL-1? in human keratinocytes (KCs). In the present study we investigated IL-1 family members in psoriasis and the effects of vitD and retinoic acid (RA) on these members. We analyzed IL-1 family members gene expression in psoriatic skin and in ex vivo skin organ culture exposed to TNF-?, IL-17 or broadband UVB; afterwards treatment with vitD or RA was performed and IL-1 family members mRNA was evaluated. Similarly, KCs were stimulated with IL-17 and subsequently treated with vitD. IL-1 family members were enhanced in psoriatic skin and in ex vivo skin organ cultures after pro-inflammatory stimuli (TNF-?, IL-17 and UVB). RA and vitD were able to suppress this enhancement.

Interleukin-1 family members are enhanced in psoriasis and suppressed by vitamin D and retinoic acid

2013

Abstract

Interleukin (IL)-1 family comprise 11 members that plays an important role in immune regulation and inflammatory process. Retinoids exert complex effects on the immune system, having anti-inflammatory effects in chronic dermatological diseases. Vitamin D (vitD) and analogs have been shown to suppress TNF-?-induced IL-1? in human keratinocytes (KCs). In the present study we investigated IL-1 family members in psoriasis and the effects of vitD and retinoic acid (RA) on these members. We analyzed IL-1 family members gene expression in psoriatic skin and in ex vivo skin organ culture exposed to TNF-?, IL-17 or broadband UVB; afterwards treatment with vitD or RA was performed and IL-1 family members mRNA was evaluated. Similarly, KCs were stimulated with IL-17 and subsequently treated with vitD. IL-1 family members were enhanced in psoriatic skin and in ex vivo skin organ cultures after pro-inflammatory stimuli (TNF-?, IL-17 and UVB). RA and vitD were able to suppress this enhancement.
2013
it
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14242/333790
Il codice NBN di questa tesi è URN:NBN:IT:BNCF-333790