Relative contribution of NF-κB and AP-1 in the modulation by curcumin and pyrrolidine dithiocarbamate of the UVB-induced cytokine expression by keratinocytes
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Grandjean-Laquerriere, A
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机构:INSERM, CNRS, Lab Biol Mol FRE 2141, F-51100 Reims, France
Grandjean-Laquerriere, A
Gangloff, SC
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机构:INSERM, CNRS, Lab Biol Mol FRE 2141, F-51100 Reims, France
Gangloff, SC
Le Naour, R
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机构:INSERM, CNRS, Lab Biol Mol FRE 2141, F-51100 Reims, France
Le Naour, R
Trentesaux, C
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机构:INSERM, CNRS, Lab Biol Mol FRE 2141, F-51100 Reims, France
Trentesaux, C
Hornebeck, W
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机构:INSERM, CNRS, Lab Biol Mol FRE 2141, F-51100 Reims, France
Hornebeck, W
Guenounou, M
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机构:INSERM, CNRS, Lab Biol Mol FRE 2141, F-51100 Reims, France
Following ultraviolet B treatment, expression of tumour necrosis factor (TNF)-alpha, interleukin (IL)-6, and IL-8 by NCTC 2544 keratinocyte cell line was significantly enhanced both at the mRNA and protein level. The UVB also increased the IL-10 steady-state mRNAs level. Radiation-induced cytokine overexpression was accompanied by NF-kappaB and AP-1 transcription factors activation as assessed by electrophoretic mobility shift assays. To investigate in keratinocytes the relative contributions of those transcription factors on UVB-mediated cytokine induction, cell cultures were supplemented with curcumin and pyrrolidine dithiocarbamate (PDTC), agents known to modulate NF-kappaB and AP-1 activation. Both compounds significantly inhibited NF-kappaB activation by UVB, but AP-1 activation was unaffected by curcumin while PDTC further stimulated its activation. In parallel, curcumin decreased, in a dose-dependent manner, the UVB-mediated overexpression of all three pro-inflammatory cytokines and only exhibited a moderate enhancing influence on IL-10 expression. In turn, the inhibitory influence of PDTC on radiation-induced TNF-alpha and IL-6 expression is much lower and in contrast to curcumin, it stimulated IL-8.