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PKC is a target of 7,8,4-trihydroxyisoflavone for the suppression of UVB-induced MMP-1 expression

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Baek,  Sohee
Huber, Robert / Structure Research, Max Planck Institute of Biochemistry, Max Planck Society;

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Citation

Lim, T.-G., Kim, Y.-A., Kim, J.-E., Baek, S., Lee, S.-Y., Lee, C. C., et al. (2018). PKC is a target of 7,8,4-trihydroxyisoflavone for the suppression of UVB-induced MMP-1 expression. Experimental Dermatology: an International Journal for Rapid Publication of Short Reports in Experimental Dermatology, 27(5), 449-452. doi:10.1111/exd.13375.


Cite as: https://hdl.handle.net/21.11116/0000-0003-E6D7-7
Abstract
The soy isoflavone daidzein is bioconverted to 7,8,4-trihydroxyisoflavone (7,8,4-THIF) by microorganisms. Here, we investigated the matrix metalloproteinase (MMP)-1 inhibitory properties of 7,8,4-THIF that arise through the suppression of UVB-induced MMP-1 expression. 7,8,4-THIF reduced UVB-induced MMP-1 expression at the transcriptional level in primary human dermal fibroblasts and inhibited UVB-induced transcriptional activity of AP-1, a major activator of MMP-1 expression. Additionally, it was observed that the mitogen-activated protein kinase (MAPK) pathway, a crucial signalling cascade for MMP-1 expression, was suppressed by 7,8,4-THIF. Protein kinase C iota (PKC) was suspected to be a direct target of 7,8,4-THIF. The direct interaction between 7,8,4-THIF and PKC was confirmed using pull-down assays and immobilized metal ion affinity-based fluorescence polarization assays. Finally, we observed that 7,8,4-THIF inhibited UVB-induced MMP-1 expression in a human skin equivalent model. Taken together, these results suggest that 7,8,4-THIF, a bioconversion product of daidzein, suppresses UVB-induced MMP-1 expression.