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The Strathprints institutional repository is a digital archive of University of Strathclyde's Open Access research outputs. Strathprints provides access to thousands of Open Access research papers by University of Strathclyde researchers, including by researchers from the Department of Computer & Information Sciences involved in mathematically structured programming, similarity and metric search, computer security, software systems, combinatronics and digital health.

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G-protein-dependent and -independent pathways regulate proteinase-activated receptor-2 mediated p65 nf kappa b serine 536 phosphorylation in human keratinocytes

Goh, F.G. and Sloss, C.M. and Cunningham, M.R. and Nilsson, M. and Cadalbert, Laurence and Plevin, R.J. (2008) G-protein-dependent and -independent pathways regulate proteinase-activated receptor-2 mediated p65 nf kappa b serine 536 phosphorylation in human keratinocytes. Cellular Signalling, 20 (7). pp. 1267-1274. ISSN 1873-3913

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Abstract

The mechanisms underpinning the coupling of GPCRs, such as PAR-2, to the phosphorylation of p65 NFκB have not been investigated. In the current study we found that trypsin and the selective PAR-2 activating peptide, 2f-LIGKV-OH, stimulated large and sustained increases in the serine 536 phosphorylation of p65/RelA in a transfected skin epithelial cell line and primary keratinocytes. Parallel experiments showed that in both cell types, p65 NFκB phosphorylation is mediated through the selective activation of IKK2. Treatment with PKC inhibitor GF109203X or PKCα siRNA reduced phosphorylation at 15 min but not 30 min, whilst rottlerin, a selective PKCδ inhibitor and PKCδ siRNA reduced the response at both time points. Pre-treatment of cells with the novel Gq/11 inhibitor YM-254890 and Gq/11 siRNA caused a similar pattern of inhibition and also reduced PAR-2-mediated NFκB transcriptional activity. Furthermore, stimulation of cells through a novel PAR-2 mutant PAR-234-43, delayed p65 phosphorylation but was without effect on the kinetics of ERK activation. Inhibition of Gi or G12/13 pathways by pertussis toxin pre-treatment or over-expression of the RGS mutant Lsc, also did not effect NFκB phosphorylation. Taken together these data indicate dependency for Gq/11 in early phosphorylation of p65 NFκB and this subsequently affects initial NFκB-dependent gene transcriptional activity, however later regulation of p65 is unaffected. Overall these novel data demonstrate an IKK2-dependent, predominantly G-protein-independent pathway involved in PAR-2 regulation of NFκB phosphorylation in keratinocytes.