Article ID Journal Published Year Pages File Type
2198000 Molecular and Cellular Endocrinology 2007 5 Pages PDF
Abstract

Using pharmaceutical and overexpression approaches we have previously reported that in H295R cells, (a) angiotensin II (AII) activates PKCɛ, PKCα and p44/42 MAPK pathway, (b) PKCɛ, PKCα and p44/42 MAPK overexpression inhibits AII-induced CYP11B2 gene transcription and (c) overexpression of PKCɛ inhibits CYP11B2 gene transcription through p44/42 MAPK activation [LeHoux, J.G., Dupuis, G., Lefebvre, A., 2001. Control of CYP11B2 gene expression through differential regulation of its promoter by atypical and conventional protein kinase C isoforms. J. Biol. Chem. 276 (11), 8021–8028; LeHoux, J.G., Lefebvre, A., 2006. Novel protein kinase C-epsilon inhibits human CYP11B2 gene expression through ERK1/2 signalling pathway and JunB. J. Mol. Endocrinol. 36 (1), 51–64]. The aim of the present work was to evaluate the physiological role of endogenous PKCɛ and PKCα isoforms in the activation of p44/42 MAPK by AII. A 50% reduction of PKCɛ protein by siRNA-PKCɛ resulted in 35% inhibition of AII-induced p44/42 MAPK activation. Knockdown of PKCɛ stimulated AII-induced CYP11B2 transcription indicating that the PKCɛ is not involved in the activation of CYP11B2 gene expression by AII. Furthermore, knockdown of PKCα enhanced AII-stimulated CYP11B2 transcription without altering p44/42 MAPK indicating that inhibition of AII-stimulated CYP11B2 gene by PKCα does not involve the p44/42 MAPK signalling pathway. These results thus establish that physiologically, PKCɛ and PKCα act through different signalling pathways to inhibit AII-stimulated CYP11B2 gene expression.

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