Prokineticin 1 modulates IL-8 expression via the calcineurin/NFAT signaling pathway

Prokineticins and their receptors are expressed in various cellular compartments in human endometrium, with prokineticin 1 (PROK1) showing a dynamic pattern of expression across the menstrual cycle and during pregnancy. Previous studies suggest that PROK1 can play an important role in implantation a...

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Published inBiochimica et biophysica acta Vol. 1793; no. 7; pp. 1315 - 1324
Main Authors Maldonado-Pérez, David, Brown, Pamela, Morgan, Kevin, Millar, Robert P., Thompson, E. Aubrey, Jabbour, Henry N.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.07.2009
Elsevier Pub. Co
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Summary:Prokineticins and their receptors are expressed in various cellular compartments in human endometrium, with prokineticin 1 (PROK1) showing a dynamic pattern of expression across the menstrual cycle and during pregnancy. Previous studies suggest that PROK1 can play an important role in implantation and early pregnancy by inducing vascular remodeling and increasing vascular permeability. Here we demonstrate that PROK1 induces the expression of IL-8, a chemokine with angiogenic properties, in endometrial epithelial Ishikawa cells stably expressing prokineticin receptor 1 and in human first trimester decidua. We also show that IL-8 promoter activity is induced by PROK1 and that this requires the presence of AP1 and NFAT motifs. The role of calcineurin/NFAT signaling pathway is confirmed by the use of specific chemical inhibitors. Additionally, PROK1 induces the expression of the regulator of calcineurin 1 isoform 4 (RCAN1-4) via the calcineurin/NFAT pathway. A modulatory role for RCAN1-4 is demonstrated by RCAN1-4 overexpression which results in the inhibition of PROK1-induced IL-8 expression whereas reduction in RCAN1-4 endogenous expression results in an increase in PROK1-induced IL-8 production. Our findings show that in endometrial cells PROK1 can activate the calcineurin/NFAT pathway to induce IL-8 expression and that this is negatively modulated by the induction of expression of RCAN1-4.
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Current address: Department of Reproductive and Developmental Sciences, University of Edinburgh, Edinburgh EH16 4TJ, UK.
ISSN:0167-4889
0006-3002
1879-2596
1878-2434
DOI:10.1016/j.bbamcr.2009.03.008