The interaction between protein kinase A and progesterone on basal and inflammation-induced myometrial oxytocin receptor expression.

Angela Yulia,Natasha Singh,Kaiyu Lei,Mark R Johnson,Rachel M Tribe,Alice J Varley,Tamas Zakar

doi:10.1371/journal.pone.0239937

Angela Yulia, Natasha Singh + Show 5 more

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https://doi.org/10.1371/journal.pone.0239937

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Journal: PloS one	Publication Date: Dec 1, 2020
Citations: 2	License type: CC BY 4.0

Affiliation: Chelsea and Westminster Hospital, King's College London

Abstract

Our previous work has shown myometrial PKA activity declines in term and twin-preterm labour in association with an increase in the expression of the oxytocin receptor (OTR). Here we investigate the action of cAMP/PKA in basal conditions, with the addition of progesterone (P4) and/or IL-1β to understand how cAMP/PKA acts to maintain pregnancy and whether the combination of cAMP and P4 would be a viable therapeutic combination for the prevention of preterm labour (PTL). Further, given that we have previously found that cAMP enhances P4 action we wanted to test the hypothesis that changes in the cAMP effector system are responsible for the functional withdrawal of myometrial P4 action. Myometrial cells were grown from biopsies obtained from women at the time of elective Caesarean section before the onset of labour. The addition of forskolin, an adenylyl cyclase activator, repressed basal OTR mRNA levels at all doses and P4 only enhanced this effect at its highest dose. Forskolin repressed the IL-1β-induced increase in OTR mRNA and protein levels in a PKA-dependent fashion and repressed IL-1β-activation and nuclear transfer of NFκB and AP-1. P4 had similar effects and the combination P4 and forskolin had greater effects on OTR and NFκB than forskolin alone. While PKA knockdown had no effect on the ability of P4 to repress IL-1β-induced OTR expression it reversed the repressive effect of the combination of P4 and forskolin and resulted in a greater increase than observed with IL-1β alone. These studies suggest that cAMP acts via PKA to repress inflammation-driven OTR expression, but that when PKA activity is reduced, the combination of cAMP and P4 actually enhances the OTR response to inflammation, promoting the onset of labour and suggesting that changes in the cAMP effector system can induce a functional P4 withdrawal.

Highlights

Preterm labor (PTL) remains the most important cause of childhood mortality [1] and current approaches to its management are relatively ineffective [2]
We found that with the reduction in myometrial PKA activity, myometrial cAMP signals through exchange proteins directly activated by cAMP (Epac1) to increase both oxytocin receptor (OTR) gene expression and protein levels and confirmed that the increase in OTR increased the response to oxytocin [3]
They are all the more important as in the paper paired with this publication we demonstrate that similar changes in the cAMP effector system occur in twin early preterm labor (PTL) (Yulia et al, unpublished observation)

Summary

Introduction

Preterm labor (PTL) remains the most important cause of childhood mortality [1] and current approaches to its management are relatively ineffective [2]. We found that with the reduction in myometrial PKA activity, myometrial cAMP signals through exchange proteins directly activated by cAMP (Epac1) to increase both OTR gene expression and protein levels and confirmed that the increase in OTR increased the response to oxytocin [3] These data are significant, as they present a plausible explanation for the increase in OTR expression and the onset of labour. They are all the more important as in the paper paired with this publication we demonstrate that similar changes in the cAMP effector system occur in twin early PTL (Yulia et al, unpublished observation). Our observations offer the prospect of therapeutic targets upstream of the OTR, the inhibition of which is only moderately effective in arresting PTL once it has started [4]

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