Placenta
Volume 30, Supplement , Pages 43-48, March 2009

Placental Endoplasmic Reticulum Stress and Oxidative Stress in the Pathophysiology of Unexplained Intrauterine Growth Restriction and Early Onset Preeclampsia

  • G.J. Burton

      Affiliations

    • Centre for Trophoblast Research, Department of Physiology, Development and Neuroscience, University of Cambridge, UK
    • Corresponding Author InformationCorresponding author. Tel.: +44 1223 333856; fax: +44 1223 333840.
  • ,
  • H.-W. Yung

      Affiliations

    • Centre for Trophoblast Research, Department of Physiology, Development and Neuroscience, University of Cambridge, UK
  • ,
  • T. Cindrova-Davies

      Affiliations

    • Centre for Trophoblast Research, Department of Physiology, Development and Neuroscience, University of Cambridge, UK
  • ,
  • D.S. Charnock-Jones

      Affiliations

    • Department of Obstetrics and Gynaecology, University of Cambridge, UK

Accepted 6 November 2008. published online 11 December 2008.

Abstract 

The pregnancy complications of unexplained intrauterine growth restriction and early onset preeclampsia are thought to share a common aetiology in placental malperfusion secondary to deficient maternal spiral artery conversion. A key question is whether the contrasting clinical manifestations reflect different placental pathologies, or whether they are due to altered maternal responses to a common factor derived from the placenta. Recently, molecular evidence of protein synthesis inhibition secondary to endoplasmic reticulum stress has provided an explanation for the small placental phenotype in both conditions. However, other pathways activated by more severe endoplasmic reticulum stress are only observed in placentas from pregnancies associated with early onset preeclampsia. Here, we review the literature and conclude that there is evidence of greater maternal vascular compromise of the placenta in these cases. We speculate that in cases of normotensive intrauterine growth restriction the placental pathology is centred predominantly around endoplasmic reticulum stress, whereas in cases complicated by preeclampsia oxidative stress is further superimposed. This causes the release of a potent mix of pro-inflammatory cytokines, anti-angiogenic factors and trophoblastic aponecrotic debris into the maternal circulation that causes the peripheral syndrome. Maternal and fetal constitutional factors may modulate how the placenta responds to the maternal vascular insult, and how the mother is affected by the placental factors released. However, the principal conclusion is that the difference between these two conditions lies in the severity of the initiating deficit in spiral arterial conversion, and the relative degrees of endoplasmic reticulum stress and oxidative stress induced in the placenta as a result.

Keywords: Endoplasmic reticulum stress, Oxidative stress, Intrauterine growth restriction, Preeclampsia, Placental pathology

 

PII: S0143-4004(08)00375-5

doi:10.1016/j.placenta.2008.11.003

Placenta
Volume 30, Supplement , Pages 43-48, March 2009