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Home › Dataset Library › Severe Preeclampsia-Related Changes in Gene Expression at the Maternal-Fetal Interface Include Siglec-6 and Pappalysin-2

Dataset: Severe Preeclampsia-Related Changes in Gene Expression at the Maternal-Fetal Interface Include Siglec-6 and Pappalysin-2

Preeclampsia (PE), which affects 4-8% of human pregnancies, causes significant maternal and neonatal morbidity and mortality. Within the...

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Preeclampsia (PE), which affects 4-8% of human pregnancies, causes significant maternal and neonatal morbidity and mortality. Within the basal plate, placental cytotrophoblasts (CTBs) of fetal origin invade the uterus and extensively remodel the maternal vasculature. In PE, CTB invasion is often shallow, and vascular remodeling is rudimentary. To better understand possible causes, we conducted a global analysis of gene expression at the maternal-fetal interface in placental samples from women with PE (n = 12; 24-36 wk) vs. samples from women who delivered due to preterm labor with no evidence of infection (n = 11; 24-36 wk), a condition that our previous work showed is associated with normal CTB invasion. Using the HG-U133A&B Affymetrix GeneChip platform, and statistical significance set at log odds-ratio of B >0, 55 genes were differentially expressed in PE. They encoded proteins previously associated with PE [e.g. Flt-1 (vascular endothelial growth factor receptor-1), leptin, CRH, and inhibin] and novel molecules [e.g. sialic acid binding Ig-like lectin 6 (Siglec-6), a potential leptin receptor, and pappalysin-2 (PAPP-A2), a protease that cleaves IGF-binding proteins]. We used quantitative PCR to validate the expression patterns of a subset of the genes. At the protein level, we confirmed PE-related changes in the expression of Siglec-6 and PAPP-A2, which localized to invasive CTBs and syncytiotrophoblasts. Notably, Siglec-6 placental expression is uniquely human, as is spontaneous PE. The functional significance of these novel observations may provide new insights into the pathogenesis of PE, and assaying the circulating levels of these proteins could have clinical utility for predicting and/or diagnosing PE. Keywords: disease state analysis Basal plate biopsies of preterm labor (24-36 weeks; n=11) and preterm severe preeclampsia (24-36 weeeks; n=12) were isolated and the global gene expression profiles determined using Affymetrix Human GeneChips. Comparisons between the preeclampsia samples and the preterm labor controls revealed genes differentially expressed in preeclampsia.

Species:
human

Samples:
23

Source:
E-GEOD-14722

PubMed:
18818296

Updated:
Jan.17, 2015

Registered:
Jan.17, 2015


Factors: (via ArrayExpress)
Sample CONDITION
GSM367781 1 24.7wk preterm
GSM367782 1 25.4wk preterm
GSM367783 1 25.6wk preterm
GSM367784 1 27.1wk preterm
GSM367785 1 29.9wk preterm
GSM367786 1 33.0wk preterm
GSM367787 1 33.3wk preterm
GSM367788 1 33.9wk preterm
GSM367789 1 35.7wk preterm
GSM367790 1 35.9wk preterm
GSM367791 1 36.6wk preterm
GSM367792 1 24.1wk preeclamptic
GSM367793 1 30.4wk preeclamptic
GSM367794 1 30.6wk preeclamptic
GSM367795 1 31.1wk preeclamptic
GSM367796 1 31.7wk preeclamptic
GSM367797 1 31.9wk preeclamptic
GSM367798 1 32.0wk preeclamptic
GSM367799 1 32.9wk preeclamptic
GSM367800 1 33.0wk preeclamptic
GSM367801 1 34.0wk preeclamptic
GSM367802 1 35.9wk preeclamptic
GSM367803 1 37.6wk preeclamptic

Tags

  • basal
  • disease
  • preeclampsia
  • protein
  • uterus
  • vasculature

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