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Related Concept Videos

Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl hydroxylase and factor...

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Disruption of the Mouse Blood-Brain Barrier by Small Extracellular Vesicles from Hypoxic Human Placentas
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Endothelial FOS expression and pre-eclampsia.

R M Mackenzie1, V C Sandrim, D M Carty

  • 1Institute of Cardiovascular and Medical Sciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, UK.

BJOG : an International Journal of Obstetrics and Gynaecology
|November 6, 2012
PubMed
Summary
This summary is machine-generated.

Plasma from women who develop pre-eclampsia alters gene expression in endothelial cells, specifically downregulating c-Fos. This reduced c-Fos expression may impair blood vessel development, contributing to pre-eclampsia.

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Trophoblast Cell Recovery from Angiogenesis-Tube Formation Assay for Differentiation Marker Expression Analysis
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Trophoblast Cell Recovery from Angiogenesis-Tube Formation Assay for Differentiation Marker Expression Analysis

Published on: November 8, 2024

Area of Science:

  • Obstetrics and Gynecology
  • Molecular Biology
  • Genetics

Background:

  • Pre-eclampsia is a serious pregnancy complication characterized by high blood pressure.
  • Endothelial cell dysfunction is implicated in the pathophysiology of pre-eclampsia.
  • Understanding molecular changes in endothelial cells exposed to pregnancy plasma is crucial.

Purpose of the Study:

  • To investigate gene expression profiles in human endothelial cells exposed to plasma from women who developed pre-eclampsia versus normotensive pregnancies.
  • To identify specific genes and pathways affected by plasma factors during gestation.

Main Methods:

  • A longitudinal nested case-control study involving 12 pregnant women (6 pre-eclampsia, 6 controls).
  • Human umbilical vein endothelial cells (HUVECs) were incubated with plasma collected at 16 and 28 weeks gestation.
  • Gene expression profiling was performed using microarrays, with validation via quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR).

Main Results:

  • Significant differences in gene expression were observed between cells incubated with plasma from cases and controls.
  • Plasma from pre-eclamptic women led to increased expression of 11 genes, while control plasma affected 25 genes.
  • A notable finding was the increased expression of the c-Fos gene (FOS) with control plasma, but not with plasma from women who developed pre-eclampsia.

Conclusions:

  • Plasma from women who later develop pre-eclampsia contains factors that dysregulate c-Fos expression in endothelial cells.
  • Reduced c-Fos expression in endothelial cells might impair vasculogenesis.
  • This dysregulation could be a contributing factor to the development of pre-eclampsia.