Publications by authors named "Alina Riedel"

Article Synopsis
  • Abnormal placental blood vessel development caused by high levels of anti-angiogenic factors like sFLT1 is associated with preeclampsia, a serious condition that affects pregnant women and their babies after 20 weeks.
  • Previous studies on mice showed that increased hsFLT1 leads to reduced placental function and symptoms similar to preeclampsia.
  • This research found elevated levels of the protein galectin-1 in specific areas of the placenta in hsFLT1 mice, suggesting that the galectin-glycan network may help counteract the harmful effects of anti-angiogenic factors during pregnancy.
View Article and Find Full Text PDF

Preeclampsia (PE) is characterized by maternal hypertension and placental dysfunction, often leading to fetal growth restriction (FGR). It is associated with an overexpression of the anti-angiogenic sFLT1 protein, which originates from the placenta and serves as a clinical biomarker to predict PE. To analyze the impact of sFLT1 on placental function and fetal growth, we generated transgenic mice with placenta-specific human sFLT1 (hsFLT1) overexpression.

View Article and Find Full Text PDF
Article Synopsis
  • - The placenta is crucial for fetal growth as it connects the embryo to the mother and significantly boosts blood flow through remodeled maternal spiral arteries.
  • - Inadequate remodeling of these arteries can cause serious pregnancy issues like pre-eclampsia, primarily due to insufficient trophoblast invasion, with the exact processes still not fully understood.
  • - A new study utilizes light sheet microscopy for 3D visualization of placental vascularization, offering a better understanding of spiral artery remodeling and paving the way for enhanced treatment insights related to pre-eclampsia.
View Article and Find Full Text PDF
Article Synopsis
  • Fetal adaptations to pregnancy complications like preeclampsia (PE) can disrupt offspring metabolism, leading to lasting metabolic issues.
  • Overexpression of sFLT1 in mice mimics PE, resulting in growth-restricted fetuses with reduced liver size, altered glycogen storage, and liver damage.
  • Male offspring showed more severe metabolic alterations post-birth, including increased weight gain and changes in hormone levels, indicating that PE may cause specific metabolic disturbances that affect males more significantly.
View Article and Find Full Text PDF