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Cleavage and Blastulation

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Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
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Fetal Circulation01:14

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Fetal circulation is a unique system that facilitates the exchange of gases, nutrients, and waste products between the developing fetus and the mother. This intricate process takes place through a special organ called the placenta.
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Three-dimensional Rendering and Analysis of Immunolabeled, Clarified Human Placental Villous Vascular Networks
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Genes, development and evolution of the placenta.

J C Cross1, D Baczyk, N Dobric

  • 1Genes & Development Research Group, Department of Biochemistry & Molecular Biology, Faculty of Medicine, University of Calgary, Alberta, Canada. jcross@ucalgary.ca

Placenta
|February 25, 2003
PubMed
Summary

Studies in mice reveal key molecular pathways controlling placental development, identifying genes crucial for trophoblast cell differentiation and function. This research aids in comparing human and mouse placentas and understanding pregnancy complications.

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Area of Science:

  • Developmental Biology
  • Genetics
  • Reproductive Biology

Background:

  • Placental development involves complex molecular pathways controlling trophoblast cell differentiation.
  • Understanding these pathways is crucial for addressing complications in human pregnancy.

Purpose of the Study:

  • To elucidate the molecular mechanisms governing trophoblast cell development and placental structure formation.
  • To compare conserved and specialized genes involved in placental development between mice and humans.

Main Methods:

  • Utilizing studies of transgenic and mutant mice to identify key genes and signaling pathways.
  • Analyzing gene expression patterns and functional roles in placental development.

Main Results:

  • Identified FGF signaling, Cdx2, Eomes, and Err2 as critical for trophoblast stem cell proliferation.
  • Highlighted bHLH transcription factors (Id1/2, Mash2, Hand1, Stra13) in trophoblast cell lineage progression.
  • Demonstrated Gcm1's role in syncytiotrophoblast differentiation and Wnt, HGF, FGF signaling in labyrinth development.

Conclusions:

  • Genes regulating placental development are often conserved, co-opted, or duplicated from other systems.
  • Conserved gene functions suggest potential mechanisms for human placental development complications.
  • Mouse models provide valuable insights for comparative placental biology and understanding human pregnancy disorders.