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Related Concept Videos

Embryonic Stem Cells00:57

Embryonic Stem Cells

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Embryonic stem (ES) cells were first discovered in mice in 1981 by Martin Evans. In 1998, James Thomson identified a method to isolate embryonic stem cells from humans. Human embryonic stem cells (hESCs) are obtained from 3-5 day old embryos that remain unused after an in vitro fertilization procedure.
ES cells are grown in a culture medium where they can divide indefinitely, creating ES cell lines. Under certain conditions, ES cells can differentiate, either spontaneously into a variety of...
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Updated: Sep 9, 2025

Derivation of Stem Cell Lines from Mouse Preimplantation Embryos
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Derivation of Stem Cell Lines from Mouse Preimplantation Embryos

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Efficient stem cell-derived mouse embryo models for environmental studies.

Victoria Jorgensen1, Min Bao1, Sergi Junyent1

  • 1Biology and Biological Engineering, California Institute of Technology, 1200 E. California Blvd, Pasadena, CA 91125, USA.

Developmental Cell
|August 29, 2025
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Summary
This summary is machine-generated.

Researchers developed iG4-blastoids, a novel stem cell model that accurately mimics mouse blastocysts. This improved model aids in studying environmental impacts on early embryogenesis.

Keywords:
GATA4blastocystblastoidembryo modelsepiblastprimitive endodermscreeningtrophectodermxenobiotics

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Area of Science:

  • Developmental Biology
  • Stem Cell Biology
  • Genetics

Background:

  • Blastoids are stem cell-derived models of blastocysts, crucial for studying early development.
  • Current blastoid models often lack proper cavitation and primitive endoderm formation.

Purpose of the Study:

  • To develop an improved blastoid model for studying early embryogenesis.
  • To investigate the effects of environmental factors on blastoid development.

Main Methods:

  • A modular approach using embryonic stem cells (ESCs), inducible GATA4-ESCs (iG4-ESCs), and trophoblast stem cells (TSCs).
  • Single-cell RNA sequencing to analyze cell composition and similarity to natural blastocysts.
  • Culturing iG4-blastoids with and without FGF4 to observe developmental changes.

Main Results:

  • The modular approach yielded cavitated blastocyst-like structures (iG4-blastoids) with 80% efficiency.
  • iG4-blastoids closely resemble mature mouse blastocysts based on single-cell RNA sequencing.
  • Culturing without FGF4 promoted mural trophectoderm specification, and 12% of structures showed post-implantation-like morphogenesis in vitro.

Conclusions:

  • iG4-blastoids represent a robust and efficient model for studying early embryogenesis.
  • This model system accurately reflects the impact of environmental factors like caffeine, alcohol, and nicotine on embryonic development.
  • The iG4-blastoid system offers new avenues for investigating embryogenesis and developmental toxicology.