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Updated: Jun 28, 2025

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Monochorionic Twinning in Bioengineered Human Embryo Models.

Dorian G Luijkx1, Asli Ak1, Ge Guo2

  • 1MERLN Institute of Technology-Inspired Regenerative Medicine, Department for Instructive Biomaterials Engineering (IBE), Maastricht University, Universiteitssingel 40, Maastricht, 6229ET, The Netherlands.

Advanced Materials (Deerfield Beach, Fla.)
|April 9, 2024
PubMed
Summary
This summary is machine-generated.

Researchers created human "twin blastoids" from stem cells to study early development. This new model efficiently generates monochorionic twins, offering insights into pregnancy complications and embryonic development.

Keywords:
blastoidsimplantation‐on‐chipmonochorionic twinningstem cell‐based embryo modelsthermoformed microwell platformstwin embryo models

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Area of Science:

  • Developmental Biology
  • Stem Cell Biology
  • Reproductive Medicine

Background:

  • Monochorionic twinning in human embryos elevates pregnancy complication risks.
  • Ethical limitations and rarity hinder in-vivo research on twinning mechanisms.
  • A significant knowledge gap exists regarding early monochorionic twin development.

Purpose of the Study:

  • To develop a model system for studying human monochorionic twinning.
  • To identify conditions that promote efficient monochorionic twin formation in vitro.
  • To investigate the early developmental characteristics of twin blastoids.

Main Methods:

  • Utilized a microthermoformed microwell platform for screening.
  • Generated human stem cell-based blastocyst models (twin blastoids).
  • Performed morphological, morphokinetic, and implantation assays.

Main Results:

  • Identified conditions for efficient induction of twin blastoids.
  • Observed twinning via splitting of the pluripotent core during cavitation.
  • Twin blastoids exhibited enhanced adhesion capacity in implantation assays.

Conclusions:

  • Developed a scalable twin blastoid model for studying monochorionic twinning.
  • The model facilitates systematic exploration of twinning origins and early phenotypes.
  • This platform offers unprecedented opportunities to understand early embryonic development and implantation potential.