Active Pregnancy, Children & Inherited Conditions Genetics & Molecular Biology

Functional interrogation of primate gastrulation and body patterning: building the embryo outside the womb

In plain English

AI plain-English summary

A marmoset embryo’s body plan is laid down in the first few days after it implants in the womb, and scientists have now mapped the molecular signals that orchestrate this process in a living primate for the first time. This matters because the equivalent stage in human development—gastrulation, when cells begin to form tissues and organs—has been nearly impossible to study directly, for both ethical and technical reasons. Without this knowledge, doctors have no way to understand why many early pregnancies fail or why certain birth defects arise. The team has created lab-grown models of human and marmoset embryos, including “printed” clusters of signalling cells that mimic the anterior visceral endoderm, a structure that directs body patterning in mice but whose role in primates was unknown. By knocking out specific genes in these models and comparing them to real embryos, they will pinpoint which signals are essential for normal development. They also plan to transfer lab-grown marmoset blastoids into live animals to test whether stem-cell-derived embryos can establish a pregnancy—a proof-of-principle that could eventually inform fertility treatments or early-pregnancy diagnostics. This is fundamental science. It will not produce a therapy tomorrow, but it fills a critical gap in understanding how a single fertilised cell becomes a structured, multi-layered primate body.

View original technical description
The human body plan is specified in the gastrulating embryo shortly after implantation. In mouse, this transformation is regulated by a dynamic signalling centre, the anterior visceral endoderm (AVE). However, the function of the primate AVE in gastrulation remains elusive. Implantation and body patterning are pivotal for healthy embryo development, but in human they have been notoriously hard to study for ethical and technical reasons. My lab recently delineated primate AVE formation by spatial transcriptome profiling of gastrulating marmoset embryos in vivo. Here, we will leverage our new extraembryonic stem cell lines to model the pre-to-postimplantation transition in human and marmoset. To interrogate the crosstalk between embryonic disc and AVE, we will engineer next-generation gastruloids by ‘printing’ AVE-like cells onto micropatterns and establish stem-cell-derived blastoid postimplantation cultures. Human and marmoset embryo models will be validated by transcriptomic comparisons to the embryo and assembled with knockout AVE-like cells to elucidate AVE-function. We will test the developmental potential of marmoset blastoids by transfer into receptive marmoset hosts and conduct lineage- tracing in vivo to determine the sequence of somatic cell-fate acquisition in primate gastrulation. Collectively, this research addresses major knowledge gaps in human development and establishes a proof-of-principle for stem-cell- derived pregnancies in primates.

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Researchers

Thorsten Boroviak (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Illuminating cell fate decisions in the implanting primate by embryo profiling and ex vivo functional analysis
An in vitro model of the interaction between the extra-embryonic lineages of the peri-implantation human embryo
Self-Organising Capacity of Stem Cells during Implantation and Early Post-implantation Development: Implications for Human Development
Towards non-human primate chimaeras: Generation of marmoset embryonic stem cells with unrestricted in vivo pluripotency
Comparative transcriptional control of establishment, maintenance and collapse of naive pluripotency in rodents and primates in vivo

Original classification

Career Development Award

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