Amniotic sac in a dish: Stem cells form structures that may aid of infertility research
The first few weeks after sperm meets egg still hold many mysteries. Among them: what causes the process to fail, leading to many cases of infertility. But scientists haven’t had a good way to explore the biology behind this phenomenon. Now, a new achievement using human stem cells could give researchers a chance to see what they couldn’t before, while avoiding ethical issues associated with studying actual embryos.
The first few weeks after sperm meets egg still hold many mysteries. Among them: what causes the process to fail, leading to many cases of infertility.
Despite the importance of this critical stage, scientists haven’t had a good way to explore what can go wrong, or even what must go right, after the newly formed ball of cells implants in the wall of the human uterus.
But a new achievement using human stem cells may help change that. Tiny lab-grown structures could give researchers a chance to see what they couldn’t before, while avoiding ethical issues associated with studying actual embryos.
A team from the University of Michigan reports in Nature Communications that they have coaxed pluripotent human stem cells to grow on a specially engineered surface into structures that resemble an early aspect of human development called the amniotic sac.
The cells spontaneously developed some of the same structural and molecular features seen in a natural amniotic sac, which is an asymmetric, hollow ball-like structure containing cells that will give rise to a part of the placenta as well as the embryo itself. But the structures grown at U-M lack other key components of the early embryo, so they can’t develop into a fetus.
It’s the first time a team has grown such a structure starting with stem cells, rather than coaxing a donated embryo to grow, as a few other teams have done.
A steady PASE
The researchers have dubbed the new structure a post-implantation amniotic sac embryoid, or PASE. They describe how a PASE develops as a hollow spherical structure with two distinct halves that remain stable even as cells divide.
One half is made of cells that will become amniotic ectoderm, the other half consists of pluripotent epiblast cells that in nature make up the embryonic disc. The hollow center resembles the amniotic cavity — which in normal development eventually gives rise to the fluid-filled sac that protects and cushions the fetus during development.
Gumucio likens a PASE to a mismatched plastic Easter egg or a blue-and-red Pokémon ball — with two clearly divided halves of two kinds of cells that maintain a stable form around a hollow center.
The team also reports details about the genes that became activated during the development of a PASE, and the signals that the cells in a PASE send to one another and to neighboring tissues. They show that a stable two-halved PASE structure relies on a signaling pathway called BMP-SMAD that’s known to be critical to embryo development.
Collaboration provides the spark
The new study follows directly from previous collaborative work between Gumucio’s lab and that of the other senior author, U-M mechanical engineering associate professor Jianping Fu, Ph.D.
In the previous work, reported in Nature Materials, the team succeeded in getting balls of stem cells to implant in a special surface engineered in Fu’s lab to resemble a simplified uterine wall. They showed that once the cells attached themselves to this substrate, they began to differentiate into hollow cysts composed entirely of amnion — a tough extraembryonic tissue that holds the amniotic fluid.
The team found that such structures could also grow from induced pluripotent stem cells (iPSCs) — cells derived from human skin and grown in the lab under conditions that give them the ability to become any type of cell, similar to how embryonic stem cells behave. This opens the door for future work using skin cells donated by couples experiencing chronic infertility, which could be grown into iPSCs and tested for their ability to form proper amniotic sacs using the methods devised by the team.
Important notes and next steps
Besides working with genetic and infertility specialists to delve deeper into PASE biology as it relates to human infertility, the team is hoping to explore additional characteristics of amnion tissue.
For example, early rupture of the amnion tissue can endanger a fetus or be the cause of a miscarriage. The team also intends to study which aspects of human amnion formation also occur in development of mouse amnion. The mouse embryo model is very attractive as an in vivo model for investigating human genetic diseases.