Pluripotent human stem cells have been coaxed to grow on a specially engineered surface into structures that resemble an early aspect of human development called the amniotic sac, reports a team from the University of Michigan.
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 the new lab-grown structures could give researchers a chance to see what they couldn’t before, while avoiding ethical issues associated with studying actual embryos.
Early Developmental Steps Critical
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. Co-senior author Deborah Gumucio, Ph.D, says:
“As many as half of all pregnancies end in the first two weeks after fertilization, often before the woman is even aware she is pregnant. For some couples, there is a chronic inability to get past these critical early developmental steps, but we have not previously had a model that would allow us to explore the reasons why. We hope this work will make it possible for many scientists to dig deeper into the pathways involved in normal and abnormal development, so we can understand some of the most fascinating biology on earth."
Gumucio is the Engel Collegiate Professor of Cell & Developmental Biology at Michigan Medicine, U-M’s academic medical center.
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.
[caption id=“attachment_91587” align=“aligncenter” width=“680”] a) Cartoon of an implanting human embryo. The amniotic ectoderm, amniotic cavity, and epiblast constitute the amniotic sac.
b) Schematic of the 3D culture system and the formation of asymmetric cysts from hPSC. The culture substrate is made of a thick layer of GeltrexTM (with a thickness >100 µm). The ECM overlay was applied from day 1 onward to provide the 3D culture environment. Asymmetric cysts were consistently observed on day 5 in all (n > 18) independent experiments.
c) Representative confocal micrographs showing an asymmetric cyst on day 5, stained for βCAT (green) and ECAD (red). HOECHST (blue) counterstains nuclei. n = 3 independent experiments. Scale bar, 50 µm.
d) Carnegie stage (CS) 5a-2, 5b, and 5c human embryo sections, showing prospective and definitive amniotic ectoderm (Am.) and epiblast (Epi.). Phase contrast image shows a representative asymmetric cyst with a distinct bipolar morphological pattern. Scale bars, 30 µm
Credit: Yue Shao et al[/caption]
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.
Gumucio notes that the PASE structures even exhibit the earliest signs of initiating a “primitive streak”, although it did not fully develop.
In a human embryo, the streak would start a process called gastrulation. That’s the division of new cells into three cell layers—endoderm, mesoderm and ectoderm—that are essential to give rise to all organs and tissues in the body.
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.
The team’s work is overseen by a panel that monitors all work done with pluripotent stem cells at U-M, and the studies are performed in accordance with laws regarding human stem cell research. The team ends experiments before the balls of cells effectively reach 14 developmental days, the cutoff used as an international limit on embryo research—even though the work involves tissue that cannot form an embryo.
The research is supported by the University of Michigan Mechanical Engineering Startup Fund and the National Institutes of Health.
Yue Shao, Kenichiro Taniguchi, Ryan F. Townshend, Toshio Miki, Deborah L. Gumucio & Jianping Fu A pluripotent stem cell-based model for post-implantation human amniotic sac development Nature Communications 8, Article number: 208 (2017) doi:10.1038/s41467-017-00236-w
Top Image: University of Michigan