Groundbreaking study: 'Mini-organs' created from amniotic fluid for the first time
Stem cells collected in late pregnancy herald advances in prenatal medicine
A pioneering approach, developed by researchers at UCL and Great Ormond Street Hospital (GOSH), means human development can be observed in late pregnancy for the first time, raising the possibility of monitoring and treating congenital conditions before birth.
The study, published in Nature Medicine, documents the first time that complex cell models, called organoids, have been grown from human stem cells during an active pregnancy. These ‘mini-organs’ also retain the baby’s biological information.
Organoids provide researchers with invaluable tools to study how organs function both when they are healthy and when impacted by disease.
The researchers say the stem cell organoids will facilitate monitoring of fetal development in late pregnancy, modelling of disease progression and testing of new treatments for diseases such as congenital diaphragmatic hernia (CDH).
Until now, organoids have been derived from adult stem cells or post-termination fetal tissue. Regulations also restrict when fetal samples can be obtained. In the UK this can be done up to 22 post-conception weeks, the legal limit for the termination of a pregnancy, but in countries like the US fetal sampling is illegal.
These restrictions have so far limited organoids’ utility for studying normal human development past 22 weeks, as well as congenital diseases at a point when there may still be an opportunity to treat them.
To overcome these issues, researchers at UCL and GOSH hypothesised that it may be possible to grow organoids from stem cells that have passed into the amniotic fluid, which surrounds the child in the womb and protects it during pregnancy. Because the child would not be touched during the collection process, sampling restrictions would be overcome and the cells would carry the same biological information as the child.
In this study, researchers extracted and characterised live cells from amniotic fluid samples taken from 12 pregnancies as part of routine diagnostic testing. They then used single-cell RNA sequencing to identify which tissues these stem cells came from. Stem cells from the lungs, kidneys and intestine were successfully extracted, which were used to grow organoids that had functional features of these tissue types.
Dr Mattia Gerli, first author of the study from UCL Surgery & Interventional Science, said: “The organoids we created from amniotic fluid cells exhibit many of the functions of the tissues they represent, including gene and protein expression. They will allow us to study what is happening during development in both health and disease, which is something that hadn’t been possible before. We know so little about late human pregnancy, so it’s incredibly exciting to open up new areas of prenatal medicine.”
To assess how the organoids might be used in the management of congenital diseases, the team worked with researchers at KU Leuven in Belgium to study the development of babies with CDH, a condition where a hole in the diaphragm means organs like the intestine and liver get displaced into the chest, putting pressure on the lungs and hindering healthy growth.
Organoids from babies with CDH both pre- and post-treatment were compared to organoids from healthy babies to study the biological characteristics of each group. As expected, there were significant developmental differences between the healthy and pre-treatment CDH organoids. But the organoids in the post-treatment CDH group were much closer to healthy ones, providing an estimate of the treatment’s effectiveness at a cellular level.
NIHR Professor Paolo de Coppi, senior author of the study from UCL Great Ormond Street Institute of Child Health and Great Ormond Street Hospital, said: “This is the first time that we’ve been able to make a functional assessment of a child’s congenital condition before birth, which is a huge step forward for prenatal medicine. Diagnosis is normally based on imaging such as ultrasound or MRI and genetic analyses.
“When we meet families with a prenatal diagnosis, we’re often unable to tell them much about the outcome because each case is different. We’re not claiming that we can do that just yet, but the ability to study functional prenatal organoids is the first step towards being able to offer a more detailed prognosis and, hopefully, provide more effective treatments in future.”
Original publication
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