Researchers have created a cellular model of the human placenta to help uncover how infections, from toxoplasmosis to the Zika virus, may pass from a mother to her unborn child.
The placenta nourishes a growing fetus, among other critical roles, and yet it’s one of the body’s least understood organs. One of its jobs is to act as a protective barrier, but sometimes pathogens sneak past. Infections such as rubella, toxoplasmosis, syphilis and HIV are well known for harming fetuses; now the Zika virus rapidly spreading through Latin America is a strong suspect, too.
“But we still don’t understand how any of those pathogens actually reach the fetus, or why that happens in one pregnancy but not another,” said senior researcher Dr. Carolyn Coyne, a virologist at the University of Pittsburgh.
Now Coyne’s team has developed a way to test that question — growing a 3-D model of the placenta’s outer boundary, the barrier that forms in very early pregnancy.
In this microscope image provided by the University of Pittsburgh, cells form a 3-D model of the placenta, developed by scientists at the University of Pittsburgh to learn more about how infections sometimes pass from a mother to her unborn child. Researchers have created a cellular model of the human placenta to help uncover how infections, from toxoplasmosis to the Zika virus, may pass from a mother to her unborn child. (Credit: University of Pittsburgh via AP)
Earlier attempts testing placental cells in lab dishes haven’t mimicked that boundary well enough to be of much use, Coyne explained. Her team succeeded in growing the cells into a 3-D structure that’s more like the real thing, the researchers reported Friday in the journal Science Advances. The trick was to grow them in a microgravity bioreactor developed by NASA, spinning the cells to mimic the forces of blood flow they’d normally experience in a mother’s body, Coyne explained.
Why not just test placentas that are expelled after childbirth? The placenta is quite different in the early weeks of pregnancy — when risks to just-forming fetal organs are thought to be especially high — than months later, said Dr. Catherine Spong of the National Institutes of Health, which helped fund the work.
“What you can learn from a placenta at the end of pregnancy may not tell you what is happening at the beginning of pregnancy,” said Spong, of NIH’s National Institute of Child Health and Human Development. The new research “has developed a neat model system to help us better understand how the placenta develops and how it might react” to a range of harmful substances.
In the first tests, the model resisted infection by a test virus and by three different strains of a parasite that causes toxoplasmosis, an infection that can trigger miscarriage or birth defects. Next up is testing how it reacts to the Zika virus.
The idea: If the model appears to protect like a healthy placenta, then researchers could manipulate it to see what it takes for various pathogens to break through.
