Researchers at NIEHS have developed a three-dimensional (3D) model that shows how exposure to cadmium might lead to congenital heart disease. Congenital heart disease is the most common birth defect in the United States, affecting nearly 40,000 newborns a year.
Cadmium is a metal that can be released into the environment through mining and various industrial processes, and it has been found in air, soil, water, and tobacco. The metal can enter the food chain when plants absorb it from soil. Previous studies suggested that maternal exposure to cadmium might be a significant risk factor for congenital heart disease.
Organoid model mimics heart
Using models derived from human cells and tissues, called in vitro models, researchers designed a 3D organoid model that mimics how the human heart develops. The researchers saw how exposure to low levels of cadmium can block usual formation of cardiomyocytes, which are the major type of cells that form the heart. In doing so, they revealed the biological mechanisms that might explain how cadmium could induce heart abnormalities.
“The models we created are useful for not only studying cadmium, but for studying other chemicals and substances as well,” said study lead Erik Tokar, Ph.D., from the Mechanistic Toxicology Branch of the NIEHS Division of Translational Toxicology (DTT).
Three models mirror developmental stages
For the study, the researchers developed three different models to evaluate the effects of cadmium on different stages of heart development.
First, they used human pluripotent stem cells to develop 3D embryoid bodies to mimic early steps in tissue and organ formation in humans. They then used a 2D cell model that included a fluorescent regulatory protein system (NKX2-5) known to be involved in heart development, which allowed them to look at cadmium toxicity after exposure.
The 3D cardiac organoid model, which can simulate the beating heart, confirmed what was seen in the other two models, showing how low doses of cadmium can inhibit the cardiomyocytes from functioning properly, affecting normal heart movement and function.
Building toward the future
The study, published in the journal Environmental Health Perspectives, builds on decades of work by toxicology researchers to advance knowledge about how environmental exposures may contribute to human diseases including cancer, cardiovascular disease, autism, and other conditions.
“These new models are leveraging advances in technology that allow us to model human biology in a way that identifies real human health hazards,” said Brian Berridge, D.V.M., Ph.D., DTT scientific director. “They also help reduce our reliance on animal testing.”
Xian Wu, Ph.D., who conducted these studies, pointed out that early exposure to human-relevant levels of cadmium lead to a dramatic inhibitory effect on cardiomyocyte differentiation, whereas later stage exposures did not have this effect. “This cadmium exposure also damaged the cardiac organoid functionality,” Wu added.
Citation: Wu X, Chen Y, Hu G, and Tokar EJ. 2022. Cardiac development in the presence of cadmium: An in vitro study using human embryonic stem cells and cardiac organoids. Environmental Health Perspectives.
(Robin Mackar is a writer and media relations coordinator in the NIEHS Office of Communications and Public Liaison.)