A team of investigators at the Medical University of South Carolina (MUSC) and Clemson University recently reported in an article in Nature Biomedical Engineering that they have developed human cardiac organoids less than 1 millimeter in diameter that closely resemble the physiological conditions that occur during a heart attack.
The team was led by bioengineer Ying Mei, Ph.D., who holds a joint faculty position at MUSC and Clemson University. He is part of the MUSC Clemson Bioengineering program, which places Clemson bioengineers and bioengineering doctoral students on the MUSC campus so that they can interact with clinicians in need of engineering solutions.
Low-oxygen cell culture conditions combined with human heart organoids recreate tissue-level features of a post-heart attack heart.
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The article's lead author, Dylan Richards, Ph.D., is a graduate of the joint program.
"We were essentially able to take that 3D complex nature of a heart attack and then downsize it into a microtissue model," said Richards.
Organoids are three-dimensional multicellular tissues that are less than 1 millimeter in diameter. These organoids, or microtissues, function like their full-size counterparts. In this case, the heart organoids actually beat and contract as the human heart does. This model uses induced pluripotent stem cells, almost like "parent cells," that divide and mature into several types of heart cells that interact and self-assemble to form the organoid.
Traditionally, biologists use cells in a dish or animal models, such as mice or rats, to model diseases being studied. These methods have their own disadvantages that the organoid model overcomes.
Cells in a dish are great for learning things at the cellular level, but it is very unnatural for cells to grow in two dimensions on a flat surface.
Animal models are very useful in taking the next steps toward recapitulating what happens in the human body, but organoids, especially those for the heart, are the closest to recreating what occurs in humans.
"The hearts of rats and mice beat five to 10 times faster than those of humans," Richards explained. "How those mechanisms work physically -the electrophysiology and the pumping action - is just different because of the scale."
In contrast, the cardiac organoid recreates a human version of the heart and closely resembles the tissue dysfunction that takes place after the oxygen shortage caused by a heart attack. Because it is very difficult to obtain a sample immediately after a heart attack occurs, most of what we know about heart attacks comes from observations made long after the initial oxygen shortage. The organoid model fills in this gap, enabling visualization immediately after oxygen deprivation.
"This can help us to understand better how cells respond in the short term and, in turn, how that makes way for long-term damage," said Richards of the organoid model.
This model also enables researchers to test whether heart drugs improve heart attack outcomes.
"It could help us determine whether a drug is effective at preventing some of this damage or preventing a detrimental response to an oxygen shortage," explained Richards.
The model could also provide a way to test whether a drug that is safe in a healthy heart is also safe in a diseased one. Such information could guide physicians in prescribing drugs more appropriately in patients who had preexisting heart conditions at the time of the heart attack.
In short, the model provides researchers with an understanding of the early events of a heart attack that they have not had before. But Mei intends to make the model even better by including immune cells. Immune cells are responsible for cleaning out any dead cells caused by the heart attack, but by doing so, they can determine how immune cells play a role in the restructuring of heart tissue after damage from an oxygen shortage. The Mei lab would like to study how they do so in hopes of preventing the death of damaged but still living areas of the heart.
MEDICA-tradefair.com; Source: Medical University of South Carolina (MUSC)