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This robot fish is made of human heart cells

"Rather than using heart imaging as a blueprint, we are identifying the key biophysical principles that make the heart work, using them as design criteria, and replicating them in a system—a living, swimming fish—where it is much easier to see if we are successful."

To learn how to make an artificial heart, researchers have created artificial fish from human cardiac muscle cells.

The fish are made from human cardiac muscle cells, painstakingly grown on laboratory tape coated with gelatin.

“Our ultimate goal is to build an artificial heart…”

The “biohybrid” fish swim by recreating the muscle contractions of a pumping heart, bringing engineers closer to creating more complex artificial pumps and providing a platform to study human diseases, such as cardiac arrhythmias.

Biomedical engineer Sung-Jin Park began working on biohybrid fish as a postdoc in Kit Parker’s lab at Harvard’s Paulson School of Engineering and Applied Sciences. Park is co-first author of a paper in Science.

“Our major achievement in this paper is that we can build a living muscle that can self-control and self-pace its movement without any additional control mechanism,” says Park, now an assistant professor in the biomedical engineering department at Georgia Tech and Emory and part of the Multi-Cellular Engineered Living Systems (M-CELS) program.

Park says his team’s research could be applied to design “biological pacemakers,” a potential alternative to electronic cardiac pacemakers. As part of a long-term implant, biological pacemakers could grow along with a pediatric patient.

“Our ultimate goal is to build an artificial heart to replace a malformed heart in a child,” says Parker, senior author of the paper. “Rather than using heart imaging as a blueprint, we are identifying the key biophysical principles that make the heart work, using them as design criteria, and replicating them in a system—a living, swimming fish—where it is much easier to see if we are successful.”

The biohybrid fish even improves with age.

The fish has two layers of muscle cells, one on each side of the tail fin. When one side contracts, the other stretches. The stretch triggers the opening of an ion channel sensitive to mechanical movement, leading to an influx of charged ions and a contraction on that side.

The researchers also engineered an “autonomous pacing node,” acting like a pacemaker, which controls the frequency and rhythm of the spontaneous contractions. Together, the two layers of muscle and the autonomous pacing node enable the generation of continuous, spontaneous, and coordinated, back-and-forth fin movements. The system can propel the fish for more than 100 days.

In addition, the biohybrid fish improves with age. Its muscle contraction strength, maximum swimming speed, and muscle coordination all increase for the first month as the cardiomyocyte cells mature. Eventually, the biohybrid fish reached speeds similar to a model organism (zebrafish) in the wild.

The biohybrid fish builds off previous research from Parker’s lab. In 2012, the Harvard team used cardiac muscle cells from rats to build a jellyfish-like biohybrid pump and in 2016 Park and his colleagues developed a swimming, artificial stingray, also from rat heart muscle cells.

The team’s discovery of the self-generated stretch/contract cycles was partly fortuitous.

“We did not expect that the mechano-electric coupling effect would be strong enough to produce our fish’s antagonistic muscle contractions,” Park says. “In the beginning, we used light to control fish movements, like what we did for our stingray. One day, after finishing this experiment, we saved the fish in the incubator for more experiments but totally forgot the fact that we saved the fish. After a couple of weeks, when we opened the incubator, we found out that the fish swam with its own pacing by itself.”

Park says he is eager to work on models of cardiac arrhythmias (sinoatrial node dysfunctions) and wants to investigate mechano-electrical signaling as a therapeutic target of heart rhythm management.

The human cardiac muscle cells used in this research are commercially available. They come from induced pluripotent stem cells, which are originally derived from skin cells.

Additional researchers from Harvard and Emory/Georgia Tech contributed to the work.

Support for the research came from the National Center for Advancing Translational Sciences and the National Science Foundation.

Source: Emory University

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Stem cells turn into beating heart cells faster in space

"These cells have the potential to treat heart disease in kids and adults, but repairing a damaged heart requires a large number of heart cells," says Chunhui Xu. "We were hoping to identify a more effective way to generate these cells by exploring the use of microgravity." (Credit: Katie Cowden/Flickr)

Researchers joined forces with NASA to turn stem cells into heart muscle cells.

In just three weeks, the stem cells became beating cardiac cells while aboard NASA’s SpaceX-20 mission.

Before trying the real thing on the International Space Station (ISS), the researchers had been using space-simulation machines to enhance the ability of pluripotent, or immature, stem cells to turn into cardiac muscle cells.

The goal was to determine the effects of zero gravity conditions on stem cells and to optimize the generation of clinically relevant cardiac muscle cells on Earth.

Stem cell-derived cardiac muscle cells have been used to treat heart failure in animal models. They’ve also been used to study inherited cardiac diseases separately from the heart of the source patient.

“These cells have the potential to treat heart disease in kids and adults, but repairing a damaged heart requires a large number of heart cells,” says Chunhui Xu, associate professor in the pediatrics department at Emory University School of Medicine. “We were hoping to identify a more effective way to generate these cells by exploring the use of microgravity.”

After the cells that were onboard the space station returned to Earth, the researchers spent the last year diving into the study outcomes.

Their results show that these stem cells grow faster in the zero gravity conditions of space.

“We think about the future of taking care of patients with heart problems,” says Kevin Maher, professor in the pediatrics department and director of the Cardiac Intensive Care Unit at Children’s Healthcare of Atlanta. . “Being able to learn how to make stem cells grow faster has the potential to increase the chance for a better treatment for patients. There’s a lot of work being done to see how we can use these types of stem cells to make the heart stronger in the future.”

The ISS National Laboratory called the spaceflight experiment a significant step for next-generation space research, as freezing cell technology offers many advantages for space research as well as research on Earth.

The potential clinical implications of this research mean that kids and teens with damaged heart valves may instead receive a replacement valve grown from their own cells.

Additionally, cells from a child with heart arrythmia could be taken by biopsy and grown to test medications and treatments, potentially opening a new door to personalized medicine.

The research appears in Biomaterials.

They shared their findings—alongside NASA astronaut Jessica U. Meir—with patients of the Children’s Healthcare of Atlanta Heart Center during a recent event, moderated by Lucky Jain, chair of the pediatrics department of at Emory School of Medicine and chief academic officer for Children’s.

Source: Emory University

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