In Washington, scientists have discovered genetic interactions that may allow heart cells to regenerate, an advance that could lead to new therapies to treat cardiac diseases.
Researchers from the University of Florida (UF) found genes known to form heart cells in humans and other animals in the gut of a muscle-less and heartless sea anemone.
The sea anemone can regenerate into a new animal if it is cut into many pieces.
Researchers analysed the function of its “heart genes,” and discovered a difference in the way these genes interact with one another, which may help explain its ability to regenerate, said Mark Martindale, a professor at UF.
“Our study shows that if we learn more about the logic of how genes that give rise to heart cells talk to each other, muscle regeneration in humans might be possible,” Martindale said.
These heart genes generate what engineers calls lockdown loops in vertebrates and flies, which means that once the genes are turned on, they tell each other to stay on in an animal’s cells for its entire lifetime.
In other words, animals with a lockdown on their genes cannot grow new heart parts or use those cells for other functions. “This ensures that heart cells always stay heart cells and cannot become any other type of cell,” Martindale said.
The finding suggests a mechanism for why the gut cells expressing heart genes in sea anemones can turn into other kinds of cells, such as those needed to regenerate damaged body parts, Martindale said.
The study supports the idea that definitive muscle cells found in the majority of animals arose from a bifunctional gut tissue that had both absorptive and contractile properties.
Researchers argue that the first animal muscle cells might have been very heart-like, Martindale said.
Continued research could one day allow scientists to coax muscles cells into regenerating different kinds of new cells, including more heart cells, Martindale said.