The animal study found it was possible to regenerate muscle cell numbers in the heart by up to 45 percent by ‘turbo-charging' a hormone that helped coordinate cell growth.
According to study lead author, associate professor Richard Harvey, PhD, UNSW, based at the Victor Chang Cardiac Research Institute, New South Wales, Australia, this is an important step toward repairing a broken heart.
"Unlike blood, hair, or skin cells, which can renew themselves throughout life, cell division in the heart virtually comes to a standstill shortly after birth, which means the heart can't fully regenerate if it is damaged later in life," Harvey says.
"Previous studies have demonstrated that it is possible to coax heart muscle cells to proliferate again, but only at very trivial levels," he says. "What the research team has been able to do is boost heart muscle cell numbers by as much as 45 percent after a heart attack."
The scientists focused on a signalling system in the heart driven by a hormone called ‘neuregulin'.
By switching the neuregulin pathway to ‘turbo charge', the researchers found that heart muscle cells continued to divide in a spectacular way in both the adolescent and adult periods. Stimulating the neuregulin pathway during a heart attack led to replacement of lost muscle.
"This big achievement will focus the attention of the field on heart muscle cell replacement as a therapeutic option for ischemic heart disease," Harvey says. "The dream is that one day we will be able to regenerate damaged heart tissue, much like a salamander can regrow a new limb if it is bitten off by a predator. Just imagine if the heart could learn to regrow and heal itself. That would be the ultimate prize."
The research, conducted at the Weizmann Institute of Science in collaboration with the Victor Chang Cardiac Research Institute, and titled "ERBB2 triggers mammalian heart regeneration by promoting cardiomyocyte dedifferentiation and proliferation," is published in Nature Cell Biology.
[Source: UNSW]