Now imagine a tiny loofah that works in much the same way inside the corridors of the human heart. As it scrubs, it alerts heart stem cells to rush to the site of dying cells to begin renewal and repair of cardiomyocytes – cells that pump blood through the heart.
While a heart loofah may remain the stuff of medical fantasy, Steven Houser, Ph.D., Director of Cardiovascular Research Center at Temple University School of Medicine, is sold on the idea that the heart – like the skin – contains its own stem cells: cells that are self-renewing and can be differentiated into different types of heart tissue. It's a controversial subject in cardiovascular circles, but for Houser, who spent thirty years studying the molecular biology of heart cells, the stakes are worth it when it comes to combating congestive heart failure (CHF).
Although stem cells have been found in many other organs in the body, including the brain, many researchers remain unconvinced that the heart contains stem cells. Houser respectfully disagrees. Abandoning his prior cell research, he has joined forces with one of the foremost investigators in cardiac stem cells, Pierro Anversa, M.D., professor of medicine and Director of the Cardiovascular Institute at New York Medical College. Anversa, who has been on the forefront of stem cell research for the past five years, has suggested that heart cells undergo an ongoing turnover fueled by cardiac stem cells. In June of this year, he published a study that actually identified cardiac stem cells in animal models that repaired tissue damaged by a heart attack.
One element that convinced Houser of Anversa's work was his own research into how the heart reacts under the stress of hypertensive diseases that can lead to congestive heart failure. Early in the disease, the heart muscle mass increases and the chambers stretch in a vain attempt to increase contracting power. While part of the enlargement is due to increased muscle mass, the question of how the chambers grow is less certain.
The traditional view holds that cardiac cells simply grow larger to accommodate the increased need, but Houser and Anversa developed a different theory – that spurred by the cardiac stem cells, cardiomyocytes actually increase in number in their response to the heart's traumatic condition.
To test this theory, Houser, with the help of Anversa, has received a new NIH grant to study if there are autologous stem cells in the heart. The two researchers have arrived at a deceptively simple idea. After inducing hypertension in an animal model to produce a distressed heart they will study the heart tissue and count cells, first in the normal heart and then in a heart that must work harder to develop excess pressure. If, according to the scientists' thesis, there are more cardiomyocytes in the heart as opposed to simply larger cells, they will conclude that stem cells had a hand in an attempt to repair and restore the heart.
"We've made a tremendous impact on cardiovascular diseases," he says. "But what we need to do now is to reverse this disease rather than just slow its progression."
Although his colleagues may remain skeptical, Houser has committed himself to the stem cell model. Inducing cells to promote repair can answer the question that has haunted his career.
"We don't know how to fix the broken heart, but stem cells might be a large part of the answer."
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