Researchers at the McEwen Centre for Regenerative Medicine at Toronto General Hospital ( TGH ) have discovered the SOS distress signal that mobilizes specific heart repair cells from the bone marrow to the injured heart after a myocardial infarction.
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While it has long been known that bone marrow cells have the ability to clear the dead tissue after a myocardial infarction, what has not been known until now is the critically important role of bone marrow adult stem cells in repairing a damaged heart, restoring its function and enhancing the growth of new blood vessels.

" These cells act like generals in a battlefield, explained Shafie Fazel, at TGH, University of Toronto and lead author of the study entitled, " Cardioprotective c-kit+ cells are from the bone marrow and regulate the myocardial balance of angiogenic cytokines," published in The Journal of Clinical Investigation. " When damaged heart tissue sends out an SOS distress signal, this subset of bone marrow cells mobilizes quickly and stimulates the growth of new blood vessels in the heart. This is the first step in repairing the heart and in preventing the vicious downward spiral of heart failure in which the heart progressively thins and dilates, eventually causing death." Despite advances in surgical procedures, mechanical assistance devices, drug therapy, and organ transplantation, more than half of patients with congestive heart failure die within five years of initial diagnosis.

" Cardiovascular diseases are the most important cause of mortality in Canada and the western world," said Ren-Ke Li, at the McEwen Centre for Regenerative Medicine and at the University of Toronto. " Each year, 70,000 Canadians suffer from a myocardial infarction and many of them are left with crushing disabilities, mainly because the heart muscle is not able to regenerate after a myocardial infarction. This study identifies the method the body employs to repair the heart and provides new therapies to stimulate cardiac regeneration and prevent heart failure in patients who have suffered a myocardial infarction," noted Li.

Li's team used genetically-engineered mice in which bone marrow cells were modified to carry a green fluorescent marker allowing researchers to easily track them. The researchers demonstrated that these bone marrow cells are quickly mobilized to the damaged heart region following a myocardial infarction. Once in the damaged area, the cells produce chemicals that trigger the growth of new blood vessels--an important step in repairing the injured heart.

The research also demonstrated that a specific molecule, called c-kit, which is located on the surface of a subset of bone marrow cells, plays a central role in this mobilization. The molecule c-kit is the switch that needs to be turned on by the SOS signals sent by the damaged heart. By binding to another molecule called the stem cell factor – much like a lock and key -- the turned on c-kit activates the bone marrow cells to migrate to the heart to help stimulate new blood vessel growth.

In the study, mice with defective c-kit bone marrow cells, could not mobilize these cells to race towards the injured site and regenerate the injured heart. Their heart function was dramatically impaired and, 42 days after a heart attack, their hearts dilated to twice the size of the normal mouse heart. However, the heart function of the c-kit defective mice could be restored to normal by restoring the c-kit cells in their bone marrow, confirming the importance of these cells in repairing the heart. This suggests that a similar treatment of an infusion of bone marrow cells after a heart attack may prevent progression of heart failure in patients who survived a heart attack.

The study may explain why some patients have mild myocardial infarctions and others develop progressive and potentially fatal congestive heart failure. " We know that the number of c-kit positive cells decreases with age and that elderly patients don't recover from heart attacks as well as younger patients. The key for the older patients would be to find new ways to restore this particular subset of cells in their bone marrow," said Fazel.

" These findings have very important implications," noted Richard Weisel, at the University of Toronto and co-author in this study. " Based on the knowledge we gained from this study, we can now design new strategies to enhance normal repair and regeneration for patients who suffered a myocardial infarction."

According to Weisel, " One treatment resulting from this discovery was to inject cells genetically modified to release large amounts of stem cell factor into the region of the heart injured by the heart attack. These cells increased the SOS signals from the heart and enhanced the intrinsic regeneration of the heart and restored function nearly to normal. These results were published in The Journal of Thoracic and Cardiovascular Surgery."

Source: University of Toronto, 2006


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